CNRS Nantes University US2B US2B
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***  CYTOKINE 2025-09-22  ***

elNémo ID: 2608031212152343365

Job options:

ID        	=	 2608031212152343365
JOBID     	=	 CYTOKINE 2025-09-22
USERID    	=	 unknown
PRIVAT    	=	 0

NMODES    	=	 5
DQMIN     	=	 -100
DQMAX     	=	 100
DQSTEP    	=	 20
DOGRAPHS  	=	 on

DOPROJMODS	=	 0
DORMSD    	=	 0

NRBL      	=	 0
CUTOFF    	=	 0
CAONLY    	=	 0


Input data for this run:


HEADER    CYTOKINE                                2025-09-22
TITLE     Crystal structure of IL-17A in complex with compound 21
EXPDTA    X-RAY DIFFRACTION
REMARK   2 RESOLUTION.    1.48 ANGSTROMS
REMARK   3  R VALUE : 0.205400
REMARK   3  FREE R VALUE : 0.226100
REMARK   4 9SQI COMPLIES WITH FORMAT V. 3.0, 1-DEC-2006
REMARK 200  TEMPERATURE           (KELVIN) : 100.00
REMARK 200  PH                             : NULL
REMARK 350 BIOMOLECULE: 1
REMARK 350 APPLY THE FOLLOWING TO CHAINS: A, B
REMARK 350   BIOMT1  1   1.000000 0.000000 0.000000   0.000000
REMARK 350   BIOMT2  1   0.000000 1.000000 0.000000   0.000000
REMARK 350   BIOMT3  1   0.000000 0.000000 1.000000   0.000000
REMARK 350 BIOMOLECULE: 2
REMARK 350 APPLY THE FOLLOWING TO CHAINS: C, D
REMARK 350   BIOMT1  1   1.000000 0.000000 0.000000   0.000000
REMARK 350   BIOMT2  1   0.000000 1.000000 0.000000   0.000000
REMARK 350   BIOMT3  1   0.000000 0.000000 1.000000   0.000000
REMARK 888
REMARK 888 WRITTEN BY MAESTRO (A PRODUCT OF SCHRODINGER, LLC)
CRYST1   61.064   59.212   70.930  90.00 101.78  90.00 P 21          8
ATOM      1  N   PRO A  42     -29.110   6.184  -6.250  1.00 51.26           N  
ANISOU    1  N   PRO A  42     6173   7300   6002    573    373    283
ATOM      2  CA  PRO A  42     -27.850   6.669  -5.663  1.00 50.47           C  
ANISOU    2  CA  PRO A  42     6184   7126   5868    590    376    201
ATOM      3  C   PRO A  42     -27.115   7.709  -6.569  1.00 48.75           C  
ANISOU    3  C   PRO A  42     6066   6802   5655    592    357    126
ATOM      4  O   PRO A  42     -26.867   7.478  -7.754  1.00 50.29           O  
ANISOU    4  O   PRO A  42     6245   6964   5900    548    332    126
ATOM      5  CB  PRO A  42     -26.985   5.411  -5.469  1.00 51.72           C  
ANISOU    5  CB  PRO A  42     6323   7261   6068    487    343    199
ATOM      6  CG  PRO A  42     -27.436   4.495  -6.597  1.00 52.13           C  
ANISOU    6  CG  PRO A  42     6304   7315   6189    405    305    242
ATOM      7  CD  PRO A  42     -28.921   4.817  -6.733  1.00 50.71           C  
ANISOU    7  CD  PRO A  42     6045   7223   5998    455    327    315
ATOM      8  H   PRO A  42     -29.904   6.255  -5.625  1.00 51.26           H  
ATOM      9  HA  PRO A  42     -28.054   7.159  -4.708  1.00 50.47           H  
ATOM     10  HB3 PRO A  42     -27.172   4.976  -4.485  1.00 51.72           H  
ATOM     11  HB2 PRO A  42     -25.910   5.605  -5.519  1.00 51.72           H  
ATOM     12  HG3 PRO A  42     -27.264   3.443  -6.370  1.00 52.13           H  
ATOM     13  HG2 PRO A  42     -26.918   4.719  -7.530  1.00 52.13           H  
ATOM     14  HD2 PRO A  42     -29.229   4.771  -7.779  1.00 50.71           H  
ATOM     15  HD3 PRO A  42     -29.538   4.103  -6.183  1.00 50.71           H  
ATOM     16  N   ARG A  43     -26.715   8.850  -5.979  1.00 46.77           N  
ANISOU   16  N   ARG A  43     5924   6497   5349    640    364     66
ATOM     17  CA  ARG A  43     -25.952   9.906  -6.653  1.00 44.82           C  
ANISOU   17  CA  ARG A  43     5780   6149   5102    632    338      1
ATOM     18  C   ARG A  43     -24.582   9.417  -7.142  1.00 40.51           C  
ANISOU   18  C   ARG A  43     5245   5538   4609    514    291    -29
ATOM     19  O   ARG A  43     -24.178   9.770  -8.245  1.00 41.20           O  
ANISOU   19  O   ARG A  43     5333   5579   4743    464    265    -41
ATOM     20  CB  ARG A  43     -25.791  11.120  -5.699  1.00 48.20           C  
ANISOU   20  CB  ARG A  43     6335   6537   5442    719    350    -47
ATOM     21  CG  ARG A  43     -24.859  12.252  -6.195  1.00 52.87           C  
ANISOU   21  CG  ARG A  43     7051   7014   6025    694    310   -112
ATOM     22  CD  ARG A  43     -24.772  13.416  -5.191  1.00 58.66           C  
ANISOU   22  CD  ARG A  43     7920   7708   6659    791    318   -151
ATOM     23  NE  ARG A  43     -23.801  14.462  -5.580  1.00 64.24           N  
ANISOU   23  NE  ARG A  43     8766   8299   7344    761    269   -209
ATOM     24  CZ  ARG A  43     -22.459  14.445  -5.457  1.00 67.57           C  
ANISOU   24  CZ  ARG A  43     9267   8654   7754    684    221   -243
ATOM     25  NH1 ARG A  43     -21.807  13.356  -5.044  1.00 68.19           N  
ANISOU   25  NH1 ARG A  43     9295   8769   7844    631    219   -230
ATOM     26  NH2 ARG A  43     -21.756  15.540  -5.752  1.00 67.33           N1+
ANISOU   26  NH2 ARG A  43     9360   8521   7701    651    169   -284
ATOM     27  H   ARG A  43     -26.964   8.991  -5.015  1.00 46.77           H  
ATOM     28  HA  ARG A  43     -26.516  10.217  -7.535  1.00 44.82           H  
ATOM     29  HB3 ARG A  43     -25.387  10.765  -4.750  1.00 48.20           H  
ATOM     30  HB2 ARG A  43     -26.775  11.534  -5.472  1.00 48.20           H  
ATOM     31  HG3 ARG A  43     -25.290  12.614  -7.125  1.00 52.87           H  
ATOM     32  HG2 ARG A  43     -23.862  11.904  -6.467  1.00 52.87           H  
ATOM     33  HD3 ARG A  43     -24.633  13.075  -4.164  1.00 58.66           H  
ATOM     34  HD2 ARG A  43     -25.733  13.933  -5.202  1.00 58.66           H  
ATOM     35 HH22 ARG A  43     -20.741  15.535  -5.777  1.00 67.33           H  
ATOM     36 HH21 ARG A  43     -22.184  16.430  -5.959  1.00 67.33           H  
ATOM     37 HH12 ARG A  43     -20.802  13.318  -4.936  1.00 68.19           H  
ATOM     38 HH11 ARG A  43     -22.266  12.453  -4.939  1.00 68.19           H  
ATOM     39  HE  ARG A  43     -24.251  15.283  -5.959  1.00 64.24           H  
ATOM     40  N   THR A  44     -23.873   8.690  -6.275  1.00 37.24           N  
ANISOU   40  N   THR A  44     4833   5132   4186    476    285    -33
ATOM     41  CA  THR A  44     -22.504   8.267  -6.492  1.00 34.99           C  
ANISOU   41  CA  THR A  44     4554   4799   3941    378    246    -53
ATOM     42  C   THR A  44     -22.461   6.744  -6.348  1.00 32.44           C  
ANISOU   42  C   THR A  44     4135   4527   3666    323    243     -8
ATOM     43  O   THR A  44     -22.973   6.213  -5.360  1.00 33.03           O  
ANISOU   43  O   THR A  44     4161   4667   3724    345    265     28
ATOM     44  CB  THR A  44     -21.551   8.934  -5.464  1.00 37.56           C  
ANISOU   44  CB  THR A  44     4966   5087   4218    368    231    -92
ATOM     45  OG1 THR A  44     -21.635  10.346  -5.637  1.00 39.14           O  
ANISOU   45  OG1 THR A  44     5275   5231   4368    419    225   -132
ATOM     46  CG2 THR A  44     -20.073   8.530  -5.603  1.00 36.90           C  
ANISOU   46  CG2 THR A  44     4881   4969   4170    271    192   -102
ATOM     47  H   THR A  44     -24.308   8.312  -5.448  1.00 37.24           H  
ATOM     48  HA  THR A  44     -22.179   8.536  -7.493  1.00 34.99           H  
ATOM     49  HB  THR A  44     -21.880   8.693  -4.450  1.00 37.56           H  
ATOM     50  HG1 THR A  44     -21.406  10.508  -6.559  1.00 39.14           H  
ATOM     51 HG21 THR A  44     -19.443   9.092  -4.912  1.00 36.90           H  
ATOM     52 HG22 THR A  44     -19.917   7.474  -5.376  1.00 36.90           H  
ATOM     53 HG23 THR A  44     -19.702   8.704  -6.614  1.00 36.90           H  
ATOM     54  N   VAL A  45     -21.897   6.087  -7.360  1.00 30.29           N  
ANISOU   54  N   VAL A  45     3842   4222   3447    255    212     -8
ATOM     55  CA  VAL A  45     -21.807   4.639  -7.451  1.00 29.61           C  
ANISOU   55  CA  VAL A  45     3689   4161   3400    201    198     29
ATOM     56  C   VAL A  45     -20.348   4.261  -7.733  1.00 29.10           C  
ANISOU   56  C   VAL A  45     3648   4055   3352    142    170      8
ATOM     57  O   VAL A  45     -19.584   5.102  -8.213  1.00 30.33           O  
ANISOU   57  O   VAL A  45     3856   4167   3501    131    158    -26
ATOM     58  CB  VAL A  45     -22.723   4.117  -8.594  1.00 29.83           C  
ANISOU   58  CB  VAL A  45     3665   4199   3471    191    187     66
ATOM     59  CG1 VAL A  45     -24.187   4.504  -8.312  1.00 31.37           C  
ANISOU   59  CG1 VAL A  45     3819   4455   3646    250    216    103
ATOM     60  CG2 VAL A  45     -22.308   4.530 -10.023  1.00 30.17           C  
ANISOU   60  CG2 VAL A  45     3742   4180   3541    173    165     37
ATOM     61  H   VAL A  45     -21.504   6.590  -8.153  1.00 30.29           H  
ATOM     62  HA  VAL A  45     -22.096   4.168  -6.509  1.00 29.61           H  
ATOM     63  HB  VAL A  45     -22.675   3.029  -8.573  1.00 29.83           H  
ATOM     64 HG11 VAL A  45     -24.884   3.987  -8.970  1.00 31.37           H  
ATOM     65 HG12 VAL A  45     -24.469   4.269  -7.286  1.00 31.37           H  
ATOM     66 HG13 VAL A  45     -24.345   5.574  -8.442  1.00 31.37           H  
ATOM     67 HG21 VAL A  45     -23.023   4.159 -10.757  1.00 30.17           H  
ATOM     68 HG22 VAL A  45     -22.263   5.612 -10.133  1.00 30.17           H  
ATOM     69 HG23 VAL A  45     -21.335   4.128 -10.304  1.00 30.17           H  
ATOM     70  N   MET A  46     -19.990   3.016  -7.413  1.00 28.19           N  
ANISOU   70  N   MET A  46     3494   3960   3256    104    159     35
ATOM     71  CA  MET A  46     -18.676   2.451  -7.685  1.00 27.67           C  
ANISOU   71  CA  MET A  46     3444   3868   3202     62    137     25
ATOM     72  C   MET A  46     -18.710   1.713  -9.025  1.00 28.37           C  
ANISOU   72  C   MET A  46     3521   3931   3329     44    114     39
ATOM     73  O   MET A  46     -19.637   0.943  -9.270  1.00 28.49           O  
ANISOU   73  O   MET A  46     3505   3956   3362     43    106     69
ATOM     74  CB  MET A  46     -18.284   1.469  -6.570  1.00 29.18           C  
ANISOU   74  CB  MET A  46     3613   4091   3383     41    137     45
ATOM     75  CG  MET A  46     -17.996   2.160  -5.234  1.00 32.66           C  
ANISOU   75  CG  MET A  46     4082   4547   3782     52    151     24
ATOM     76  SD  MET A  46     -17.394   1.030  -3.950  1.00 30.47           S  
ANISOU   76  SD  MET A  46     3776   4312   3490     30    154     49
ATOM     77  CE  MET A  46     -18.927   0.149  -3.559  1.00 31.27           C  
ANISOU   77  CE  MET A  46     3825   4458   3597     52    170     90
ATOM     78  H   MET A  46     -20.708   2.357  -7.109  1.00 28.19           H  
ATOM     79  HA  MET A  46     -17.934   3.247  -7.723  1.00 27.67           H  
ATOM     80  HB3 MET A  46     -17.397   0.912  -6.873  1.00 29.18           H  
ATOM     81  HB2 MET A  46     -19.072   0.725  -6.447  1.00 29.18           H  
ATOM     82  HG3 MET A  46     -18.885   2.672  -4.868  1.00 32.66           H  
ATOM     83  HG2 MET A  46     -17.236   2.928  -5.373  1.00 32.66           H  
ATOM     84  HE1 MET A  46     -18.756  -0.558  -2.747  1.00 31.27           H  
ATOM     85  HE2 MET A  46     -19.703   0.850  -3.246  1.00 31.27           H  
ATOM     86  HE3 MET A  46     -19.291  -0.408  -4.422  1.00 31.27           H  
ATOM     87  N   VAL A  47     -17.681   1.921  -9.842  1.00 27.13           N  
ANISOU   87  N   VAL A  47     3389   3744   3175     30    101     23
ATOM     88  CA  VAL A  47     -17.489   1.221 -11.100  1.00 26.87           C  
ANISOU   88  CA  VAL A  47     3359   3684   3168     25     80     33
ATOM     89  C   VAL A  47     -16.125   0.519 -11.050  1.00 27.66           C  
ANISOU   89  C   VAL A  47     3466   3786   3258     15     70     40
ATOM     90  O   VAL A  47     -15.111   1.171 -10.799  1.00 28.10           O  
ANISOU   90  O   VAL A  47     3530   3851   3296      7     75     31
ATOM     91  CB  VAL A  47     -17.523   2.193 -12.310  1.00 27.02           C  
ANISOU   91  CB  VAL A  47     3397   3671   3197     39     77     15
ATOM     92  CG1 VAL A  47     -17.212   1.504 -13.656  1.00 27.81           C  
ANISOU   92  CG1 VAL A  47     3507   3744   3316     41     55     25
ATOM     93  CG2 VAL A  47     -18.880   2.920 -12.382  1.00 27.27           C  
ANISOU   93  CG2 VAL A  47     3419   3708   3234     60     90     13
ATOM     94  H   VAL A  47     -16.959   2.589  -9.578  1.00 27.13           H  
ATOM     95  HA  VAL A  47     -18.268   0.474 -11.252  1.00 26.87           H  
ATOM     96  HB  VAL A  47     -16.758   2.960 -12.167  1.00 27.02           H  
ATOM     97 HG11 VAL A  47     -17.309   2.202 -14.488  1.00 27.81           H  
ATOM     98 HG12 VAL A  47     -16.192   1.122 -13.699  1.00 27.81           H  
ATOM     99 HG13 VAL A  47     -17.878   0.662 -13.839  1.00 27.81           H  
ATOM    100 HG21 VAL A  47     -18.958   3.540 -13.274  1.00 27.27           H  
ATOM    101 HG22 VAL A  47     -19.710   2.214 -12.400  1.00 27.27           H  
ATOM    102 HG23 VAL A  47     -19.030   3.573 -11.522  1.00 27.27           H  
ATOM    103  N   ASN A  48     -16.135  -0.794 -11.283  1.00 27.74           N  
ANISOU  103  N   ASN A  48     3478   3787   3274     17     53     61
ATOM    104  CA  ASN A  48     -14.961  -1.634 -11.492  1.00 26.28           C  
ANISOU  104  CA  ASN A  48     3306   3606   3073     26     46     73
ATOM    105  C   ASN A  48     -14.502  -1.451 -12.951  1.00 26.40           C  
ANISOU  105  C   ASN A  48     3344   3595   3090     51     38     69
ATOM    106  O   ASN A  48     -15.269  -1.759 -13.871  1.00 28.14           O  
ANISOU  106  O   ASN A  48     3586   3779   3326     61     20     69
ATOM    107  CB  ASN A  48     -15.380  -3.078 -11.136  1.00 27.90           C  
ANISOU  107  CB  ASN A  48     3522   3802   3277     25     26     96
ATOM    108  CG  ASN A  48     -14.313  -4.165 -11.249  1.00 30.77           C  
ANISOU  108  CG  ASN A  48     3906   4170   3614     49     21    110
ATOM    109  OD1 ASN A  48     -13.155  -3.928 -11.584  1.00 28.81           O  
ANISOU  109  OD1 ASN A  48     3672   3924   3353     80     26    110
ATOM    110  ND2 ASN A  48     -14.710  -5.401 -10.966  1.00 32.34           N  
ANISOU  110  ND2 ASN A  48     4107   4381   3802     41     14    128
ATOM    111  H   ASN A  48     -17.038  -1.252 -11.406  1.00 27.74           H  
ATOM    112  HA  ASN A  48     -14.171  -1.317 -10.812  1.00 26.28           H  
ATOM    113  HB3 ASN A  48     -16.219  -3.383 -11.756  1.00 27.90           H  
ATOM    114  HB2 ASN A  48     -15.752  -3.092 -10.112  1.00 27.90           H  
ATOM    115 HD22 ASN A  48     -14.101  -6.180 -11.139  1.00 32.34           H  
ATOM    116 HD21 ASN A  48     -15.686  -5.636 -10.742  1.00 32.34           H  
ATOM    117  N   LEU A  49     -13.296  -0.897 -13.132  1.00 27.24           N  
ANISOU  117  N   LEU A  49     3444   3726   3178     58     49     73
ATOM    118  CA  LEU A  49     -12.741  -0.525 -14.434  1.00 28.62           C  
ANISOU  118  CA  LEU A  49     3633   3892   3351     84     47     76
ATOM    119  C   LEU A  49     -12.174  -1.713 -15.226  1.00 27.69           C  
ANISOU  119  C   LEU A  49     3542   3769   3211    134     39     97
ATOM    120  O   LEU A  49     -11.871  -1.539 -16.405  1.00 27.49           O  
ANISOU  120  O   LEU A  49     3527   3744   3172    169     41    107
ATOM    121  CB  LEU A  49     -11.636   0.547 -14.271  1.00 30.57           C  
ANISOU  121  CB  LEU A  49     3855   4177   3583     63     58     85
ATOM    122  CG  LEU A  49     -12.097   1.934 -13.772  1.00 34.34           C  
ANISOU  122  CG  LEU A  49     4335   4642   4073     22     58     60
ATOM    123  CD1 LEU A  49     -10.900   2.906 -13.765  1.00 35.32           C  
ANISOU  123  CD1 LEU A  49     4450   4791   4179     -7     53     76
ATOM    124  CD2 LEU A  49     -13.254   2.505 -14.615  1.00 34.93           C  
ANISOU  124  CD2 LEU A  49     4429   4670   4173     34     55     34
ATOM    125  H   LEU A  49     -12.705  -0.714 -12.324  1.00 27.24           H  
ATOM    126  HA  LEU A  49     -13.544  -0.113 -15.044  1.00 28.62           H  
ATOM    127  HB3 LEU A  49     -11.154   0.692 -15.240  1.00 30.57           H  
ATOM    128  HB2 LEU A  49     -10.851   0.167 -13.612  1.00 30.57           H  
ATOM    129  HG  LEU A  49     -12.454   1.838 -12.744  1.00 34.34           H  
ATOM    130 HD11 LEU A  49     -11.179   3.930 -14.011  1.00 35.32           H  
ATOM    131 HD12 LEU A  49     -10.425   2.931 -12.787  1.00 35.32           H  
ATOM    132 HD13 LEU A  49     -10.126   2.611 -14.474  1.00 35.32           H  
ATOM    133 HD21 LEU A  49     -13.281   3.594 -14.613  1.00 34.93           H  
ATOM    134 HD22 LEU A  49     -13.169   2.193 -15.655  1.00 34.93           H  
ATOM    135 HD23 LEU A  49     -14.216   2.165 -14.235  1.00 34.93           H  
ATOM    136  N   ASN A  50     -12.015  -2.887 -14.601  1.00 27.79           N  
ANISOU  136  N   ASN A  50     3571   3777   3211    145     29    108
ATOM    137  CA  ASN A  50     -11.456  -4.075 -15.254  1.00 28.26           C  
ANISOU  137  CA  ASN A  50     3676   3823   3237    205     18    126
ATOM    138  C   ASN A  50     -12.526  -4.702 -16.158  1.00 28.55           C  
ANISOU  138  C   ASN A  50     3770   3790   3286    212    -15    114
ATOM    139  O   ASN A  50     -13.226  -5.624 -15.727  1.00 29.74           O  
ANISOU  139  O   ASN A  50     3948   3905   3445    189    -44    115
ATOM    140  CB  ASN A  50     -10.921  -5.059 -14.187  1.00 29.46           C  
ANISOU  140  CB  ASN A  50     3831   3996   3367    210     18    144
ATOM    141  CG  ASN A  50      -9.612  -4.617 -13.522  1.00 32.00           C  
ANISOU  141  CG  ASN A  50     4101   4394   3665    215     47    168
ATOM    142  OD1 ASN A  50      -8.892  -3.758 -14.011  1.00 31.75           O  
ANISOU  142  OD1 ASN A  50     4041   4402   3619    232     63    184
ATOM    143  ND2 ASN A  50      -9.253  -5.219 -12.396  1.00 34.39           N  
ANISOU  143  ND2 ASN A  50     4387   4723   3958    199     51    178
ATOM    144  H   ASN A  50     -12.317  -2.972 -13.640  1.00 27.79           H  
ATOM    145  HA  ASN A  50     -10.617  -3.741 -15.868  1.00 28.26           H  
ATOM    146  HB3 ASN A  50     -10.700  -6.014 -14.664  1.00 29.46           H  
ATOM    147  HB2 ASN A  50     -11.683  -5.248 -13.430  1.00 29.46           H  
ATOM    148 HD22 ASN A  50      -8.359  -4.951 -12.010  1.00 34.39           H  
ATOM    149 HD21 ASN A  50      -9.799  -5.962 -12.001  1.00 34.39           H  
ATOM    150  N   ILE A  51     -12.647  -4.147 -17.370  1.00 25.52           N  
ANISOU  150  N   ILE A  51     3403   3389   2906    236    -16    106
ATOM    151  CA  ILE A  51     -13.650  -4.458 -18.385  1.00 26.82           C  
ANISOU  151  CA  ILE A  51     3618   3487   3084    235    -52     94
ATOM    152  C   ILE A  51     -13.797  -5.970 -18.662  1.00 27.86           C  
ANISOU  152  C   ILE A  51     3836   3564   3186    266    -94    104
ATOM    153  O   ILE A  51     -12.806  -6.702 -18.714  1.00 28.64           O  
ANISOU  153  O   ILE A  51     3974   3670   3238    332    -87    116
ATOM    154  CB  ILE A  51     -13.345  -3.718 -19.735  1.00 27.78           C  
ANISOU  154  CB  ILE A  51     3750   3606   3200    274    -42     88
ATOM    155  CG1 ILE A  51     -13.384  -2.180 -19.578  1.00 29.33           C  
ANISOU  155  CG1 ILE A  51     3878   3841   3427    233    -13     78
ATOM    156  CG2 ILE A  51     -14.252  -4.109 -20.926  1.00 28.48           C  
ANISOU  156  CG2 ILE A  51     3897   3625   3298    274    -83     77
ATOM    157  CD1 ILE A  51     -12.553  -1.440 -20.635  1.00 29.47           C  
ANISOU  157  CD1 ILE A  51     3893   3874   3430    270      3     84
ATOM    158  H   ILE A  51     -12.082  -3.325 -17.556  1.00 25.52           H  
ATOM    159  HA  ILE A  51     -14.582  -4.079 -17.980  1.00 26.82           H  
ATOM    160  HB  ILE A  51     -12.326  -3.992 -20.012  1.00 27.78           H  
ATOM    161 HG13 ILE A  51     -13.008  -1.879 -18.605  1.00 29.33           H  
ATOM    162 HG12 ILE A  51     -14.414  -1.826 -19.608  1.00 29.33           H  
ATOM    163 HG21 ILE A  51     -14.037  -3.516 -21.813  1.00 28.48           H  
ATOM    164 HG22 ILE A  51     -14.110  -5.146 -21.226  1.00 28.48           H  
ATOM    165 HG23 ILE A  51     -15.306  -3.965 -20.684  1.00 28.48           H  
ATOM    166 HD11 ILE A  51     -12.526  -0.371 -20.428  1.00 29.47           H  
ATOM    167 HD12 ILE A  51     -11.520  -1.792 -20.641  1.00 29.47           H  
ATOM    168 HD13 ILE A  51     -12.951  -1.563 -21.641  1.00 29.47           H  
ATOM    169  N   HIS A  52     -15.038  -6.409 -18.867  1.00 27.96           N  
ANISOU  169  N   HIS A  52     3880   3524   3219    221   -139    104
ATOM    170  CA  HIS A  52     -15.349  -7.706 -19.456  1.00 29.45           C  
ANISOU  170  CA  HIS A  52     4175   3639   3375    242   -197    113
ATOM    171  C   HIS A  52     -15.915  -7.467 -20.862  1.00 28.94           C  
ANISOU  171  C   HIS A  52     4163   3518   3314    248   -233    104
ATOM    172  O   HIS A  52     -16.535  -6.435 -21.103  1.00 28.66           O  
ANISOU  172  O   HIS A  52     4078   3490   3323    193   -236    102
ATOM    173  CB  HIS A  52     -16.309  -8.467 -18.519  1.00 30.66           C  
ANISOU  173  CB  HIS A  52     4334   3768   3545    172   -240    134
ATOM    174  CG  HIS A  52     -15.631  -9.120 -17.333  1.00 32.98           C  
ANISOU  174  CG  HIS A  52     4612   4097   3821    179   -220    145
ATOM    175  ND1 HIS A  52     -14.280  -8.972 -17.045  1.00 36.51           N  
ANISOU  175  ND1 HIS A  52     5079   4522   4271    126   -261    170
ATOM    176  CD2 HIS A  52     -16.120  -9.979 -16.373  1.00 35.10           C  
ANISOU  176  CD2 HIS A  52     4845   4423   4068    227   -168    141
ATOM    177  CE1 HIS A  52     -14.008  -9.765 -16.007  1.00 36.35           C  
ANISOU  177  CE1 HIS A  52     5038   4542   4232    150   -229    174
ATOM    178  NE2 HIS A  52     -15.080 -10.386 -15.537  1.00 36.93           N  
ANISOU  178  NE2 HIS A  52     5072   4669   4292    207   -172    158
ATOM    179  H   HIS A  52     -15.809  -5.750 -18.817  1.00 27.96           H  
ATOM    180  HA  HIS A  52     -14.451  -8.312 -19.602  1.00 29.45           H  
ATOM    181  HB3 HIS A  52     -16.828  -9.255 -19.070  1.00 30.66           H  
ATOM    182  HB2 HIS A  52     -17.093  -7.803 -18.149  1.00 30.66           H  
ATOM    183  HD1 HIS A  52     -13.618  -8.384 -17.542  1.00 36.51           H  
ATOM    184  HD2 HIS A  52     -17.125 -10.352 -16.235  1.00 35.10           H  
ATOM    185  HE1 HIS A  52     -13.020  -9.880 -15.588  1.00 36.35           H  
ATOM    186  N   ASN A  53     -15.655  -8.378 -21.801  1.00 27.93           N  
ANISOU  186  N   ASN A  53     4139   3337   3136    320   -260    101
ATOM    187  CA  ASN A  53     -16.243  -8.301 -23.142  1.00 28.29           C  
ANISOU  187  CA  ASN A  53     4247   3321   3180    321   -303     93
ATOM    188  C   ASN A  53     -17.516  -9.141 -23.106  1.00 29.13           C  
ANISOU  188  C   ASN A  53     4403   3361   3303    238   -383    111
ATOM    189  O   ASN A  53     -17.472 -10.284 -22.655  1.00 30.19           O  
ANISOU  189  O   ASN A  53     4573   3474   3425    211   -417    129
ATOM    190  CB  ASN A  53     -15.244  -8.818 -24.199  1.00 29.98           C  
ANISOU  190  CB  ASN A  53     4576   3494   3323    431   -314     86
ATOM    191  CG  ASN A  53     -14.180  -7.797 -24.616  1.00 34.96           C  
ANISOU  191  CG  ASN A  53     5148   4199   3936    509   -240     82
ATOM    192  OD1 ASN A  53     -13.938  -7.581 -25.800  1.00 35.44           O  
ANISOU  192  OD1 ASN A  53     5092   4336   4037    474   -187     83
ATOM    193  ND2 ASN A  53     -13.521  -7.147 -23.665  1.00 38.64           N  
ANISOU  193  ND2 ASN A  53     5698   4645   4337    616   -239     82
ATOM    194  H   ASN A  53     -15.274  -9.276 -21.540  1.00 27.93           H  
ATOM    195  HA  ASN A  53     -16.475  -7.261 -23.383  1.00 28.29           H  
ATOM    196  HB3 ASN A  53     -15.803  -9.057 -25.102  1.00 29.98           H  
ATOM    197  HB2 ASN A  53     -14.778  -9.753 -23.888  1.00 29.98           H  
ATOM    198 HD22 ASN A  53     -12.769  -6.530 -23.920  1.00 38.64           H  
ATOM    199 HD21 ASN A  53     -13.715  -7.322 -22.689  1.00 38.64           H  
ATOM    200  N   ARG A  54     -18.620  -8.555 -23.566  1.00 28.97           N  
ANISOU  200  N   ARG A  54     4386   3313   3309    196   -418    112
ATOM    201  CA  ARG A  54     -19.933  -9.168 -23.603  1.00 30.15           C  
ANISOU  201  CA  ARG A  54     4572   3410   3474    106   -501    143
ATOM    202  C   ARG A  54     -20.334  -9.290 -25.075  1.00 30.61           C  
ANISOU  202  C   ARG A  54     4725   3394   3511    119   -560    137
ATOM    203  O   ARG A  54     -20.717  -8.301 -25.695  1.00 31.30           O  
ANISOU  203  O   ARG A  54     4763   3504   3627    116   -539    127
ATOM    204  CB  ARG A  54     -20.907  -8.296 -22.780  1.00 32.33           C  
ANISOU  204  CB  ARG A  54     4712   3758   3814     21   -478    166
ATOM    205  CG  ARG A  54     -22.403  -8.679 -22.870  1.00 38.91           C  
ANISOU  205  CG  ARG A  54     5549   4565   4670    -78   -558    214
ATOM    206  CD  ARG A  54     -22.752 -10.057 -22.292  1.00 40.63           C  
ANISOU  206  CD  ARG A  54     5826   4745   4867   -128   -622    250
ATOM    207  NE  ARG A  54     -22.525 -10.106 -20.837  1.00 38.22           N  
ANISOU  207  NE  ARG A  54     5426   4514   4582   -148   -571    264
ATOM    208  CZ  ARG A  54     -22.563 -11.169 -20.028  1.00 41.42           C  
ANISOU  208  CZ  ARG A  54     5861   4902   4974   -198   -617    301
ATOM    209  NH1 ARG A  54     -22.917 -12.370 -20.488  1.00 40.91           N  
ANISOU  209  NH1 ARG A  54     5924   4743   4876   -236   -718    328
ATOM    210  NH2 ARG A  54     -22.229 -11.022 -18.751  1.00 40.10           N1+
ANISOU  210  NH2 ARG A  54     5604   4806   4824   -212   -568    313
ATOM    211  H   ARG A  54     -18.602  -7.597 -23.922  1.00 28.97           H  
ATOM    212  HA  ARG A  54     -19.910 -10.165 -23.160  1.00 30.15           H  
ATOM    213  HB3 ARG A  54     -20.809  -7.259 -23.095  1.00 32.33           H  
ATOM    214  HB2 ARG A  54     -20.583  -8.295 -21.739  1.00 32.33           H  
ATOM    215  HG3 ARG A  54     -22.793  -8.598 -23.887  1.00 38.91           H  
ATOM    216  HG2 ARG A  54     -22.949  -7.918 -22.311  1.00 38.91           H  
ATOM    217  HD3 ARG A  54     -22.093 -10.807 -22.730  1.00 40.63           H  
ATOM    218  HD2 ARG A  54     -23.768 -10.351 -22.563  1.00 40.63           H  
ATOM    219 HH22 ARG A  54     -22.262 -11.737 -18.044  1.00 40.10           H  
ATOM    220 HH21 ARG A  54     -21.827 -10.106 -18.449  1.00 40.10           H  
ATOM    221 HH12 ARG A  54     -22.934 -13.196 -19.910  1.00 40.91           H  
ATOM    222 HH11 ARG A  54     -23.162 -12.476 -21.465  1.00 40.91           H  
ATOM    223  HE  ARG A  54     -22.318  -9.181 -20.422  1.00 38.22           H  
ATOM    224  N   ASN A  55     -20.237 -10.515 -25.605  1.00 31.69           N  
ANISOU  224  N   ASN A  55     5015   3434   3593    133   -640    144
ATOM    225  CA  ASN A  55     -20.766 -10.924 -26.917  1.00 33.94           C  
ANISOU  225  CA  ASN A  55     5415   3634   3849    138   -714    141
ATOM    226  C   ASN A  55     -20.146 -10.178 -28.114  1.00 34.66           C  
ANISOU  226  C   ASN A  55     5511   3736   3921    235   -661    103
ATOM    227  O   ASN A  55     -20.740 -10.166 -29.186  1.00 36.51           O  
ANISOU  227  O   ASN A  55     5784   3930   4156    222   -702    101
ATOM    228  CB  ASN A  55     -22.320 -10.870 -26.923  1.00 37.55           C  
ANISOU  228  CB  ASN A  55     5827   4086   4356     11   -780    182
ATOM    229  CG  ASN A  55     -22.943 -12.027 -26.150  1.00 45.75           C  
ANISOU  229  CG  ASN A  55     6901   5087   5394    -93   -866    234
ATOM    230  OD1 ASN A  55     -23.159 -11.937 -24.943  1.00 48.05           O  
ANISOU  230  OD1 ASN A  55     7070   5452   5736   -172   -849    272
ATOM    231  ND2 ASN A  55     -23.225 -13.132 -26.831  1.00 48.44           N  
ANISOU  231  ND2 ASN A  55     7415   5314   5675    -93   -964    241
ATOM    232  H   ASN A  55     -19.852 -11.254 -25.036  1.00 31.69           H  
ATOM    233  HA  ASN A  55     -20.454 -11.966 -26.989  1.00 33.94           H  
ATOM    234  HB3 ASN A  55     -22.713 -10.932 -27.938  1.00 37.55           H  
ATOM    235  HB2 ASN A  55     -22.694  -9.920 -26.541  1.00 37.55           H  
ATOM    236 HD22 ASN A  55     -23.668 -13.907 -26.366  1.00 48.44           H  
ATOM    237 HD21 ASN A  55     -23.038 -13.191 -27.834  1.00 48.44           H  
ATOM    238  N   THR A  56     -18.927  -9.653 -27.968  1.00 35.30           N  
ANISOU  238  N   THR A  56     5558   3874   3980    334   -576     80
ATOM    239  CA  THR A  56     -18.200  -8.941 -29.022  1.00 36.57           C  
ANISOU  239  CA  THR A  56     5719   4058   4119    428   -524     56
ATOM    240  C   THR A  56     -17.812  -9.847 -30.220  1.00 39.77           C  
ANISOU  240  C   THR A  56     6302   4372   4438    523   -577     44
ATOM    241  O   THR A  56     -17.583  -9.339 -31.315  1.00 40.12           O  
ANISOU  241  O   THR A  56     6362   4423   4457    598   -550     29
ATOM    242  CB  THR A  56     -16.925  -8.325 -28.398  1.00 37.42           C  
ANISOU  242  CB  THR A  56     5720   4268   4232    490   -422     49
ATOM    243  OG1 THR A  56     -16.245  -9.295 -27.612  1.00 39.68           O  
ANISOU  243  OG1 THR A  56     6066   4552   4460    563   -412     55
ATOM    244  CG2 THR A  56     -17.261  -7.175 -27.435  1.00 35.60           C  
ANISOU  244  CG2 THR A  56     5329   4119   4080    401   -373     55
ATOM    245  H   THR A  56     -18.429  -9.700 -27.090  1.00 35.30           H  
ATOM    246  HA  THR A  56     -18.842  -8.147 -29.409  1.00 36.57           H  
ATOM    247  HB  THR A  56     -16.254  -7.963 -29.181  1.00 37.42           H  
ATOM    248  HG1 THR A  56     -15.343  -8.980 -27.466  1.00 39.68           H  
ATOM    249 HG21 THR A  56     -16.356  -6.786 -26.978  1.00 35.60           H  
ATOM    250 HG22 THR A  56     -17.747  -6.352 -27.961  1.00 35.60           H  
ATOM    251 HG23 THR A  56     -17.927  -7.488 -26.630  1.00 35.60           H  
ATOM    252  N   ASN A  57     -17.817 -11.173 -30.018  1.00 40.84           N  
ANISOU  252  N   ASN A  57     6578   4417   4524    519   -657     53
ATOM    253  CA  ASN A  57     -17.647 -12.184 -31.070  1.00 44.33           C  
ANISOU  253  CA  ASN A  57     7218   4751   4875    606   -724     41
ATOM    254  C   ASN A  57     -18.992 -12.757 -31.555  1.00 46.63           C  
ANISOU  254  C   ASN A  57     7621   4929   5166    507   -849     53
ATOM    255  O   ASN A  57     -18.977 -13.723 -32.315  1.00 49.06           O  
ANISOU  255  O   ASN A  57     8124   5125   5392    561   -929     45
ATOM    256  CB  ASN A  57     -16.692 -13.298 -30.589  1.00 47.64           C  
ANISOU  256  CB  ASN A  57     7741   5144   5214    707   -720     40
ATOM    257  CG  ASN A  57     -15.240 -12.829 -30.535  1.00 53.04           C  
ANISOU  257  CG  ASN A  57     8375   5921   5859    852   -614     31
ATOM    258  OD1 ASN A  57     -14.726 -12.505 -29.473  1.00 54.62           O  
ANISOU  258  OD1 ASN A  57     8614   6121   6017    945   -594     20
ATOM    259  ND2 ASN A  57     -14.558 -12.777 -31.675  1.00 54.07           N  
ANISOU  259  ND2 ASN A  57     8411   6136   6000    873   -546     44
ATOM    260  H   ASN A  57     -17.936 -11.491 -29.070  1.00 40.84           H  
ATOM    261  HA  ASN A  57     -17.176 -11.697 -31.924  1.00 44.33           H  
ATOM    262  HB3 ASN A  57     -16.718 -14.153 -31.266  1.00 47.64           H  
ATOM    263  HB2 ASN A  57     -16.997 -13.681 -29.614  1.00 47.64           H  
ATOM    264 HD22 ASN A  57     -13.607 -12.444 -31.639  1.00 54.07           H  
ATOM    265 HD21 ASN A  57     -14.959 -13.069 -32.550  1.00 54.07           H  
ATOM    266  N   THR A  58     -20.130 -12.175 -31.155  1.00 46.49           N  
ANISOU  266  N   THR A  58     7488   4943   5234    366   -871     76
ATOM    267  CA  THR A  58     -21.431 -12.454 -31.761  1.00 47.41           C  
ANISOU  267  CA  THR A  58     7675   4979   5361    258   -985    101
ATOM    268  C   THR A  58     -21.673 -11.373 -32.827  1.00 49.52           C  
ANISOU  268  C   THR A  58     7885   5278   5651    283   -949     83
ATOM    269  O   THR A  58     -21.701 -10.197 -32.478  1.00 49.96           O  
ANISOU  269  O   THR A  58     7769   5442   5772    275   -856     79
ATOM    270  CB  THR A  58     -22.566 -12.363 -30.708  1.00 48.62           C  
ANISOU  270  CB  THR A  58     7699   5180   5595    100  -1012    151
ATOM    271  OG1 THR A  58     -22.217 -13.196 -29.611  1.00 49.26           O  
ANISOU  271  OG1 THR A  58     7785   5262   5668     78  -1017    168
ATOM    272  CG2 THR A  58     -23.948 -12.794 -31.232  1.00 48.92           C  
ANISOU  272  CG2 THR A  58     7796   5149   5643    -24  -1137    194
ATOM    273  H   THR A  58     -20.093 -11.297 -30.638  1.00 46.49           H  
ATOM    274  HA  THR A  58     -21.451 -13.441 -32.229  1.00 47.41           H  
ATOM    275  HB  THR A  58     -22.656 -11.339 -30.338  1.00 48.62           H  
ATOM    276  HG1 THR A  58     -21.253 -13.162 -29.568  1.00 49.26           H  
ATOM    277 HG21 THR A  58     -24.697 -12.758 -30.441  1.00 48.92           H  
ATOM    278 HG22 THR A  58     -24.294 -12.137 -32.031  1.00 48.92           H  
ATOM    279 HG23 THR A  58     -23.927 -13.810 -31.626  1.00 48.92           H  
ATOM    280  N   ASN A  59     -21.791 -11.774 -34.103  1.00 49.73           N  
ANISOU  280  N   ASN A  59     8065   5209   5620    319  -1022     71
ATOM    281  CA  ASN A  59     -21.910 -10.877 -35.269  1.00 50.66           C  
ANISOU  281  CA  ASN A  59     8162   5342   5744    358   -997     51
ATOM    282  C   ASN A  59     -20.794  -9.799 -35.323  1.00 51.72           C  
ANISOU  282  C   ASN A  59     8175   5585   5892    467   -858     23
ATOM    283  O   ASN A  59     -21.116  -8.610 -35.366  1.00 50.74           O  
ANISOU  283  O   ASN A  59     7888   5550   5841    426   -792     26
ATOM    284  CB  ASN A  59     -23.319 -10.223 -35.328  1.00 52.96           C  
ANISOU  284  CB  ASN A  59     8351   5659   6113    221  -1036     84
ATOM    285  CG  ASN A  59     -24.469 -11.223 -35.405  1.00 57.33           C  
ANISOU  285  CG  ASN A  59     9017   6113   6651    101  -1183    127
ATOM    286  OD1 ASN A  59     -24.347 -12.289 -35.998  1.00 59.97           O  
ANISOU  286  OD1 ASN A  59     9247   6489   7051    -34  -1217    177
ATOM    287  ND2 ASN A  59     -25.611 -10.893 -34.813  1.00 56.45           N  
ANISOU  287  ND2 ASN A  59     9125   5873   6452    147  -1277    113
ATOM    288  H   ASN A  59     -21.781 -12.761 -34.313  1.00 49.73           H  
ATOM    289  HA  ASN A  59     -21.787 -11.485 -36.165  1.00 50.66           H  
ATOM    290  HB3 ASN A  59     -23.388  -9.591 -36.216  1.00 52.96           H  
ATOM    291  HB2 ASN A  59     -23.459  -9.558 -34.474  1.00 52.96           H  
ATOM    292 HD22 ASN A  59     -26.392 -11.522 -34.889  1.00 56.45           H  
ATOM    293 HD21 ASN A  59     -25.690 -10.019 -34.319  1.00 56.45           H  
ATOM    294  N   PRO A  60     -19.499 -10.201 -35.249  1.00 53.35           N  
ANISOU  294  N   PRO A  60     8455   5790   6026    602   -814      4
ATOM    295  CA  PRO A  60     -18.379  -9.240 -35.117  1.00 54.39           C  
ANISOU  295  CA  PRO A  60     8461   6037   6167    692   -688     -7
ATOM    296  C   PRO A  60     -18.102  -8.306 -36.287  1.00 55.57           C  
ANISOU  296  C   PRO A  60     8606   6207   6299    768   -652    -21
ATOM    297  O   PRO A  60     -18.725  -8.342 -37.350  1.00 56.27           O  
ANISOU  297  O   PRO A  60     8695   6265   6421    705   -695    -23
ATOM    298  CB  PRO A  60     -17.174 -10.160 -34.831  1.00 54.93           C  
ANISOU  298  CB  PRO A  60     8610   6103   6158    807   -663     -9
ATOM    299  CG  PRO A  60     -17.509 -11.463 -35.539  1.00 55.48           C  
ANISOU  299  CG  PRO A  60     8894   6033   6153    817   -778    -12
ATOM    300  CD  PRO A  60     -19.010 -11.581 -35.329  1.00 53.42           C  
ANISOU  300  CD  PRO A  60     8668   5696   5934    681   -880     -3
ATOM    301  HA  PRO A  60     -18.545  -8.614 -34.238  1.00 54.39           H  
ATOM    302  HXT PRO A  60     -17.291  -7.597 -36.125  1.00 55.57           H  
ATOM    303  HB3 PRO A  60     -17.110 -10.337 -33.758  1.00 54.93           H  
ATOM    304  HB2 PRO A  60     -16.207  -9.756 -35.136  1.00 54.93           H  
ATOM    305  HG3 PRO A  60     -16.953 -12.321 -35.164  1.00 55.48           H  
ATOM    306  HG2 PRO A  60     -17.299 -11.363 -36.605  1.00 55.48           H  
ATOM    307  HD2 PRO A  60     -19.483 -12.160 -36.122  1.00 53.42           H  
ATOM    308  HD3 PRO A  60     -19.198 -12.079 -34.381  1.00 53.42           H  
ATOM    309  N   ASP A  65     -14.847  -3.442 -43.219  1.00 54.40           N  
ANISOU  309  N   ASP A  65     8292   6390   5988   1331   -304      0
ATOM    310  CA  ASP A  65     -14.333  -2.519 -44.269  1.00 53.88           C  
ANISOU  310  CA  ASP A  65     8174   6387   5911   1387   -255     19
ATOM    311  C   ASP A  65     -15.477  -1.634 -44.885  1.00 51.38           C  
ANISOU  311  C   ASP A  65     7827   6027   5669   1280   -292     -3
ATOM    312  O   ASP A  65     -15.342  -1.020 -45.947  1.00 50.83           O  
ANISOU  312  O   ASP A  65     7757   5976   5579   1329   -274      4
ATOM    313  CB  ASP A  65     -13.480  -3.325 -45.274  1.00 58.74           C  
ANISOU  313  CB  ASP A  65     8936   6982   6399   1563   -257     26
ATOM    314  CG  ASP A  65     -12.674  -2.471 -46.254  1.00 67.50           C  
ANISOU  314  CG  ASP A  65     9964   8205   7478   1654   -178     69
ATOM    315  OD1 ASP A  65     -11.878  -1.636 -45.768  1.00 70.78           O  
ANISOU  315  OD1 ASP A  65    10222   8740   7931   1630   -105    112
ATOM    316  OD2 ASP A  65     -12.915  -2.620 -47.468  1.00 70.82           O1-
ANISOU  316  OD2 ASP A  65    10477   8596   7836   1744   -192     65
ATOM    317  H1  ASP A  65     -14.728  -4.392 -43.547  1.00 54.40           H  
ATOM    318  H2  ASP A  65     -14.225  -3.401 -42.419  1.00 54.40           H  
ATOM    319  HA  ASP A  65     -13.693  -1.789 -43.770  1.00 53.88           H  
ATOM    320  HB3 ASP A  65     -14.098  -4.033 -45.829  1.00 58.74           H  
ATOM    321  HB2 ASP A  65     -12.746  -3.926 -44.738  1.00 58.74           H  
ATOM    322  N   TYR A  66     -16.596  -1.515 -44.158  1.00 49.81           N  
ANISOU  322  N   TYR A  66     7593   5781   5552   1139   -338    -24
ATOM    323  CA  TYR A  66     -17.754  -0.695 -44.527  1.00 49.71           C  
ANISOU  323  CA  TYR A  66     7542   5737   5608   1042   -371    -38
ATOM    324  C   TYR A  66     -17.414   0.791 -44.731  1.00 48.70           C  
ANISOU  324  C   TYR A  66     7284   5698   5523   1036   -300    -20
ATOM    325  O   TYR A  66     -18.085   1.444 -45.522  1.00 47.85           O  
ANISOU  325  O   TYR A  66     7183   5574   5425   1033   -312    -26
ATOM    326  CB  TYR A  66     -18.878  -0.831 -43.480  1.00 50.09           C  
ANISOU  326  CB  TYR A  66     7539   5755   5737    901   -413    -47
ATOM    327  CG  TYR A  66     -19.440  -2.223 -43.220  1.00 50.51           C  
ANISOU  327  CG  TYR A  66     7720   5712   5758    876   -502    -57
ATOM    328  CD1 TYR A  66     -19.482  -3.207 -44.232  1.00 52.00           C  
ANISOU  328  CD1 TYR A  66     8085   5816   5858    958   -563    -68
ATOM    329  CD2 TYR A  66     -19.990  -2.517 -41.954  1.00 51.99           C  
ANISOU  329  CD2 TYR A  66     7861   5891   6001    767   -531    -52
ATOM    330  CE1 TYR A  66     -20.075  -4.460 -43.980  1.00 53.01           C  
ANISOU  330  CE1 TYR A  66     8346   5845   5950    928   -656    -74
ATOM    331  CE2 TYR A  66     -20.570  -3.774 -41.701  1.00 52.81           C  
ANISOU  331  CE2 TYR A  66     8083   5907   6077    731   -621    -53
ATOM    332  CZ  TYR A  66     -20.622  -4.743 -42.716  1.00 54.16           C  
ANISOU  332  CZ  TYR A  66     8434   5985   6158    806   -687    -63
ATOM    333  OH  TYR A  66     -21.218  -5.945 -42.474  1.00 56.72           O  
ANISOU  333  OH  TYR A  66     8889   6211   6451    760   -788    -61
ATOM    334  H   TYR A  66     -16.636  -2.098 -43.328  1.00 49.81           H  
ATOM    335  HA  TYR A  66     -18.115  -1.050 -45.493  1.00 49.71           H  
ATOM    336  HB3 TYR A  66     -19.720  -0.204 -43.780  1.00 50.09           H  
ATOM    337  HB2 TYR A  66     -18.530  -0.422 -42.529  1.00 50.09           H  
ATOM    338  HD1 TYR A  66     -19.094  -3.005 -45.218  1.00 52.00           H  
ATOM    339  HD2 TYR A  66     -19.993  -1.778 -41.164  1.00 51.99           H  
ATOM    340  HE1 TYR A  66     -20.136  -5.191 -44.769  1.00 53.01           H  
ATOM    341  HE2 TYR A  66     -21.003  -3.981 -40.732  1.00 52.81           H  
ATOM    342  HH  TYR A  66     -21.383  -6.485 -43.248  1.00 56.72           H  
ATOM    343  N   TYR A  67     -16.367   1.293 -44.062  1.00 49.24           N  
ANISOU  343  N   TYR A  67     7240   5859   5612   1034   -230      4
ATOM    344  CA  TYR A  67     -15.908   2.677 -44.202  1.00 50.13           C  
ANISOU  344  CA  TYR A  67     7231   6052   5763   1014   -170     28
ATOM    345  C   TYR A  67     -15.330   2.987 -45.601  1.00 48.65           C  
ANISOU  345  C   TYR A  67     7076   5891   5518   1114   -148     48
ATOM    346  O   TYR A  67     -15.411   4.140 -46.020  1.00 46.68           O  
ANISOU  346  O   TYR A  67     6756   5676   5305   1082   -124     60
ATOM    347  CB  TYR A  67     -14.932   3.028 -43.053  1.00 51.63           C  
ANISOU  347  CB  TYR A  67     7313   6334   5971    995   -111     59
ATOM    348  CG  TYR A  67     -13.525   2.460 -43.166  1.00 54.72           C  
ANISOU  348  CG  TYR A  67     7717   6795   6279   1114    -68    100
ATOM    349  CD1 TYR A  67     -13.282   1.088 -42.946  1.00 56.63           C  
ANISOU  349  CD1 TYR A  67     8045   7011   6461   1182    -84     94
ATOM    350  CD2 TYR A  67     -12.449   3.302 -43.514  1.00 56.61           C  
ANISOU  350  CD2 TYR A  67     7878   7134   6496   1157    -11    152
ATOM    351  CE1 TYR A  67     -11.991   0.559 -43.134  1.00 58.12           C  
ANISOU  351  CE1 TYR A  67     8242   7275   6566   1306    -38    138
ATOM    352  CE2 TYR A  67     -11.157   2.776 -43.692  1.00 58.05           C  
ANISOU  352  CE2 TYR A  67     8056   7402   6599   1271     34    204
ATOM    353  CZ  TYR A  67     -10.932   1.399 -43.522  1.00 59.64           C  
ANISOU  353  CZ  TYR A  67     8344   7580   6737   1352     23    196
ATOM    354  OH  TYR A  67      -9.697   0.877 -43.768  1.00 61.81           O  
ANISOU  354  OH  TYR A  67     8611   7950   6925   1480     73    254
ATOM    355  H   TYR A  67     -15.803   0.678 -43.496  1.00 49.24           H  
ATOM    356  HA  TYR A  67     -16.783   3.316 -44.092  1.00 50.13           H  
ATOM    357  HB3 TYR A  67     -15.359   2.740 -42.092  1.00 51.63           H  
ATOM    358  HB2 TYR A  67     -14.849   4.115 -43.009  1.00 51.63           H  
ATOM    359  HD1 TYR A  67     -14.079   0.424 -42.651  1.00 56.63           H  
ATOM    360  HD2 TYR A  67     -12.610   4.356 -43.658  1.00 56.61           H  
ATOM    361  HE1 TYR A  67     -11.821  -0.499 -43.003  1.00 58.12           H  
ATOM    362  HE2 TYR A  67     -10.342   3.421 -43.983  1.00 58.05           H  
ATOM    363  HH  TYR A  67      -9.723  -0.082 -43.869  1.00 61.81           H  
ATOM    364  N   ASN A  68     -14.792   1.968 -46.294  1.00 48.09           N  
ANISOU  364  N   ASN A  68     7117   5804   5351   1240   -156     54
ATOM    365  CA  ASN A  68     -14.289   2.062 -47.670  1.00 48.80           C  
ANISOU  365  CA  ASN A  68     7253   5922   5365   1361   -133     77
ATOM    366  C   ASN A  68     -15.382   1.701 -48.677  1.00 47.18           C  
ANISOU  366  C   ASN A  68     7187   5610   5130   1385   -203     39
ATOM    367  O   ASN A  68     -15.540   2.412 -49.662  1.00 47.44           O  
ANISOU  367  O   ASN A  68     7232   5656   5135   1439   -191     49
ATOM    368  CB  ASN A  68     -13.092   1.102 -47.867  1.00 52.00           C  
ANISOU  368  CB  ASN A  68     7707   6384   5666   1509    -95    112
ATOM    369  CG  ASN A  68     -11.762   1.656 -47.374  1.00 59.65           C  
ANISOU  369  CG  ASN A  68     8534   7499   6630   1537    -11    180
ATOM    370  OD1 ASN A  68     -11.427   2.807 -47.646  1.00 62.64           O  
ANISOU  370  OD1 ASN A  68     8809   7942   7049   1492     22    210
ATOM    371  ND2 ASN A  68     -10.979   0.862 -46.663  1.00 61.33           N  
ANISOU  371  ND2 ASN A  68     8743   7771   6789   1609     22    212
ATOM    372  H   ASN A  68     -14.776   1.040 -45.887  1.00 48.09           H  
ATOM    373  HA  ASN A  68     -13.965   3.092 -47.827  1.00 48.80           H  
ATOM    374  HB3 ASN A  68     -12.940   0.914 -48.932  1.00 52.00           H  
ATOM    375  HB2 ASN A  68     -13.304   0.127 -47.428  1.00 52.00           H  
ATOM    376 HD22 ASN A  68     -10.108   1.186 -46.277  1.00 61.33           H  
ATOM    377 HD21 ASN A  68     -11.285  -0.103 -46.428  1.00 61.33           H  
ATOM    378  N   ARG A  69     -16.092   0.594 -48.431  1.00 45.57           N  
ANISOU  378  N   ARG A  69     7096   5298   4920   1351   -280      0
ATOM    379  CA  ARG A  69     -17.026  -0.006 -49.389  1.00 44.34           C  
ANISOU  379  CA  ARG A  69     7089   5029   4728   1361   -365    -32
ATOM    380  C   ARG A  69     -18.379   0.714 -49.496  1.00 41.69           C  
ANISOU  380  C   ARG A  69     6701   4657   4483   1230   -406    -48
ATOM    381  O   ARG A  69     -19.194   0.319 -50.331  1.00 42.46           O  
ANISOU  381  O   ARG A  69     6896   4681   4557   1234   -468    -65
ATOM    382  CB  ARG A  69     -17.275  -1.466 -48.977  1.00 47.63           C  
ANISOU  382  CB  ARG A  69     7649   5347   5103   1360   -442    -55
ATOM    383  CG  ARG A  69     -16.053  -2.390 -49.130  1.00 52.31           C  
ANISOU  383  CG  ARG A  69     8346   5950   5580   1521   -417    -44
ATOM    384  CD  ARG A  69     -16.173  -3.691 -48.323  1.00 54.84           C  
ANISOU  384  CD  ARG A  69     8781   6186   5870   1507   -482    -62
ATOM    385  NE  ARG A  69     -17.474  -4.372 -48.551  1.00 57.15           N  
ANISOU  385  NE  ARG A  69     9209   6340   6163   1428   -601    -93
ATOM    386  CZ  ARG A  69     -18.203  -5.081 -47.681  1.00 59.32           C  
ANISOU  386  CZ  ARG A  69     9544   6537   6460   1334   -679   -104
ATOM    387  NH1 ARG A  69     -19.391  -5.549 -48.065  1.00 58.73           N  
ANISOU  387  NH1 ARG A  69     9586   6345   6383   1252   -794   -118
ATOM    388  NH2 ARG A  69     -17.761  -5.309 -46.441  1.00 58.27           N1+
ANISOU  388  NH2 ARG A  69     9351   6444   6346   1317   -645    -94
ATOM    389  H   ARG A  69     -15.859   0.044 -47.612  1.00 45.57           H  
ATOM    390  HA  ARG A  69     -16.583   0.016 -50.388  1.00 44.34           H  
ATOM    391  HB3 ARG A  69     -18.071  -1.874 -49.602  1.00 47.63           H  
ATOM    392  HB2 ARG A  69     -17.649  -1.493 -47.953  1.00 47.63           H  
ATOM    393  HG3 ARG A  69     -15.201  -1.855 -48.708  1.00 52.31           H  
ATOM    394  HG2 ARG A  69     -15.779  -2.565 -50.172  1.00 52.31           H  
ATOM    395  HD3 ARG A  69     -15.907  -3.519 -47.282  1.00 54.84           H  
ATOM    396  HD2 ARG A  69     -15.422  -4.382 -48.708  1.00 54.84           H  
ATOM    397 HH22 ARG A  69     -18.255  -5.856 -45.752  1.00 58.27           H  
ATOM    398 HH21 ARG A  69     -16.872  -4.913 -46.161  1.00 58.27           H  
ATOM    399 HH12 ARG A  69     -20.000  -6.108 -47.489  1.00 58.73           H  
ATOM    400 HH11 ARG A  69     -19.750  -5.286 -48.992  1.00 58.73           H  
ATOM    401  HE  ARG A  69     -17.828  -4.233 -49.497  1.00 57.15           H  
ATOM    402  N   SER A  70     -18.636   1.683 -48.614  1.00 39.20           N  
ANISOU  402  N   SER A  70     6241   4391   4263   1120   -375    -42
ATOM    403  CA  SER A  70     -19.864   2.460 -48.601  1.00 37.39           C  
ANISOU  403  CA  SER A  70     5949   4140   4117   1003   -405    -52
ATOM    404  C   SER A  70     -19.964   3.405 -49.809  1.00 36.38           C  
ANISOU  404  C   SER A  70     5795   4032   3995   1026   -385    -47
ATOM    405  O   SER A  70     -18.959   3.933 -50.280  1.00 37.84           O  
ANISOU  405  O   SER A  70     5941   4284   4150   1102   -321    -26
ATOM    406  CB  SER A  70     -19.970   3.204 -47.254  1.00 36.51           C  
ANISOU  406  CB  SER A  70     5693   4090   4091    909   -361    -44
ATOM    407  OG  SER A  70     -21.074   4.082 -47.161  1.00 35.26           O  
ANISOU  407  OG  SER A  70     5471   3921   4007    812   -382    -49
ATOM    408  H   SER A  70     -17.895   1.982 -47.998  1.00 39.20           H  
ATOM    409  HA  SER A  70     -20.695   1.761 -48.654  1.00 37.39           H  
ATOM    410  HB3 SER A  70     -19.054   3.761 -47.052  1.00 36.51           H  
ATOM    411  HB2 SER A  70     -20.094   2.481 -46.451  1.00 36.51           H  
ATOM    412  HG  SER A  70     -21.761   3.658 -46.611  1.00 35.26           H  
ATOM    413  N   THR A  71     -21.210   3.657 -50.212  1.00 34.30           N  
ANISOU  413  N   THR A  71     5542   3718   3773    953   -441    -59
ATOM    414  CA  THR A  71     -21.608   4.748 -51.098  1.00 33.66           C  
ANISOU  414  CA  THR A  71     5421   3658   3711    958   -422    -54
ATOM    415  C   THR A  71     -21.415   6.131 -50.429  1.00 32.04           C  
ANISOU  415  C   THR A  71     5059   3531   3582    901   -351    -40
ATOM    416  O   THR A  71     -21.290   7.128 -51.135  1.00 32.66           O  
ANISOU  416  O   THR A  71     5092   3641   3677    910   -320    -30
ATOM    417  CB  THR A  71     -23.102   4.599 -51.476  1.00 35.29           C  
ANISOU  417  CB  THR A  71     5676   3793   3939    893   -503    -64
ATOM    418  OG1 THR A  71     -23.887   4.425 -50.304  1.00 35.32           O  
ANISOU  418  OG1 THR A  71     5597   3801   4020    776   -523    -60
ATOM    419  CG2 THR A  71     -23.354   3.371 -52.355  1.00 36.88           C  
ANISOU  419  CG2 THR A  71     6050   3900   4062    933   -592    -77
ATOM    420  H   THR A  71     -21.961   3.159 -49.752  1.00 34.30           H  
ATOM    421  HA  THR A  71     -20.995   4.705 -51.997  1.00 33.66           H  
ATOM    422  HB  THR A  71     -23.448   5.490 -52.006  1.00 35.29           H  
ATOM    423  HG1 THR A  71     -23.752   3.521 -49.997  1.00 35.32           H  
ATOM    424 HG21 THR A  71     -24.410   3.284 -52.617  1.00 36.88           H  
ATOM    425 HG22 THR A  71     -22.798   3.450 -53.292  1.00 36.88           H  
ATOM    426 HG23 THR A  71     -23.049   2.446 -51.866  1.00 36.88           H  
ATOM    427  N   SER A  72     -21.312   6.176 -49.097  1.00 30.60           N  
ANISOU  427  N   SER A  72     4807   3377   3442    843   -330    -38
ATOM    428  CA  SER A  72     -21.021   7.356 -48.297  1.00 30.22           C  
ANISOU  428  CA  SER A  72     4634   3394   3453    794   -270    -27
ATOM    429  C   SER A  72     -19.798   7.069 -47.398  1.00 30.13           C  
ANISOU  429  C   SER A  72     4591   3435   3423    819   -225    -12
ATOM    430  O   SER A  72     -19.979   6.926 -46.185  1.00 30.02           O  
ANISOU  430  O   SER A  72     4536   3428   3443    761   -223    -18
ATOM    431  CB  SER A  72     -22.301   7.699 -47.505  1.00 29.85           C  
ANISOU  431  CB  SER A  72     4535   3329   3476    695   -296    -37
ATOM    432  OG  SER A  72     -22.758   6.574 -46.761  1.00 29.97           O  
ANISOU  432  OG  SER A  72     4584   3314   3491    661   -338    -43
ATOM    433  H   SER A  72     -21.410   5.320 -48.555  1.00 30.60           H  
ATOM    434  HA  SER A  72     -20.772   8.209 -48.929  1.00 30.22           H  
ATOM    435  HB3 SER A  72     -23.083   8.029 -48.187  1.00 29.85           H  
ATOM    436  HB2 SER A  72     -22.117   8.530 -46.822  1.00 29.85           H  
ATOM    437  HG  SER A  72     -21.978   6.204 -46.325  1.00 29.97           H  
ATOM    438  N   PRO A  73     -18.596   6.879 -47.993  1.00 32.80           N  
ANISOU  438  N   PRO A  73     4952   3815   3697    912   -190     11
ATOM    439  CA  PRO A  73     -17.415   6.419 -47.244  1.00 33.35           C  
ANISOU  439  CA  PRO A  73     4997   3940   3736    948   -151     33
ATOM    440  C   PRO A  73     -16.890   7.470 -46.253  1.00 32.49           C  
ANISOU  440  C   PRO A  73     4767   3898   3678    881   -103     54
ATOM    441  O   PRO A  73     -17.114   8.673 -46.435  1.00 31.87           O  
ANISOU  441  O   PRO A  73     4631   3831   3648    826    -92     57
ATOM    442  CB  PRO A  73     -16.402   6.087 -48.348  1.00 35.63           C  
ANISOU  442  CB  PRO A  73     5334   4266   3937   1074   -125     62
ATOM    443  CG  PRO A  73     -16.744   7.046 -49.477  1.00 35.92           C  
ANISOU  443  CG  PRO A  73     5362   4301   3985   1077   -124     67
ATOM    444  CD  PRO A  73     -18.262   7.135 -49.398  1.00 33.57           C  
ANISOU  444  CD  PRO A  73     5097   3917   3741    997   -184     24
ATOM    445  HA  PRO A  73     -17.654   5.517 -46.681  1.00 33.35           H  
ATOM    446  HB3 PRO A  73     -16.556   5.058 -48.681  1.00 35.63           H  
ATOM    447  HB2 PRO A  73     -15.367   6.161 -48.022  1.00 35.63           H  
ATOM    448  HG3 PRO A  73     -16.383   6.721 -50.454  1.00 35.92           H  
ATOM    449  HG2 PRO A  73     -16.315   8.023 -49.267  1.00 35.92           H  
ATOM    450  HD2 PRO A  73     -18.626   8.100 -49.748  1.00 33.57           H  
ATOM    451  HD3 PRO A  73     -18.697   6.367 -50.030  1.00 33.57           H  
ATOM    452  N   TRP A  74     -16.192   7.001 -45.217  1.00 31.07           N  
ANISOU  452  N   TRP A  74     4560   3758   3487    883    -81     69
ATOM    453  CA  TRP A  74     -15.707   7.840 -44.129  1.00 31.88           C  
ANISOU  453  CA  TRP A  74     4561   3920   3633    814    -46     90
ATOM    454  C   TRP A  74     -14.303   7.408 -43.704  1.00 33.85           C  
ANISOU  454  C   TRP A  74     4777   4249   3835    861     -7    134
ATOM    455  O   TRP A  74     -13.789   6.389 -44.170  1.00 34.04           O  
ANISOU  455  O   TRP A  74     4861   4280   3793    954     -6    144
ATOM    456  CB  TRP A  74     -16.721   7.819 -42.962  1.00 31.72           C  
ANISOU  456  CB  TRP A  74     4522   3855   3674    722    -70     53
ATOM    457  CG  TRP A  74     -16.901   6.549 -42.182  1.00 30.65           C  
ANISOU  457  CG  TRP A  74     4431   3693   3522    731    -92     37
ATOM    458  CD1 TRP A  74     -16.214   6.209 -41.069  1.00 31.72           C  
ANISOU  458  CD1 TRP A  74     4531   3865   3655    717    -72     48
ATOM    459  CD2 TRP A  74     -17.825   5.447 -42.433  1.00 31.16           C  
ANISOU  459  CD2 TRP A  74     4582   3681   3577    737   -148      8
ATOM    460  NE1 TRP A  74     -16.680   5.004 -40.585  1.00 32.87           N  
ANISOU  460  NE1 TRP A  74     4739   3962   3787    724   -108     27
ATOM    461  CE2 TRP A  74     -17.669   4.483 -41.390  1.00 32.37           C  
ANISOU  461  CE2 TRP A  74     4751   3828   3721    728   -158      4
ATOM    462  CE3 TRP A  74     -18.797   5.171 -43.421  1.00 31.91           C  
ANISOU  462  CE3 TRP A  74     4746   3712   3668    744   -195    -10
ATOM    463  CZ2 TRP A  74     -18.441   3.312 -41.330  1.00 32.92           C  
ANISOU  463  CZ2 TRP A  74     4905   3826   3778    721   -218    -16
ATOM    464  CZ3 TRP A  74     -19.576   3.998 -43.375  1.00 32.42           C  
ANISOU  464  CZ3 TRP A  74     4891   3708   3720    731   -258    -28
ATOM    465  CH2 TRP A  74     -19.395   3.067 -42.333  1.00 33.09           C  
ANISOU  465  CH2 TRP A  74     4993   3784   3795    719   -270    -29
ATOM    466  H   TRP A  74     -15.907   6.025 -45.204  1.00 31.07           H  
ATOM    467  HA  TRP A  74     -15.610   8.866 -44.485  1.00 31.88           H  
ATOM    468  HB3 TRP A  74     -17.697   8.110 -43.345  1.00 31.72           H  
ATOM    469  HB2 TRP A  74     -16.463   8.587 -42.235  1.00 31.72           H  
ATOM    470  HD1 TRP A  74     -15.453   6.826 -40.610  1.00 31.72           H  
ATOM    471  HE1 TRP A  74     -16.371   4.611 -39.700  1.00 32.87           H  
ATOM    472  HE3 TRP A  74     -18.944   5.875 -44.225  1.00 31.91           H  
ATOM    473  HZ2 TRP A  74     -18.308   2.611 -40.519  1.00 32.92           H  
ATOM    474  HZ3 TRP A  74     -20.315   3.816 -44.144  1.00 32.42           H  
ATOM    475  HH2 TRP A  74     -19.991   2.168 -42.301  1.00 33.09           H  
ATOM    476  N   ASN A  75     -13.697   8.214 -42.832  1.00 34.51           N  
ANISOU  476  N   ASN A  75     4772   4395   3945    802     21    167
ATOM    477  CA  ASN A  75     -12.429   7.933 -42.161  1.00 35.16           C  
ANISOU  477  CA  ASN A  75     4806   4559   3992    825     53    215
ATOM    478  C   ASN A  75     -12.620   8.298 -40.692  1.00 34.88           C  
ANISOU  478  C   ASN A  75     4725   4518   4011    726     48    198
ATOM    479  O   ASN A  75     -13.336   9.257 -40.390  1.00 33.72           O  
ANISOU  479  O   ASN A  75     4569   4322   3922    647     29    164
ATOM    480  CB  ASN A  75     -11.263   8.747 -42.767  1.00 36.40           C  
ANISOU  480  CB  ASN A  75     4897   4820   4115    851     90    292
ATOM    481  CG  ASN A  75     -10.882   8.300 -44.175  1.00 40.91           C  
ANISOU  481  CG  ASN A  75     5516   5404   4623    965    101    310
ATOM    482  OD1 ASN A  75     -11.536   8.675 -45.140  1.00 45.16           O  
ANISOU  482  OD1 ASN A  75     6069   5912   5177    957     90    300
ATOM    483  ND2 ASN A  75      -9.837   7.495 -44.335  1.00 42.50           N  
ANISOU  483  ND2 ASN A  75     5753   5648   4749   1080    120    336
ATOM    484  H   ASN A  75     -14.178   9.052 -42.516  1.00 34.51           H  
ATOM    485  HA  ASN A  75     -12.212   6.866 -42.244  1.00 35.16           H  
ATOM    486  HB3 ASN A  75     -10.383   8.663 -42.129  1.00 36.40           H  
ATOM    487  HB2 ASN A  75     -11.514   9.808 -42.788  1.00 36.40           H  
ATOM    488 HD22 ASN A  75      -9.574   7.217 -45.268  1.00 42.50           H  
ATOM    489 HD21 ASN A  75      -9.254   7.222 -43.558  1.00 42.50           H  
ATOM    490  N   LEU A  76     -11.976   7.527 -39.813  1.00 33.83           N  
ANISOU  490  N   LEU A  76     4570   4431   3851    742     63    221
ATOM    491  CA  LEU A  76     -11.992   7.745 -38.373  1.00 33.86           C  
ANISOU  491  CA  LEU A  76     4534   4432   3899    654     58    206
ATOM    492  C   LEU A  76     -10.784   8.607 -37.992  1.00 35.03           C  
ANISOU  492  C   LEU A  76     4598   4672   4043    608     81    271
ATOM    493  O   LEU A  76      -9.679   8.330 -38.458  1.00 35.84           O  
ANISOU  493  O   LEU A  76     4667   4860   4093    667    106    336
ATOM    494  CB  LEU A  76     -11.926   6.386 -37.644  1.00 35.46           C  
ANISOU  494  CB  LEU A  76     4770   4621   4081    686     53    188
ATOM    495  CG  LEU A  76     -13.165   5.481 -37.830  1.00 37.81           C  
ANISOU  495  CG  LEU A  76     5155   4824   4387    703     15    130
ATOM    496  CD1 LEU A  76     -12.927   4.097 -37.203  1.00 38.61           C  
ANISOU  496  CD1 LEU A  76     5290   4919   4462    731      9    124
ATOM    497  CD2 LEU A  76     -14.459   6.121 -37.289  1.00 38.24           C  
ANISOU  497  CD2 LEU A  76     5199   4819   4511    611    -10     87
ATOM    498  H   LEU A  76     -11.328   6.821 -40.127  1.00 33.83           H  
ATOM    499  HA  LEU A  76     -12.908   8.259 -38.085  1.00 33.86           H  
ATOM    500  HB3 LEU A  76     -11.798   6.562 -36.576  1.00 35.46           H  
ATOM    501  HB2 LEU A  76     -11.029   5.854 -37.966  1.00 35.46           H  
ATOM    502  HG  LEU A  76     -13.300   5.315 -38.900  1.00 37.81           H  
ATOM    503 HD11 LEU A  76     -13.496   3.328 -37.727  1.00 38.61           H  
ATOM    504 HD12 LEU A  76     -11.877   3.804 -37.241  1.00 38.61           H  
ATOM    505 HD13 LEU A  76     -13.227   4.070 -36.154  1.00 38.61           H  
ATOM    506 HD21 LEU A  76     -15.040   5.433 -36.673  1.00 38.24           H  
ATOM    507 HD22 LEU A  76     -14.266   7.000 -36.674  1.00 38.24           H  
ATOM    508 HD23 LEU A  76     -15.102   6.428 -38.111  1.00 38.24           H  
ATOM    509  N   HIS A  77     -11.024   9.616 -37.155  1.00 35.28           N  
ANISOU  509  N   HIS A  77     4598   4684   4123    506     67    258
ATOM    510  CA  HIS A  77     -10.016  10.514 -36.608  1.00 36.81           C  
ANISOU  510  CA  HIS A  77     4724   4948   4314    439     71    318
ATOM    511  C   HIS A  77     -10.009  10.319 -35.089  1.00 33.60           C  
ANISOU  511  C   HIS A  77     4304   4535   3926    380     63    300
ATOM    512  O   HIS A  77     -11.072  10.115 -34.504  1.00 32.60           O  
ANISOU  512  O   HIS A  77     4214   4335   3836    353     49    236
ATOM    513  CB  HIS A  77     -10.352  11.967 -36.995  1.00 41.55           C  
ANISOU  513  CB  HIS A  77     5321   5520   4945    370     53    320
ATOM    514  CG  HIS A  77     -10.394  12.205 -38.486  1.00 50.13           C  
ANISOU  514  CG  HIS A  77     6413   6624   6009    428     63    347
ATOM    515  ND1 HIS A  77     -11.454  11.795 -39.281  1.00 53.39           N  
ANISOU  515  ND1 HIS A  77     6883   6961   6441    463     55    291
ATOM    516  CD2 HIS A  77      -9.487  12.784 -39.346  1.00 52.54           C  
ANISOU  516  CD2 HIS A  77     6671   7024   6268    470     84    428
ATOM    517  CE1 HIS A  77     -11.138  12.096 -40.540  1.00 54.22           C  
ANISOU  517  CE1 HIS A  77     6981   7107   6514    517     68    333
ATOM    518  NE2 HIS A  77      -9.976  12.725 -40.654  1.00 54.21           N  
ANISOU  518  NE2 HIS A  77     6916   7211   6471    527     88    417
ATOM    519  H   HIS A  77     -11.966   9.772 -36.797  1.00 35.28           H  
ATOM    520  HA  HIS A  77      -9.028  10.266 -37.002  1.00 36.81           H  
ATOM    521  HB3 HIS A  77      -9.609  12.640 -36.562  1.00 41.55           H  
ATOM    522  HB2 HIS A  77     -11.310  12.260 -36.560  1.00 41.55           H  
ATOM    523  HD1 HIS A  77     -12.281  11.298 -38.972  1.00 53.39           H  
ATOM    524  HD2 HIS A  77      -8.524  13.225 -39.129  1.00 52.54           H  
ATOM    525  HE1 HIS A  77     -11.757  11.842 -41.386  1.00 54.22           H  
ATOM    526  N   ARG A  78      -8.813  10.330 -34.496  1.00 32.35           N  
ANISOU  526  N   ARG A  78     4088   4461   3741    359     73    363
ATOM    527  CA  ARG A  78      -8.594  10.060 -33.080  1.00 32.16           C  
ANISOU  527  CA  ARG A  78     4049   4443   3727    309     66    355
ATOM    528  C   ARG A  78      -8.757  11.353 -32.270  1.00 33.51           C  
ANISOU  528  C   ARG A  78     4219   4582   3932    195     35    346
ATOM    529  O   ARG A  78      -8.003  12.296 -32.501  1.00 36.56           O  
ANISOU  529  O   ARG A  78     4581   4996   4313    142     20    396
ATOM    530  CB  ARG A  78      -7.176   9.467 -32.929  1.00 33.36           C  
ANISOU  530  CB  ARG A  78     4137   4711   3827    343     88    437
ATOM    531  CG  ARG A  78      -6.840   8.935 -31.526  1.00 35.04           C  
ANISOU  531  CG  ARG A  78     4334   4941   4041    313     87    433
ATOM    532  CD  ARG A  78      -5.440   8.286 -31.483  1.00 38.05           C  
ANISOU  532  CD  ARG A  78     4648   5447   4363    365    113    522
ATOM    533  NE  ARG A  78      -4.980   7.957 -30.118  1.00 36.68           N  
ANISOU  533  NE  ARG A  78     4451   5302   4184    341    113    529
ATOM    534  CZ  ARG A  78      -4.350   8.777 -29.257  1.00 35.48           C  
ANISOU  534  CZ  ARG A  78     4247   5195   4037    243     92    573
ATOM    535  NH1 ARG A  78      -3.979   8.336 -28.056  1.00 36.51           N  
ANISOU  535  NH1 ARG A  78     4358   5358   4157    233     95    581
ATOM    536  NH2 ARG A  78      -4.102  10.045 -29.569  1.00 35.50           N1+
ANISOU  536  NH2 ARG A  78     4224   5214   4052    152     64    614
ATOM    537  H   ARG A  78      -8.000  10.593 -35.027  1.00 32.35           H  
ATOM    538  HA  ARG A  78      -9.323   9.318 -32.742  1.00 32.16           H  
ATOM    539  HB3 ARG A  78      -6.438  10.220 -33.214  1.00 33.36           H  
ATOM    540  HB2 ARG A  78      -7.057   8.651 -33.639  1.00 33.36           H  
ATOM    541  HG3 ARG A  78      -7.578   8.151 -31.348  1.00 35.04           H  
ATOM    542  HG2 ARG A  78      -6.983   9.678 -30.739  1.00 35.04           H  
ATOM    543  HD3 ARG A  78      -4.701   8.833 -32.072  1.00 38.05           H  
ATOM    544  HD2 ARG A  78      -5.525   7.309 -31.958  1.00 38.05           H  
ATOM    545 HH22 ARG A  78      -3.751  10.702 -28.836  1.00 35.50           H  
ATOM    546 HH21 ARG A  78      -4.347  10.462 -30.450  1.00 35.50           H  
ATOM    547 HH12 ARG A  78      -3.727   9.028 -27.314  1.00 36.51           H  
ATOM    548 HH11 ARG A  78      -4.020   7.383 -27.741  1.00 36.51           H  
ATOM    549  HE  ARG A  78      -5.238   7.034 -29.801  1.00 36.68           H  
ATOM    550  N   ASN A  79      -9.700  11.348 -31.329  1.00 32.26           N  
ANISOU  550  N   ASN A  79     4094   4361   3803    160     23    285
ATOM    551  CA  ASN A  79      -9.970  12.430 -30.389  1.00 32.58           C  
ANISOU  551  CA  ASN A  79     4156   4358   3865     69     -7    268
ATOM    552  C   ASN A  79      -9.415  11.966 -29.033  1.00 32.42           C  
ANISOU  552  C   ASN A  79     4116   4367   3835     36    -10    274
ATOM    553  O   ASN A  79      -9.833  10.905 -28.564  1.00 32.29           O  
ANISOU  553  O   ASN A  79     4110   4333   3826     76      6    233
ATOM    554  CB  ASN A  79     -11.503  12.643 -30.359  1.00 34.47           C  
ANISOU  554  CB  ASN A  79     4457   4500   4140     80    -12    188
ATOM    555  CG  ASN A  79     -11.964  13.842 -29.534  1.00 39.82           C  
ANISOU  555  CG  ASN A  79     5179   5121   4832     16    -38    155
ATOM    556  OD1 ASN A  79     -11.682  13.925 -28.339  1.00 38.26           O  
ANISOU  556  OD1 ASN A  79     4983   4930   4626    -26    -49    154
ATOM    557  ND2 ASN A  79     -12.714  14.753 -30.135  1.00 44.20           N  
ANISOU  557  ND2 ASN A  79     5778   5613   5402     18    -48    123
ATOM    558  H   ASN A  79     -10.265  10.511 -31.176  1.00 32.26           H  
ATOM    559  HA  ASN A  79      -9.478  13.362 -30.677  1.00 32.58           H  
ATOM    560  HB3 ASN A  79     -12.020  11.756 -29.993  1.00 34.47           H  
ATOM    561  HB2 ASN A  79     -11.850  12.786 -31.382  1.00 34.47           H  
ATOM    562 HD22 ASN A  79     -13.070  15.550 -29.642  1.00 44.20           H  
ATOM    563 HD21 ASN A  79     -13.159  14.523 -31.042  1.00 44.20           H  
ATOM    564  N   GLU A  80      -8.492  12.725 -28.429  1.00 31.25           N  
ANISOU  564  N   GLU A  80     3941   4262   3670    -42    -34    328
ATOM    565  CA  GLU A  80      -7.839  12.393 -27.162  1.00 32.91           C  
ANISOU  565  CA  GLU A  80     4132   4506   3869    -79    -41    342
ATOM    566  C   GLU A  80      -8.109  13.504 -26.143  1.00 34.04           C  
ANISOU  566  C   GLU A  80     4325   4589   4019   -169    -83    317
ATOM    567  O   GLU A  80      -8.079  14.676 -26.510  1.00 35.20           O  
ANISOU  567  O   GLU A  80     4496   4718   4161   -234   -120    344
ATOM    568  CB  GLU A  80      -6.334  12.151 -27.384  1.00 35.53           C  
ANISOU  568  CB  GLU A  80     4383   4956   4163    -91    -38    443
ATOM    569  CG  GLU A  80      -5.546  11.788 -26.097  1.00 40.27           C  
ANISOU  569  CG  GLU A  80     4950   5605   4745   -127    -44    470
ATOM    570  CD  GLU A  80      -4.133  11.284 -26.383  1.00 43.10           C  
ANISOU  570  CD  GLU A  80     5218   6095   5062   -143    -44    585
ATOM    571  OE1 GLU A  80      -3.506  11.785 -27.336  1.00 44.82           O  
ANISOU  571  OE1 GLU A  80     5391   6378   5259   -104    -27    647
ATOM    572  OE2 GLU A  80      -3.763  10.242 -25.805  1.00 43.37           O1-
ANISOU  572  OE2 GLU A  80     5223   6173   5081   -193    -59    617
ATOM    573  H   GLU A  80      -8.283  13.651 -28.777  1.00 31.25           H  
ATOM    574  HA  GLU A  80      -8.248  11.465 -26.775  1.00 32.91           H  
ATOM    575  HB3 GLU A  80      -5.886  13.035 -27.843  1.00 35.53           H  
ATOM    576  HB2 GLU A  80      -6.221  11.340 -28.104  1.00 35.53           H  
ATOM    577  HG3 GLU A  80      -6.091  11.025 -25.539  1.00 40.27           H  
ATOM    578  HG2 GLU A  80      -5.458  12.655 -25.443  1.00 40.27           H  
ATOM    579  N   ASP A  81      -8.369  13.109 -24.893  1.00 33.11           N  
ANISOU  579  N   ASP A  81     4232   4441   3906   -171    -81    269
ATOM    580  CA  ASP A  81      -8.761  14.000 -23.801  1.00 33.43           C  
ANISOU  580  CA  ASP A  81     4335   4422   3942   -242   -120    242
ATOM    581  C   ASP A  81      -8.334  13.310 -22.487  1.00 34.66           C  
ANISOU  581  C   ASP A  81     4473   4612   4085   -259   -119    245
ATOM    582  O   ASP A  81      -8.952  12.303 -22.126  1.00 34.28           O  
ANISOU  582  O   ASP A  81     4420   4555   4049   -202    -86    200
ATOM    583  CB  ASP A  81     -10.284  14.267 -23.891  1.00 34.62           C  
ANISOU  583  CB  ASP A  81     4561   4479   4116   -203   -113    159
ATOM    584  CG  ASP A  81     -10.959  15.148 -22.838  1.00 38.31           C  
ANISOU  584  CG  ASP A  81     5112   4878   4567   -251   -149    124
ATOM    585  OD1 ASP A  81     -10.390  15.439 -21.761  1.00 39.79           O  
ANISOU  585  OD1 ASP A  81     5306   5083   4728   -320   -184    156
ATOM    586  OD2 ASP A  81     -12.158  15.430 -23.047  1.00 42.59           O1-
ANISOU  586  OD2 ASP A  81     5717   5351   5116   -215   -145     69
ATOM    587  H   ASP A  81      -8.396  12.116 -24.679  1.00 33.11           H  
ATOM    588  HA  ASP A  81      -8.263  14.960 -23.928  1.00 33.43           H  
ATOM    589  HB3 ASP A  81     -10.796  13.306 -23.893  1.00 34.62           H  
ATOM    590  HB2 ASP A  81     -10.502  14.706 -24.866  1.00 34.62           H  
ATOM    591  N   PRO A  82      -7.262  13.784 -21.810  1.00 35.45           N  
ANISOU  591  N   PRO A  82     4557   4752   4158   -343   -158    303
ATOM    592  CA  PRO A  82      -6.758  13.118 -20.591  1.00 36.50           C  
ANISOU  592  CA  PRO A  82     4669   4925   4277   -360   -158    311
ATOM    593  C   PRO A  82      -7.684  13.225 -19.364  1.00 36.16           C  
ANISOU  593  C   PRO A  82     4702   4802   4236   -359   -164    234
ATOM    594  O   PRO A  82      -7.582  12.386 -18.465  1.00 38.26           O  
ANISOU  594  O   PRO A  82     4951   5094   4493   -360   -157    230
ATOM    595  CB  PRO A  82      -5.392  13.777 -20.352  1.00 38.32           C  
ANISOU  595  CB  PRO A  82     4872   5214   4476   -466   -211    399
ATOM    596  CG  PRO A  82      -5.515  15.160 -20.970  1.00 38.96           C  
ANISOU  596  CG  PRO A  82     4994   5255   4555   -519   -251    419
ATOM    597  CD  PRO A  82      -6.437  14.942 -22.166  1.00 36.92           C  
ANISOU  597  CD  PRO A  82     4744   4958   4325   -432   -209    373
ATOM    598  HA  PRO A  82      -6.601  12.055 -20.783  1.00 36.50           H  
ATOM    599  HB3 PRO A  82      -4.627  13.207 -20.881  1.00 38.32           H  
ATOM    600  HB2 PRO A  82      -5.100  13.819 -19.301  1.00 38.32           H  
ATOM    601  HG3 PRO A  82      -4.554  15.602 -21.237  1.00 38.96           H  
ATOM    602  HG2 PRO A  82      -5.996  15.830 -20.255  1.00 38.96           H  
ATOM    603  HD2 PRO A  82      -7.026  15.841 -22.360  1.00 36.92           H  
ATOM    604  HD3 PRO A  82      -5.864  14.703 -23.064  1.00 36.92           H  
ATOM    605  N   GLU A  83      -8.585  14.216 -19.358  1.00 34.54           N  
ANISOU  605  N   GLU A  83     4581   4508   4035   -359   -180    181
ATOM    606  CA  GLU A  83      -9.568  14.453 -18.304  1.00 34.41           C  
ANISOU  606  CA  GLU A  83     4640   4424   4010   -338   -180    112
ATOM    607  C   GLU A  83     -10.849  13.623 -18.487  1.00 34.85           C  
ANISOU  607  C   GLU A  83     4681   4465   4096   -241   -124     56
ATOM    608  O   GLU A  83     -11.771  13.758 -17.681  1.00 34.62           O  
ANISOU  608  O   GLU A  83     4701   4393   4060   -207   -114      5
ATOM    609  CB  GLU A  83      -9.862  15.968 -18.225  1.00 37.22           C  
ANISOU  609  CB  GLU A  83     5107   4692   4344   -376   -228     87
ATOM    610  CG  GLU A  83      -8.674  16.801 -17.702  1.00 38.92           C  
ANISOU  610  CG  GLU A  83     5359   4906   4521   -488   -300    140
ATOM    611  CD  GLU A  83      -8.303  16.425 -16.270  1.00 46.89           C  
ANISOU  611  CD  GLU A  83     6383   5931   5505   -518   -315    137
ATOM    612  OE1 GLU A  83      -9.187  16.527 -15.392  1.00 44.86           O  
ANISOU  612  OE1 GLU A  83     6192   5619   5233   -469   -302     72
ATOM    613  OE2 GLU A  83      -7.165  15.964 -16.056  1.00 49.72           O1-
ANISOU  613  OE2 GLU A  83     6678   6361   5853   -586   -339    205
ATOM    614  H   GLU A  83      -8.678  14.825 -20.164  1.00 34.54           H  
ATOM    615  HA  GLU A  83      -9.161  14.129 -17.349  1.00 34.41           H  
ATOM    616  HB3 GLU A  83     -10.734  16.158 -17.598  1.00 37.22           H  
ATOM    617  HB2 GLU A  83     -10.115  16.341 -19.214  1.00 37.22           H  
ATOM    618  HG3 GLU A  83      -8.929  17.861 -17.716  1.00 38.92           H  
ATOM    619  HG2 GLU A  83      -7.809  16.689 -18.358  1.00 38.92           H  
ATOM    620  N   ARG A  84     -10.898  12.784 -19.526  1.00 34.17           N  
ANISOU  620  N   ARG A  84     4531   4417   4036   -195    -91     71
ATOM    621  CA  ARG A  84     -12.046  11.970 -19.882  1.00 33.42           C  
ANISOU  621  CA  ARG A  84     4425   4306   3968   -119    -52     30
ATOM    622  C   ARG A  84     -11.691  10.482 -19.792  1.00 32.36           C  
ANISOU  622  C   ARG A  84     4227   4227   3842    -87    -26     48
ATOM    623  O   ARG A  84     -10.551  10.091 -20.050  1.00 33.40           O  
ANISOU  623  O   ARG A  84     4313   4416   3962   -100    -27     98
ATOM    624  CB  ARG A  84     -12.458  12.375 -21.305  1.00 32.53           C  
ANISOU  624  CB  ARG A  84     4317   4170   3875    -91    -48     28
ATOM    625  CG  ARG A  84     -13.712  11.700 -21.891  1.00 32.28           C  
ANISOU  625  CG  ARG A  84     4274   4121   3870    -21    -18     -5
ATOM    626  CD  ARG A  84     -14.002  12.167 -23.329  1.00 31.87           C  
ANISOU  626  CD  ARG A  84     4226   4052   3833      1    -18     -1
ATOM    627  NE  ARG A  84     -13.021  11.656 -24.308  1.00 30.06           N  
ANISOU  627  NE  ARG A  84     3954   3871   3598     -2    -17     47
ATOM    628  CZ  ARG A  84     -12.657  12.221 -25.472  1.00 33.80           C  
ANISOU  628  CZ  ARG A  84     4427   4343   4072     -2    -24     69
ATOM    629  NH1 ARG A  84     -11.705  11.658 -26.203  1.00 34.43           N  
ANISOU  629  NH1 ARG A  84     4464   4480   4139      9    -18    119
ATOM    630  NH2 ARG A  84     -13.208  13.345 -25.932  1.00 33.15           N1+
ANISOU  630  NH2 ARG A  84     4390   4208   3998     -9    -37     46
ATOM    631  H   ARG A  84     -10.101  12.724 -20.148  1.00 34.17           H  
ATOM    632  HA  ARG A  84     -12.872  12.183 -19.209  1.00 33.42           H  
ATOM    633  HB3 ARG A  84     -11.611  12.214 -21.973  1.00 32.53           H  
ATOM    634  HB2 ARG A  84     -12.642  13.447 -21.291  1.00 32.53           H  
ATOM    635  HG3 ARG A  84     -14.585  11.849 -21.256  1.00 32.28           H  
ATOM    636  HG2 ARG A  84     -13.544  10.624 -21.911  1.00 32.28           H  
ATOM    637  HD3 ARG A  84     -13.889  13.250 -23.330  1.00 31.87           H  
ATOM    638  HD2 ARG A  84     -15.030  11.976 -23.628  1.00 31.87           H  
ATOM    639 HH22 ARG A  84     -12.870  13.763 -26.803  1.00 33.15           H  
ATOM    640 HH21 ARG A  84     -13.850  13.890 -25.382  1.00 33.15           H  
ATOM    641 HH12 ARG A  84     -11.429  12.079 -27.087  1.00 34.43           H  
ATOM    642 HH11 ARG A  84     -11.062  10.962 -25.833  1.00 34.43           H  
ATOM    643  HE  ARG A  84     -12.647  10.735 -24.065  1.00 30.06           H  
ATOM    644  N   TYR A  85     -12.694   9.658 -19.487  1.00 31.03           N  
ANISOU  644  N   TYR A  85     4056   4045   3690    -40     -3     14
ATOM    645  CA  TYR A  85     -12.665   8.216 -19.689  1.00 30.44           C  
ANISOU  645  CA  TYR A  85     3940   4003   3622     -5     16     27
ATOM    646  C   TYR A  85     -13.923   7.835 -20.514  1.00 29.61           C  
ANISOU  646  C   TYR A  85     3842   3865   3543     45     26      3
ATOM    647  O   TYR A  85     -15.025   8.182 -20.083  1.00 28.99           O  
ANISOU  647  O   TYR A  85     3783   3756   3476     54     30    -27
ATOM    648  CB  TYR A  85     -12.590   7.503 -18.325  1.00 32.41           C  
ANISOU  648  CB  TYR A  85     4181   4270   3864    -11     23     19
ATOM    649  CG  TYR A  85     -12.569   5.991 -18.447  1.00 31.63           C  
ANISOU  649  CG  TYR A  85     4054   4195   3770     26     35     32
ATOM    650  CD1 TYR A  85     -13.772   5.263 -18.578  1.00 33.54           C  
ANISOU  650  CD1 TYR A  85     4303   4408   4032     61     40     12
ATOM    651  CD2 TYR A  85     -11.336   5.312 -18.476  1.00 32.22           C  
ANISOU  651  CD2 TYR A  85     4099   4321   3823     26     38     69
ATOM    652  CE1 TYR A  85     -13.738   3.871 -18.778  1.00 33.62           C  
ANISOU  652  CE1 TYR A  85     4307   4425   4040     92     40     26
ATOM    653  CE2 TYR A  85     -11.304   3.918 -18.657  1.00 33.44           C  
ANISOU  653  CE2 TYR A  85     4245   4487   3973     72     47     80
ATOM    654  CZ  TYR A  85     -12.501   3.200 -18.821  1.00 35.78           C  
ANISOU  654  CZ  TYR A  85     4566   4741   4289    102     44     56
ATOM    655  OH  TYR A  85     -12.444   1.858 -19.029  1.00 37.07           O  
ANISOU  655  OH  TYR A  85     4742   4901   4441    144     41     66
ATOM    656  H   TYR A  85     -13.601  10.054 -19.227  1.00 31.03           H  
ATOM    657  HA  TYR A  85     -11.749   7.938 -20.196  1.00 30.44           H  
ATOM    658  HB3 TYR A  85     -13.401   7.786 -17.667  1.00 32.41           H  
ATOM    659  HB2 TYR A  85     -11.688   7.825 -17.801  1.00 32.41           H  
ATOM    660  HD1 TYR A  85     -14.725   5.773 -18.551  1.00 33.54           H  
ATOM    661  HD2 TYR A  85     -10.407   5.852 -18.367  1.00 32.22           H  
ATOM    662  HE1 TYR A  85     -14.667   3.335 -18.899  1.00 33.62           H  
ATOM    663  HE2 TYR A  85     -10.357   3.397 -18.676  1.00 33.44           H  
ATOM    664  HH  TYR A  85     -13.297   1.418 -19.044  1.00 37.07           H  
ATOM    665  N   PRO A  86     -13.784   7.120 -21.657  1.00 30.04           N  
ANISOU  665  N   PRO A  86     3886   3925   3601     79     29     19
ATOM    666  CA  PRO A  86     -12.523   6.725 -22.312  1.00 30.50           C  
ANISOU  666  CA  PRO A  86     3922   4030   3638     91     31     61
ATOM    667  C   PRO A  86     -11.742   7.944 -22.830  1.00 30.22           C  
ANISOU  667  C   PRO A  86     3880   4009   3592     56     22     87
ATOM    668  O   PRO A  86     -12.335   8.872 -23.380  1.00 29.59           O  
ANISOU  668  O   PRO A  86     3826   3890   3527     46     14     68
ATOM    669  CB  PRO A  86     -12.976   5.796 -23.452  1.00 32.37           C  
ANISOU  669  CB  PRO A  86     4171   4251   3877    149     34     59
ATOM    670  CG  PRO A  86     -14.385   6.248 -23.786  1.00 34.35           C  
ANISOU  670  CG  PRO A  86     4447   4446   4157    151     26     22
ATOM    671  CD  PRO A  86     -14.944   6.676 -22.434  1.00 31.01           C  
ANISOU  671  CD  PRO A  86     4024   4013   3746    115     28     -1
ATOM    672  HA  PRO A  86     -11.903   6.153 -21.620  1.00 30.50           H  
ATOM    673  HB3 PRO A  86     -13.001   4.767 -23.095  1.00 32.37           H  
ATOM    674  HB2 PRO A  86     -12.326   5.817 -24.328  1.00 32.37           H  
ATOM    675  HG3 PRO A  86     -14.981   5.482 -24.284  1.00 34.35           H  
ATOM    676  HG2 PRO A  86     -14.338   7.112 -24.452  1.00 34.35           H  
ATOM    677  HD2 PRO A  86     -15.699   7.456 -22.549  1.00 31.01           H  
ATOM    678  HD3 PRO A  86     -15.410   5.831 -21.923  1.00 31.01           H  
ATOM    679  N   SER A  87     -10.427   7.949 -22.595  1.00 30.54           N  
ANISOU  679  N   SER A  87     3885   4113   3607     37     21    138
ATOM    680  CA ASER A  87      -9.572   9.080 -22.946  0.50 31.24           C  
ANISOU  680  CA ASER A  87     3961   4226   3683    -11      3    180
ATOM    681  CA BSER A  87      -9.530   9.019 -23.013  0.50 30.98           C  
ANISOU  681  CA BSER A  87     3927   4196   3650    -10      4    181
ATOM    682  C   SER A  87      -9.428   9.248 -24.468  1.00 31.04           C  
ANISOU  682  C   SER A  87     3931   4205   3658     31     11    198
ATOM    683  O   SER A  87      -9.357  10.380 -24.939  1.00 32.29           O  
ANISOU  683  O   SER A  87     4098   4353   3819     -7     -6    212
ATOM    684  CB ASER A  87      -8.223   8.940 -22.215  0.50 33.87           C  
ANISOU  684  CB ASER A  87     4243   4642   3985    -46     -3    247
ATOM    685  CB BSER A  87      -8.100   8.763 -22.557  0.50 32.89           C  
ANISOU  685  CB BSER A  87     4114   4523   3859    -36      1    249
ATOM    686  OG ASER A  87      -7.400  10.066 -22.405  0.50 36.92           O  
ANISOU  686  OG ASER A  87     4620   5047   4360   -110    -31    293
ATOM    687  OG BSER A  87      -7.555   7.599 -23.154  0.50 35.08           O  
ANISOU  687  OG BSER A  87     4355   4857   4114     38     29    282
ATOM    688  H   SER A  87      -9.983   7.185 -22.113  1.00 30.54           H  
ATOM    689  HA ASER A  87     -10.060   9.986 -22.582  0.50 31.24           H  
ATOM    690  HA BSER A  87      -9.892   9.944 -22.563  0.50 30.98           H  
ATOM    691  HB3ASER A  87      -7.682   8.057 -22.559  0.50 33.87           H  
ATOM    692  HB3BSER A  87      -8.079   8.658 -21.472  0.50 32.89           H  
ATOM    693  HB2ASER A  87      -8.384   8.829 -21.143  0.50 33.87           H  
ATOM    694  HB2BSER A  87      -7.480   9.624 -22.808  0.50 32.89           H  
ATOM    695  HG ASER A  87      -7.929  10.857 -22.198  0.50 36.92           H  
ATOM    696  HG BSER A  87      -6.656   7.471 -22.844  0.50 35.08           H  
ATOM    697  N   VAL A  88      -9.489   8.140 -25.213  1.00 28.96           N  
ANISOU  697  N   VAL A  88     3663   3952   3388    108     33    197
ATOM    698  CA  VAL A  88      -9.455   8.130 -26.667  1.00 30.64           C  
ANISOU  698  CA  VAL A  88     3878   4169   3593    158     41    214
ATOM    699  C   VAL A  88     -10.854   7.752 -27.171  1.00 29.94           C  
ANISOU  699  C   VAL A  88     3840   4007   3530    199     40    156
ATOM    700  O   VAL A  88     -11.413   6.764 -26.696  1.00 30.79           O  
ANISOU  700  O   VAL A  88     3968   4090   3641    231     42    129
ATOM    701  CB  VAL A  88      -8.430   7.088 -27.193  1.00 32.43           C  
ANISOU  701  CB  VAL A  88     4071   4477   3775    228     64    272
ATOM    702  CG1 VAL A  88      -8.412   6.964 -28.731  1.00 33.89           C  
ANISOU  702  CG1 VAL A  88     4270   4666   3943    299     75    286
ATOM    703  CG2 VAL A  88      -7.018   7.423 -26.681  1.00 33.01           C  
ANISOU  703  CG2 VAL A  88     4079   4642   3821    182     63    347
ATOM    704  H   VAL A  88      -9.734   7.265 -24.779  1.00 28.96           H  
ATOM    705  HA  VAL A  88      -9.167   9.108 -27.049  1.00 30.64           H  
ATOM    706  HB  VAL A  88      -8.693   6.105 -26.797  1.00 32.43           H  
ATOM    707 HG11 VAL A  88      -7.597   6.329 -29.074  1.00 33.89           H  
ATOM    708 HG12 VAL A  88      -9.333   6.531 -29.122  1.00 33.89           H  
ATOM    709 HG13 VAL A  88      -8.295   7.946 -29.190  1.00 33.89           H  
ATOM    710 HG21 VAL A  88      -6.285   6.699 -27.033  1.00 33.01           H  
ATOM    711 HG22 VAL A  88      -6.707   8.416 -27.010  1.00 33.01           H  
ATOM    712 HG23 VAL A  88      -6.968   7.419 -25.592  1.00 33.01           H  
ATOM    713  N   ILE A  89     -11.371   8.537 -28.116  1.00 27.49           N  
ANISOU  713  N   ILE A  89     3548   3661   3236    195     33    144
ATOM    714  CA  ILE A  89     -12.582   8.264 -28.882  1.00 28.78           C  
ANISOU  714  CA  ILE A  89     3753   3762   3421    230     28    100
ATOM    715  C   ILE A  89     -12.190   8.398 -30.365  1.00 31.15           C  
ANISOU  715  C   ILE A  89     4056   4075   3704    274     33    125
ATOM    716  O   ILE A  89     -11.283   9.170 -30.683  1.00 32.93           O  
ANISOU  716  O   ILE A  89     4256   4334   3922    246     33    162
ATOM    717  CB  ILE A  89     -13.721   9.269 -28.517  1.00 31.13           C  
ANISOU  717  CB  ILE A  89     4072   4004   3753    186     16     59
ATOM    718  CG1 ILE A  89     -14.162   9.045 -27.052  1.00 33.42           C  
ANISOU  718  CG1 ILE A  89     4359   4286   4051    157     16     35
ATOM    719  CG2 ILE A  89     -14.954   9.221 -29.455  1.00 33.77           C  
ANISOU  719  CG2 ILE A  89     4435   4287   4108    221     10     27
ATOM    720  CD1 ILE A  89     -15.227  10.019 -26.546  1.00 35.32           C  
ANISOU  720  CD1 ILE A  89     4624   4486   4313    133     10      1
ATOM    721  H   ILE A  89     -10.825   9.321 -28.476  1.00 27.49           H  
ATOM    722  HA  ILE A  89     -12.925   7.241 -28.703  1.00 28.78           H  
ATOM    723  HB  ILE A  89     -13.313  10.279 -28.589  1.00 31.13           H  
ATOM    724 HG13 ILE A  89     -13.306   9.105 -26.381  1.00 33.42           H  
ATOM    725 HG12 ILE A  89     -14.537   8.028 -26.947  1.00 33.42           H  
ATOM    726 HG21 ILE A  89     -15.711   9.946 -29.161  1.00 33.77           H  
ATOM    727 HG22 ILE A  89     -14.707   9.476 -30.484  1.00 33.77           H  
ATOM    728 HG23 ILE A  89     -15.424   8.238 -29.456  1.00 33.77           H  
ATOM    729 HD11 ILE A  89     -15.208  10.074 -25.460  1.00 35.32           H  
ATOM    730 HD12 ILE A  89     -15.074  11.025 -26.942  1.00 35.32           H  
ATOM    731 HD13 ILE A  89     -16.223   9.690 -26.842  1.00 35.32           H  
ATOM    732  N   TRP A  90     -12.849   7.635 -31.243  1.00 31.54           N  
ANISOU  732  N   TRP A  90     4140   4099   3746    337     31    111
ATOM    733  CA  TRP A  90     -12.652   7.703 -32.688  1.00 33.18           C  
ANISOU  733  CA  TRP A  90     4360   4315   3931    391     36    132
ATOM    734  C   TRP A  90     -13.934   8.251 -33.319  1.00 35.80           C  
ANISOU  734  C   TRP A  90     4724   4580   4297    377     19     92
ATOM    735  O   TRP A  90     -15.006   7.698 -33.074  1.00 38.22           O  
ANISOU  735  O   TRP A  90     5061   4836   4624    377      2     54
ATOM    736  CB  TRP A  90     -12.301   6.316 -33.249  1.00 34.42           C  
ANISOU  736  CB  TRP A  90     4554   4481   4043    480     40    141
ATOM    737  CG  TRP A  90     -10.937   5.809 -32.887  1.00 37.17           C  
ANISOU  737  CG  TRP A  90     4865   4911   4347    512     64    193
ATOM    738  CD1 TRP A  90     -10.626   5.088 -31.788  1.00 38.95           C  
ANISOU  738  CD1 TRP A  90     5081   5154   4566    504     67    194
ATOM    739  CD2 TRP A  90      -9.677   6.025 -33.593  1.00 38.29           C  
ANISOU  739  CD2 TRP A  90     4967   5140   4442    561     90    260
ATOM    740  NE1 TRP A  90      -9.275   4.799 -31.790  1.00 39.67           N  
ANISOU  740  NE1 TRP A  90     5127   5338   4609    544     93    257
ATOM    741  CE2 TRP A  90      -8.640   5.348 -32.882  1.00 39.68           C  
ANISOU  741  CE2 TRP A  90     5104   5388   4583    579    108    303
ATOM    742  CE3 TRP A  90      -9.308   6.706 -34.773  1.00 39.94           C  
ANISOU  742  CE3 TRP A  90     5163   5380   4633    590    100    295
ATOM    743  CZ2 TRP A  90      -7.310   5.328 -33.339  1.00 41.26           C  
ANISOU  743  CZ2 TRP A  90     5248   5699   4729    629    137    385
ATOM    744  CZ3 TRP A  90      -7.982   6.683 -35.250  1.00 41.02           C  
ANISOU  744  CZ3 TRP A  90     5246   5626   4716    640    129    376
ATOM    745  CH2 TRP A  90      -6.983   5.992 -34.534  1.00 41.45           C  
ANISOU  745  CH2 TRP A  90     5257   5758   4734    660    148    423
ATOM    746  H   TRP A  90     -13.663   7.117 -30.949  1.00 31.54           H  
ATOM    747  HA  TRP A  90     -11.830   8.372 -32.939  1.00 33.18           H  
ATOM    748  HB3 TRP A  90     -12.346   6.346 -34.338  1.00 34.42           H  
ATOM    749  HB2 TRP A  90     -13.046   5.579 -32.948  1.00 34.42           H  
ATOM    750  HD1 TRP A  90     -11.352   4.772 -31.051  1.00 38.95           H  
ATOM    751  HE1 TRP A  90      -8.857   4.196 -31.095  1.00 39.67           H  
ATOM    752  HE3 TRP A  90     -10.060   7.245 -35.326  1.00 39.94           H  
ATOM    753  HZ2 TRP A  90      -6.553   4.788 -32.790  1.00 41.26           H  
ATOM    754  HZ3 TRP A  90      -7.738   7.196 -36.170  1.00 41.02           H  
ATOM    755  HH2 TRP A  90      -5.969   5.968 -34.909  1.00 41.45           H  
ATOM    756  N   GLU A  91     -13.786   9.332 -34.089  1.00 33.46           N  
ANISOU  756  N   GLU A  91     4419   4289   4006    366     21    107
ATOM    757  CA  GLU A  91     -14.877  10.101 -34.677  1.00 33.74           C  
ANISOU  757  CA  GLU A  91     4480   4265   4073    354      6     73
ATOM    758  C   GLU A  91     -14.816   9.984 -36.209  1.00 33.80           C  
ANISOU  758  C   GLU A  91     4512   4269   4061    411      6     84
ATOM    759  O   GLU A  91     -13.765  10.228 -36.809  1.00 34.66           O  
ANISOU  759  O   GLU A  91     4600   4431   4137    439     21    130
ATOM    760  CB  GLU A  91     -14.757  11.564 -34.192  1.00 37.75           C  
ANISOU  760  CB  GLU A  91     4972   4774   4598    292      4     81
ATOM    761  CG  GLU A  91     -14.875  11.675 -32.651  1.00 47.63           C  
ANISOU  761  CG  GLU A  91     6212   6025   5860    239      2     69
ATOM    762  CD  GLU A  91     -14.771  13.089 -32.073  1.00 61.47           C  
ANISOU  762  CD  GLU A  91     7980   7750   7627    183    -10     58
ATOM    763  OE1 GLU A  91     -14.047  13.930 -32.647  1.00 64.91           O  
ANISOU  763  OE1 GLU A  91     8409   8206   8050    146    -19     96
ATOM    764  OE2 GLU A  91     -15.348  13.292 -30.985  1.00 65.90           O1-
ANISOU  764  OE2 GLU A  91     8564   8268   8207    177    -14     17
ATOM    765  H   GLU A  91     -12.855   9.724 -34.215  1.00 33.46           H  
ATOM    766  HA  GLU A  91     -15.840   9.714 -34.340  1.00 33.74           H  
ATOM    767  HB3 GLU A  91     -15.531  12.179 -34.653  1.00 37.75           H  
ATOM    768  HB2 GLU A  91     -13.806  11.991 -34.517  1.00 37.75           H  
ATOM    769  HG3 GLU A  91     -14.076  11.108 -32.175  1.00 47.63           H  
ATOM    770  HG2 GLU A  91     -15.810  11.219 -32.321  1.00 47.63           H  
ATOM    771  N   ALA A  92     -15.930   9.575 -36.823  1.00 33.20           N  
ANISOU  771  N   ALA A  92     4476   4137   3999    432    -14     50
ATOM    772  CA  ALA A  92     -16.079   9.444 -38.265  1.00 32.54           C  
ANISOU  772  CA  ALA A  92     4427   4042   3893    490    -19     57
ATOM    773  C   ALA A  92     -16.325  10.803 -38.926  1.00 33.79           C  
ANISOU  773  C   ALA A  92     4574   4195   4071    469    -17     63
ATOM    774  O   ALA A  92     -17.189  11.554 -38.474  1.00 34.02           O  
ANISOU  774  O   ALA A  92     4596   4194   4137    420    -24     40
ATOM    775  CB  ALA A  92     -17.262   8.521 -38.570  1.00 32.81           C  
ANISOU  775  CB  ALA A  92     4518   4017   3933    512    -52     24
ATOM    776  H   ALA A  92     -16.751   9.352 -36.261  1.00 33.20           H  
ATOM    777  HA  ALA A  92     -15.175   8.989 -38.669  1.00 32.54           H  
ATOM    778  HB1 ALA A  92     -17.394   8.390 -39.644  1.00 32.81           H  
ATOM    779  HB2 ALA A  92     -17.118   7.535 -38.130  1.00 32.81           H  
ATOM    780  HB3 ALA A  92     -18.194   8.929 -38.178  1.00 32.81           H  
ATOM    781  N   LYS A  93     -15.622  11.054 -40.032  1.00 33.00           N  
ANISOU  781  N   LYS A  93     4476   4123   3939    515     -6     94
ATOM    782  CA  LYS A  93     -15.894  12.161 -40.938  1.00 34.59           C  
ANISOU  782  CA  LYS A  93     4673   4315   4154    501     -7    103
ATOM    783  C   LYS A  93     -16.080  11.560 -42.336  1.00 33.14           C  
ANISOU  783  C   LYS A  93     4534   4114   3944    572    -15     99
ATOM    784  O   LYS A  93     -15.234  10.766 -42.759  1.00 32.61           O  
ANISOU  784  O   LYS A  93     4481   4082   3826    641     -3    126
ATOM    785  CB  LYS A  93     -14.707  13.144 -40.899  1.00 39.51           C  
ANISOU  785  CB  LYS A  93     5249   5004   4761    476     11    161
ATOM    786  CG  LYS A  93     -14.936  14.445 -41.687  1.00 49.18           C  
ANISOU  786  CG  LYS A  93     6475   6206   6004    445      3    167
ATOM    787  CD  LYS A  93     -13.698  15.353 -41.676  1.00 56.44           C  
ANISOU  787  CD  LYS A  93     7350   7186   6909    398      8    233
ATOM    788  CE  LYS A  93     -13.955  16.693 -42.385  1.00 61.63           C  
ANISOU  788  CE  LYS A  93     8024   7805   7587    360     -8    233
ATOM    789  NZ  LYS A  93     -12.729  17.512 -42.459  1.00 65.27           N1+
ANISOU  789  NZ  LYS A  93     8445   8328   8027    316    -11    312
ATOM    790  H   LYS A  93     -14.923  10.385 -40.338  1.00 33.00           H  
ATOM    791  HA  LYS A  93     -16.807  12.688 -40.653  1.00 34.59           H  
ATOM    792  HB3 LYS A  93     -13.820  12.642 -41.281  1.00 39.51           H  
ATOM    793  HB2 LYS A  93     -14.494  13.399 -39.859  1.00 39.51           H  
ATOM    794  HG3 LYS A  93     -15.790  14.971 -41.257  1.00 49.18           H  
ATOM    795  HG2 LYS A  93     -15.203  14.218 -42.720  1.00 49.18           H  
ATOM    796  HD3 LYS A  93     -12.872  14.820 -42.152  1.00 56.44           H  
ATOM    797  HD2 LYS A  93     -13.395  15.525 -40.641  1.00 56.44           H  
ATOM    798  HE3 LYS A  93     -14.729  17.251 -41.854  1.00 61.63           H  
ATOM    799  HE2 LYS A  93     -14.327  16.517 -43.397  1.00 61.63           H  
ATOM    800  HZ1 LYS A  93     -12.027  17.029 -43.003  1.00 65.27           H  
ATOM    801  HZ2 LYS A  93     -12.932  18.400 -42.898  1.00 65.27           H  
ATOM    802  HZ3 LYS A  93     -12.373  17.676 -41.527  1.00 65.27           H  
ATOM    803  N   CYS A  94     -17.161  11.941 -43.028  1.00 32.76           N  
ANISOU  803  N   CYS A  94     4512   4012   3923    563    -35     70
ATOM    804  CA  CYS A  94     -17.458  11.491 -44.392  1.00 32.82           C  
ANISOU  804  CA  CYS A  94     4569   3996   3905    625    -50     65
ATOM    805  C   CYS A  94     -16.451  12.096 -45.390  1.00 33.62           C  
ANISOU  805  C   CYS A  94     4656   4151   3968    670    -24    113
ATOM    806  O   CYS A  94     -16.022  13.236 -45.196  1.00 33.77           O  
ANISOU  806  O   CYS A  94     4627   4202   4002    626     -9    142
ATOM    807  CB  CYS A  94     -18.908  11.860 -44.776  1.00 33.80           C  
ANISOU  807  CB  CYS A  94     4714   4063   4068    599    -76     32
ATOM    808  SG  CYS A  94     -20.169  11.668 -43.469  1.00 34.47           S  
ANISOU  808  SG  CYS A  94     4796   4104   4196    545   -104     -5
ATOM    809  H   CYS A  94     -17.839  12.565 -42.616  1.00 32.76           H  
ATOM    810  HA  CYS A  94     -17.372  10.405 -44.416  1.00 32.82           H  
ATOM    811  HB3 CYS A  94     -19.206  11.255 -45.632  1.00 33.80           H  
ATOM    812  HB2 CYS A  94     -18.961  12.896 -45.116  1.00 33.80           H  
ATOM    813  N   ARG A  95     -16.080  11.337 -46.427  1.00 33.43           N  
ANISOU  813  N   ARG A  95     4677   4136   3888    758    -24    124
ATOM    814  CA  ARG A  95     -15.095  11.770 -47.428  1.00 34.63           C  
ANISOU  814  CA  ARG A  95     4810   4354   3995    813      5    178
ATOM    815  C   ARG A  95     -15.637  12.790 -48.439  1.00 34.43           C  
ANISOU  815  C   ARG A  95     4788   4308   3987    804     -2    179
ATOM    816  O   ARG A  95     -14.851  13.543 -49.011  1.00 35.70           O  
ANISOU  816  O   ARG A  95     4906   4528   4130    810     22    232
ATOM    817  CB  ARG A  95     -14.575  10.558 -48.219  1.00 38.09           C  
ANISOU  817  CB  ARG A  95     5310   4805   4357    929      9    188
ATOM    818  CG  ARG A  95     -13.843   9.535 -47.362  1.00 43.73           C  
ANISOU  818  CG  ARG A  95     6013   5566   5038    960     28    209
ATOM    819  CD  ARG A  95     -13.289   8.374 -48.195  1.00 47.14           C  
ANISOU  819  CD  ARG A  95     6496   6039   5376   1096     47    241
ATOM    820  NE  ARG A  95     -12.834   7.311 -47.298  1.00 50.22           N  
ANISOU  820  NE  ARG A  95     6912   6430   5741   1124     46    232
ATOM    821  CZ  ARG A  95     -12.546   6.034 -47.552  1.00 50.78           C  
ANISOU  821  CZ  ARG A  95     7080   6473   5742   1228     35    218
ATOM    822  NH1 ARG A  95     -12.556   5.527 -48.785  1.00 50.18           N  
ANISOU  822  NH1 ARG A  95     7088   6375   5604   1328     27    217
ATOM    823  NH2 ARG A  95     -12.234   5.262 -46.521  1.00 48.14           N1+
ANISOU  823  NH2 ARG A  95     6767   6130   5392   1238     30    208
ATOM    824  H   ARG A  95     -16.468  10.400 -46.532  1.00 33.43           H  
ATOM    825  HA  ARG A  95     -14.256  12.245 -46.915  1.00 34.63           H  
ATOM    826  HB3 ARG A  95     -13.899  10.897 -49.006  1.00 38.09           H  
ATOM    827  HB2 ARG A  95     -15.408  10.075 -48.730  1.00 38.09           H  
ATOM    828  HG3 ARG A  95     -14.441   9.188 -46.519  1.00 43.73           H  
ATOM    829  HG2 ARG A  95     -12.999  10.074 -46.927  1.00 43.73           H  
ATOM    830  HD3 ARG A  95     -12.381   8.713 -48.698  1.00 47.14           H  
ATOM    831  HD2 ARG A  95     -13.975   8.043 -48.975  1.00 47.14           H  
ATOM    832 HH22 ARG A  95     -11.904   4.302 -46.672  1.00 48.14           H  
ATOM    833 HH21 ARG A  95     -12.550   5.516 -45.588  1.00 48.14           H  
ATOM    834 HH12 ARG A  95     -12.260   4.567 -48.947  1.00 50.18           H  
ATOM    835 HH11 ARG A  95     -12.879   6.066 -49.575  1.00 50.18           H  
ATOM    836  HE  ARG A  95     -12.548   7.681 -46.385  1.00 50.22           H  
ATOM    837  N   HIS A  96     -16.945  12.741 -48.695  1.00 32.08           N  
ANISOU  837  N   HIS A  96     4539   3931   3719    789    -37    127
ATOM    838  CA  HIS A  96     -17.609  13.498 -49.745  1.00 33.18           C  
ANISOU  838  CA  HIS A  96     4689   4046   3871    791    -46    125
ATOM    839  C   HIS A  96     -18.826  14.205 -49.149  1.00 32.42           C  
ANISOU  839  C   HIS A  96     4587   3893   3839    717    -69     86
ATOM    840  O   HIS A  96     -19.319  13.808 -48.093  1.00 32.53           O  
ANISOU  840  O   HIS A  96     4600   3877   3882    678    -85     56
ATOM    841  CB  HIS A  96     -18.030  12.533 -50.878  1.00 35.17           C  
ANISOU  841  CB  HIS A  96     5024   4260   4078    871    -71    107
ATOM    842  CG  HIS A  96     -16.904  11.701 -51.442  1.00 38.12           C  
ANISOU  842  CG  HIS A  96     5427   4684   4372    972    -49    141
ATOM    843  ND1 HIS A  96     -15.892  12.221 -52.233  1.00 40.37           N  
ANISOU  843  ND1 HIS A  96     5687   5036   4615   1028    -15    194
ATOM    844  CD2 HIS A  96     -16.613  10.365 -51.299  1.00 39.60           C  
ANISOU  844  CD2 HIS A  96     5672   4865   4511   1034    -57    132
ATOM    845  CE1 HIS A  96     -15.041  11.226 -52.490  1.00 40.92           C  
ANISOU  845  CE1 HIS A  96     5792   5146   4608   1129      3    218
ATOM    846  NE2 HIS A  96     -15.405  10.077 -51.934  1.00 40.25           N  
ANISOU  846  NE2 HIS A  96     5765   5013   4515   1139    -23    179
ATOM    847  H   HIS A  96     -17.557  12.186 -48.119  1.00 32.08           H  
ATOM    848  HA  HIS A  96     -16.939  14.258 -50.152  1.00 33.18           H  
ATOM    849  HB3 HIS A  96     -18.495  13.082 -51.697  1.00 35.17           H  
ATOM    850  HB2 HIS A  96     -18.798  11.847 -50.511  1.00 35.17           H  
ATOM    851  HD1 HIS A  96     -15.790  13.173 -52.549  1.00 40.37           H  
ATOM    852  HD2 HIS A  96     -17.159   9.607 -50.760  1.00 39.60           H  
ATOM    853  HE1 HIS A  96     -14.140  11.345 -53.075  1.00 40.92           H  
ATOM    854  N   LEU A  97     -19.291  15.233 -49.868  1.00 31.27           N  
ANISOU  854  N   LEU A  97     4435   3735   3711    705    -71     91
ATOM    855  CA  LEU A  97     -20.595  15.846 -49.628  1.00 31.18           C  
ANISOU  855  CA  LEU A  97     4425   3671   3749    659    -91     58
ATOM    856  C   LEU A  97     -21.691  14.984 -50.275  1.00 31.70           C  
ANISOU  856  C   LEU A  97     4542   3692   3809    688   -129     30
ATOM    857  O   LEU A  97     -22.718  14.743 -49.648  1.00 32.16           O  
ANISOU  857  O   LEU A  97     4599   3719   3902    653   -152      5
ATOM    858  CB  LEU A  97     -20.619  17.280 -50.208  1.00 32.43           C  
ANISOU  858  CB  LEU A  97     4571   3830   3922    642    -83     75
ATOM    859  CG  LEU A  97     -19.584  18.247 -49.592  1.00 37.16           C  
ANISOU  859  CG  LEU A  97     5130   4462   4526    595    -62    109
ATOM    860  CD1 LEU A  97     -19.545  19.568 -50.377  1.00 38.96           C  
ANISOU  860  CD1 LEU A  97     5360   4684   4758    583    -62    132
ATOM    861  CD2 LEU A  97     -19.836  18.501 -48.093  1.00 39.09           C  
ANISOU  861  CD2 LEU A  97     5362   4686   4803    539    -64     84
ATOM    862  H   LEU A  97     -18.798  15.536 -50.690  1.00 31.27           H  
ATOM    863  HA  LEU A  97     -20.792  15.884 -48.554  1.00 31.18           H  
ATOM    864  HB3 LEU A  97     -21.619  17.699 -50.072  1.00 32.43           H  
ATOM    865  HB2 LEU A  97     -20.469  17.236 -51.288  1.00 32.43           H  
ATOM    866  HG  LEU A  97     -18.591  17.805 -49.688  1.00 37.16           H  
ATOM    867 HD11 LEU A  97     -18.854  20.281 -49.925  1.00 38.96           H  
ATOM    868 HD12 LEU A  97     -19.215  19.408 -51.404  1.00 38.96           H  
ATOM    869 HD13 LEU A  97     -20.528  20.040 -50.417  1.00 38.96           H  
ATOM    870 HD21 LEU A  97     -19.838  19.564 -47.847  1.00 39.09           H  
ATOM    871 HD22 LEU A  97     -20.796  18.104 -47.761  1.00 39.09           H  
ATOM    872 HD23 LEU A  97     -19.063  18.031 -47.485  1.00 39.09           H  
ATOM    873  N   GLY A  98     -21.426  14.514 -51.502  1.00 31.34           N  
ANISOU  873  N   GLY A  98     4543   3645   3719    752   -138     39
ATOM    874  CA  GLY A  98     -22.318  13.648 -52.269  1.00 32.28           C  
ANISOU  874  CA  GLY A  98     4728   3714   3825    774   -187     15
ATOM    875  C   GLY A  98     -22.096  12.173 -51.907  1.00 32.86           C  
ANISOU  875  C   GLY A  98     4853   3770   3862    798   -211      4
ATOM    876  O   GLY A  98     -21.405  11.862 -50.933  1.00 32.17           O  
ANISOU  876  O   GLY A  98     4740   3710   3772    790   -188      9
ATOM    877  H   GLY A  98     -20.528  14.700 -51.910  1.00 31.34           H  
ATOM    878  HA3 GLY A  98     -22.119  13.804 -53.327  1.00 32.28           H  
ATOM    879  HA2 GLY A  98     -23.356  13.915 -52.091  1.00 32.28           H  
ATOM    880  N   CYS A  99     -22.672  11.267 -52.703  1.00 32.55           N  
ANISOU  880  N   CYS A  99     4895   3680   3792    825   -263    -10
ATOM    881  CA  CYS A  99     -22.530   9.812 -52.548  1.00 34.39           C  
ANISOU  881  CA  CYS A  99     5208   3880   3980    854   -300    -21
ATOM    882  C   CYS A  99     -21.896   9.217 -53.810  1.00 37.47           C  
ANISOU  882  C   CYS A  99     5693   4255   4287    957   -310    -16
ATOM    883  O   CYS A  99     -22.080   9.767 -54.891  1.00 39.16           O  
ANISOU  883  O   CYS A  99     5923   4464   4490    984   -313    -12
ATOM    884  CB  CYS A  99     -23.904   9.158 -52.337  1.00 33.16           C  
ANISOU  884  CB  CYS A  99     5085   3665   3851    788   -371    -37
ATOM    885  SG  CYS A  99     -24.855   9.764 -50.921  1.00 33.01           S  
ANISOU  885  SG  CYS A  99     4954   3671   3917    685   -359    -36
ATOM    886  H   CYS A  99     -23.149  11.580 -53.549  1.00 32.55           H  
ATOM    887  HA  CYS A  99     -21.893   9.573 -51.696  1.00 34.39           H  
ATOM    888  HB3 CYS A  99     -23.771   8.084 -52.204  1.00 33.16           H  
ATOM    889  HB2 CYS A  99     -24.522   9.272 -53.231  1.00 33.16           H  
ATOM    890  N   ILE A 100     -21.190   8.095 -53.669  1.00 37.37           N  
ANISOU  890  N   ILE A 100     5756   4231   4213   1018   -319    -19
ATOM    891  CA  ILE A 100     -20.587   7.361 -54.776  1.00 41.42           C  
ANISOU  891  CA  ILE A 100     6379   4728   4630   1138   -328    -15
ATOM    892  C   ILE A 100     -21.667   6.533 -55.506  1.00 44.97           C  
ANISOU  892  C   ILE A 100     6958   5079   5049   1136   -419    -42
ATOM    893  O   ILE A 100     -22.394   5.782 -54.851  1.00 45.44           O  
ANISOU  893  O   ILE A 100     7059   5081   5124   1072   -480    -58
ATOM    894  CB  ILE A 100     -19.449   6.417 -54.283  1.00 43.68           C  
ANISOU  894  CB  ILE A 100     6702   5045   4849   1222   -299     -2
ATOM    895  CG1 ILE A 100     -18.389   7.165 -53.438  1.00 46.23           C  
ANISOU  895  CG1 ILE A 100     6891   5472   5204   1208   -217     33
ATOM    896  CG2 ILE A 100     -18.765   5.638 -55.424  1.00 45.66           C  
ANISOU  896  CG2 ILE A 100     7077   5285   4988   1368   -303      5
ATOM    897  CD1 ILE A 100     -17.783   8.397 -54.123  1.00 49.10           C  
ANISOU  897  CD1 ILE A 100     7172   5909   5574   1227   -162     71
ATOM    898  H   ILE A 100     -21.135   7.651 -52.754  1.00 37.37           H  
ATOM    899  HA  ILE A 100     -20.158   8.084 -55.467  1.00 41.42           H  
ATOM    900  HB  ILE A 100     -19.892   5.666 -53.632  1.00 43.68           H  
ATOM    901 HG13 ILE A 100     -17.594   6.477 -53.146  1.00 46.23           H  
ATOM    902 HG12 ILE A 100     -18.841   7.485 -52.499  1.00 46.23           H  
ATOM    903 HG21 ILE A 100     -17.921   5.053 -55.059  1.00 45.66           H  
ATOM    904 HG22 ILE A 100     -19.448   4.933 -55.896  1.00 45.66           H  
ATOM    905 HG23 ILE A 100     -18.397   6.310 -56.199  1.00 45.66           H  
ATOM    906 HD11 ILE A 100     -16.776   8.592 -53.757  1.00 49.10           H  
ATOM    907 HD12 ILE A 100     -17.714   8.284 -55.205  1.00 49.10           H  
ATOM    908 HD13 ILE A 100     -18.391   9.279 -53.920  1.00 49.10           H  
ATOM    909  N   ASN A 101     -21.752   6.715 -56.830  1.00 46.98           N  
ANISOU  909  N   ASN A 101     7277   5315   5257   1198   -433    -41
ATOM    910  CA  ASN A 101     -22.690   6.034 -57.726  1.00 51.12           C  
ANISOU  910  CA  ASN A 101     7933   5743   5748   1192   -528    -63
ATOM    911  C   ASN A 101     -22.094   4.711 -58.268  1.00 54.94           C  
ANISOU  911  C   ASN A 101     8591   6170   6116   1309   -567    -75
ATOM    912  O   ASN A 101     -20.951   4.376 -57.949  1.00 55.79           O  
ANISOU  912  O   ASN A 101     8705   6322   6171   1399   -512    -64
ATOM    913  CB  ASN A 101     -23.181   7.025 -58.832  1.00 52.49           C  
ANISOU  913  CB  ASN A 101     8084   5918   5941   1183   -533    -58
ATOM    914  CG  ASN A 101     -22.335   7.145 -60.110  1.00 56.17           C  
ANISOU  914  CG  ASN A 101     8568   6433   6343   1306   -476    -41
ATOM    915  OD1 ASN A 101     -21.139   6.872 -60.105  1.00 57.11           O  
ANISOU  915  OD1 ASN A 101     8748   6573   6378   1421   -445    -32
ATOM    916  ND2 ASN A 101     -22.949   7.522 -61.227  1.00 56.82           N  
ANISOU  916  ND2 ASN A 101     8592   6541   6458   1291   -457    -30
ATOM    917  H   ASN A 101     -21.075   7.329 -57.283  1.00 46.98           H  
ATOM    918  HA  ASN A 101     -23.570   5.695 -57.177  1.00 51.12           H  
ATOM    919  HB3 ASN A 101     -23.314   8.021 -58.410  1.00 52.49           H  
ATOM    920  HB2 ASN A 101     -24.174   6.706 -59.147  1.00 52.49           H  
ATOM    921 HD22 ASN A 101     -22.462   7.456 -62.132  1.00 56.82           H  
ATOM    922 HD21 ASN A 101     -23.935   7.723 -61.264  1.00 56.82           H  
ATOM    923  N   ALA A 102     -22.855   3.991 -59.110  1.00 57.45           N  
ANISOU  923  N   ALA A 102     9055   6387   6384   1310   -664    -95
ATOM    924  CA  ALA A 102     -22.446   2.718 -59.724  1.00 60.27           C  
ANISOU  924  CA  ALA A 102     9613   6668   6620   1423   -717   -112
ATOM    925  C   ALA A 102     -21.203   2.817 -60.630  1.00 63.01           C  
ANISOU  925  C   ALA A 102     9995   7072   6874   1597   -642    -98
ATOM    926  O   ALA A 102     -20.447   1.853 -60.734  1.00 63.97           O  
ANISOU  926  O   ALA A 102    10231   7180   6897   1720   -637   -101
ATOM    927  CB  ALA A 102     -23.632   2.134 -60.506  1.00 60.37           C  
ANISOU  927  CB  ALA A 102     9770   6563   6603   1377   -841   -130
ATOM    928  H   ALA A 102     -23.764   4.334 -59.371  1.00 57.45           H  
ATOM    929  HA  ALA A 102     -22.195   2.024 -58.919  1.00 60.27           H  
ATOM    930  HB1 ALA A 102     -23.367   1.174 -60.953  1.00 60.37           H  
ATOM    931  HB2 ALA A 102     -24.493   1.966 -59.858  1.00 60.37           H  
ATOM    932  HB3 ALA A 102     -23.938   2.795 -61.320  1.00 60.37           H  
ATOM    933  N   ASP A 103     -20.998   3.996 -61.229  1.00 64.01           N  
ANISOU  933  N   ASP A 103    10023   7271   7029   1612   -583    -78
ATOM    934  CA  ASP A 103     -19.859   4.337 -62.093  1.00 65.02           C  
ANISOU  934  CA  ASP A 103    10158   7475   7073   1770   -505    -50
ATOM    935  C   ASP A 103     -18.593   4.651 -61.269  1.00 65.14           C  
ANISOU  935  C   ASP A 103    10044   7614   7092   1819   -398     -9
ATOM    936  O   ASP A 103     -17.535   4.908 -61.845  1.00 65.96           O  
ANISOU  936  O   ASP A 103    10142   7800   7121   1954   -330     29
ATOM    937  CB  ASP A 103     -20.134   5.548 -63.028  1.00 67.66           C  
ANISOU  937  CB  ASP A 103    10423   7846   7439   1757   -482    -35
ATOM    938  CG  ASP A 103     -21.499   5.587 -63.720  1.00 74.32           C  
ANISOU  938  CG  ASP A 103    11397   8582   8260   1734   -581    -66
ATOM    939  OD1 ASP A 103     -22.010   4.516 -64.114  1.00 75.37           O  
ANISOU  939  OD1 ASP A 103    11716   8618   8302   1794   -658    -93
ATOM    940  OD2 ASP A 103     -21.995   6.723 -63.898  1.00 76.87           O1-
ANISOU  940  OD2 ASP A 103    11641   8914   8650   1657   -585    -61
ATOM    941  H   ASP A 103     -21.678   4.733 -61.124  1.00 64.01           H  
ATOM    942  HA  ASP A 103     -19.640   3.473 -62.723  1.00 65.02           H  
ATOM    943  HB3 ASP A 103     -19.387   5.563 -63.822  1.00 67.66           H  
ATOM    944  HB2 ASP A 103     -20.006   6.477 -62.471  1.00 67.66           H  
ATOM    945  N   GLY A 104     -18.718   4.706 -59.936  1.00 63.51           N  
ANISOU  945  N   GLY A 104     9730   7430   6972   1709   -385     -9
ATOM    946  CA  GLY A 104     -17.646   5.062 -59.009  1.00 61.91           C  
ANISOU  946  CA  GLY A 104     9397   7342   6785   1728   -294     32
ATOM    947  C   GLY A 104     -17.442   6.583 -58.933  1.00 59.75           C  
ANISOU  947  C   GLY A 104     8944   7162   6594   1656   -229     69
ATOM    948  O   GLY A 104     -16.447   7.034 -58.366  1.00 60.06           O  
ANISOU  948  O   GLY A 104     8872   7305   6645   1664   -158    114
ATOM    949  H   GLY A 104     -19.631   4.523 -59.533  1.00 63.51           H  
ATOM    950  HA3 GLY A 104     -16.713   4.577 -59.299  1.00 61.91           H  
ATOM    951  HA2 GLY A 104     -17.907   4.692 -58.019  1.00 61.91           H  
ATOM    952  N   ASN A 105     -18.360   7.372 -59.507  1.00 57.59           N  
ANISOU  952  N   ASN A 105     8648   6853   6380   1578   -258     54
ATOM    953  CA  ASN A 105     -18.329   8.836 -59.539  1.00 55.79           C  
ANISOU  953  CA  ASN A 105     8273   6698   6228   1508   -207     85
ATOM    954  C   ASN A 105     -19.170   9.365 -58.371  1.00 52.53           C  
ANISOU  954  C   ASN A 105     7772   6260   5928   1355   -225     62
ATOM    955  O   ASN A 105     -20.008   8.639 -57.837  1.00 51.78           O  
ANISOU  955  O   ASN A 105     7729   6088   5857   1297   -285     24
ATOM    956  CB  ASN A 105     -18.888   9.323 -60.898  1.00 57.97           C  
ANISOU  956  CB  ASN A 105     8576   6957   6492   1532   -221     86
ATOM    957  CG  ASN A 105     -17.911   9.198 -62.070  1.00 62.66           C  
ANISOU  957  CG  ASN A 105     9253   7584   6972   1690   -198    112
ATOM    958  OD1 ASN A 105     -17.766  10.125 -62.857  1.00 64.21           O  
ANISOU  958  OD1 ASN A 105     9563   7713   7120   1739   -247     88
ATOM    959  ND2 ASN A 105     -17.213   8.078 -62.219  1.00 63.31           N  
ANISOU  959  ND2 ASN A 105     9282   7772   7002   1776   -125    167
ATOM    960  H   ASN A 105     -19.239   6.955 -59.813  1.00 57.59           H  
ATOM    961  HA  ASN A 105     -17.288   9.153 -59.446  1.00 55.79           H  
ATOM    962  HB3 ASN A 105     -19.143  10.382 -60.824  1.00 57.97           H  
ATOM    963  HB2 ASN A 105     -19.823   8.823 -61.151  1.00 57.97           H  
ATOM    964 HD22 ASN A 105     -16.622   7.978 -63.026  1.00 63.31           H  
ATOM    965 HD21 ASN A 105     -17.358   7.276 -61.616  1.00 63.31           H  
ATOM    966  N   VAL A 106     -18.945  10.623 -57.974  1.00 50.46           N  
ANISOU  966  N   VAL A 106     7382   6060   5729   1291   -177     90
ATOM    967  CA  VAL A 106     -19.739  11.260 -56.927  1.00 48.75           C  
ANISOU  967  CA  VAL A 106     7090   5823   5611   1163   -189     70
ATOM    968  C   VAL A 106     -21.037  11.815 -57.549  1.00 45.94           C  
ANISOU  968  C   VAL A 106     6752   5406   5298   1110   -236     43
ATOM    969  O   VAL A 106     -20.969  12.735 -58.365  1.00 47.37           O  
ANISOU  969  O   VAL A 106     6933   5597   5469   1137   -227     57
ATOM    970  CB  VAL A 106     -18.972  12.426 -56.231  1.00 49.91           C  
ANISOU  970  CB  VAL A 106     7113   6047   5802   1112   -130    107
ATOM    971  CG1 VAL A 106     -19.802  13.120 -55.128  1.00 50.54           C  
ANISOU  971  CG1 VAL A 106     7137   6097   5971    996   -144     81
ATOM    972  CG2 VAL A 106     -17.631  11.959 -55.633  1.00 50.75           C  
ANISOU  972  CG2 VAL A 106     7196   6222   5865   1158    -89    140
ATOM    973  H   VAL A 106     -18.328  11.217 -58.502  1.00 50.46           H  
ATOM    974  HA  VAL A 106     -19.988  10.523 -56.161  1.00 48.75           H  
ATOM    975  HB  VAL A 106     -18.739  13.179 -56.987  1.00 49.91           H  
ATOM    976 HG11 VAL A 106     -19.212  13.864 -54.595  1.00 50.54           H  
ATOM    977 HG12 VAL A 106     -20.670  13.639 -55.537  1.00 50.54           H  
ATOM    978 HG13 VAL A 106     -20.166  12.393 -54.400  1.00 50.54           H  
ATOM    979 HG21 VAL A 106     -17.071  12.800 -55.225  1.00 50.75           H  
ATOM    980 HG22 VAL A 106     -17.785  11.246 -54.825  1.00 50.75           H  
ATOM    981 HG23 VAL A 106     -16.995  11.482 -56.378  1.00 50.75           H  
ATOM    982  N   ASP A 107     -22.181  11.273 -57.124  1.00 41.58           N  
ANISOU  982  N   ASP A 107     6217   4794   4787   1037   -288     11
ATOM    983  CA  ASP A 107     -23.509  11.842 -57.334  1.00 39.64           C  
ANISOU  983  CA  ASP A 107     5971   4503   4588    976   -334     -4
ATOM    984  C   ASP A 107     -23.679  12.983 -56.317  1.00 36.81           C  
ANISOU  984  C   ASP A 107     5501   4177   4307    898   -299      1
ATOM    985  O   ASP A 107     -23.515  12.758 -55.115  1.00 35.79           O  
ANISOU  985  O   ASP A 107     5332   4053   4213    845   -296     -6
ATOM    986  CB  ASP A 107     -24.630  10.784 -57.177  1.00 41.97           C  
ANISOU  986  CB  ASP A 107     6338   4729   4878    938   -413    -27
ATOM    987  CG  ASP A 107     -26.067  11.318 -57.244  1.00 47.95           C  
ANISOU  987  CG  ASP A 107     7077   5456   5687    862   -464    -29
ATOM    988  OD1 ASP A 107     -26.289  12.380 -57.870  1.00 47.28           O  
ANISOU  988  OD1 ASP A 107     6932   5395   5638    850   -438    -21
ATOM    989  OD2 ASP A 107     -26.957  10.608 -56.741  1.00 51.79           O1-
ANISOU  989  OD2 ASP A 107     7607   5898   6175    813   -533    -34
ATOM    990  H   ASP A 107     -22.139  10.568 -56.387  1.00 41.58           H  
ATOM    991  HA  ASP A 107     -23.561  12.242 -58.349  1.00 39.64           H  
ATOM    992  HB3 ASP A 107     -24.495  10.238 -56.242  1.00 41.97           H  
ATOM    993  HB2 ASP A 107     -24.527  10.042 -57.967  1.00 41.97           H  
ATOM    994  N   TYR A 108     -23.979  14.181 -56.822  1.00 35.99           N  
ANISOU  994  N   TYR A 108     5355   4094   4226    895   -273     15
ATOM    995  CA  TYR A 108     -24.166  15.388 -56.025  1.00 36.55           C  
ANISOU  995  CA  TYR A 108     5342   4187   4358    835   -242     20
ATOM    996  C   TYR A 108     -25.632  15.626 -55.623  1.00 35.61           C  
ANISOU  996  C   TYR A 108     5203   4037   4289    777   -276      4
ATOM    997  O   TYR A 108     -25.862  16.525 -54.812  1.00 36.63           O  
ANISOU  997  O   TYR A 108     5274   4181   4463    738   -251      6
ATOM    998  CB  TYR A 108     -23.570  16.593 -56.791  1.00 37.65           C  
ANISOU  998  CB  TYR A 108     5452   4359   4496    855   -202     46
ATOM    999  CG  TYR A 108     -24.212  16.917 -58.133  1.00 40.11           C  
ANISOU  999  CG  TYR A 108     5796   4646   4798    881   -226     47
ATOM   1000  CD1 TYR A 108     -23.671  16.401 -59.330  1.00 41.58           C  
ANISOU 1000  CD1 TYR A 108     6043   4832   4923    954   -235     56
ATOM   1001  CD2 TYR A 108     -25.362  17.733 -58.185  1.00 41.94           C  
ANISOU 1001  CD2 TYR A 108     6001   4859   5077    841   -236     40
ATOM   1002  CE1 TYR A 108     -24.295  16.674 -60.563  1.00 42.55           C  
ANISOU 1002  CE1 TYR A 108     6199   4932   5036    977   -258     56
ATOM   1003  CE2 TYR A 108     -25.990  17.993 -59.416  1.00 43.89           C  
ANISOU 1003  CE2 TYR A 108     6275   5085   5316    864   -258     43
ATOM   1004  CZ  TYR A 108     -25.465  17.454 -60.604  1.00 45.01           C  
ANISOU 1004  CZ  TYR A 108     6477   5224   5400    928   -270     50
ATOM   1005  OH  TYR A 108     -26.121  17.643 -61.782  1.00 49.16           O  
ANISOU 1005  OH  TYR A 108     7031   5730   5917    950   -293     53
ATOM   1006  H   TYR A 108     -24.205  14.245 -57.803  1.00 35.99           H  
ATOM   1007  HA  TYR A 108     -23.611  15.289 -55.090  1.00 36.55           H  
ATOM   1008  HB3 TYR A 108     -22.502  16.431 -56.944  1.00 37.65           H  
ATOM   1009  HB2 TYR A 108     -23.638  17.483 -56.162  1.00 37.65           H  
ATOM   1010  HD1 TYR A 108     -22.786  15.780 -59.311  1.00 41.58           H  
ATOM   1011  HD2 TYR A 108     -25.787  18.136 -57.278  1.00 41.94           H  
ATOM   1012  HE1 TYR A 108     -23.895  16.258 -61.476  1.00 42.55           H  
ATOM   1013  HE2 TYR A 108     -26.894  18.583 -59.438  1.00 43.89           H  
ATOM   1014  HH  TYR A 108     -27.072  17.700 -61.633  1.00 49.16           H  
ATOM   1015  N   HIS A 109     -26.597  14.871 -56.176  1.00 33.59           N  
ANISOU 1015  N   HIS A 109     4999   3743   4023    772   -336     -5
ATOM   1016  CA  HIS A 109     -28.016  15.028 -55.838  1.00 34.50           C  
ANISOU 1016  CA  HIS A 109     5082   3845   4179    717   -372     -4
ATOM   1017  C   HIS A 109     -28.361  14.393 -54.482  1.00 33.92           C  
ANISOU 1017  C   HIS A 109     4979   3778   4130    666   -384     -6
ATOM   1018  O   HIS A 109     -29.284  14.860 -53.819  1.00 36.23           O  
ANISOU 1018  O   HIS A 109     5233   4077   4456    621   -408      5
ATOM   1019  CB  HIS A 109     -28.916  14.441 -56.940  1.00 37.75           C  
ANISOU 1019  CB  HIS A 109     5560   4218   4567    719   -444      0
ATOM   1020  CG  HIS A 109     -28.667  14.994 -58.319  1.00 43.90           C  
ANISOU 1020  CG  HIS A 109     6375   4989   5318    772   -438      2
ATOM   1021  ND1 HIS A 109     -27.816  14.373 -59.209  1.00 47.90           N  
ANISOU 1021  ND1 HIS A 109     6832   5512   5856    768   -415     12
ATOM   1022  CD2 HIS A 109     -29.167  16.094 -58.979  1.00 44.87           C  
ANISOU 1022  CD2 HIS A 109     6579   5091   5380    836   -450     -2
ATOM   1023  CE1 HIS A 109     -27.821  15.095 -60.331  1.00 47.61           C  
ANISOU 1023  CE1 HIS A 109     6842   5464   5782    821   -416     14
ATOM   1024  NE2 HIS A 109     -28.616  16.162 -60.262  1.00 47.25           N  
ANISOU 1024  NE2 HIS A 109     6875   5399   5678    866   -434      6
ATOM   1025  H   HIS A 109     -26.375  14.113 -56.823  1.00 33.59           H  
ATOM   1026  HA  HIS A 109     -28.236  16.095 -55.766  1.00 34.50           H  
ATOM   1027  HB3 HIS A 109     -29.964  14.608 -56.691  1.00 37.75           H  
ATOM   1028  HB2 HIS A 109     -28.788  13.356 -56.976  1.00 37.75           H  
ATOM   1029  HD1 HIS A 109     -27.266  13.532 -58.991  1.00 47.90           H  
ATOM   1030  HD2 HIS A 109     -29.868  16.838 -58.631  1.00 44.87           H  
ATOM   1031  HE1 HIS A 109     -27.224  14.850 -61.198  1.00 47.61           H  
ATOM   1032  N   MET A 110     -27.614  13.358 -54.096  1.00 32.01           N  
ANISOU 1032  N   MET A 110     4755   3541   3868    677   -368    -15
ATOM   1033  CA  MET A 110     -27.694  12.707 -52.793  1.00 31.53           C  
ANISOU 1033  CA  MET A 110     4670   3484   3825    631   -379    -16
ATOM   1034  C   MET A 110     -26.634  13.297 -51.850  1.00 30.70           C  
ANISOU 1034  C   MET A 110     4521   3415   3727    639   -314    -21
ATOM   1035  O   MET A 110     -25.762  14.049 -52.293  1.00 30.53           O  
ANISOU 1035  O   MET A 110     4504   3411   3686    680   -275    -18
ATOM   1036  CB  MET A 110     -27.508  11.197 -52.999  1.00 33.95           C  
ANISOU 1036  CB  MET A 110     5062   3750   4087    637   -436    -21
ATOM   1037  CG  MET A 110     -28.627  10.567 -53.842  1.00 35.68           C  
ANISOU 1037  CG  MET A 110     5338   3926   4292    618   -514    -12
ATOM   1038  SD  MET A 110     -30.254  10.558 -53.035  1.00 38.04           S  
ANISOU 1038  SD  MET A 110     5567   4243   4645    524   -560     19
ATOM   1039  CE  MET A 110     -30.004   9.162 -51.911  1.00 37.88           C  
ANISOU 1039  CE  MET A 110     5580   4203   4611    482   -598     20
ATOM   1040  H   MET A 110     -26.884  13.036 -54.717  1.00 32.01           H  
ATOM   1041  HA  MET A 110     -28.671  12.887 -52.341  1.00 31.53           H  
ATOM   1042  HB3 MET A 110     -27.481  10.707 -52.028  1.00 33.95           H  
ATOM   1043  HB2 MET A 110     -26.544  10.999 -53.472  1.00 33.95           H  
ATOM   1044  HG3 MET A 110     -28.354   9.546 -54.111  1.00 35.68           H  
ATOM   1045  HG2 MET A 110     -28.728  11.093 -54.793  1.00 35.68           H  
ATOM   1046  HE1 MET A 110     -30.921   8.932 -51.371  1.00 37.88           H  
ATOM   1047  HE2 MET A 110     -29.712   8.285 -52.486  1.00 37.88           H  
ATOM   1048  HE3 MET A 110     -29.221   9.377 -51.185  1.00 37.88           H  
ATOM   1049  N   ASN A 111     -26.744  13.019 -50.545  1.00 29.14           N  
ANISOU 1049  N   ASN A 111     4279   3234   3558    596   -306    -23
ATOM   1050  CA  ASN A 111     -25.859  13.586 -49.524  1.00 28.64           C  
ANISOU 1050  CA  ASN A 111     4175   3202   3503    594   -251    -26
ATOM   1051  C   ASN A 111     -25.315  12.465 -48.638  1.00 29.61           C  
ANISOU 1051  C   ASN A 111     4309   3330   3612    585   -254    -30
ATOM   1052  O   ASN A 111     -26.105  11.685 -48.109  1.00 30.03           O  
ANISOU 1052  O   ASN A 111     4366   3371   3675    551   -290    -30
ATOM   1053  CB  ASN A 111     -26.620  14.587 -48.621  1.00 28.07           C  
ANISOU 1053  CB  ASN A 111     4042   3148   3475    559   -226    -26
ATOM   1054  CG  ASN A 111     -27.137  15.880 -49.261  1.00 31.14           C  
ANISOU 1054  CG  ASN A 111     4420   3535   3878    573   -213    -23
ATOM   1055  OD1 ASN A 111     -27.881  16.608 -48.609  1.00 33.56           O  
ANISOU 1055  OD1 ASN A 111     4757   3827   4165    603   -222    -18
ATOM   1056  ND2 ASN A 111     -26.787  16.200 -50.505  1.00 31.87           N  
ANISOU 1056  ND2 ASN A 111     4476   3638   3996    559   -191    -24
ATOM   1057  H   ASN A 111     -27.484  12.405 -50.205  1.00 29.14           H  
ATOM   1058  HA  ASN A 111     -25.024  14.106 -49.990  1.00 28.64           H  
ATOM   1059  HB3 ASN A 111     -25.968  14.898 -47.802  1.00 28.07           H  
ATOM   1060  HB2 ASN A 111     -27.465  14.086 -48.149  1.00 28.07           H  
ATOM   1061 HD22 ASN A 111     -27.161  17.029 -50.934  1.00 31.87           H  
ATOM   1062 HD21 ASN A 111     -26.239  15.567 -51.086  1.00 31.87           H  
ATOM   1063  N   SER A 112     -23.997  12.458 -48.414  1.00 27.94           N  
ANISOU 1063  N   SER A 112     4096   3144   3377    611   -216    -26
ATOM   1064  CA  SER A 112     -23.368  11.722 -47.321  1.00 26.55           C  
ANISOU 1064  CA  SER A 112     3915   2981   3192    601   -209    -28
ATOM   1065  C   SER A 112     -23.585  12.496 -46.014  1.00 26.90           C  
ANISOU 1065  C   SER A 112     3894   3048   3278    551   -182    -31
ATOM   1066  O   SER A 112     -23.153  13.648 -45.936  1.00 27.86           O  
ANISOU 1066  O   SER A 112     3984   3187   3414    544   -149    -26
ATOM   1067  CB  SER A 112     -21.852  11.622 -47.569  1.00 29.90           C  
ANISOU 1067  CB  SER A 112     4348   3439   3573    650   -175    -12
ATOM   1068  OG  SER A 112     -21.534  10.629 -48.520  1.00 30.11           O  
ANISOU 1068  OG  SER A 112     4449   3447   3544    716   -197    -10
ATOM   1069  H   SER A 112     -23.425  13.175 -48.852  1.00 27.94           H  
ATOM   1070  HA  SER A 112     -23.799  10.722 -47.234  1.00 26.55           H  
ATOM   1071  HB3 SER A 112     -21.330  11.372 -46.645  1.00 29.90           H  
ATOM   1072  HB2 SER A 112     -21.460  12.583 -47.898  1.00 29.90           H  
ATOM   1073  HG  SER A 112     -21.615  11.040 -49.402  1.00 30.11           H  
ATOM   1074  N   VAL A 113     -24.202  11.875 -45.007  1.00 26.12           N  
ANISOU 1074  N   VAL A 113     3783   2948   3196    516   -198    -37
ATOM   1075  CA  VAL A 113     -24.385  12.484 -43.689  1.00 26.48           C  
ANISOU 1075  CA  VAL A 113     3774   3015   3272    479   -171    -41
ATOM   1076  C   VAL A 113     -23.815  11.554 -42.593  1.00 26.54           C  
ANISOU 1076  C   VAL A 113     3776   3037   3272    463   -167    -42
ATOM   1077  O   VAL A 113     -23.933  10.331 -42.733  1.00 26.36           O  
ANISOU 1077  O   VAL A 113     3787   2997   3230    467   -200    -40
ATOM   1078  CB  VAL A 113     -25.887  12.748 -43.407  1.00 28.03           C  
ANISOU 1078  CB  VAL A 113     3942   3209   3500    453   -189    -38
ATOM   1079  CG1 VAL A 113     -26.424  13.888 -44.293  1.00 27.24           C  
ANISOU 1079  CG1 VAL A 113     3842   3100   3409    471   -186    -36
ATOM   1080  CG2 VAL A 113     -26.791  11.506 -43.505  1.00 29.17           C  
ANISOU 1080  CG2 VAL A 113     4102   3339   3641    432   -242    -27
ATOM   1081  H   VAL A 113     -24.566  10.931 -45.127  1.00 26.12           H  
ATOM   1082  HA  VAL A 113     -23.870  13.442 -43.660  1.00 26.48           H  
ATOM   1083  HB  VAL A 113     -25.956  13.103 -42.378  1.00 28.03           H  
ATOM   1084 HG11 VAL A 113     -27.464  14.118 -44.060  1.00 27.24           H  
ATOM   1085 HG12 VAL A 113     -25.845  14.801 -44.148  1.00 27.24           H  
ATOM   1086 HG13 VAL A 113     -26.368  13.631 -45.352  1.00 27.24           H  
ATOM   1087 HG21 VAL A 113     -27.831  11.761 -43.313  1.00 29.17           H  
ATOM   1088 HG22 VAL A 113     -26.746  11.057 -44.496  1.00 29.17           H  
ATOM   1089 HG23 VAL A 113     -26.520  10.745 -42.776  1.00 29.17           H  
ATOM   1090  N   PRO A 114     -23.161  12.127 -41.554  1.00 27.34           N  
ANISOU 1090  N   PRO A 114     3842   3165   3383    445   -132    -44
ATOM   1091  CA  PRO A 114     -22.662  11.336 -40.419  1.00 27.85           C  
ANISOU 1091  CA  PRO A 114     3896   3246   3441    428   -127    -44
ATOM   1092  C   PRO A 114     -23.809  10.862 -39.511  1.00 29.74           C  
ANISOU 1092  C   PRO A 114     4114   3483   3704    395   -146    -46
ATOM   1093  O   PRO A 114     -24.694  11.646 -39.174  1.00 31.34           O  
ANISOU 1093  O   PRO A 114     4287   3691   3929    384   -140    -46
ATOM   1094  CB  PRO A 114     -21.699  12.297 -39.704  1.00 28.76           C  
ANISOU 1094  CB  PRO A 114     3983   3389   3557    413    -89    -41
ATOM   1095  CG  PRO A 114     -22.270  13.682 -39.977  1.00 29.84           C  
ANISOU 1095  CG  PRO A 114     4113   3512   3712    407    -80    -46
ATOM   1096  CD  PRO A 114     -22.857  13.553 -41.382  1.00 27.86           C  
ANISOU 1096  CD  PRO A 114     3886   3239   3460    436   -102    -44
ATOM   1097  HA  PRO A 114     -22.101  10.475 -40.777  1.00 27.85           H  
ATOM   1098  HB3 PRO A 114     -20.708  12.206 -40.152  1.00 28.76           H  
ATOM   1099  HB2 PRO A 114     -21.595  12.093 -38.637  1.00 28.76           H  
ATOM   1100  HG3 PRO A 114     -21.538  14.486 -39.881  1.00 29.84           H  
ATOM   1101  HG2 PRO A 114     -23.074  13.882 -39.265  1.00 29.84           H  
ATOM   1102  HD2 PRO A 114     -23.738  14.188 -41.491  1.00 27.86           H  
ATOM   1103  HD3 PRO A 114     -22.120  13.851 -42.130  1.00 27.86           H  
ATOM   1104  N   ILE A 115     -23.771   9.585 -39.123  1.00 30.70           N  
ANISOU 1104  N   ILE A 115     4248   3602   3815    384   -168    -42
ATOM   1105  CA  ILE A 115     -24.652   9.023 -38.111  1.00 32.48           C  
ANISOU 1105  CA  ILE A 115     4444   3837   4060    346   -186    -33
ATOM   1106  C   ILE A 115     -23.999   9.322 -36.755  1.00 31.86           C  
ANISOU 1106  C   ILE A 115     4331   3788   3985    334   -147    -40
ATOM   1107  O   ILE A 115     -22.944   8.759 -36.441  1.00 34.33           O  
ANISOU 1107  O   ILE A 115     4658   4106   4279    340   -138    -43
ATOM   1108  CB  ILE A 115     -24.851   7.490 -38.294  1.00 34.73           C  
ANISOU 1108  CB  ILE A 115     4773   4096   4327    333   -237    -22
ATOM   1109  CG1 ILE A 115     -25.549   7.201 -39.643  1.00 35.55           C  
ANISOU 1109  CG1 ILE A 115     4927   4161   4419    344   -284    -16
ATOM   1110  CG2 ILE A 115     -25.642   6.830 -37.137  1.00 36.28           C  
ANISOU 1110  CG2 ILE A 115     4930   4313   4543    284   -257     -1
ATOM   1111  CD1 ILE A 115     -25.439   5.745 -40.104  1.00 37.61           C  
ANISOU 1111  CD1 ILE A 115     5262   4379   4649    340   -341    -10
ATOM   1112  H   ILE A 115     -22.951   9.027 -39.355  1.00 30.70           H  
ATOM   1113  HA  ILE A 115     -25.633   9.502 -38.161  1.00 32.48           H  
ATOM   1114  HB  ILE A 115     -23.863   7.025 -38.324  1.00 34.73           H  
ATOM   1115 HG13 ILE A 115     -25.118   7.825 -40.428  1.00 35.55           H  
ATOM   1116 HG12 ILE A 115     -26.597   7.496 -39.584  1.00 35.55           H  
ATOM   1117 HG21 ILE A 115     -25.813   5.767 -37.304  1.00 36.28           H  
ATOM   1118 HG22 ILE A 115     -25.120   6.903 -36.181  1.00 36.28           H  
ATOM   1119 HG23 ILE A 115     -26.619   7.297 -37.009  1.00 36.28           H  
ATOM   1120 HD11 ILE A 115     -26.393   5.372 -40.478  1.00 37.61           H  
ATOM   1121 HD12 ILE A 115     -24.714   5.672 -40.912  1.00 37.61           H  
ATOM   1122 HD13 ILE A 115     -25.107   5.070 -39.314  1.00 37.61           H  
ATOM   1123  N   GLN A 116     -24.608  10.259 -36.028  1.00 31.52           N  
ANISOU 1123  N   GLN A 116     4249   3767   3962    325   -124    -41
ATOM   1124  CA  GLN A 116     -24.186  10.664 -34.699  1.00 32.85           C  
ANISOU 1124  CA  GLN A 116     4394   3958   4129    314    -92    -49
ATOM   1125  C   GLN A 116     -25.026   9.919 -33.665  1.00 33.06           C  
ANISOU 1125  C   GLN A 116     4389   4010   4163    292   -101    -34
ATOM   1126  O   GLN A 116     -26.243   9.843 -33.825  1.00 34.90           O  
ANISOU 1126  O   GLN A 116     4595   4257   4407    285   -118    -13
ATOM   1127  CB  GLN A 116     -24.346  12.182 -34.539  1.00 36.54           C  
ANISOU 1127  CB  GLN A 116     4859   4426   4599    328    -64    -61
ATOM   1128  CG  GLN A 116     -23.501  12.971 -35.555  1.00 42.21           C  
ANISOU 1128  CG  GLN A 116     5607   5121   5308    340    -59    -68
ATOM   1129  CD  GLN A 116     -23.112  14.328 -34.990  1.00 49.78           C  
ANISOU 1129  CD  GLN A 116     6578   6073   6264    342    -38    -79
ATOM   1130  OE1 GLN A 116     -23.964  15.158 -34.706  1.00 51.12           O  
ANISOU 1130  OE1 GLN A 116     6747   6238   6438    362    -32    -84
ATOM   1131  NE2 GLN A 116     -21.818  14.557 -34.805  1.00 51.22           N  
ANISOU 1131  NE2 GLN A 116     6774   6255   6432    321    -30    -79
ATOM   1132  H   GLN A 116     -25.482  10.659 -36.338  1.00 31.52           H  
ATOM   1133  HA  GLN A 116     -23.138  10.420 -34.551  1.00 32.85           H  
ATOM   1134  HB3 GLN A 116     -24.041  12.436 -33.522  1.00 36.54           H  
ATOM   1135  HB2 GLN A 116     -25.392  12.484 -34.617  1.00 36.54           H  
ATOM   1136  HG3 GLN A 116     -24.051  13.121 -36.483  1.00 42.21           H  
ATOM   1137  HG2 GLN A 116     -22.601  12.414 -35.815  1.00 42.21           H  
ATOM   1138 HE22 GLN A 116     -21.533  15.422 -34.376  1.00 51.22           H  
ATOM   1139 HE21 GLN A 116     -21.125  13.872 -35.101  1.00 51.22           H  
ATOM   1140  N   GLN A 117     -24.360   9.403 -32.635  1.00 30.69           N  
ANISOU 1140  N   GLN A 117     4082   3724   3854    278    -87    -39
ATOM   1141  CA  GLN A 117     -24.977   8.700 -31.522  1.00 30.44           C  
ANISOU 1141  CA  GLN A 117     4020   3719   3827    255    -93    -23
ATOM   1142  C   GLN A 117     -24.728   9.530 -30.256  1.00 30.18           C  
ANISOU 1142  C   GLN A 117     3968   3712   3788    259    -54    -35
ATOM   1143  O   GLN A 117     -23.605  10.009 -30.075  1.00 30.59           O  
ANISOU 1143  O   GLN A 117     4040   3754   3828    260    -36    -54
ATOM   1144  CB  GLN A 117     -24.327   7.296 -31.456  1.00 31.21           C  
ANISOU 1144  CB  GLN A 117     4143   3803   3913    238   -119    -18
ATOM   1145  CG  GLN A 117     -24.755   6.371 -30.301  1.00 33.62           C  
ANISOU 1145  CG  GLN A 117     4421   4135   4221    206   -129      2
ATOM   1146  CD  GLN A 117     -26.269   6.226 -30.172  1.00 39.29           C  
ANISOU 1146  CD  GLN A 117     5102   4874   4954    182   -157     39
ATOM   1147  OE1 GLN A 117     -26.947   5.783 -31.089  1.00 43.29           O  
ANISOU 1147  OE1 GLN A 117     5628   5356   5463    168   -203     58
ATOM   1148  NE2 GLN A 117     -26.822   6.615 -29.031  1.00 36.89           N  
ANISOU 1148  NE2 GLN A 117     4742   4620   4654    178   -133     57
ATOM   1149  H   GLN A 117     -23.353   9.527 -32.565  1.00 30.69           H  
ATOM   1150  HA  GLN A 117     -26.053   8.597 -31.679  1.00 30.44           H  
ATOM   1151  HB3 GLN A 117     -23.241   7.398 -31.421  1.00 31.21           H  
ATOM   1152  HB2 GLN A 117     -24.544   6.777 -32.392  1.00 31.21           H  
ATOM   1153  HG3 GLN A 117     -24.328   6.712 -29.359  1.00 33.62           H  
ATOM   1154  HG2 GLN A 117     -24.332   5.382 -30.474  1.00 33.62           H  
ATOM   1155 HE22 GLN A 117     -27.811   6.476 -28.903  1.00 36.89           H  
ATOM   1156 HE21 GLN A 117     -26.239   6.977 -28.276  1.00 36.89           H  
ATOM   1157  N   GLU A 118     -25.750   9.659 -29.393  1.00 31.12           N  
ANISOU 1157  N   GLU A 118     4048   3865   3909    263    -43    -19
ATOM   1158  CA  GLU A 118     -25.588  10.151 -28.022  1.00 31.59           C  
ANISOU 1158  CA  GLU A 118     4100   3947   3954    275     -9    -31
ATOM   1159  C   GLU A 118     -24.778   9.121 -27.223  1.00 29.99           C  
ANISOU 1159  C   GLU A 118     3892   3756   3748    243    -14    -28
ATOM   1160  O   GLU A 118     -25.184   7.956 -27.161  1.00 29.99           O  
ANISOU 1160  O   GLU A 118     3873   3766   3756    219    -41     -3
ATOM   1161  CB  GLU A 118     -26.937  10.359 -27.297  1.00 37.14           C  
ANISOU 1161  CB  GLU A 118     4761   4699   4653    302      6     -4
ATOM   1162  CG  GLU A 118     -27.814  11.535 -27.785  1.00 47.00           C  
ANISOU 1162  CG  GLU A 118     6019   5944   5897    349     21     -8
ATOM   1163  CD  GLU A 118     -28.908  11.941 -26.785  1.00 58.68           C  
ANISOU 1163  CD  GLU A 118     7460   7480   7356    400     49     19
ATOM   1164  OE1 GLU A 118     -29.230  11.168 -25.854  1.00 59.47           O  
ANISOU 1164  OE1 GLU A 118     7515   7631   7451    392     55     48
ATOM   1165  OE2 GLU A 118     -29.310  13.120 -26.793  1.00 61.86           O1-
ANISOU 1165  OE2 GLU A 118     7880   7879   7744    453     67     14
ATOM   1166  H   GLU A 118     -26.621   9.192 -29.598  1.00 31.12           H  
ATOM   1167  HA  GLU A 118     -25.048  11.098 -28.050  1.00 31.59           H  
ATOM   1168  HB3 GLU A 118     -26.723  10.513 -26.237  1.00 37.14           H  
ATOM   1169  HB2 GLU A 118     -27.528   9.442 -27.341  1.00 37.14           H  
ATOM   1170  HG3 GLU A 118     -28.273  11.299 -28.745  1.00 47.00           H  
ATOM   1171  HG2 GLU A 118     -27.191  12.415 -27.940  1.00 47.00           H  
ATOM   1172  N   ILE A 119     -23.664   9.560 -26.645  1.00 29.20           N  
ANISOU 1172  N   ILE A 119     3815   3646   3633    239      3    -51
ATOM   1173  CA  ILE A 119     -22.717   8.729 -25.924  1.00 27.94           C  
ANISOU 1173  CA  ILE A 119     3652   3497   3466    214      1    -50
ATOM   1174  C   ILE A 119     -22.425   9.370 -24.563  1.00 29.20           C  
ANISOU 1174  C   ILE A 119     3814   3673   3607    215     26    -63
ATOM   1175  O   ILE A 119     -22.229  10.585 -24.493  1.00 29.83           O  
ANISOU 1175  O   ILE A 119     3923   3737   3674    231     39    -81
ATOM   1176  CB  ILE A 119     -21.417   8.560 -26.768  1.00 29.97           C  
ANISOU 1176  CB  ILE A 119     3937   3732   3718    207     -8    -56
ATOM   1177  CG1 ILE A 119     -21.623   7.575 -27.943  1.00 30.11           C  
ANISOU 1177  CG1 ILE A 119     3967   3731   3743    213    -37    -44
ATOM   1178  CG2 ILE A 119     -20.145   8.200 -25.988  1.00 31.35           C  
ANISOU 1178  CG2 ILE A 119     4113   3922   3876    191      0    -56
ATOM   1179  CD1 ILE A 119     -21.840   6.105 -27.541  1.00 33.61           C  
ANISOU 1179  CD1 ILE A 119     4406   4178   4186    197    -62    -26
ATOM   1180  H   ILE A 119     -23.402  10.542 -26.739  1.00 29.20           H  
ATOM   1181  HA  ILE A 119     -23.149   7.753 -25.727  1.00 27.94           H  
ATOM   1182  HB  ILE A 119     -21.211   9.529 -27.224  1.00 29.97           H  
ATOM   1183 HG13 ILE A 119     -20.761   7.629 -28.608  1.00 30.11           H  
ATOM   1184 HG12 ILE A 119     -22.465   7.905 -28.551  1.00 30.11           H  
ATOM   1185 HG21 ILE A 119     -19.311   8.022 -26.667  1.00 31.35           H  
ATOM   1186 HG22 ILE A 119     -19.834   9.004 -25.322  1.00 31.35           H  
ATOM   1187 HG23 ILE A 119     -20.300   7.307 -25.385  1.00 31.35           H  
ATOM   1188 HD11 ILE A 119     -22.129   5.516 -28.409  1.00 33.61           H  
ATOM   1189 HD12 ILE A 119     -20.933   5.660 -27.129  1.00 33.61           H  
ATOM   1190 HD13 ILE A 119     -22.637   5.976 -26.811  1.00 33.61           H  
ATOM   1191  N   LEU A 120     -22.393   8.550 -23.505  1.00 27.42           N  
ANISOU 1191  N   LEU A 120     3568   3475   3377    198     29    -54
ATOM   1192  CA  LEU A 120     -21.954   8.990 -22.188  1.00 27.49           C  
ANISOU 1192  CA  LEU A 120     3586   3496   3362    199     49    -67
ATOM   1193  C   LEU A 120     -20.434   8.808 -22.102  1.00 27.30           C  
ANISOU 1193  C   LEU A 120     3579   3464   3328    168     44    -74
ATOM   1194  O   LEU A 120     -19.900   7.838 -22.632  1.00 27.37           O  
ANISOU 1194  O   LEU A 120     3578   3475   3345    156     31    -61
ATOM   1195  CB  LEU A 120     -22.678   8.194 -21.076  1.00 28.34           C  
ANISOU 1195  CB  LEU A 120     3655   3646   3466    200     58    -47
ATOM   1196  CG  LEU A 120     -24.192   8.469 -20.961  1.00 30.53           C  
ANISOU 1196  CG  LEU A 120     3897   3956   3748    230     66    -22
ATOM   1197  CD1 LEU A 120     -24.865   7.504 -19.964  1.00 32.83           C  
ANISOU 1197  CD1 LEU A 120     4139   4297   4036    219     69     12
ATOM   1198  CD2 LEU A 120     -24.499   9.943 -20.629  1.00 32.68           C  
ANISOU 1198  CD2 LEU A 120     4198   4226   3993    284     94    -41
ATOM   1199  H   LEU A 120     -22.443   7.536 -23.636  1.00 27.42           H  
ATOM   1200  HA  LEU A 120     -22.186  10.043 -22.064  1.00 27.49           H  
ATOM   1201  HB3 LEU A 120     -22.204   8.410 -20.118  1.00 28.34           H  
ATOM   1202  HB2 LEU A 120     -22.529   7.129 -21.245  1.00 28.34           H  
ATOM   1203  HG  LEU A 120     -24.631   8.258 -21.938  1.00 30.53           H  
ATOM   1204 HD11 LEU A 120     -25.716   7.016 -20.436  1.00 32.83           H  
ATOM   1205 HD12 LEU A 120     -24.188   6.719 -19.625  1.00 32.83           H  
ATOM   1206 HD13 LEU A 120     -25.241   8.006 -19.072  1.00 32.83           H  
ATOM   1207 HD21 LEU A 120     -25.295  10.053 -19.895  1.00 32.68           H  
ATOM   1208 HD22 LEU A 120     -23.627  10.468 -20.237  1.00 32.68           H  
ATOM   1209 HD23 LEU A 120     -24.819  10.467 -21.529  1.00 32.68           H  
ATOM   1210  N   VAL A 121     -19.750   9.724 -21.432  1.00 27.02           N  
ANISOU 1210  N   VAL A 121     3574   3421   3270    158     49    -89
ATOM   1211  CA  VAL A 121     -18.339   9.627 -21.091  1.00 26.99           C  
ANISOU 1211  CA  VAL A 121     3576   3426   3254    122     41    -82
ATOM   1212  C   VAL A 121     -18.216  10.028 -19.617  1.00 29.54           C  
ANISOU 1212  C   VAL A 121     3915   3757   3550    110     47    -93
ATOM   1213  O   VAL A 121     -19.067  10.761 -19.113  1.00 29.65           O  
ANISOU 1213  O   VAL A 121     3953   3763   3551    139     58   -110
ATOM   1214  CB  VAL A 121     -17.465  10.572 -21.968  1.00 28.29           C  
ANISOU 1214  CB  VAL A 121     3765   3570   3413    102     27    -78
ATOM   1215  CG1 VAL A 121     -17.517  10.165 -23.448  1.00 27.68           C  
ANISOU 1215  CG1 VAL A 121     3673   3488   3356    121     24    -66
ATOM   1216  CG2 VAL A 121     -17.757  12.081 -21.820  1.00 28.67           C  
ANISOU 1216  CG2 VAL A 121     3869   3580   3445    103     21    -99
ATOM   1217  H   VAL A 121     -20.233  10.538 -21.048  1.00 27.02           H  
ATOM   1218  HA  VAL A 121     -17.983   8.599 -21.197  1.00 26.99           H  
ATOM   1219  HB  VAL A 121     -16.433  10.424 -21.652  1.00 28.29           H  
ATOM   1220 HG11 VAL A 121     -16.892  10.802 -24.069  1.00 27.68           H  
ATOM   1221 HG12 VAL A 121     -17.176   9.140 -23.582  1.00 27.68           H  
ATOM   1222 HG13 VAL A 121     -18.529  10.230 -23.847  1.00 27.68           H  
ATOM   1223 HG21 VAL A 121     -17.140  12.670 -22.498  1.00 28.67           H  
ATOM   1224 HG22 VAL A 121     -18.798  12.312 -22.051  1.00 28.67           H  
ATOM   1225 HG23 VAL A 121     -17.549  12.443 -20.813  1.00 28.67           H  
ATOM   1226  N   LEU A 122     -17.175   9.551 -18.943  1.00 28.75           N  
ANISOU 1226  N   LEU A 122     3809   3677   3439     75     40    -81
ATOM   1227  CA  LEU A 122     -16.817  10.013 -17.613  1.00 29.72           C  
ANISOU 1227  CA  LEU A 122     3956   3805   3532     58     39    -91
ATOM   1228  C   LEU A 122     -15.840  11.180 -17.776  1.00 31.80           C  
ANISOU 1228  C   LEU A 122     4270   4041   3772     17     12    -91
ATOM   1229  O   LEU A 122     -14.899  11.044 -18.560  1.00 32.40           O  
ANISOU 1229  O   LEU A 122     4327   4130   3854    -16     -2    -64
ATOM   1230  CB  LEU A 122     -16.116   8.866 -16.867  1.00 30.87           C  
ANISOU 1230  CB  LEU A 122     4061   3992   3678     37     42    -71
ATOM   1231  CG  LEU A 122     -16.956   7.609 -16.604  1.00 33.56           C  
ANISOU 1231  CG  LEU A 122     4360   4355   4038     64     57    -63
ATOM   1232  CD1 LEU A 122     -16.125   6.527 -15.889  1.00 35.86           C  
ANISOU 1232  CD1 LEU A 122     4623   4680   4320     44     57    -45
ATOM   1233  CD2 LEU A 122     -18.224   7.936 -15.817  1.00 35.35           C  
ANISOU 1233  CD2 LEU A 122     4588   4584   4261     95     73    -76
ATOM   1234  H   LEU A 122     -16.466   8.995 -19.419  1.00 28.75           H  
ATOM   1235  HA  LEU A 122     -17.693  10.342 -17.054  1.00 29.72           H  
ATOM   1236  HB3 LEU A 122     -15.740   9.234 -15.919  1.00 30.87           H  
ATOM   1237  HB2 LEU A 122     -15.245   8.588 -17.445  1.00 30.87           H  
ATOM   1238  HG  LEU A 122     -17.249   7.208 -17.572  1.00 33.56           H  
ATOM   1239 HD11 LEU A 122     -16.487   5.528 -16.132  1.00 35.86           H  
ATOM   1240 HD12 LEU A 122     -15.070   6.570 -16.165  1.00 35.86           H  
ATOM   1241 HD13 LEU A 122     -16.170   6.643 -14.806  1.00 35.86           H  
ATOM   1242 HD21 LEU A 122     -18.722   7.027 -15.481  1.00 35.35           H  
ATOM   1243 HD22 LEU A 122     -17.995   8.545 -14.943  1.00 35.35           H  
ATOM   1244 HD23 LEU A 122     -18.929   8.493 -16.431  1.00 35.35           H  
ATOM   1245  N   ARG A 123     -16.037  12.260 -17.019  1.00 31.62           N  
ANISOU 1245  N   ARG A 123     4314   3982   3717     19      2   -115
ATOM   1246  CA  ARG A 123     -15.056  13.325 -16.840  1.00 32.58           C  
ANISOU 1246  CA  ARG A 123     4500   4070   3811    -35    -39   -110
ATOM   1247  C   ARG A 123     -14.651  13.351 -15.368  1.00 32.52           C  
ANISOU 1247  C   ARG A 123     4523   4068   3767    -68    -56   -112
ATOM   1248  O   ARG A 123     -15.518  13.136 -14.521  1.00 32.92           O  
ANISOU 1248  O   ARG A 123     4595   4116   3798    -23    -36   -138
ATOM   1249  CB  ARG A 123     -15.640  14.678 -17.282  1.00 36.78           C  
ANISOU 1249  CB  ARG A 123     5116   4536   4322     -7    -51   -139
ATOM   1250  CG  ARG A 123     -14.615  15.830 -17.129  1.00 41.45           C  
ANISOU 1250  CG  ARG A 123     5780   5086   4884    -79   -106   -125
ATOM   1251  CD  ARG A 123     -14.884  17.085 -17.966  1.00 43.61           C  
ANISOU 1251  CD  ARG A 123     6103   5309   5159    -80   -126   -128
ATOM   1252  NE  ARG A 123     -15.048  16.775 -19.396  1.00 41.36           N  
ANISOU 1252  NE  ARG A 123     5741   5054   4919    -58    -99   -112
ATOM   1253  CZ  ARG A 123     -14.131  16.435 -20.315  1.00 40.27           C  
ANISOU 1253  CZ  ARG A 123     5554   4947   4801   -107   -113    -69
ATOM   1254  NH1 ARG A 123     -12.826  16.384 -20.050  1.00 37.82           N  
ANISOU 1254  NH1 ARG A 123     5247   4653   4472   -188   -153    -28
ATOM   1255  NH2 ARG A 123     -14.537  16.135 -21.541  1.00 39.63           N1+
ANISOU 1255  NH2 ARG A 123     5420   4884   4752    -74    -89    -60
ATOM   1256  H   ARG A 123     -16.848  12.305 -16.401  1.00 31.62           H  
ATOM   1257  HA  ARG A 123     -14.170  13.119 -17.438  1.00 32.58           H  
ATOM   1258  HB3 ARG A 123     -16.538  14.915 -16.709  1.00 36.78           H  
ATOM   1259  HB2 ARG A 123     -15.965  14.569 -18.315  1.00 36.78           H  
ATOM   1260  HG3 ARG A 123     -13.586  15.501 -17.277  1.00 41.45           H  
ATOM   1261  HG2 ARG A 123     -14.658  16.140 -16.083  1.00 41.45           H  
ATOM   1262  HD3 ARG A 123     -14.018  17.741 -17.893  1.00 43.61           H  
ATOM   1263  HD2 ARG A 123     -15.720  17.658 -17.566  1.00 43.61           H  
ATOM   1264 HH22 ARG A 123     -13.801  15.907 -22.239  1.00 39.63           H  
ATOM   1265 HH21 ARG A 123     -15.508  16.147 -21.809  1.00 39.63           H  
ATOM   1266 HH12 ARG A 123     -12.121  16.139 -20.772  1.00 37.82           H  
ATOM   1267 HH11 ARG A 123     -12.471  16.539 -19.121  1.00 37.82           H  
ATOM   1268  HE  ARG A 123     -16.052  16.742 -19.639  1.00 41.36           H  
ATOM   1269  N   ARG A 124     -13.363  13.590 -15.092  1.00 32.71           N  
ANISOU 1269  N   ARG A 124     4543   4107   3778   -144    -91    -78
ATOM   1270  CA  ARG A 124     -12.816  13.697 -13.738  1.00 33.96           C  
ANISOU 1270  CA  ARG A 124     4730   4272   3901   -184   -114    -75
ATOM   1271  C   ARG A 124     -13.495  14.835 -12.960  1.00 35.82           C  
ANISOU 1271  C   ARG A 124     5084   4438   4087   -168   -138   -116
ATOM   1272  O   ARG A 124     -13.582  15.951 -13.475  1.00 35.94           O  
ANISOU 1272  O   ARG A 124     5177   4393   4086   -176   -167   -126
ATOM   1273  CB  ARG A 124     -11.289  13.905 -13.805  1.00 33.77           C  
ANISOU 1273  CB  ARG A 124     4684   4280   3866   -278   -159    -19
ATOM   1274  CG  ARG A 124     -10.555  12.775 -14.542  1.00 35.58           C  
ANISOU 1274  CG  ARG A 124     4801   4588   4130   -277   -132     26
ATOM   1275  CD  ARG A 124      -9.033  12.990 -14.611  1.00 36.10           C  
ANISOU 1275  CD  ARG A 124     4830   4705   4180   -361   -172     96
ATOM   1276  NE  ARG A 124      -8.391  12.064 -15.559  1.00 37.86           N  
ANISOU 1276  NE  ARG A 124     4956   5003   4427   -337   -141    143
ATOM   1277  CZ  ARG A 124      -8.197  10.746 -15.462  1.00 40.23           C  
ANISOU 1277  CZ  ARG A 124     5192   5358   4736   -295   -105    152
ATOM   1278  NH1 ARG A 124      -8.523  10.077 -14.352  1.00 39.27           N  
ANISOU 1278  NH1 ARG A 124     5082   5233   4607   -284    -95    124
ATOM   1279  NH2 ARG A 124      -7.690  10.107 -16.515  1.00 42.33           N1+
ANISOU 1279  NH2 ARG A 124     5391   5681   5013   -259    -80    191
ATOM   1280  H   ARG A 124     -12.718  13.788 -15.850  1.00 32.71           H  
ATOM   1281  HA  ARG A 124     -13.010  12.755 -13.224  1.00 33.96           H  
ATOM   1282  HB3 ARG A 124     -10.888  13.992 -12.795  1.00 33.77           H  
ATOM   1283  HB2 ARG A 124     -11.075  14.857 -14.293  1.00 33.77           H  
ATOM   1284  HG3 ARG A 124     -10.972  12.571 -15.526  1.00 35.58           H  
ATOM   1285  HG2 ARG A 124     -10.752  11.881 -13.949  1.00 35.58           H  
ATOM   1286  HD3 ARG A 124      -8.587  12.772 -13.647  1.00 36.10           H  
ATOM   1287  HD2 ARG A 124      -8.772  14.024 -14.813  1.00 36.10           H  
ATOM   1288 HH22 ARG A 124      -7.494   9.122 -16.549  1.00 42.33           H  
ATOM   1289 HH21 ARG A 124      -7.492  10.653 -17.358  1.00 42.33           H  
ATOM   1290 HH12 ARG A 124      -8.443   9.081 -14.227  1.00 39.27           H  
ATOM   1291 HH11 ARG A 124      -8.912  10.593 -13.555  1.00 39.27           H  
ATOM   1292  HE  ARG A 124      -8.043  12.557 -16.385  1.00 37.86           H  
ATOM   1293  N   GLU A 125     -13.973  14.522 -11.753  1.00 37.42           N  
ANISOU 1293  N   GLU A 125     5307   4648   4264   -133   -120   -140
ATOM   1294  CA  GLU A 125     -14.569  15.470 -10.819  1.00 38.51           C  
ANISOU 1294  CA  GLU A 125     5568   4721   4341    -97   -138   -180
ATOM   1295  C   GLU A 125     -14.022  15.111  -9.423  1.00 39.90           C  
ANISOU 1295  C   GLU A 125     5759   4918   4483   -114   -146   -182
ATOM   1296  O   GLU A 125     -14.416  14.055  -8.918  1.00 39.91           O  
ANISOU 1296  O   GLU A 125     5683   4978   4503    -77   -101   -179
ATOM   1297  CB  GLU A 125     -16.117  15.389 -10.900  1.00 41.25           C  
ANISOU 1297  CB  GLU A 125     5923   5062   4687     15    -86   -213
ATOM   1298  CG  GLU A 125     -16.849  16.182  -9.787  1.00 48.30           C  
ANISOU 1298  CG  GLU A 125     6958   5888   5507     75   -101   -254
ATOM   1299  CD  GLU A 125     -18.357  16.310  -9.999  1.00 57.72           C  
ANISOU 1299  CD  GLU A 125     8160   7080   6689    194    -50   -276
ATOM   1300  OE1 GLU A 125     -18.771  17.056 -10.909  1.00 57.90           O  
ANISOU 1300  OE1 GLU A 125     8149   7101   6751    206    -39   -270
ATOM   1301  OE2 GLU A 125     -19.145  15.706  -9.234  1.00 63.83           O1-
ANISOU 1301  OE2 GLU A 125     8972   7866   7416    279    -20   -295
ATOM   1302  H   GLU A 125     -13.800  13.593 -11.375  1.00 37.42           H  
ATOM   1303  HA  GLU A 125     -14.296  16.485 -11.099  1.00 38.51           H  
ATOM   1304  HB3 GLU A 125     -16.438  14.348 -10.863  1.00 41.25           H  
ATOM   1305  HB2 GLU A 125     -16.436  15.761 -11.875  1.00 41.25           H  
ATOM   1306  HG3 GLU A 125     -16.438  17.189  -9.719  1.00 48.30           H  
ATOM   1307  HG2 GLU A 125     -16.674  15.710  -8.820  1.00 48.30           H  
ATOM   1308  N   PRO A 126     -13.146  15.939  -8.804  1.00 41.58           N  
ANISOU 1308  N   PRO A 126     6071   5084   4645   -179   -210   -181
ATOM   1309  CA  PRO A 126     -12.542  17.175  -9.351  1.00 41.32           C  
ANISOU 1309  CA  PRO A 126     6141   4974   4583   -244   -281   -175
ATOM   1310  C   PRO A 126     -11.565  16.912 -10.525  1.00 42.22           C  
ANISOU 1310  C   PRO A 126     6169   5128   4746   -334   -304   -116
ATOM   1311  O   PRO A 126     -11.212  15.750 -10.754  1.00 40.31           O  
ANISOU 1311  O   PRO A 126     5796   4970   4549   -347   -271    -81
ATOM   1312  CB  PRO A 126     -11.816  17.778  -8.130  1.00 42.26           C  
ANISOU 1312  CB  PRO A 126     6376   5048   4632   -298   -346   -181
ATOM   1313  CG  PRO A 126     -11.462  16.588  -7.258  1.00 43.67           C  
ANISOU 1313  CG  PRO A 126     6459   5307   4826   -306   -316   -163
ATOM   1314  CD  PRO A 126     -12.650  15.658  -7.453  1.00 41.91           C  
ANISOU 1314  CD  PRO A 126     6132   5142   4649   -201   -224   -181
ATOM   1315  HA  PRO A 126     -13.332  17.854  -9.671  1.00 41.32           H  
ATOM   1316  HB3 PRO A 126     -12.496  18.442  -7.594  1.00 42.26           H  
ATOM   1317  HB2 PRO A 126     -10.925  18.357  -8.380  1.00 42.26           H  
ATOM   1318  HG3 PRO A 126     -11.279  16.850  -6.216  1.00 43.67           H  
ATOM   1319  HG2 PRO A 126     -10.558  16.114  -7.646  1.00 43.67           H  
ATOM   1320  HD2 PRO A 126     -12.350  14.620  -7.310  1.00 41.91           H  
ATOM   1321  HD3 PRO A 126     -13.443  15.882  -6.738  1.00 41.91           H  
ATOM   1322  N   PRO A 127     -11.114  17.989 -11.216  1.00 43.33           N  
ANISOU 1322  N   PRO A 127     6379   5210   4872   -391   -361   -101
ATOM   1323  CA  PRO A 127     -10.053  17.896 -12.238  1.00 43.53           C  
ANISOU 1323  CA  PRO A 127     6315   5285   4939   -469   -379    -37
ATOM   1324  C   PRO A 127      -8.811  17.115 -11.778  1.00 43.04           C  
ANISOU 1324  C   PRO A 127     6162   5307   4883   -550   -397     26
ATOM   1325  O   PRO A 127      -8.405  17.233 -10.620  1.00 43.11           O  
ANISOU 1325  O   PRO A 127     6222   5305   4851   -597   -437     29
ATOM   1326  CB  PRO A 127      -9.711  19.361 -12.549  1.00 45.22           C  
ANISOU 1326  CB  PRO A 127     6652   5414   5117   -540   -460    -25
ATOM   1327  CG  PRO A 127     -10.995  20.117 -12.262  1.00 46.35           C  
ANISOU 1327  CG  PRO A 127     6933   5459   5217   -453   -456    -99
ATOM   1328  CD  PRO A 127     -11.568  19.376 -11.060  1.00 44.45           C  
ANISOU 1328  CD  PRO A 127     6691   5240   4956   -379   -411   -139
ATOM   1329  HA  PRO A 127     -10.494  17.420 -13.117  1.00 43.53           H  
ATOM   1330  HB3 PRO A 127      -9.366  19.496 -13.575  1.00 45.22           H  
ATOM   1331  HB2 PRO A 127      -8.918  19.719 -11.888  1.00 45.22           H  
ATOM   1332  HG3 PRO A 127     -11.672  20.010 -13.111  1.00 46.35           H  
ATOM   1333  HG2 PRO A 127     -10.840  21.182 -12.087  1.00 46.35           H  
ATOM   1334  HD2 PRO A 127     -11.154  19.789 -10.141  1.00 44.45           H  
ATOM   1335  HD3 PRO A 127     -12.653  19.477 -11.031  1.00 44.45           H  
ATOM   1336  N   HIS A 128      -8.271  16.297 -12.684  1.00 42.35           N  
ANISOU 1336  N   HIS A 128     5940   5306   4844   -553   -361     75
ATOM   1337  CA  HIS A 128      -7.083  15.457 -12.515  1.00 42.49           C  
ANISOU 1337  CA  HIS A 128     5852   5423   4869   -609   -364    144
ATOM   1338  C   HIS A 128      -7.281  14.248 -11.575  1.00 41.06           C  
ANISOU 1338  C   HIS A 128     5621   5288   4693   -558   -317    123
ATOM   1339  O   HIS A 128      -6.342  13.465 -11.430  1.00 41.75           O  
ANISOU 1339  O   HIS A 128     5622   5458   4781   -593   -316    179
ATOM   1340  CB  HIS A 128      -5.836  16.293 -12.122  1.00 45.53           C  
ANISOU 1340  CB  HIS A 128     6279   5809   5212   -742   -456    209
ATOM   1341  CG  HIS A 128      -5.638  17.589 -12.879  1.00 51.72           C  
ANISOU 1341  CG  HIS A 128     7138   6531   5981   -809   -519    231
ATOM   1342  ND1 HIS A 128      -5.855  17.714 -14.241  1.00 54.89           N  
ANISOU 1342  ND1 HIS A 128     7478   6960   6417   -793   -497    261
ATOM   1343  CD2 HIS A 128      -5.289  18.849 -12.445  1.00 53.84           C  
ANISOU 1343  CD2 HIS A 128     7545   6711   6201   -891   -609    230
ATOM   1344  CE1 HIS A 128      -5.644  18.991 -14.560  1.00 55.58           C  
ANISOU 1344  CE1 HIS A 128     7659   6980   6480   -870   -570    279
ATOM   1345  NE2 HIS A 128      -5.287  19.740 -13.521  1.00 55.71           N  
ANISOU 1345  NE2 HIS A 128     7802   6920   6444   -933   -643    263
ATOM   1346  H   HIS A 128      -8.634  16.340 -13.647  1.00 42.35           H  
ATOM   1347  HA  HIS A 128      -6.890  15.036 -13.502  1.00 42.49           H  
ATOM   1348  HB3 HIS A 128      -4.939  15.686 -12.255  1.00 45.53           H  
ATOM   1349  HB2 HIS A 128      -5.877  16.532 -11.058  1.00 45.53           H  
ATOM   1350  HD1 HIS A 128      -6.222  16.999 -14.885  1.00 54.89           H  
ATOM   1351  HD2 HIS A 128      -5.048  19.181 -11.446  1.00 53.84           H  
ATOM   1352  HE1 HIS A 128      -5.767  19.376 -15.561  1.00 55.58           H  
ATOM   1353  N   SER A 129      -8.476  14.065 -10.982  1.00 38.61           N  
ANISOU 1353  N   SER A 129     5358   4931   4381   -474   -278     50
ATOM   1354  CA  SER A 129      -8.769  12.951 -10.074  1.00 37.35           C  
ANISOU 1354  CA  SER A 129     5148   4818   4225   -432   -236     37
ATOM   1355  C   SER A 129      -8.596  11.582 -10.771  1.00 36.29           C  
ANISOU 1355  C   SER A 129     4890   4763   4136   -394   -184     67
ATOM   1356  O   SER A 129      -9.275  11.331 -11.775  1.00 34.15           O  
ANISOU 1356  O   SER A 129     4591   4487   3899   -341   -149     54
ATOM   1357  CB  SER A 129     -10.199  13.072  -9.514  1.00 37.63           C  
ANISOU 1357  CB  SER A 129     5241   4805   4251   -344   -199    -33
ATOM   1358  OG  SER A 129     -10.443  12.010  -8.602  1.00 38.13           O  
ANISOU 1358  OG  SER A 129     5253   4917   4319   -310   -161    -39
ATOM   1359  H   SER A 129      -9.188  14.776 -11.102  1.00 38.61           H  
ATOM   1360  HA  SER A 129      -8.098  13.068  -9.227  1.00 37.35           H  
ATOM   1361  HB3 SER A 129     -10.940  13.041 -10.315  1.00 37.63           H  
ATOM   1362  HB2 SER A 129     -10.327  14.017  -8.987  1.00 37.63           H  
ATOM   1363  HG  SER A 129     -11.334  12.121  -8.207  1.00 38.13           H  
ATOM   1364  N   PRO A 130      -7.718  10.698 -10.245  1.00 36.58           N  
ANISOU 1364  N   PRO A 130     4861   4869   4170   -414   -178    104
ATOM   1365  CA  PRO A 130      -7.617   9.320 -10.748  1.00 36.47           C  
ANISOU 1365  CA  PRO A 130     4748   4922   4188   -364   -129    129
ATOM   1366  C   PRO A 130      -8.919   8.500 -10.684  1.00 34.63           C  
ANISOU 1366  C   PRO A 130     4504   4675   3978   -281    -78     81
ATOM   1367  O   PRO A 130      -9.126   7.669 -11.568  1.00 35.96           O  
ANISOU 1367  O   PRO A 130     4619   4871   4174   -233    -44     90
ATOM   1368  CB  PRO A 130      -6.520   8.681  -9.875  1.00 38.40           C  
ANISOU 1368  CB  PRO A 130     4936   5244   4412   -410   -144    188
ATOM   1369  CG  PRO A 130      -5.711   9.848  -9.342  1.00 39.97           C  
ANISOU 1369  CG  PRO A 130     5199   5416   4571   -498   -206    198
ATOM   1370  CD  PRO A 130      -6.754  10.942  -9.170  1.00 37.91           C  
ANISOU 1370  CD  PRO A 130     5049   5057   4300   -481   -219    128
ATOM   1371  HA  PRO A 130      -7.267   9.372 -11.780  1.00 36.47           H  
ATOM   1372  HB3 PRO A 130      -5.901   7.974 -10.427  1.00 38.40           H  
ATOM   1373  HB2 PRO A 130      -6.959   8.142  -9.031  1.00 38.40           H  
ATOM   1374  HG3 PRO A 130      -4.986  10.161 -10.096  1.00 39.97           H  
ATOM   1375  HG2 PRO A 130      -5.166   9.622  -8.424  1.00 39.97           H  
ATOM   1376  HD2 PRO A 130      -7.264  10.857  -8.209  1.00 37.91           H  
ATOM   1377  HD3 PRO A 130      -6.273  11.919  -9.224  1.00 37.91           H  
ATOM   1378  N   ASN A 131      -9.733   8.710  -9.640  1.00 31.61           N  
ANISOU 1378  N   ASN A 131     4178   4250   3580   -263    -74     34
ATOM   1379  CA  ASN A 131     -10.735   7.741  -9.190  1.00 29.79           C  
ANISOU 1379  CA  ASN A 131     3923   4028   3367   -199    -31      7
ATOM   1380  C   ASN A 131     -12.116   8.335  -8.874  1.00 29.23           C  
ANISOU 1380  C   ASN A 131     3905   3910   3292   -150    -14    -41
ATOM   1381  O   ASN A 131     -12.941   7.609  -8.311  1.00 30.96           O  
ANISOU 1381  O   ASN A 131     4108   4143   3512   -109     14    -54
ATOM   1382  CB  ASN A 131     -10.182   6.919  -7.991  1.00 31.80           C  
ANISOU 1382  CB  ASN A 131     4159   4323   3600   -217    -31     20
ATOM   1383  CG  ASN A 131     -10.004   7.710  -6.689  1.00 32.28           C  
ANISOU 1383  CG  ASN A 131     4297   4353   3614   -255    -66      2
ATOM   1384  OD1 ASN A 131      -9.866   8.928  -6.702  1.00 32.22           O  
ANISOU 1384  OD1 ASN A 131     4368   4288   3588   -264    -91    -22
ATOM   1385  ND2 ASN A 131      -9.959   7.034  -5.546  1.00 32.55           N  
ANISOU 1385  ND2 ASN A 131     4323   4419   3626   -270    -68     10
ATOM   1386  H   ASN A 131      -9.538   9.457  -8.978  1.00 31.61           H  
ATOM   1387  HA  ASN A 131     -10.953   7.046  -9.998  1.00 29.79           H  
ATOM   1388  HB3 ASN A 131      -9.218   6.485  -8.247  1.00 31.80           H  
ATOM   1389  HB2 ASN A 131     -10.849   6.078  -7.795  1.00 31.80           H  
ATOM   1390 HD22 ASN A 131      -9.815   7.552  -4.692  1.00 32.55           H  
ATOM   1391 HD21 ASN A 131     -10.063   6.031  -5.513  1.00 32.55           H  
ATOM   1392  N   SER A 132     -12.387   9.591  -9.241  1.00 29.74           N  
ANISOU 1392  N   SER A 132     4033   3921   3346   -149    -32    -62
ATOM   1393  CA  SER A 132     -13.701  10.191  -9.044  1.00 30.48           C  
ANISOU 1393  CA  SER A 132     4176   3977   3428    -85    -11   -103
ATOM   1394  C   SER A 132     -14.102  10.963 -10.305  1.00 31.53           C  
ANISOU 1394  C   SER A 132     4335   4068   3575    -70    -17   -113
ATOM   1395  O   SER A 132     -13.341  11.801 -10.793  1.00 33.26           O  
ANISOU 1395  O   SER A 132     4590   4260   3787   -122    -55   -102
ATOM   1396  CB  SER A 132     -13.744  10.981  -7.720  1.00 33.29           C  
ANISOU 1396  CB  SER A 132     4622   4300   3725    -78    -29   -130
ATOM   1397  OG  SER A 132     -12.967  12.160  -7.733  1.00 36.80           O  
ANISOU 1397  OG  SER A 132     5136   4705   4140   -148    -86   -124
ATOM   1398  H   SER A 132     -11.701  10.186  -9.691  1.00 29.74           H  
ATOM   1399  HA  SER A 132     -14.434   9.399  -8.922  1.00 30.48           H  
ATOM   1400  HB3 SER A 132     -13.408  10.352  -6.896  1.00 33.29           H  
ATOM   1401  HB2 SER A 132     -14.775  11.264  -7.500  1.00 33.29           H  
ATOM   1402  HG  SER A 132     -13.494  12.845  -8.194  1.00 36.80           H  
ATOM   1403  N   PHE A 133     -15.283  10.631 -10.831  1.00 29.87           N  
ANISOU 1403  N   PHE A 133     4106   3857   3384     -6     18   -127
ATOM   1404  CA  PHE A 133     -15.786  11.140 -12.098  1.00 29.35           C  
ANISOU 1404  CA  PHE A 133     4051   3760   3339     14     18   -134
ATOM   1405  C   PHE A 133     -17.246  11.590 -11.955  1.00 31.31           C  
ANISOU 1405  C   PHE A 133     4324   3996   3576     94     47   -157
ATOM   1406  O   PHE A 133     -17.944  11.152 -11.038  1.00 32.95           O  
ANISOU 1406  O   PHE A 133     4517   4233   3768    138     74   -160
ATOM   1407  CB  PHE A 133     -15.726  10.012 -13.155  1.00 28.99           C  
ANISOU 1407  CB  PHE A 133     3919   3751   3346     10     33   -107
ATOM   1408  CG  PHE A 133     -14.354   9.436 -13.473  1.00 29.19           C  
ANISOU 1408  CG  PHE A 133     3905   3805   3379    -45     15    -74
ATOM   1409  CD1 PHE A 133     -13.796   8.437 -12.650  1.00 31.07           C  
ANISOU 1409  CD1 PHE A 133     4102   4088   3616    -56     23    -57
ATOM   1410  CD2 PHE A 133     -13.571   9.974 -14.516  1.00 30.28           C  
ANISOU 1410  CD2 PHE A 133     4044   3935   3525    -77     -6    -54
ATOM   1411  CE1 PHE A 133     -12.513   7.971 -12.897  1.00 30.92           C  
ANISOU 1411  CE1 PHE A 133     4045   4104   3597    -94     10    -20
ATOM   1412  CE2 PHE A 133     -12.297   9.483 -14.760  1.00 30.90           C  
ANISOU 1412  CE2 PHE A 133     4077   4059   3604   -115    -16    -12
ATOM   1413  CZ  PHE A 133     -11.775   8.483 -13.954  1.00 30.55           C  
ANISOU 1413  CZ  PHE A 133     3995   4059   3553   -121     -8      4
ATOM   1414  H   PHE A 133     -15.843   9.902 -10.401  1.00 29.87           H  
ATOM   1415  HA  PHE A 133     -15.191  11.992 -12.418  1.00 29.35           H  
ATOM   1416  HB3 PHE A 133     -16.159  10.384 -14.084  1.00 28.99           H  
ATOM   1417  HB2 PHE A 133     -16.370   9.190 -12.843  1.00 28.99           H  
ATOM   1418  HD1 PHE A 133     -14.359   8.041 -11.817  1.00 31.07           H  
ATOM   1419  HD2 PHE A 133     -13.964  10.753 -15.147  1.00 30.28           H  
ATOM   1420  HE1 PHE A 133     -12.082   7.213 -12.264  1.00 30.92           H  
ATOM   1421  HE2 PHE A 133     -11.715   9.889 -15.575  1.00 30.90           H  
ATOM   1422  HZ  PHE A 133     -10.779   8.108 -14.133  1.00 30.55           H  
ATOM   1423  N   ARG A 134     -17.714  12.370 -12.930  1.00 31.59           N  
ANISOU 1423  N   ARG A 134     4386   3997   3621    115     44   -167
ATOM   1424  CA  ARG A 134     -19.128  12.529 -13.247  1.00 33.15           C  
ANISOU 1424  CA  ARG A 134     4584   4197   3815    195     75   -176
ATOM   1425  C   ARG A 134     -19.341  12.075 -14.696  1.00 33.95           C  
ANISOU 1425  C   ARG A 134     4625   4306   3967    192     80   -159
ATOM   1426  O   ARG A 134     -18.441  12.227 -15.522  1.00 34.52           O  
ANISOU 1426  O   ARG A 134     4700   4356   4060    144     56   -154
ATOM   1427  CB  ARG A 134     -19.561  13.998 -13.051  1.00 36.34           C  
ANISOU 1427  CB  ARG A 134     5099   4542   4166    239     64   -207
ATOM   1428  CG  ARG A 134     -21.074  14.252 -13.266  1.00 42.22           C  
ANISOU 1428  CG  ARG A 134     5837   5303   4903    335    102   -209
ATOM   1429  CD  ARG A 134     -21.443  15.733 -13.410  1.00 47.51           C  
ANISOU 1429  CD  ARG A 134     6626   5906   5519    389     90   -239
ATOM   1430  NE  ARG A 134     -21.312  16.456 -12.138  1.00 51.32           N  
ANISOU 1430  NE  ARG A 134     7210   6357   5932    409     76   -264
ATOM   1431  CZ  ARG A 134     -22.248  16.838 -11.270  1.00 53.22           C  
ANISOU 1431  CZ  ARG A 134     7477   6626   6119    505    112   -270
ATOM   1432  NH1 ARG A 134     -23.530  16.503 -11.435  1.00 51.39           N  
ANISOU 1432  NH1 ARG A 134     7167   6464   5897    586    163   -245
ATOM   1433  NH2 ARG A 134     -21.866  17.556 -10.216  1.00 52.46           N1+
ANISOU 1433  NH2 ARG A 134     7489   6492   5953    523     93   -296
ATOM   1434  H   ARG A 134     -17.062  12.702 -13.643  1.00 31.59           H  
ATOM   1435  HA  ARG A 134     -19.724  11.882 -12.607  1.00 33.15           H  
ATOM   1436  HB3 ARG A 134     -18.985  14.633 -13.728  1.00 36.34           H  
ATOM   1437  HB2 ARG A 134     -19.294  14.319 -12.043  1.00 36.34           H  
ATOM   1438  HG3 ARG A 134     -21.574  13.852 -12.383  1.00 42.22           H  
ATOM   1439  HG2 ARG A 134     -21.520  13.706 -14.089  1.00 42.22           H  
ATOM   1440  HD3 ARG A 134     -22.388  15.886 -13.932  1.00 47.51           H  
ATOM   1441  HD2 ARG A 134     -20.698  16.209 -14.048  1.00 47.51           H  
ATOM   1442 HH22 ARG A 134     -22.468  18.155  -9.679  1.00 52.46           H  
ATOM   1443 HH21 ARG A 134     -20.846  17.666 -10.115  1.00 52.46           H  
ATOM   1444 HH12 ARG A 134     -24.281  16.856 -10.870  1.00 51.39           H  
ATOM   1445 HH11 ARG A 134     -23.775  15.898 -12.229  1.00 51.39           H  
ATOM   1446  HE  ARG A 134     -20.322  16.662 -11.886  1.00 51.32           H  
ATOM   1447  N   LEU A 135     -20.535  11.551 -14.990  1.00 33.48           N  
ANISOU 1447  N   LEU A 135     4513   4282   3926    241    109   -145
ATOM   1448  CA  LEU A 135     -21.002  11.360 -16.361  1.00 34.27           C  
ANISOU 1448  CA  LEU A 135     4568   4384   4069    240    107   -130
ATOM   1449  C   LEU A 135     -21.212  12.700 -17.092  1.00 33.41           C  
ANISOU 1449  C   LEU A 135     4518   4228   3949    268    101   -149
ATOM   1450  O   LEU A 135     -21.854  13.604 -16.548  1.00 34.48           O  
ANISOU 1450  O   LEU A 135     4708   4349   4045    324    113   -165
ATOM   1451  CB  LEU A 135     -22.354  10.618 -16.359  1.00 36.05           C  
ANISOU 1451  CB  LEU A 135     4722   4664   4312    276    130    -99
ATOM   1452  CG  LEU A 135     -22.302   9.116 -16.039  1.00 39.70           C  
ANISOU 1452  CG  LEU A 135     5122   5166   4798    237    126    -72
ATOM   1453  CD1 LEU A 135     -23.720   8.595 -15.793  1.00 40.80           C  
ANISOU 1453  CD1 LEU A 135     5197   5361   4945    265    140    -32
ATOM   1454  CD2 LEU A 135     -21.620   8.294 -17.147  1.00 40.43           C  
ANISOU 1454  CD2 LEU A 135     5201   5237   4925    189    100    -66
ATOM   1455  H   LEU A 135     -21.216  11.424 -14.251  1.00 33.48           H  
ATOM   1456  HA  LEU A 135     -20.254  10.777 -16.896  1.00 34.27           H  
ATOM   1457  HB3 LEU A 135     -22.819  10.721 -17.342  1.00 36.05           H  
ATOM   1458  HB2 LEU A 135     -23.026  11.123 -15.663  1.00 36.05           H  
ATOM   1459  HG  LEU A 135     -21.739   8.993 -15.114  1.00 39.70           H  
ATOM   1460 HD11 LEU A 135     -23.689   7.618 -15.316  1.00 40.80           H  
ATOM   1461 HD12 LEU A 135     -24.304   9.259 -15.158  1.00 40.80           H  
ATOM   1462 HD13 LEU A 135     -24.274   8.495 -16.726  1.00 40.80           H  
ATOM   1463 HD21 LEU A 135     -20.961   7.540 -16.718  1.00 40.43           H  
ATOM   1464 HD22 LEU A 135     -22.351   7.762 -17.754  1.00 40.43           H  
ATOM   1465 HD23 LEU A 135     -21.032   8.903 -17.834  1.00 40.43           H  
ATOM   1466  N   GLU A 136     -20.780  12.750 -18.350  1.00 31.61           N  
ANISOU 1466  N   GLU A 136     4279   3978   3753    240     84   -144
ATOM   1467  CA  GLU A 136     -21.187  13.749 -19.323  1.00 31.63           C  
ANISOU 1467  CA  GLU A 136     4330   3938   3752    264     77   -158
ATOM   1468  C   GLU A 136     -21.750  13.042 -20.557  1.00 31.98           C  
ANISOU 1468  C   GLU A 136     4317   3996   3838    268     79   -139
ATOM   1469  O   GLU A 136     -21.255  11.974 -20.904  1.00 30.85           O  
ANISOU 1469  O   GLU A 136     4122   3877   3724    235     73   -120
ATOM   1470  CB  GLU A 136     -20.004  14.645 -19.706  1.00 35.46           C  
ANISOU 1470  CB  GLU A 136     4873   4374   4227    210     44   -167
ATOM   1471  CG  GLU A 136     -19.428  15.415 -18.507  1.00 44.87           C  
ANISOU 1471  CG  GLU A 136     6144   5536   5369    198     27   -186
ATOM   1472  CD  GLU A 136     -18.530  16.582 -18.904  1.00 54.81           C  
ANISOU 1472  CD  GLU A 136     7481   6735   6609    148    -16   -190
ATOM   1473  OE1 GLU A 136     -17.982  16.625 -20.032  1.00 52.62           O  
ANISOU 1473  OE1 GLU A 136     7169   6461   6362    103    -31   -168
ATOM   1474  OE2 GLU A 136     -18.387  17.507 -18.085  1.00 59.61           O1-
ANISOU 1474  OE2 GLU A 136     8188   7292   7167    155    -38   -212
ATOM   1475  H   GLU A 136     -20.227  11.981 -18.732  1.00 31.61           H  
ATOM   1476  HA  GLU A 136     -21.968  14.351 -18.881  1.00 31.63           H  
ATOM   1477  HB3 GLU A 136     -20.328  15.352 -20.470  1.00 35.46           H  
ATOM   1478  HB2 GLU A 136     -19.211  14.052 -20.163  1.00 35.46           H  
ATOM   1479  HG3 GLU A 136     -18.863  14.738 -17.865  1.00 44.87           H  
ATOM   1480  HG2 GLU A 136     -20.245  15.801 -17.896  1.00 44.87           H  
ATOM   1481  N   LYS A 137     -22.757  13.636 -21.205  1.00 32.73           N  
ANISOU 1481  N   LYS A 137     4426   4078   3933    313     86   -142
ATOM   1482  CA  LYS A 137     -23.291  13.154 -22.479  1.00 33.08           C  
ANISOU 1482  CA  LYS A 137     4421   4132   4014    315     82   -122
ATOM   1483  C   LYS A 137     -22.708  14.012 -23.611  1.00 33.01           C  
ANISOU 1483  C   LYS A 137     4452   4075   4014    299     63   -134
ATOM   1484  O   LYS A 137     -22.867  15.230 -23.548  1.00 34.32           O  
ANISOU 1484  O   LYS A 137     4683   4202   4154    318     60   -153
ATOM   1485  CB  LYS A 137     -24.833  13.251 -22.475  1.00 37.60           C  
ANISOU 1485  CB  LYS A 137     4961   4744   4583    377    104   -103
ATOM   1486  CG  LYS A 137     -25.478  12.657 -23.746  1.00 45.29           C  
ANISOU 1486  CG  LYS A 137     5881   5736   5593    371     92    -75
ATOM   1487  CD  LYS A 137     -26.825  13.285 -24.110  1.00 54.69           C  
ANISOU 1487  CD  LYS A 137     7031   6976   6773    430    112    -44
ATOM   1488  CE  LYS A 137     -28.002  12.829 -23.240  1.00 62.47           C  
ANISOU 1488  CE  LYS A 137     7974   8026   7737    455    135    -17
ATOM   1489  NZ  LYS A 137     -29.265  13.370 -23.768  1.00 67.50           N1+
ANISOU 1489  NZ  LYS A 137     8571   8723   8352    529    162     21
ATOM   1490  H   LYS A 137     -23.057  14.552 -20.888  1.00 32.73           H  
ATOM   1491  HA  LYS A 137     -23.019  12.112 -22.641  1.00 33.08           H  
ATOM   1492  HB3 LYS A 137     -25.116  14.299 -22.379  1.00 37.60           H  
ATOM   1493  HB2 LYS A 137     -25.243  12.750 -21.600  1.00 37.60           H  
ATOM   1494  HG3 LYS A 137     -25.581  11.575 -23.643  1.00 45.29           H  
ATOM   1495  HG2 LYS A 137     -24.831  12.784 -24.615  1.00 45.29           H  
ATOM   1496  HD3 LYS A 137     -27.015  13.053 -25.158  1.00 54.69           H  
ATOM   1497  HD2 LYS A 137     -26.733  14.372 -24.075  1.00 54.69           H  
ATOM   1498  HE3 LYS A 137     -27.865  13.146 -22.206  1.00 62.47           H  
ATOM   1499  HE2 LYS A 137     -28.062  11.740 -23.255  1.00 62.47           H  
ATOM   1500  HZ1 LYS A 137     -29.260  14.381 -23.764  1.00 67.50           H  
ATOM   1501  HZ2 LYS A 137     -29.328  13.059 -24.752  1.00 67.50           H  
ATOM   1502  HZ3 LYS A 137     -30.071  12.995 -23.301  1.00 67.50           H  
ATOM   1503  N   ILE A 138     -22.127  13.373 -24.627  1.00 28.90           N  
ANISOU 1503  N   ILE A 138     3902   3555   3524    266     48   -121
ATOM   1504  CA  ILE A 138     -21.659  13.982 -25.871  1.00 30.00           C  
ANISOU 1504  CA  ILE A 138     4069   3660   3670    253     33   -123
ATOM   1505  C   ILE A 138     -22.326  13.291 -27.080  1.00 30.37           C  
ANISOU 1505  C   ILE A 138     4080   3715   3746    265     27   -108
ATOM   1506  O   ILE A 138     -22.974  12.255 -26.910  1.00 30.45           O  
ANISOU 1506  O   ILE A 138     4049   3753   3769    272     27    -94
ATOM   1507  CB  ILE A 138     -20.116  13.818 -26.005  1.00 30.08           C  
ANISOU 1507  CB  ILE A 138     4085   3669   3675    200     17   -114
ATOM   1508  CG1 ILE A 138     -19.622  12.349 -25.942  1.00 29.41           C  
ANISOU 1508  CG1 ILE A 138     3949   3622   3605    187     18    -95
ATOM   1509  CG2 ILE A 138     -19.378  14.696 -24.980  1.00 31.34           C  
ANISOU 1509  CG2 ILE A 138     4287   3816   3804    173     11   -123
ATOM   1510  CD1 ILE A 138     -18.190  12.164 -26.461  1.00 31.36           C  
ANISOU 1510  CD1 ILE A 138     4189   3884   3841    153      8    -73
ATOM   1511  H   ILE A 138     -22.121  12.352 -24.636  1.00 28.90           H  
ATOM   1512  HA  ILE A 138     -21.930  15.039 -25.908  1.00 30.00           H  
ATOM   1513  HB  ILE A 138     -19.833  14.209 -26.986  1.00 30.08           H  
ATOM   1514 HG13 ILE A 138     -20.263  11.688 -26.525  1.00 29.41           H  
ATOM   1515 HG12 ILE A 138     -19.693  11.985 -24.917  1.00 29.41           H  
ATOM   1516 HG21 ILE A 138     -18.302  14.682 -25.147  1.00 31.34           H  
ATOM   1517 HG22 ILE A 138     -19.705  15.732 -25.064  1.00 31.34           H  
ATOM   1518 HG23 ILE A 138     -19.567  14.366 -23.958  1.00 31.34           H  
ATOM   1519 HD11 ILE A 138     -17.989  11.109 -26.635  1.00 31.36           H  
ATOM   1520 HD12 ILE A 138     -18.041  12.683 -27.410  1.00 31.36           H  
ATOM   1521 HD13 ILE A 138     -17.450  12.532 -25.752  1.00 31.36           H  
ATOM   1522  N   LEU A 139     -22.139  13.857 -28.277  1.00 29.96           N  
ANISOU 1522  N   LEU A 139     4046   3636   3699    265     16   -108
ATOM   1523  CA  LEU A 139     -22.437  13.211 -29.554  1.00 31.92           C  
ANISOU 1523  CA  LEU A 139     4274   3885   3969    277      5    -95
ATOM   1524  C   LEU A 139     -21.108  12.714 -30.137  1.00 32.36           C  
ANISOU 1524  C   LEU A 139     4331   3942   4023    255     -5    -84
ATOM   1525  O   LEU A 139     -20.126  13.453 -30.077  1.00 33.83           O  
ANISOU 1525  O   LEU A 139     4537   4122   4197    235     -6    -81
ATOM   1526  CB  LEU A 139     -23.074  14.235 -30.523  1.00 34.40           C  
ANISOU 1526  CB  LEU A 139     4612   4174   4286    305      5   -101
ATOM   1527  CG  LEU A 139     -24.541  14.573 -30.199  1.00 38.04           C  
ANISOU 1527  CG  LEU A 139     5057   4649   4748    345     16    -99
ATOM   1528  CD1 LEU A 139     -25.016  15.784 -31.020  1.00 39.19           C  
ANISOU 1528  CD1 LEU A 139     5233   4767   4891    379     16   -104
ATOM   1529  CD2 LEU A 139     -25.461  13.359 -30.424  1.00 38.19           C  
ANISOU 1529  CD2 LEU A 139     5024   4699   4787    341      2    -73
ATOM   1530  H   LEU A 139     -21.519  14.648 -28.360  1.00 29.96           H  
ATOM   1531  HA  LEU A 139     -23.108  12.365 -29.414  1.00 31.92           H  
ATOM   1532  HB3 LEU A 139     -23.028  13.855 -31.546  1.00 34.40           H  
ATOM   1533  HB2 LEU A 139     -22.474  15.146 -30.529  1.00 34.40           H  
ATOM   1534  HG  LEU A 139     -24.607  14.860 -29.147  1.00 38.04           H  
ATOM   1535 HD11 LEU A 139     -26.057  16.030 -30.804  1.00 39.19           H  
ATOM   1536 HD12 LEU A 139     -24.424  16.673 -30.796  1.00 39.19           H  
ATOM   1537 HD13 LEU A 139     -24.935  15.595 -32.091  1.00 39.19           H  
ATOM   1538 HD21 LEU A 139     -26.401  13.632 -30.903  1.00 38.19           H  
ATOM   1539 HD22 LEU A 139     -24.995  12.593 -31.046  1.00 38.19           H  
ATOM   1540 HD23 LEU A 139     -25.707  12.892 -29.474  1.00 38.19           H  
ATOM   1541  N   VAL A 140     -21.111  11.507 -30.709  1.00 31.29           N  
ANISOU 1541  N   VAL A 140     4179   3815   3894    260    -17    -73
ATOM   1542  CA  VAL A 140     -19.979  10.942 -31.443  1.00 32.85           C  
ANISOU 1542  CA  VAL A 140     4383   4020   4078    261    -22    -58
ATOM   1543  C   VAL A 140     -20.484  10.484 -32.826  1.00 33.32           C  
ANISOU 1543  C   VAL A 140     4458   4060   4141    289    -40    -54
ATOM   1544  O   VAL A 140     -21.466   9.742 -32.889  1.00 32.87           O  
ANISOU 1544  O   VAL A 140     4401   3993   4096    293    -59    -55
ATOM   1545  CB  VAL A 140     -19.377   9.712 -30.696  1.00 35.18           C  
ANISOU 1545  CB  VAL A 140     4665   4339   4362    253    -23    -50
ATOM   1546  CG1 VAL A 140     -18.275   8.964 -31.478  1.00 35.13           C  
ANISOU 1546  CG1 VAL A 140     4669   4347   4332    277    -25    -30
ATOM   1547  CG2 VAL A 140     -18.823  10.116 -29.317  1.00 34.90           C  
ANISOU 1547  CG2 VAL A 140     4617   4324   4320    223     -8    -53
ATOM   1548  H   VAL A 140     -21.955  10.942 -30.684  1.00 31.29           H  
ATOM   1549  HA  VAL A 140     -19.195  11.690 -31.583  1.00 32.85           H  
ATOM   1550  HB  VAL A 140     -20.183   8.996 -30.527  1.00 35.18           H  
ATOM   1551 HG11 VAL A 140     -17.841   8.163 -30.881  1.00 35.13           H  
ATOM   1552 HG12 VAL A 140     -18.647   8.503 -32.393  1.00 35.13           H  
ATOM   1553 HG13 VAL A 140     -17.463   9.637 -31.753  1.00 35.13           H  
ATOM   1554 HG21 VAL A 140     -18.381   9.267 -28.794  1.00 34.90           H  
ATOM   1555 HG22 VAL A 140     -18.055  10.884 -29.414  1.00 34.90           H  
ATOM   1556 HG23 VAL A 140     -19.605  10.518 -28.674  1.00 34.90           H  
ATOM   1557  N   SER A 141     -19.808  10.916 -33.900  1.00 32.83           N  
ANISOU 1557  N   SER A 141     4410   3997   4067    306    -38    -44
ATOM   1558  CA  SER A 141     -20.051  10.448 -35.267  1.00 32.20           C  
ANISOU 1558  CA  SER A 141     4355   3896   3982    340    -57    -41
ATOM   1559  C   SER A 141     -19.444   9.042 -35.445  1.00 32.73           C  
ANISOU 1559  C   SER A 141     4442   3970   4023    364    -68    -31
ATOM   1560  O   SER A 141     -18.222   8.915 -35.354  1.00 33.81           O  
ANISOU 1560  O   SER A 141     4572   4139   4134    377    -50    -13
ATOM   1561  CB  SER A 141     -19.387  11.428 -36.253  1.00 34.60           C  
ANISOU 1561  CB  SER A 141     4667   4202   4276    356    -48    -29
ATOM   1562  OG  SER A 141     -19.933  12.736 -36.178  1.00 41.20           O  
ANISOU 1562  OG  SER A 141     5500   5021   5132    337    -43    -40
ATOM   1563  H   SER A 141     -19.022  11.537 -33.778  1.00 32.83           H  
ATOM   1564  HA  SER A 141     -21.120  10.411 -35.467  1.00 32.20           H  
ATOM   1565  HB3 SER A 141     -19.513  11.062 -37.274  1.00 34.60           H  
ATOM   1566  HB2 SER A 141     -18.313  11.491 -36.070  1.00 34.60           H  
ATOM   1567  HG  SER A 141     -19.432  13.272 -36.804  1.00 41.20           H  
ATOM   1568  N   VAL A 142     -20.273   8.021 -35.685  1.00 32.01           N  
ANISOU 1568  N   VAL A 142     4381   3850   3932    371   -101    -36
ATOM   1569  CA  VAL A 142     -19.820   6.624 -35.715  1.00 33.86           C  
ANISOU 1569  CA  VAL A 142     4656   4074   4135    396   -121    -30
ATOM   1570  C   VAL A 142     -19.483   6.147 -37.148  1.00 34.54           C  
ANISOU 1570  C   VAL A 142     4806   4133   4184    453   -142    -26
ATOM   1571  O   VAL A 142     -18.567   5.347 -37.345  1.00 36.96           O  
ANISOU 1571  O   VAL A 142     5160   4434   4448    497   -151    -19
ATOM   1572  CB  VAL A 142     -20.913   5.685 -35.134  1.00 36.58           C  
ANISOU 1572  CB  VAL A 142     5006   4398   4495    359   -156    -31
ATOM   1573  CG1 VAL A 142     -20.464   4.213 -35.029  1.00 38.85           C  
ANISOU 1573  CG1 VAL A 142     5353   4663   4744    383   -184    -26
ATOM   1574  CG2 VAL A 142     -21.413   6.176 -33.759  1.00 37.43           C  
ANISOU 1574  CG2 VAL A 142     5054   4538   4629    316   -131    -33
ATOM   1575  H   VAL A 142     -21.273   8.197 -35.774  1.00 32.01           H  
ATOM   1576  HA  VAL A 142     -18.917   6.512 -35.110  1.00 33.86           H  
ATOM   1577  HB  VAL A 142     -21.768   5.711 -35.811  1.00 36.58           H  
ATOM   1578 HG11 VAL A 142     -21.269   3.582 -34.666  1.00 38.85           H  
ATOM   1579 HG12 VAL A 142     -20.165   3.791 -35.986  1.00 38.85           H  
ATOM   1580 HG13 VAL A 142     -19.619   4.106 -34.350  1.00 38.85           H  
ATOM   1581 HG21 VAL A 142     -22.074   5.449 -33.286  1.00 37.43           H  
ATOM   1582 HG22 VAL A 142     -20.582   6.359 -33.077  1.00 37.43           H  
ATOM   1583 HG23 VAL A 142     -21.977   7.105 -33.841  1.00 37.43           H  
ATOM   1584  N   GLY A 143     -20.213   6.658 -38.137  1.00 31.96           N  
ANISOU 1584  N   GLY A 143     4487   3789   3869    459   -150    -30
ATOM   1585  CA  GLY A 143     -20.035   6.305 -39.538  1.00 30.59           C  
ANISOU 1585  CA  GLY A 143     4377   3587   3657    515   -171    -27
ATOM   1586  C   GLY A 143     -20.931   7.246 -40.338  1.00 29.56           C  
ANISOU 1586  C   GLY A 143     4240   3438   3554    500   -182    -33
ATOM   1587  O   GLY A 143     -21.490   8.187 -39.773  1.00 30.32           O  
ANISOU 1587  O   GLY A 143     4281   3550   3691    459   -165    -37
ATOM   1588  H   GLY A 143     -20.904   7.374 -37.947  1.00 31.96           H  
ATOM   1589  HA3 GLY A 143     -20.298   5.262 -39.714  1.00 30.59           H  
ATOM   1590  HA2 GLY A 143     -18.998   6.460 -39.834  1.00 30.59           H  
ATOM   1591  N   CYS A 144     -21.077   7.010 -41.647  1.00 28.97           N  
ANISOU 1591  N   CYS A 144     4224   3333   3450    544   -207    -33
ATOM   1592  CA  CYS A 144     -21.897   7.843 -42.530  1.00 29.07           C  
ANISOU 1592  CA  CYS A 144     4231   3329   3485    535   -218    -36
ATOM   1593  C   CYS A 144     -22.878   6.973 -43.321  1.00 29.05           C  
ANISOU 1593  C   CYS A 144     4298   3271   3470    533   -283    -40
ATOM   1594  O   CYS A 144     -22.633   5.778 -43.514  1.00 27.97           O  
ANISOU 1594  O   CYS A 144     4240   3099   3290    561   -320    -41
ATOM   1595  CB  CYS A 144     -20.992   8.668 -43.471  1.00 31.75           C  
ANISOU 1595  CB  CYS A 144     4568   3695   3803    586   -182    -26
ATOM   1596  SG  CYS A 144     -19.868   9.824 -42.626  1.00 33.10           S  
ANISOU 1596  SG  CYS A 144     4656   3930   3990    564   -120    -10
ATOM   1597  H   CYS A 144     -20.682   6.186 -42.082  1.00 28.97           H  
ATOM   1598  HA  CYS A 144     -22.502   8.525 -41.938  1.00 29.07           H  
ATOM   1599  HB3 CYS A 144     -21.605   9.234 -44.177  1.00 31.75           H  
ATOM   1600  HB2 CYS A 144     -20.378   7.998 -44.066  1.00 31.75           H  
ATOM   1601  N   THR A 145     -23.968   7.600 -43.763  1.00 26.99           N  
ANISOU 1601  N   THR A 145     4013   3001   3242    499   -301    -38
ATOM   1602  CA  THR A 145     -24.992   6.982 -44.589  1.00 27.16           C  
ANISOU 1602  CA  THR A 145     4093   2973   3255    484   -371    -32
ATOM   1603  C   THR A 145     -25.384   7.994 -45.690  1.00 28.46           C  
ANISOU 1603  C   THR A 145     4251   3136   3426    505   -364    -33
ATOM   1604  O   THR A 145     -25.223   9.205 -45.496  1.00 28.61           O  
ANISOU 1604  O   THR A 145     4218   3191   3462    521   -308    -36
ATOM   1605  CB  THR A 145     -26.200   6.556 -43.707  1.00 29.45           C  
ANISOU 1605  CB  THR A 145     4347   3263   3579    407   -412    -14
ATOM   1606  OG1 THR A 145     -27.073   5.665 -44.378  1.00 30.31           O  
ANISOU 1606  OG1 THR A 145     4531   3318   3666    381   -497      0
ATOM   1607  CG2 THR A 145     -27.038   7.710 -43.137  1.00 29.36           C  
ANISOU 1607  CG2 THR A 145     4242   3296   3617    376   -382     -3
ATOM   1608  H   THR A 145     -24.098   8.600 -43.610  1.00 26.99           H  
ATOM   1609  HA  THR A 145     -24.596   6.092 -45.077  1.00 27.16           H  
ATOM   1610  HB  THR A 145     -25.805   5.992 -42.864  1.00 29.45           H  
ATOM   1611  HG1 THR A 145     -26.987   4.799 -43.934  1.00 30.31           H  
ATOM   1612 HG21 THR A 145     -27.812   7.339 -42.470  1.00 29.36           H  
ATOM   1613 HG22 THR A 145     -26.417   8.401 -42.565  1.00 29.36           H  
ATOM   1614 HG23 THR A 145     -27.535   8.278 -43.918  1.00 29.36           H  
ATOM   1615  N   CYS A 146     -25.825   7.479 -46.843  1.00 28.54           N  
ANISOU 1615  N   CYS A 146     4328   3100   3416    505   -427    -28
ATOM   1616  CA  CYS A 146     -26.244   8.262 -47.999  1.00 28.50           C  
ANISOU 1616  CA  CYS A 146     4321   3093   3416    527   -423    -28
ATOM   1617  C   CYS A 146     -27.748   8.529 -47.861  1.00 28.19           C  
ANISOU 1617  C   CYS A 146     4233   3059   3418    464   -458     -7
ATOM   1618  O   CYS A 146     -28.497   7.555 -47.802  1.00 30.35           O  
ANISOU 1618  O   CYS A 146     4535   3309   3689    416   -526     11
ATOM   1619  CB  CYS A 146     -25.953   7.474 -49.295  1.00 29.89           C  
ANISOU 1619  CB  CYS A 146     4609   3216   3531    581   -467    -35
ATOM   1620  SG  CYS A 146     -26.355   8.401 -50.797  1.00 32.98           S  
ANISOU 1620  SG  CYS A 146     5007   3603   3921    612   -467    -33
ATOM   1621  H   CYS A 146     -25.973   6.483 -46.911  1.00 28.54           H  
ATOM   1622  HA  CYS A 146     -25.687   9.198 -48.030  1.00 28.50           H  
ATOM   1623  HB3 CYS A 146     -26.528   6.549 -49.314  1.00 29.89           H  
ATOM   1624  HB2 CYS A 146     -24.907   7.174 -49.351  1.00 29.89           H  
ATOM   1625  N   VAL A 147     -28.158   9.800 -47.799  1.00 27.45           N  
ANISOU 1625  N   VAL A 147     4068   3002   3361    464   -417     -4
ATOM   1626  CA  VAL A 147     -29.552  10.221 -47.691  1.00 28.79           C  
ANISOU 1626  CA  VAL A 147     4182   3192   3563    419   -442     24
ATOM   1627  C   VAL A 147     -29.943  11.150 -48.851  1.00 28.92           C  
ANISOU 1627  C   VAL A 147     4200   3205   3584    443   -443     27
ATOM   1628  O   VAL A 147     -29.094  11.850 -49.408  1.00 29.08           O  
ANISOU 1628  O   VAL A 147     4234   3221   3593    492   -401      7
ATOM   1629  CB  VAL A 147     -29.830  10.992 -46.358  1.00 29.36           C  
ANISOU 1629  CB  VAL A 147     4163   3319   3673    402   -389     30
ATOM   1630  CG1 VAL A 147     -29.654  10.101 -45.121  1.00 28.91           C  
ANISOU 1630  CG1 VAL A 147     4098   3271   3616    370   -393     33
ATOM   1631  CG2 VAL A 147     -29.038  12.305 -46.186  1.00 29.89           C  
ANISOU 1631  CG2 VAL A 147     4210   3400   3747    446   -317      5
ATOM   1632  H   VAL A 147     -27.475  10.547 -47.928  1.00 27.45           H  
ATOM   1633  HA  VAL A 147     -30.199   9.352 -47.756  1.00 28.79           H  
ATOM   1634  HB  VAL A 147     -30.881  11.278 -46.361  1.00 29.36           H  
ATOM   1635 HG11 VAL A 147     -29.855  10.646 -44.200  1.00 28.91           H  
ATOM   1636 HG12 VAL A 147     -30.327   9.248 -45.141  1.00 28.91           H  
ATOM   1637 HG13 VAL A 147     -28.636   9.723 -45.072  1.00 28.91           H  
ATOM   1638 HG21 VAL A 147     -29.224  12.754 -45.211  1.00 29.89           H  
ATOM   1639 HG22 VAL A 147     -27.967  12.127 -46.264  1.00 29.89           H  
ATOM   1640 HG23 VAL A 147     -29.303  13.051 -46.935  1.00 29.89           H  
ATOM   1641  N   THR A 148     -31.246  11.194 -49.140  1.00 29.21           N  
ANISOU 1641  N   THR A 148     4208   3254   3636    406   -487     60
ATOM   1642  CA  THR A 148     -31.865  12.232 -49.957  1.00 30.20           C  
ANISOU 1642  CA  THR A 148     4314   3390   3772    428   -480     69
ATOM   1643  C   THR A 148     -31.830  13.578 -49.178  1.00 29.96           C  
ANISOU 1643  C   THR A 148     4209   3404   3770    454   -404     63
ATOM   1644  O   THR A 148     -32.039  13.571 -47.955  1.00 31.34           O  
ANISOU 1644  O   THR A 148     4330   3617   3963    436   -380     73
ATOM   1645  CB  THR A 148     -33.350  11.839 -50.207  1.00 33.57           C  
ANISOU 1645  CB  THR A 148     4715   3833   4207    376   -549    118
ATOM   1646  OG1 THR A 148     -34.089  11.693 -49.000  1.00 36.15           O  
ANISOU 1646  OG1 THR A 148     4966   4213   4558    331   -548    153
ATOM   1647  CG2 THR A 148     -33.508  10.529 -50.991  1.00 33.74           C  
ANISOU 1647  CG2 THR A 148     4829   3796   4193    346   -636    124
ATOM   1648  H   THR A 148     -31.897  10.556 -48.695  1.00 29.21           H  
ATOM   1649  HA  THR A 148     -31.322  12.286 -50.899  1.00 30.20           H  
ATOM   1650  HB  THR A 148     -33.822  12.632 -50.791  1.00 33.57           H  
ATOM   1651  HG1 THR A 148     -34.289  12.575 -48.671  1.00 36.15           H  
ATOM   1652 HG21 THR A 148     -34.559  10.297 -51.165  1.00 33.74           H  
ATOM   1653 HG22 THR A 148     -33.029  10.596 -51.967  1.00 33.74           H  
ATOM   1654 HG23 THR A 148     -33.075   9.678 -50.464  1.00 33.74           H  
ATOM   1655  N   PRO A 149     -31.550  14.711 -49.858  1.00 31.18           N  
ANISOU 1655  N   PRO A 149     4371   3552   3924    498   -367     46
ATOM   1656  CA  PRO A 149     -31.584  16.038 -49.213  1.00 31.03           C  
ANISOU 1656  CA  PRO A 149     4304   3561   3924    523   -306     41
ATOM   1657  C   PRO A 149     -32.994  16.446 -48.742  1.00 31.68           C  
ANISOU 1657  C   PRO A 149     4322   3690   4024    521   -308     76
ATOM   1658  O   PRO A 149     -33.985  15.875 -49.201  1.00 33.32           O  
ANISOU 1658  O   PRO A 149     4517   3911   4233    502   -357    110
ATOM   1659  CB  PRO A 149     -31.056  16.982 -50.307  1.00 33.05           C  
ANISOU 1659  CB  PRO A 149     4596   3791   4171    563   -284     23
ATOM   1660  CG  PRO A 149     -31.408  16.295 -51.615  1.00 34.53           C  
ANISOU 1660  CG  PRO A 149     4822   3955   4342    562   -337     34
ATOM   1661  CD  PRO A 149     -31.228  14.818 -51.282  1.00 31.53           C  
ANISOU 1661  CD  PRO A 149     4474   3560   3945    529   -383     35
ATOM   1662  HA  PRO A 149     -30.905  16.053 -48.359  1.00 31.03           H  
ATOM   1663  HB3 PRO A 149     -29.971  17.060 -50.221  1.00 33.05           H  
ATOM   1664  HB2 PRO A 149     -31.462  17.993 -50.251  1.00 33.05           H  
ATOM   1665  HG3 PRO A 149     -30.796  16.624 -52.455  1.00 34.53           H  
ATOM   1666  HG2 PRO A 149     -32.452  16.491 -51.861  1.00 34.53           H  
ATOM   1667  HD2 PRO A 149     -31.850  14.200 -51.931  1.00 31.53           H  
ATOM   1668  HD3 PRO A 149     -30.188  14.518 -51.414  1.00 31.53           H  
ATOM   1669  N   ILE A 150     -33.062  17.442 -47.850  1.00 30.17           N  
ANISOU 1669  N   ILE A 150     4096   3525   3840    546   -257     71
ATOM   1670  CA  ILE A 150     -34.308  18.142 -47.543  1.00 31.08           C  
ANISOU 1670  CA  ILE A 150     4155   3692   3962    573   -244    106
ATOM   1671  C   ILE A 150     -34.377  19.330 -48.513  1.00 30.52           C  
ANISOU 1671  C   ILE A 150     4110   3599   3886    621   -226     95
ATOM   1672  O   ILE A 150     -33.495  20.190 -48.487  1.00 29.89           O  
ANISOU 1672  O   ILE A 150     4078   3479   3801    643   -194     59
ATOM   1673  CB  ILE A 150     -34.354  18.663 -46.074  1.00 33.57           C  
ANISOU 1673  CB  ILE A 150     4443   4037   4275    597   -194    100
ATOM   1674  CG1 ILE A 150     -34.355  17.500 -45.057  1.00 35.73           C  
ANISOU 1674  CG1 ILE A 150     4682   4339   4553    549   -211    116
ATOM   1675  CG2 ILE A 150     -35.521  19.634 -45.774  1.00 34.06           C  
ANISOU 1675  CG2 ILE A 150     4460   4153   4329    655   -167    133
ATOM   1676  CD1 ILE A 150     -35.560  16.550 -45.151  1.00 39.52           C  
ANISOU 1676  CD1 ILE A 150     5099   4877   5039    515   -258    180
ATOM   1677  H   ILE A 150     -32.225  17.956 -47.619  1.00 30.17           H  
ATOM   1678  HA  ILE A 150     -35.171  17.495 -47.712  1.00 31.08           H  
ATOM   1679  HB  ILE A 150     -33.439  19.231 -45.894  1.00 33.57           H  
ATOM   1680 HG13 ILE A 150     -34.297  17.895 -44.042  1.00 35.73           H  
ATOM   1681 HG12 ILE A 150     -33.449  16.915 -45.192  1.00 35.73           H  
ATOM   1682 HG21 ILE A 150     -35.559  19.889 -44.714  1.00 34.06           H  
ATOM   1683 HG22 ILE A 150     -35.421  20.576 -46.313  1.00 34.06           H  
ATOM   1684 HG23 ILE A 150     -36.488  19.211 -46.046  1.00 34.06           H  
ATOM   1685 HD11 ILE A 150     -35.646  15.962 -44.237  1.00 39.52           H  
ATOM   1686 HD12 ILE A 150     -36.506  17.076 -45.271  1.00 39.52           H  
ATOM   1687 HD13 ILE A 150     -35.454  15.849 -45.978  1.00 39.52           H  
ATOM   1688  N   VAL A 151     -35.390  19.321 -49.378  1.00 29.80           N  
ANISOU 1688  N   VAL A 151     3989   3536   3796    631   -251    133
ATOM   1689  CA  VAL A 151     -35.607  20.335 -50.395  1.00 30.76           C  
ANISOU 1689  CA  VAL A 151     4134   3640   3913    675   -240    129
ATOM   1690  C   VAL A 151     -36.782  21.214 -49.939  1.00 32.34           C  
ANISOU 1690  C   VAL A 151     4287   3893   4107    732   -214    163
ATOM   1691  O   VAL A 151     -37.747  20.691 -49.382  1.00 35.38           O  
ANISOU 1691  O   VAL A 151     4602   4349   4494    725   -225    212
ATOM   1692  CB  VAL A 151     -35.963  19.666 -51.754  1.00 34.07           C  
ANISOU 1692  CB  VAL A 151     4567   4045   4332    644   -300    146
ATOM   1693  CG1 VAL A 151     -36.270  20.669 -52.886  1.00 36.39           C  
ANISOU 1693  CG1 VAL A 151     4882   4324   4621    689   -292    146
ATOM   1694  CG2 VAL A 151     -34.846  18.703 -52.203  1.00 35.82           C  
ANISOU 1694  CG2 VAL A 151     4849   4215   4547    607   -326    114
ATOM   1695  H   VAL A 151     -36.110  18.619 -49.309  1.00 29.80           H  
ATOM   1696  HA  VAL A 151     -34.718  20.957 -50.524  1.00 30.76           H  
ATOM   1697  HB  VAL A 151     -36.864  19.066 -51.613  1.00 34.07           H  
ATOM   1698 HG11 VAL A 151     -36.421  20.155 -53.835  1.00 36.39           H  
ATOM   1699 HG12 VAL A 151     -37.181  21.239 -52.698  1.00 36.39           H  
ATOM   1700 HG13 VAL A 151     -35.453  21.377 -53.024  1.00 36.39           H  
ATOM   1701 HG21 VAL A 151     -35.070  18.256 -53.172  1.00 35.82           H  
ATOM   1702 HG22 VAL A 151     -33.888  19.216 -52.289  1.00 35.82           H  
ATOM   1703 HG23 VAL A 151     -34.712  17.878 -51.502  1.00 35.82           H  
ATOM   1704  N   HIS A 152     -36.670  22.522 -50.185  1.00 30.68           N  
ANISOU 1704  N   HIS A 152     4116   3654   3886    791   -176    140
ATOM   1705  CA  HIS A 152     -37.704  23.498 -49.878  1.00 34.38           C  
ANISOU 1705  CA  HIS A 152     4552   4172   4339    865   -148    173
ATOM   1706  C   HIS A 152     -38.257  23.971 -51.224  1.00 40.02           C  
ANISOU 1706  C   HIS A 152     5268   4883   5054    879   -173    193
ATOM   1707  O   HIS A 152     -37.582  24.718 -51.930  1.00 41.91           O  
ANISOU 1707  O   HIS A 152     5572   5059   5293    883   -172    158
ATOM   1708  CB  HIS A 152     -37.095  24.664 -49.070  1.00 34.71           C  
ANISOU 1708  CB  HIS A 152     4650   4181   4358    927    -96    137
ATOM   1709  CG  HIS A 152     -36.525  24.285 -47.724  1.00 33.07           C  
ANISOU 1709  CG  HIS A 152     4453   3963   4150    901    -80    111
ATOM   1710  ND1 HIS A 152     -35.313  23.630 -47.560  1.00 36.00           N  
ANISOU 1710  ND1 HIS A 152     4797   4382   4500    948    -47    127
ATOM   1711  CD2 HIS A 152     -37.007  24.491 -46.451  1.00 34.17           C  
ANISOU 1711  CD2 HIS A 152     4623   4057   4303    836    -92     76
ATOM   1712  CE1 HIS A 152     -35.122  23.468 -46.250  1.00 37.40           C  
ANISOU 1712  CE1 HIS A 152     4990   4537   4683    904    -44     98
ATOM   1713  NE2 HIS A 152     -36.111  23.966 -45.520  1.00 36.37           N  
ANISOU 1713  NE2 HIS A 152     4898   4349   4573    838    -68     66
ATOM   1714  H   HIS A 152     -35.901  22.876 -50.733  1.00 30.68           H  
ATOM   1715  HA  HIS A 152     -38.514  23.058 -49.291  1.00 34.38           H  
ATOM   1716  HB3 HIS A 152     -37.858  25.425 -48.901  1.00 34.71           H  
ATOM   1717  HB2 HIS A 152     -36.308  25.160 -49.640  1.00 34.71           H  
ATOM   1718  HD1 HIS A 152     -34.686  23.314 -48.283  1.00 36.00           H  
ATOM   1719  HD2 HIS A 152     -37.923  24.969 -46.134  1.00 34.17           H  
ATOM   1720  HE1 HIS A 152     -34.259  22.974 -45.827  1.00 37.40           H  
ATOM   1721  N   HIS A 153     -39.454  23.496 -51.588  1.00 42.24           N  
ANISOU 1721  N   HIS A 153     5474   5238   5335    880   -198    255
ATOM   1722  CA  HIS A 153     -40.131  23.778 -52.866  1.00 44.26           C  
ANISOU 1722  CA  HIS A 153     5727   5497   5592    886   -229    280
ATOM   1723  C   HIS A 153     -40.829  25.130 -52.751  1.00 44.15           C  
ANISOU 1723  C   HIS A 153     5715   5505   5557    984   -187    294
ATOM   1724  O   HIS A 153     -41.837  25.421 -53.395  1.00 44.27           O  
ANISOU 1724  O   HIS A 153     5652   5608   5558   1025   -181    358
ATOM   1725  CB  HIS A 153     -41.111  22.628 -53.207  1.00 48.21           C  
ANISOU 1725  CB  HIS A 153     6148   6068   6100    827   -290    350
ATOM   1726  CG  HIS A 153     -40.502  21.248 -53.199  1.00 55.06           C  
ANISOU 1726  CG  HIS A 153     7032   6906   6982    734   -342    338
ATOM   1727  ND1 HIS A 153     -40.362  20.506 -52.024  1.00 58.19           N  
ANISOU 1727  ND1 HIS A 153     7502   7226   7381    692   -382    299
ATOM   1728  CD2 HIS A 153     -39.994  20.516 -54.249  1.00 57.26           C  
ANISOU 1728  CD2 HIS A 153     7268   7221   7266    683   -360    363
ATOM   1729  CE1 HIS A 153     -39.799  19.364 -52.396  1.00 59.17           C  
ANISOU 1729  CE1 HIS A 153     7634   7339   7509    623   -424    300
ATOM   1730  NE2 HIS A 153     -39.560  19.317 -53.708  1.00 59.03           N  
ANISOU 1730  NE2 HIS A 153     7547   7386   7497    609   -415    337
ATOM   1731  H   HIS A 153     -39.871  22.757 -51.033  1.00 42.24           H  
ATOM   1732  HA  HIS A 153     -39.390  23.841 -53.666  1.00 44.26           H  
ATOM   1733  HXT HIS A 153     -40.375  25.835 -52.054  1.00 44.15           H  
ATOM   1734  HB3 HIS A 153     -41.546  22.792 -54.194  1.00 48.21           H  
ATOM   1735  HB2 HIS A 153     -41.951  22.621 -52.510  1.00 48.21           H  
ATOM   1736  HD2 HIS A 153     -39.921  20.744 -55.305  1.00 57.26           H  
ATOM   1737  HE1 HIS A 153     -39.561  18.566 -51.706  1.00 59.17           H  
ATOM   1738  HE2 HIS A 153     -39.153  18.536 -54.203  1.00 59.03           H  
TER    1739      HIS A 153
ATOM   1740  N   PHE B  41      -3.043   2.539 -11.933  1.00 47.44           N  
ANISOU 1740  N   PHE B  41     5256   7640   5127    368     15    113
ATOM   1741  CA  PHE B  41      -4.467   2.948 -12.069  1.00 46.64           C  
ANISOU 1741  CA  PHE B  41     5277   7315   5128    310     15     74
ATOM   1742  C   PHE B  41      -5.390   2.220 -11.028  1.00 45.36           C  
ANISOU 1742  C   PHE B  41     5206   7002   5027    358      8     44
ATOM   1743  O   PHE B  41      -5.158   1.062 -10.665  1.00 47.36           O  
ANISOU 1743  O   PHE B  41     5464   7279   5252    478      2     42
ATOM   1744  CB  PHE B  41      -5.001   2.706 -13.502  1.00 47.53           C  
ANISOU 1744  CB  PHE B  41     5428   7368   5261    385     28     53
ATOM   1745  CG  PHE B  41      -4.460   3.657 -14.560  1.00 50.09           C  
ANISOU 1745  CG  PHE B  41     5688   7798   5545    303     34     79
ATOM   1746  CD1 PHE B  41      -4.777   5.031 -14.515  1.00 51.85           C  
ANISOU 1746  CD1 PHE B  41     5925   7992   5782    128     21     93
ATOM   1747  CD2 PHE B  41      -3.587   3.189 -15.563  1.00 51.71           C  
ANISOU 1747  CD2 PHE B  41     5822   8148   5679    402     48     95
ATOM   1748  CE1 PHE B  41      -4.254   5.897 -15.466  1.00 52.92           C  
ANISOU 1748  CE1 PHE B  41     6012   8227   5867     34     17    125
ATOM   1749  CE2 PHE B  41      -3.082   4.067 -16.511  1.00 52.60           C  
ANISOU 1749  CE2 PHE B  41     5865   8379   5742    312     54    128
ATOM   1750  CZ  PHE B  41      -3.417   5.414 -16.462  1.00 52.67           C  
ANISOU 1750  CZ  PHE B  41     5897   8341   5773    121     36    144
ATOM   1751  H1  PHE B  41      -2.483   2.832 -12.724  1.00 47.44           H  
ATOM   1752  H2  PHE B  41      -2.593   2.880 -11.094  1.00 47.44           H  
ATOM   1753  HA  PHE B  41      -4.493   4.020 -11.877  1.00 46.64           H  
ATOM   1754  HB3 PHE B  41      -6.086   2.814 -13.531  1.00 47.53           H  
ATOM   1755  HB2 PHE B  41      -4.808   1.673 -13.799  1.00 47.53           H  
ATOM   1756  HD1 PHE B  41      -5.428   5.418 -13.747  1.00 51.85           H  
ATOM   1757  HD2 PHE B  41      -3.315   2.145 -15.608  1.00 51.71           H  
ATOM   1758  HE1 PHE B  41      -4.495   6.949 -15.431  1.00 52.92           H  
ATOM   1759  HE2 PHE B  41      -2.425   3.704 -17.288  1.00 52.60           H  
ATOM   1760  HZ  PHE B  41      -3.015   6.089 -17.203  1.00 52.67           H  
ATOM   1761  N   PRO B  42      -6.457   2.913 -10.563  1.00 41.26           N  
ANISOU 1761  N   PRO B  42     4765   6332   4580    273      6     22
ATOM   1762  CA  PRO B  42      -7.426   2.317  -9.628  1.00 39.12           C  
ANISOU 1762  CA  PRO B  42     4569   5938   4358    307      1      1
ATOM   1763  C   PRO B  42      -8.298   1.230 -10.286  1.00 37.07           C  
ANISOU 1763  C   PRO B  42     4385   5566   4132    399     -2    -19
ATOM   1764  O   PRO B  42      -8.859   1.459 -11.356  1.00 37.97           O  
ANISOU 1764  O   PRO B  42     4520   5639   4266    406      4    -29
ATOM   1765  CB  PRO B  42      -8.269   3.524  -9.178  1.00 39.57           C  
ANISOU 1765  CB  PRO B  42     4669   5905   4460    192      2    -11
ATOM   1766  CG  PRO B  42      -8.232   4.475 -10.362  1.00 40.49           C  
ANISOU 1766  CG  PRO B  42     4783   6024   4577    128      5    -12
ATOM   1767  CD  PRO B  42      -6.826   4.290 -10.911  1.00 40.12           C  
ANISOU 1767  CD  PRO B  42     4648   6131   4464    149      5     18
ATOM   1768  HA  PRO B  42      -6.905   1.890  -8.770  1.00 39.12           H  
ATOM   1769  HB3 PRO B  42      -7.799   3.996  -8.315  1.00 39.57           H  
ATOM   1770  HB2 PRO B  42      -9.290   3.265  -8.893  1.00 39.57           H  
ATOM   1771  HG3 PRO B  42      -8.463   5.508 -10.115  1.00 40.49           H  
ATOM   1772  HG2 PRO B  42      -8.953   4.147 -11.112  1.00 40.49           H  
ATOM   1773  HD2 PRO B  42      -6.810   4.482 -11.983  1.00 40.12           H  
ATOM   1774  HD3 PRO B  42      -6.135   4.981 -10.425  1.00 40.12           H  
ATOM   1775  N   ARG B  43      -8.458   0.088  -9.601  1.00 35.24           N  
ANISOU 1775  N   ARG B  43     4210   5276   3904    454    -18    -22
ATOM   1776  CA  ARG B  43      -9.399  -0.970  -9.989  1.00 33.18           C  
ANISOU 1776  CA  ARG B  43     4047   4896   3665    509    -37    -33
ATOM   1777  C   ARG B  43     -10.860  -0.486  -9.964  1.00 30.40           C  
ANISOU 1777  C   ARG B  43     3731   4439   3381    415    -30    -41
ATOM   1778  O   ARG B  43     -11.663  -0.921 -10.788  1.00 30.03           O  
ANISOU 1778  O   ARG B  43     3731   4320   3361    417    -36    -47
ATOM   1779  CB  ARG B  43      -9.226  -2.179  -9.033  1.00 36.93           C  
ANISOU 1779  CB  ARG B  43     4583   5344   4106    577    -68    -25
ATOM   1780  CG  ARG B  43     -10.232  -3.346  -9.209  1.00 40.65           C  
ANISOU 1780  CG  ARG B  43     5181   5676   4587    595   -105    -25
ATOM   1781  CD  ARG B  43     -10.081  -4.402  -8.098  1.00 44.86           C  
ANISOU 1781  CD  ARG B  43     5787   6183   5074    648   -144    -14
ATOM   1782  NE  ARG B  43     -11.135  -5.441  -8.109  1.00 47.09           N  
ANISOU 1782  NE  ARG B  43     6212   6329   5349    639   -194     -3
ATOM   1783  CZ  ARG B  43     -12.345  -5.397  -7.522  1.00 47.60           C  
ANISOU 1783  CZ  ARG B  43     6312   6333   5441    534   -207     17
ATOM   1784  NH1 ARG B  43     -12.806  -4.281  -6.950  1.00 46.00           N  
ANISOU 1784  NH1 ARG B  43     6015   6185   5279    448   -167     19
ATOM   1785  NH2 ARG B  43     -13.114  -6.488  -7.505  1.00 47.01           N1+
ANISOU 1785  NH2 ARG B  43     6371   6146   5343    507   -264     37
ATOM   1786  H   ARG B  43      -7.902  -0.055  -8.773  1.00 35.24           H  
ATOM   1787  HA  ARG B  43      -9.170  -1.280 -11.012  1.00 33.18           H  
ATOM   1788  HB3 ARG B  43      -9.320  -1.813  -8.009  1.00 36.93           H  
ATOM   1789  HB2 ARG B  43      -8.207  -2.563  -9.121  1.00 36.93           H  
ATOM   1790  HG3 ARG B  43      -9.984  -3.799 -10.169  1.00 40.65           H  
ATOM   1791  HG2 ARG B  43     -11.273  -3.035  -9.299  1.00 40.65           H  
ATOM   1792  HD3 ARG B  43      -9.926  -3.960  -7.112  1.00 44.86           H  
ATOM   1793  HD2 ARG B  43      -9.169  -4.962  -8.313  1.00 44.86           H  
ATOM   1794 HH22 ARG B  43     -14.046  -6.481  -7.107  1.00 47.01           H  
ATOM   1795 HH21 ARG B  43     -12.818  -7.377  -7.881  1.00 47.01           H  
ATOM   1796 HH12 ARG B  43     -13.685  -4.229  -6.456  1.00 46.00           H  
ATOM   1797 HH11 ARG B  43     -12.370  -3.371  -7.100  1.00 46.00           H  
ATOM   1798  HE  ARG B  43     -10.838  -6.286  -8.574  1.00 47.09           H  
ATOM   1799  N   THR B  44     -11.197   0.333  -8.964  1.00 29.35           N  
ANISOU 1799  N   THR B  44     3575   4308   3267    341    -18    -40
ATOM   1800  CA  THR B  44     -12.556   0.754  -8.683  1.00 27.93           C  
ANISOU 1800  CA  THR B  44     3419   4061   3132    275     -9    -46
ATOM   1801  C   THR B  44     -12.559   2.267  -8.462  1.00 29.58           C  
ANISOU 1801  C   THR B  44     3594   4294   3350    215     11    -60
ATOM   1802  O   THR B  44     -11.692   2.776  -7.749  1.00 30.86           O  
ANISOU 1802  O   THR B  44     3726   4517   3483    187     12    -56
ATOM   1803  CB  THR B  44     -13.111   0.025  -7.430  1.00 30.31           C  
ANISOU 1803  CB  THR B  44     3745   4340   3430    257    -18    -34
ATOM   1804  OG1 THR B  44     -13.040  -1.376  -7.674  1.00 32.82           O  
ANISOU 1804  OG1 THR B  44     4125   4618   3729    303    -51    -18
ATOM   1805  CG2 THR B  44     -14.561   0.377  -7.065  1.00 30.72           C  
ANISOU 1805  CG2 THR B  44     3803   4357   3511    204     -5    -35
ATOM   1806  H   THR B  44     -10.489   0.768  -8.390  1.00 29.35           H  
ATOM   1807  HA  THR B  44     -13.189   0.533  -9.537  1.00 27.93           H  
ATOM   1808  HB  THR B  44     -12.479   0.251  -6.568  1.00 30.31           H  
ATOM   1809  HG1 THR B  44     -13.339  -1.485  -8.586  1.00 32.82           H  
ATOM   1810 HG21 THR B  44     -14.914  -0.234  -6.233  1.00 30.72           H  
ATOM   1811 HG22 THR B  44     -14.655   1.418  -6.752  1.00 30.72           H  
ATOM   1812 HG23 THR B  44     -15.238   0.225  -7.907  1.00 30.72           H  
ATOM   1813  N   VAL B  45     -13.502   2.944  -9.115  1.00 28.49           N  
ANISOU 1813  N   VAL B  45     3475   4107   3243    192     20    -73
ATOM   1814  CA  VAL B  45     -13.616   4.394  -9.133  1.00 28.61           C  
ANISOU 1814  CA  VAL B  45     3495   4119   3256    145     28    -89
ATOM   1815  C   VAL B  45     -15.062   4.782  -8.808  1.00 28.75           C  
ANISOU 1815  C   VAL B  45     3540   4092   3292    144     37   -102
ATOM   1816  O   VAL B  45     -15.966   3.962  -8.984  1.00 27.67           O  
ANISOU 1816  O   VAL B  45     3402   3938   3175    162     39    -92
ATOM   1817  CB  VAL B  45     -13.224   4.956 -10.529  1.00 29.89           C  
ANISOU 1817  CB  VAL B  45     3655   4284   3417    132     25    -94
ATOM   1818  CG1 VAL B  45     -11.772   4.577 -10.860  1.00 30.29           C  
ANISOU 1818  CG1 VAL B  45     3657   4421   3431    141     20    -75
ATOM   1819  CG2 VAL B  45     -14.160   4.563 -11.693  1.00 28.99           C  
ANISOU 1819  CG2 VAL B  45     3560   4113   3340    165     28   -100
ATOM   1820  H   VAL B  45     -14.192   2.451  -9.678  1.00 28.49           H  
ATOM   1821  HA  VAL B  45     -12.978   4.840  -8.368  1.00 28.61           H  
ATOM   1822  HB  VAL B  45     -13.261   6.044 -10.462  1.00 29.89           H  
ATOM   1823 HG11 VAL B  45     -11.402   5.091 -11.747  1.00 30.29           H  
ATOM   1824 HG12 VAL B  45     -11.105   4.811 -10.032  1.00 30.29           H  
ATOM   1825 HG13 VAL B  45     -11.684   3.506 -11.037  1.00 30.29           H  
ATOM   1826 HG21 VAL B  45     -13.801   4.975 -12.635  1.00 28.99           H  
ATOM   1827 HG22 VAL B  45     -14.220   3.482 -11.812  1.00 28.99           H  
ATOM   1828 HG23 VAL B  45     -15.173   4.941 -11.555  1.00 28.99           H  
ATOM   1829  N   MET B  46     -15.246   6.013  -8.330  1.00 27.49           N  
ANISOU 1829  N   MET B  46     3411   3922   3112    123     38   -121
ATOM   1830  CA  MET B  46     -16.552   6.580  -8.034  1.00 27.02           C  
ANISOU 1830  CA  MET B  46     3375   3839   3051    151     48   -137
ATOM   1831  C   MET B  46     -17.042   7.361  -9.255  1.00 28.22           C  
ANISOU 1831  C   MET B  46     3559   3951   3213    164     44   -154
ATOM   1832  O   MET B  46     -16.280   8.146  -9.817  1.00 29.13           O  
ANISOU 1832  O   MET B  46     3708   4045   3316    131     28   -162
ATOM   1833  CB  MET B  46     -16.447   7.505  -6.810  1.00 27.27           C  
ANISOU 1833  CB  MET B  46     3450   3873   3037    147     45   -154
ATOM   1834  CG  MET B  46     -16.171   6.737  -5.513  1.00 27.86           C  
ANISOU 1834  CG  MET B  46     3492   3990   3105    144     53   -137
ATOM   1835  SD  MET B  46     -16.139   7.778  -4.030  1.00 32.67           S  
ANISOU 1835  SD  MET B  46     4160   4600   3653    147     48   -158
ATOM   1836  CE  MET B  46     -14.518   8.567  -4.226  1.00 31.50           C  
ANISOU 1836  CE  MET B  46     4047   4442   3480     68     14   -154
ATOM   1837  H   MET B  46     -14.458   6.662  -8.303  1.00 27.49           H  
ATOM   1838  HA  MET B  46     -17.259   5.786  -7.801  1.00 27.02           H  
ATOM   1839  HB3 MET B  46     -17.375   8.064  -6.694  1.00 27.27           H  
ATOM   1840  HB2 MET B  46     -15.670   8.253  -6.977  1.00 27.27           H  
ATOM   1841  HG3 MET B  46     -15.229   6.192  -5.580  1.00 27.86           H  
ATOM   1842  HG2 MET B  46     -16.947   5.985  -5.366  1.00 27.86           H  
ATOM   1843  HE1 MET B  46     -14.311   9.220  -3.378  1.00 31.50           H  
ATOM   1844  HE2 MET B  46     -13.732   7.814  -4.277  1.00 31.50           H  
ATOM   1845  HE3 MET B  46     -14.480   9.168  -5.134  1.00 31.50           H  
ATOM   1846  N   VAL B  47     -18.305   7.160  -9.627  1.00 28.14           N  
ANISOU 1846  N   VAL B  47     3537   3941   3216    204     55   -156
ATOM   1847  CA  VAL B  47     -18.960   7.906 -10.686  1.00 28.53           C  
ANISOU 1847  CA  VAL B  47     3614   3956   3270    229     51   -173
ATOM   1848  C   VAL B  47     -20.213   8.568 -10.102  1.00 30.57           C  
ANISOU 1848  C   VAL B  47     3884   4237   3495    296     61   -189
ATOM   1849  O   VAL B  47     -21.061   7.881  -9.530  1.00 31.63           O  
ANISOU 1849  O   VAL B  47     3958   4436   3626    316     78   -169
ATOM   1850  CB  VAL B  47     -19.371   6.994 -11.870  1.00 28.89           C  
ANISOU 1850  CB  VAL B  47     3622   3997   3359    223     50   -153
ATOM   1851  CG1 VAL B  47     -20.178   7.732 -12.962  1.00 30.67           C  
ANISOU 1851  CG1 VAL B  47     3875   4191   3588    252     45   -169
ATOM   1852  CG2 VAL B  47     -18.128   6.329 -12.490  1.00 29.79           C  
ANISOU 1852  CG2 VAL B  47     3728   4101   3489    188     41   -140
ATOM   1853  H   VAL B  47     -18.877   6.476  -9.133  1.00 28.14           H  
ATOM   1854  HA  VAL B  47     -18.303   8.681 -11.081  1.00 28.53           H  
ATOM   1855  HB  VAL B  47     -20.009   6.193 -11.490  1.00 28.89           H  
ATOM   1856 HG11 VAL B  47     -20.388   7.079 -13.808  1.00 30.67           H  
ATOM   1857 HG12 VAL B  47     -21.144   8.081 -12.600  1.00 30.67           H  
ATOM   1858 HG13 VAL B  47     -19.643   8.606 -13.333  1.00 30.67           H  
ATOM   1859 HG21 VAL B  47     -18.381   5.757 -13.380  1.00 29.79           H  
ATOM   1860 HG22 VAL B  47     -17.387   7.074 -12.777  1.00 29.79           H  
ATOM   1861 HG23 VAL B  47     -17.645   5.648 -11.788  1.00 29.79           H  
ATOM   1862  N   ASN B  48     -20.303   9.889 -10.265  1.00 31.07           N  
ANISOU 1862  N   ASN B  48     4028   4253   3522    334     46   -221
ATOM   1863  CA  ASN B  48     -21.493  10.695 -10.023  1.00 32.26           C  
ANISOU 1863  CA  ASN B  48     4201   4432   3626    432     53   -243
ATOM   1864  C   ASN B  48     -22.436  10.543 -11.236  1.00 33.96           C  
ANISOU 1864  C   ASN B  48     4377   4660   3868    460     55   -235
ATOM   1865  O   ASN B  48     -22.072  10.940 -12.347  1.00 33.48           O  
ANISOU 1865  O   ASN B  48     4361   4532   3828    436     36   -244
ATOM   1866  CB  ASN B  48     -21.026  12.142  -9.753  1.00 33.13           C  
ANISOU 1866  CB  ASN B  48     4451   4466   3671    468     22   -284
ATOM   1867  CG  ASN B  48     -22.115  13.182  -9.499  1.00 39.36           C  
ANISOU 1867  CG  ASN B  48     5293   5272   4389    603     21   -316
ATOM   1868  OD1 ASN B  48     -23.313  12.907  -9.438  1.00 39.82           O  
ANISOU 1868  OD1 ASN B  48     5275   5405   4449    673     42   -307
ATOM   1869  ND2 ASN B  48     -21.690  14.428  -9.346  1.00 42.46           N  
ANISOU 1869  ND2 ASN B  48     5826   5600   4706    647    -10   -352
ATOM   1870  H   ASN B  48     -19.510  10.375 -10.684  1.00 31.07           H  
ATOM   1871  HA  ASN B  48     -21.969  10.324  -9.119  1.00 32.26           H  
ATOM   1872  HB3 ASN B  48     -20.425  12.502 -10.587  1.00 33.13           H  
ATOM   1873  HB2 ASN B  48     -20.358  12.145  -8.890  1.00 33.13           H  
ATOM   1874 HD22 ASN B  48     -22.334  15.194  -9.312  1.00 42.46           H  
ATOM   1875 HD21 ASN B  48     -20.684  14.680  -9.403  1.00 42.46           H  
ATOM   1876  N   LEU B  49     -23.600   9.923 -11.012  1.00 36.08           N  
ANISOU 1876  N   LEU B  49     4551   5026   4132    495     77   -209
ATOM   1877  CA  LEU B  49     -24.554   9.542 -12.058  1.00 37.12           C  
ANISOU 1877  CA  LEU B  49     4632   5190   4283    508     76   -192
ATOM   1878  C   LEU B  49     -25.436  10.700 -12.556  1.00 38.81           C  
ANISOU 1878  C   LEU B  49     4887   5414   4445    622     70   -223
ATOM   1879  O   LEU B  49     -26.198  10.500 -13.501  1.00 39.56           O  
ANISOU 1879  O   LEU B  49     4930   5552   4548    640     68   -206
ATOM   1880  CB  LEU B  49     -25.459   8.387 -11.568  1.00 36.83           C  
ANISOU 1880  CB  LEU B  49     4476   5270   4248    474     91   -139
ATOM   1881  CG  LEU B  49     -24.772   7.021 -11.376  1.00 38.66           C  
ANISOU 1881  CG  LEU B  49     4686   5479   4525    367     85   -104
ATOM   1882  CD1 LEU B  49     -25.818   5.988 -10.922  1.00 40.81           C  
ANISOU 1882  CD1 LEU B  49     4865   5862   4779    317     85    -45
ATOM   1883  CD2 LEU B  49     -24.077   6.523 -12.655  1.00 37.88           C  
ANISOU 1883  CD2 LEU B  49     4632   5279   4483    313     63   -107
ATOM   1884  H   LEU B  49     -23.842   9.655 -10.060  1.00 36.08           H  
ATOM   1885  HA  LEU B  49     -23.986   9.205 -12.924  1.00 37.12           H  
ATOM   1886  HB3 LEU B  49     -26.271   8.246 -12.283  1.00 36.83           H  
ATOM   1887  HB2 LEU B  49     -25.941   8.682 -10.634  1.00 36.83           H  
ATOM   1888  HG  LEU B  49     -24.020   7.114 -10.591  1.00 38.66           H  
ATOM   1889 HD11 LEU B  49     -25.474   4.963 -11.058  1.00 40.81           H  
ATOM   1890 HD12 LEU B  49     -26.062   6.115  -9.868  1.00 40.81           H  
ATOM   1891 HD13 LEU B  49     -26.752   6.091 -11.476  1.00 40.81           H  
ATOM   1892 HD21 LEU B  49     -23.903   5.447 -12.640  1.00 37.88           H  
ATOM   1893 HD22 LEU B  49     -24.686   6.734 -13.533  1.00 37.88           H  
ATOM   1894 HD23 LEU B  49     -23.107   6.995 -12.792  1.00 37.88           H  
ATOM   1895  N   ASN B  50     -25.356  11.879 -11.928  1.00 38.90           N  
ANISOU 1895  N   ASN B  50     5003   5382   4396    702     59   -267
ATOM   1896  CA  ASN B  50     -26.112  13.068 -12.335  1.00 40.81           C  
ANISOU 1896  CA  ASN B  50     5320   5613   4572    833     43   -304
ATOM   1897  C   ASN B  50     -25.426  13.704 -13.551  1.00 42.55           C  
ANISOU 1897  C   ASN B  50     5647   5697   4822    787      6   -323
ATOM   1898  O   ASN B  50     -24.594  14.600 -13.379  1.00 42.77           O  
ANISOU 1898  O   ASN B  50     5808   5613   4830    753    -26   -350
ATOM   1899  CB  ASN B  50     -26.213  14.049 -11.148  1.00 42.40           C  
ANISOU 1899  CB  ASN B  50     5624   5805   4679    942     35   -345
ATOM   1900  CG  ASN B  50     -27.284  13.659 -10.134  1.00 47.54           C  
ANISOU 1900  CG  ASN B  50     6157   6627   5278   1026     76   -326
ATOM   1901  OD1 ASN B  50     -28.439  13.464 -10.481  1.00 49.96           O  
ANISOU 1901  OD1 ASN B  50     6316   7072   5593   1032    102   -285
ATOM   1902  ND2 ASN B  50     -26.936  13.566  -8.858  1.00 47.63           N  
ANISOU 1902  ND2 ASN B  50     6226   6644   5227   1079     79   -348
ATOM   1903  H   ASN B  50     -24.669  11.984 -11.193  1.00 38.90           H  
ATOM   1904  HA  ASN B  50     -27.117  12.731 -12.603  1.00 40.81           H  
ATOM   1905  HB3 ASN B  50     -26.524  15.026 -11.520  1.00 42.40           H  
ATOM   1906  HB2 ASN B  50     -25.241  14.192 -10.677  1.00 42.40           H  
ATOM   1907 HD22 ASN B  50     -27.664  13.327  -8.200  1.00 47.63           H  
ATOM   1908 HD21 ASN B  50     -25.967  13.609  -8.594  1.00 47.63           H  
ATOM   1909  N   ILE B  51     -25.776  13.194 -14.739  1.00 43.54           N  
ANISOU 1909  N   ILE B  51     5709   5840   4994    764      8   -302
ATOM   1910  CA  ILE B  51     -25.239  13.558 -16.050  1.00 44.10           C  
ANISOU 1910  CA  ILE B  51     5853   5801   5101    706    -21   -311
ATOM   1911  C   ILE B  51     -25.267  15.082 -16.319  1.00 45.27           C  
ANISOU 1911  C   ILE B  51     6169   5849   5182    782    -64   -357
ATOM   1912  O   ILE B  51     -26.250  15.755 -16.003  1.00 46.45           O  
ANISOU 1912  O   ILE B  51     6353   6036   5261    925    -69   -381
ATOM   1913  CB  ILE B  51     -26.024  12.843 -17.201  1.00 44.66           C  
ANISOU 1913  CB  ILE B  51     5828   5923   5219    693    -13   -281
ATOM   1914  CG1 ILE B  51     -26.007  11.301 -17.069  1.00 45.52           C  
ANISOU 1914  CG1 ILE B  51     5807   6103   5385    602     11   -231
ATOM   1915  CG2 ILE B  51     -25.557  13.224 -18.627  1.00 44.84           C  
ANISOU 1915  CG2 ILE B  51     5926   5839   5273    644    -41   -291
ATOM   1916  CD1 ILE B  51     -27.205  10.614 -17.748  1.00 46.97           C  
ANISOU 1916  CD1 ILE B  51     5895   6366   5584    603     11   -195
ATOM   1917  H   ILE B  51     -26.401  12.397 -14.735  1.00 43.54           H  
ATOM   1918  HA  ILE B  51     -24.209  13.212 -16.058  1.00 44.10           H  
ATOM   1919  HB  ILE B  51     -27.066  13.157 -17.115  1.00 44.66           H  
ATOM   1920 HG13 ILE B  51     -26.014  10.995 -16.025  1.00 45.52           H  
ATOM   1921 HG12 ILE B  51     -25.080  10.894 -17.471  1.00 45.52           H  
ATOM   1922 HG21 ILE B  51     -26.043  12.619 -19.390  1.00 44.84           H  
ATOM   1923 HG22 ILE B  51     -25.781  14.260 -18.877  1.00 44.84           H  
ATOM   1924 HG23 ILE B  51     -24.481  13.076 -18.739  1.00 44.84           H  
ATOM   1925 HD11 ILE B  51     -26.971   9.577 -17.989  1.00 46.97           H  
ATOM   1926 HD12 ILE B  51     -28.072  10.608 -17.087  1.00 46.97           H  
ATOM   1927 HD13 ILE B  51     -27.503  11.100 -18.676  1.00 46.97           H  
ATOM   1928  N   HIS B  52     -24.207  15.601 -16.940  1.00 45.44           N  
ANISOU 1928  N   HIS B  52     6299   5753   5213    689    -98   -364
ATOM   1929  CA  HIS B  52     -24.188  16.933 -17.537  1.00 46.90           C  
ANISOU 1929  CA  HIS B  52     6667   5824   5329    733   -153   -400
ATOM   1930  C   HIS B  52     -24.193  16.775 -19.064  1.00 46.77           C  
ANISOU 1930  C   HIS B  52     6648   5766   5356    683   -167   -389
ATOM   1931  O   HIS B  52     -23.450  15.956 -19.595  1.00 46.21           O  
ANISOU 1931  O   HIS B  52     6521   5689   5346    554   -157   -360
ATOM   1932  CB  HIS B  52     -22.966  17.712 -17.016  1.00 50.00           C  
ANISOU 1932  CB  HIS B  52     7205   6116   5676    642   -196   -410
ATOM   1933  CG  HIS B  52     -23.140  18.310 -15.637  1.00 55.66           C  
ANISOU 1933  CG  HIS B  52     8010   6827   6311    734   -209   -439
ATOM   1934  ND1 HIS B  52     -24.226  18.043 -14.814  1.00 58.02           N  
ANISOU 1934  ND1 HIS B  52     8515   7006   6525    698   -274   -461
ATOM   1935  CD2 HIS B  52     -22.370  19.218 -14.945  1.00 57.86           C  
ANISOU 1935  CD2 HIS B  52     8203   7211   6571    853   -168   -447
ATOM   1936  CE1 HIS B  52     -24.099  18.807 -13.729  1.00 58.60           C  
ANISOU 1936  CE1 HIS B  52     8627   7103   6535    807   -269   -486
ATOM   1937  NE2 HIS B  52     -22.990  19.534 -13.735  1.00 58.48           N  
ANISOU 1937  NE2 HIS B  52     8432   7230   6556    907   -202   -479
ATOM   1938  H   HIS B  52     -23.413  15.006 -17.157  1.00 45.44           H  
ATOM   1939  HA  HIS B  52     -25.087  17.500 -17.283  1.00 46.90           H  
ATOM   1940  HB3 HIS B  52     -22.733  18.534 -17.696  1.00 50.00           H  
ATOM   1941  HB2 HIS B  52     -22.079  17.077 -17.008  1.00 50.00           H  
ATOM   1942  HD1 HIS B  52     -24.990  17.410 -15.018  1.00 58.02           H  
ATOM   1943  HD2 HIS B  52     -21.436  19.680 -15.232  1.00 57.86           H  
ATOM   1944  HE1 HIS B  52     -24.821  18.828 -12.926  1.00 58.60           H  
ATOM   1945  N   ASN B  53     -25.062  17.509 -19.768  1.00 46.81           N  
ANISOU 1945  N   ASN B  53     6708   5753   5324    794   -188   -411
ATOM   1946  CA  ASN B  53     -25.120  17.433 -21.234  1.00 48.52           C  
ANISOU 1946  CA  ASN B  53     6934   5924   5578    745   -204   -401
ATOM   1947  C   ASN B  53     -24.015  18.347 -21.775  1.00 49.71           C  
ANISOU 1947  C   ASN B  53     7242   5943   5701    626   -256   -404
ATOM   1948  O   ASN B  53     -23.996  19.534 -21.449  1.00 48.33           O  
ANISOU 1948  O   ASN B  53     7231   5685   5446    634   -303   -428
ATOM   1949  CB  ASN B  53     -26.537  17.791 -21.745  1.00 50.61           C  
ANISOU 1949  CB  ASN B  53     7218   6209   5804    895   -217   -421
ATOM   1950  CG  ASN B  53     -27.565  16.656 -21.586  1.00 55.21           C  
ANISOU 1950  CG  ASN B  53     7604   6949   6423    954   -167   -393
ATOM   1951  OD1 ASN B  53     -28.221  16.243 -22.540  1.00 56.76           O  
ANISOU 1951  OD1 ASN B  53     7662   7227   6676    879   -126   -359
ATOM   1952  ND2 ASN B  53     -27.729  16.111 -20.385  1.00 56.21           N  
ANISOU 1952  ND2 ASN B  53     7718   7128   6512   1081   -176   -402
ATOM   1953  H   ASN B  53     -25.535  18.289 -19.336  1.00 46.81           H  
ATOM   1954  HA  ASN B  53     -24.923  16.398 -21.521  1.00 48.52           H  
ATOM   1955  HB3 ASN B  53     -26.482  18.005 -22.813  1.00 50.61           H  
ATOM   1956  HB2 ASN B  53     -26.907  18.705 -21.281  1.00 50.61           H  
ATOM   1957 HD22 ASN B  53     -28.439  15.411 -20.248  1.00 56.21           H  
ATOM   1958 HD21 ASN B  53     -27.195  16.431 -19.591  1.00 56.21           H  
ATOM   1959  N   ARG B  54     -23.090  17.762 -22.537  1.00 51.08           N  
ANISOU 1959  N   ARG B  54     7364   6111   5934    506   -250   -375
ATOM   1960  CA  ARG B  54     -21.890  18.387 -23.060  1.00 53.42           C  
ANISOU 1960  CA  ARG B  54     7772   6325   6202    369   -294   -363
ATOM   1961  C   ARG B  54     -22.063  18.497 -24.578  1.00 56.07           C  
ANISOU 1961  C   ARG B  54     8126   6622   6555    344   -310   -356
ATOM   1962  O   ARG B  54     -21.595  17.642 -25.324  1.00 55.47           O  
ANISOU 1962  O   ARG B  54     7923   6607   6548    288   -273   -329
ATOM   1963  CB  ARG B  54     -20.667  17.531 -22.638  1.00 54.46           C  
ANISOU 1963  CB  ARG B  54     7797   6524   6373    236   -263   -327
ATOM   1964  CG  ARG B  54     -19.293  17.992 -23.171  1.00 57.37           C  
ANISOU 1964  CG  ARG B  54     8238   6858   6704     78   -302   -299
ATOM   1965  CD  ARG B  54     -18.840  19.369 -22.666  1.00 59.82           C  
ANISOU 1965  CD  ARG B  54     8744   7073   6913     34   -373   -311
ATOM   1966  NE  ARG B  54     -18.569  19.353 -21.216  1.00 61.89           N  
ANISOU 1966  NE  ARG B  54     8982   7374   7161     23   -361   -309
ATOM   1967  CZ  ARG B  54     -18.356  20.390 -20.397  1.00 64.46           C  
ANISOU 1967  CZ  ARG B  54     9474   7621   7396     -9   -422   -319
ATOM   1968  NH1 ARG B  54     -18.389  21.646 -20.848  1.00 65.39           N  
ANISOU 1968  NH1 ARG B  54     9812   7608   7423    -33   -504   -333
ATOM   1969  NH2 ARG B  54     -18.112  20.171 -19.111  1.00 62.90           N1+
ANISOU 1969  NH2 ARG B  54     9241   7466   7191    -22   -407   -316
ATOM   1970  H   ARG B  54     -23.185  16.788 -22.831  1.00 51.08           H  
ATOM   1971  HA  ARG B  54     -21.777  19.392 -22.650  1.00 53.42           H  
ATOM   1972  HB3 ARG B  54     -20.804  16.503 -22.967  1.00 54.46           H  
ATOM   1973  HB2 ARG B  54     -20.633  17.479 -21.550  1.00 54.46           H  
ATOM   1974  HG3 ARG B  54     -19.237  17.962 -24.260  1.00 57.37           H  
ATOM   1975  HG2 ARG B  54     -18.566  17.246 -22.843  1.00 57.37           H  
ATOM   1976  HD3 ARG B  54     -19.638  20.091 -22.843  1.00 59.82           H  
ATOM   1977  HD2 ARG B  54     -17.981  19.724 -23.236  1.00 59.82           H  
ATOM   1978 HH22 ARG B  54     -17.905  20.871 -18.419  1.00 62.90           H  
ATOM   1979 HH21 ARG B  54     -18.175  19.197 -18.742  1.00 62.90           H  
ATOM   1980 HH12 ARG B  54     -18.227  22.447 -20.258  1.00 65.39           H  
ATOM   1981 HH11 ARG B  54     -18.588  21.816 -21.823  1.00 65.39           H  
ATOM   1982  HE  ARG B  54     -18.472  18.399 -20.822  1.00 61.89           H  
ATOM   1983  N   ASN B  55     -22.761  19.558 -25.010  1.00 58.03           N  
ANISOU 1983  N   ASN B  55     8544   6771   6736    406   -367   -384
ATOM   1984  CA  ASN B  55     -22.928  19.994 -26.412  1.00 60.92           C  
ANISOU 1984  CA  ASN B  55     8952   7088   7107    387   -392   -379
ATOM   1985  C   ASN B  55     -23.834  19.009 -27.142  1.00 62.00           C  
ANISOU 1985  C   ASN B  55     8921   7309   7325    456   -340   -372
ATOM   1986  O   ASN B  55     -23.953  19.001 -28.368  1.00 62.67           O  
ANISOU 1986  O   ASN B  55     8987   7382   7441    401   -341   -356
ATOM   1987  CB  ASN B  55     -21.578  20.214 -27.170  1.00 63.54           C  
ANISOU 1987  CB  ASN B  55     9314   7394   7432    198   -413   -342
ATOM   1988  CG  ASN B  55     -20.541  21.104 -26.475  1.00 69.43           C  
ANISOU 1988  CG  ASN B  55    10248   8051   8079     97   -484   -339
ATOM   1989  OD1 ASN B  55     -20.754  21.641 -25.391  1.00 71.26           O  
ANISOU 1989  OD1 ASN B  55    10619   8213   8243    177   -524   -371
ATOM   1990  ND2 ASN B  55     -19.375  21.275 -27.088  1.00 71.06           N  
ANISOU 1990  ND2 ASN B  55    10468   8268   8264    -84   -506   -295
ATOM   1991  H   ASN B  55     -23.098  20.204 -24.311  1.00 58.03           H  
ATOM   1992  HA  ASN B  55     -23.454  20.950 -26.380  1.00 60.92           H  
ATOM   1993  HXT ASN B  55     -24.384  18.308 -26.511  1.00 62.00           H  
ATOM   1994  HB3 ASN B  55     -21.783  20.651 -28.149  1.00 63.54           H  
ATOM   1995  HB2 ASN B  55     -21.105  19.251 -27.369  1.00 63.54           H  
ATOM   1996 HD22 ASN B  55     -18.687  21.875 -26.663  1.00 71.06           H  
ATOM   1997 HD21 ASN B  55     -19.181  20.853 -27.984  1.00 71.06           H  
ATOM   1998  N   SER B  64     -32.539  12.082 -35.746  1.00 49.15           N  
ANISOU 1998  N   SER B  64     6439   6250   5985    648   -328   -151
ATOM   1999  CA  SER B  64     -32.900  12.645 -37.079  1.00 48.79           C  
ANISOU 1999  CA  SER B  64     6460   6129   5950    636   -359   -156
ATOM   2000  C   SER B  64     -33.932  11.725 -37.810  1.00 47.27           C  
ANISOU 2000  C   SER B  64     6188   5998   5776    554   -382   -101
ATOM   2001  O   SER B  64     -34.370  10.696 -37.285  1.00 48.84           O  
ANISOU 2001  O   SER B  64     6298   6275   5982    482   -378    -58
ATOM   2002  CB  SER B  64     -31.624  12.849 -37.938  1.00 51.02           C  
ANISOU 2002  CB  SER B  64     6865   6258   6264    573   -353   -187
ATOM   2003  OG  SER B  64     -31.011  11.588 -38.146  1.00 51.57           O  
ANISOU 2003  OG  SER B  64     6923   6294   6378    464   -349   -162
ATOM   2004  H1  SER B  64     -32.384  12.805 -35.054  1.00 49.15           H  
ATOM   2005  H2  SER B  64     -33.327  11.546 -35.403  1.00 49.15           H  
ATOM   2006  HA  SER B  64     -33.394  13.611 -36.952  1.00 48.79           H  
ATOM   2007  HB3 SER B  64     -30.919  13.515 -37.439  1.00 51.02           H  
ATOM   2008  HB2 SER B  64     -31.852  13.306 -38.903  1.00 51.02           H  
ATOM   2009  HG  SER B  64     -30.939  11.219 -37.252  1.00 51.57           H  
ATOM   2010  N   ASP B  65     -34.280  12.114 -39.038  1.00 42.81           N  
ANISOU 2010  N   ASP B  65     5667   5391   5209    561   -415   -102
ATOM   2011  CA  ASP B  65     -35.095  11.394 -40.010  1.00 40.09           C  
ANISOU 2011  CA  ASP B  65     5278   5085   4871    490   -450    -54
ATOM   2012  C   ASP B  65     -34.221  10.570 -40.985  1.00 36.59           C  
ANISOU 2012  C   ASP B  65     4921   4508   4472    383   -459    -55
ATOM   2013  O   ASP B  65     -34.771   9.950 -41.903  1.00 35.24           O  
ANISOU 2013  O   ASP B  65     4753   4333   4302    328   -496    -25
ATOM   2014  CB  ASP B  65     -36.040  12.346 -40.794  1.00 42.49           C  
ANISOU 2014  CB  ASP B  65     5583   5427   5135    584   -483    -59
ATOM   2015  CG  ASP B  65     -35.433  13.621 -41.406  1.00 48.79           C  
ANISOU 2015  CG  ASP B  65     6523   6089   5926    664   -484   -121
ATOM   2016  OD1 ASP B  65     -34.222  13.894 -41.226  1.00 45.94           O  
ANISOU 2016  OD1 ASP B  65     6252   5611   5593    623   -460   -153
ATOM   2017  OD2 ASP B  65     -36.177  14.311 -42.128  1.00 54.36           O1-
ANISOU 2017  OD2 ASP B  65     7254   6812   6587    766   -514   -133
ATOM   2018  H   ASP B  65     -33.925  12.985 -39.430  1.00 42.81           H  
ATOM   2019  HA  ASP B  65     -35.724  10.684 -39.475  1.00 40.09           H  
ATOM   2020  HB3 ASP B  65     -36.833  12.676 -40.124  1.00 42.49           H  
ATOM   2021  HB2 ASP B  65     -36.545  11.801 -41.592  1.00 42.49           H  
ATOM   2022  N   TYR B  66     -32.889  10.519 -40.781  1.00 35.22           N  
ANISOU 2022  N   TYR B  66     4812   4243   4325    356   -426    -85
ATOM   2023  CA  TYR B  66     -31.926   9.780 -41.618  1.00 33.56           C  
ANISOU 2023  CA  TYR B  66     4679   3932   4141    282   -430    -87
ATOM   2024  C   TYR B  66     -32.277   8.295 -41.807  1.00 33.31           C  
ANISOU 2024  C   TYR B  66     4624   3922   4111    196   -459    -40
ATOM   2025  O   TYR B  66     -32.053   7.759 -42.889  1.00 32.58           O  
ANISOU 2025  O   TYR B  66     4598   3760   4020    152   -486    -32
ATOM   2026  CB  TYR B  66     -30.494   9.872 -41.044  1.00 32.85           C  
ANISOU 2026  CB  TYR B  66     4633   3784   4063    272   -389   -117
ATOM   2027  CG  TYR B  66     -29.786  11.219 -41.044  1.00 33.32           C  
ANISOU 2027  CG  TYR B  66     4751   3799   4112    318   -370   -158
ATOM   2028  CD1 TYR B  66     -30.230  12.309 -41.827  1.00 32.98           C  
ANISOU 2028  CD1 TYR B  66     4761   3721   4048    360   -395   -174
ATOM   2029  CD2 TYR B  66     -28.623  11.364 -40.256  1.00 33.54           C  
ANISOU 2029  CD2 TYR B  66     4796   3808   4138    304   -336   -177
ATOM   2030  CE1 TYR B  66     -29.514  13.520 -41.818  1.00 33.20           C  
ANISOU 2030  CE1 TYR B  66     4872   3691   4051    384   -392   -206
ATOM   2031  CE2 TYR B  66     -27.920  12.582 -40.237  1.00 34.10           C  
ANISOU 2031  CE2 TYR B  66     4934   3837   4185    318   -331   -205
ATOM   2032  CZ  TYR B  66     -28.358  13.657 -41.028  1.00 34.18           C  
ANISOU 2032  CZ  TYR B  66     5015   3801   4171    351   -362   -219
ATOM   2033  OH  TYR B  66     -27.656  14.825 -41.037  1.00 35.64           O  
ANISOU 2033  OH  TYR B  66     5293   3929   4319    343   -370   -241
ATOM   2034  H   TYR B  66     -32.490  11.060 -40.017  1.00 35.22           H  
ATOM   2035  HA  TYR B  66     -31.945  10.223 -42.614  1.00 33.56           H  
ATOM   2036  HB3 TYR B  66     -29.843   9.206 -41.613  1.00 32.85           H  
ATOM   2037  HB2 TYR B  66     -30.491   9.488 -40.022  1.00 32.85           H  
ATOM   2038  HD1 TYR B  66     -31.116  12.242 -42.440  1.00 32.98           H  
ATOM   2039  HD2 TYR B  66     -28.273  10.549 -39.640  1.00 33.54           H  
ATOM   2040  HE1 TYR B  66     -29.851  14.339 -42.431  1.00 33.20           H  
ATOM   2041  HE2 TYR B  66     -27.033  12.685 -39.627  1.00 34.10           H  
ATOM   2042  HH  TYR B  66     -27.970  15.468 -41.673  1.00 35.64           H  
ATOM   2043  N   TYR B  67     -32.875   7.674 -40.782  1.00 34.31           N  
ANISOU 2043  N   TYR B  67     4668   4141   4226    168   -462     -4
ATOM   2044  CA  TYR B  67     -33.338   6.286 -40.807  1.00 35.75           C  
ANISOU 2044  CA  TYR B  67     4852   4336   4397     62   -505     49
ATOM   2045  C   TYR B  67     -34.400   6.001 -41.893  1.00 36.25           C  
ANISOU 2045  C   TYR B  67     4917   4418   4439     12   -564     90
ATOM   2046  O   TYR B  67     -34.536   4.843 -42.282  1.00 35.12           O  
ANISOU 2046  O   TYR B  67     4833   4230   4280    -82   -613    126
ATOM   2047  CB  TYR B  67     -33.814   5.871 -39.396  1.00 37.44           C  
ANISOU 2047  CB  TYR B  67     4969   4666   4592     29   -502     89
ATOM   2048  CG  TYR B  67     -35.165   6.415 -38.953  1.00 40.52           C  
ANISOU 2048  CG  TYR B  67     5228   5221   4946     51   -514    126
ATOM   2049  CD1 TYR B  67     -35.272   7.697 -38.377  1.00 41.67           C  
ANISOU 2049  CD1 TYR B  67     5319   5430   5084    177   -475     90
ATOM   2050  CD2 TYR B  67     -36.326   5.634 -39.118  1.00 43.10           C  
ANISOU 2050  CD2 TYR B  67     5491   5653   5232    -53   -570    203
ATOM   2051  CE1 TYR B  67     -36.533   8.207 -38.011  1.00 43.62           C  
ANISOU 2051  CE1 TYR B  67     5443   5848   5281    229   -485    122
ATOM   2052  CE2 TYR B  67     -37.585   6.139 -38.749  1.00 45.49           C  
ANISOU 2052  CE2 TYR B  67     5650   6148   5487    -27   -579    245
ATOM   2053  CZ  TYR B  67     -37.693   7.433 -38.209  1.00 47.22           C  
ANISOU 2053  CZ  TYR B  67     5808   6437   5697    129   -532    202
ATOM   2054  OH  TYR B  67     -38.926   7.933 -37.904  1.00 50.72           O  
ANISOU 2054  OH  TYR B  67     6106   7089   6077    188   -538    240
ATOM   2055  H   TYR B  67     -33.066   8.200 -39.943  1.00 34.31           H  
ATOM   2056  HA  TYR B  67     -32.475   5.674 -41.061  1.00 35.75           H  
ATOM   2057  HB3 TYR B  67     -33.060   6.126 -38.651  1.00 37.44           H  
ATOM   2058  HB2 TYR B  67     -33.876   4.782 -39.368  1.00 37.44           H  
ATOM   2059  HD1 TYR B  67     -34.392   8.301 -38.209  1.00 41.67           H  
ATOM   2060  HD2 TYR B  67     -36.261   4.649 -39.545  1.00 43.10           H  
ATOM   2061  HE1 TYR B  67     -36.589   9.195 -37.574  1.00 43.62           H  
ATOM   2062  HE2 TYR B  67     -38.469   5.538 -38.900  1.00 45.49           H  
ATOM   2063  HH  TYR B  67     -38.890   8.765 -37.422  1.00 50.72           H  
ATOM   2064  N   ASN B  68     -35.114   7.038 -42.365  1.00 36.08           N  
ANISOU 2064  N   ASN B  68     4837   4466   4407     77   -567     86
ATOM   2065  CA  ASN B  68     -36.090   6.948 -43.457  1.00 36.60           C  
ANISOU 2065  CA  ASN B  68     4892   4566   4449     34   -623    126
ATOM   2066  C   ASN B  68     -35.508   7.453 -44.779  1.00 35.56           C  
ANISOU 2066  C   ASN B  68     4868   4308   4337     73   -627     84
ATOM   2067  O   ASN B  68     -35.847   6.883 -45.810  1.00 36.67           O  
ANISOU 2067  O   ASN B  68     5049   4417   4465     14   -676    111
ATOM   2068  CB  ASN B  68     -37.353   7.777 -43.124  1.00 39.76           C  
ANISOU 2068  CB  ASN B  68     5158   5140   4811     99   -629    152
ATOM   2069  CG  ASN B  68     -38.252   7.131 -42.075  1.00 44.90           C  
ANISOU 2069  CG  ASN B  68     5678   5966   5414     15   -658    231
ATOM   2070  OD1 ASN B  68     -38.401   5.912 -42.046  1.00 46.41           O  
ANISOU 2070  OD1 ASN B  68     5896   6145   5593   -130   -705    285
ATOM   2071  ND2 ASN B  68     -38.874   7.931 -41.217  1.00 46.26           N  
ANISOU 2071  ND2 ASN B  68     5717   6311   5547    106   -635    241
ATOM   2072  H   ASN B  68     -34.921   7.967 -42.006  1.00 36.08           H  
ATOM   2073  HA  ASN B  68     -36.371   5.901 -43.588  1.00 36.60           H  
ATOM   2074  HB3 ASN B  68     -37.972   7.868 -44.019  1.00 39.76           H  
ATOM   2075  HB2 ASN B  68     -37.081   8.795 -42.837  1.00 39.76           H  
ATOM   2076 HD22 ASN B  68     -39.407   7.533 -40.454  1.00 46.26           H  
ATOM   2077 HD21 ASN B  68     -38.751   8.931 -41.248  1.00 46.26           H  
ATOM   2078  N   ARG B  69     -34.685   8.511 -44.738  1.00 33.06           N  
ANISOU 2078  N   ARG B  69     4597   3924   4041    165   -579     22
ATOM   2079  CA  ARG B  69     -34.153   9.165 -45.943  1.00 32.01           C  
ANISOU 2079  CA  ARG B  69     4564   3682   3918    193   -583    -15
ATOM   2080  C   ARG B  69     -32.955   8.435 -46.566  1.00 31.38           C  
ANISOU 2080  C   ARG B  69     4589   3480   3852    146   -573    -34
ATOM   2081  O   ARG B  69     -32.563   8.787 -47.678  1.00 30.92           O  
ANISOU 2081  O   ARG B  69     4611   3345   3792    149   -581    -52
ATOM   2082  CB  ARG B  69     -33.697  10.591 -45.593  1.00 32.13           C  
ANISOU 2082  CB  ARG B  69     4601   3677   3931    292   -548    -65
ATOM   2083  CG  ARG B  69     -34.829  11.570 -45.249  1.00 34.18           C  
ANISOU 2083  CG  ARG B  69     4795   4034   4157    384   -565    -61
ATOM   2084  CD  ARG B  69     -34.325  12.812 -44.502  1.00 36.55           C  
ANISOU 2084  CD  ARG B  69     5137   4309   4443    480   -534   -110
ATOM   2085  NE  ARG B  69     -33.228  13.518 -45.191  1.00 34.08           N  
ANISOU 2085  NE  ARG B  69     4953   3858   4136    469   -530   -149
ATOM   2086  CZ  ARG B  69     -32.407  14.433 -44.658  1.00 33.58           C  
ANISOU 2086  CZ  ARG B  69     4962   3735   4062    492   -509   -185
ATOM   2087  NH1 ARG B  69     -31.444  14.944 -45.423  1.00 31.27           N  
ANISOU 2087  NH1 ARG B  69     4777   3339   3765    453   -511   -205
ATOM   2088  NH2 ARG B  69     -32.518  14.827 -43.388  1.00 31.71           N1+
ANISOU 2088  NH2 ARG B  69     4688   3548   3811    543   -488   -196
ATOM   2089  H   ARG B  69     -34.463   8.936 -43.849  1.00 33.06           H  
ATOM   2090  HA  ARG B  69     -34.928   9.215 -46.713  1.00 32.01           H  
ATOM   2091  HB3 ARG B  69     -33.168  11.010 -46.450  1.00 32.13           H  
ATOM   2092  HB2 ARG B  69     -32.969  10.550 -44.781  1.00 32.13           H  
ATOM   2093  HG3 ARG B  69     -35.505  11.058 -44.563  1.00 34.18           H  
ATOM   2094  HG2 ARG B  69     -35.439  11.832 -46.115  1.00 34.18           H  
ATOM   2095  HD3 ARG B  69     -34.065  12.536 -43.484  1.00 36.55           H  
ATOM   2096  HD2 ARG B  69     -35.139  13.537 -44.459  1.00 36.55           H  
ATOM   2097 HH22 ARG B  69     -31.938  15.511 -42.938  1.00 31.71           H  
ATOM   2098 HH21 ARG B  69     -33.265  14.463 -42.758  1.00 31.71           H  
ATOM   2099 HH12 ARG B  69     -30.794  15.649 -45.111  1.00 31.27           H  
ATOM   2100 HH11 ARG B  69     -31.368  14.616 -46.386  1.00 31.27           H  
ATOM   2101  HE  ARG B  69     -33.135  13.299 -46.182  1.00 34.08           H  
ATOM   2102  N   SER B  70     -32.348   7.509 -45.816  1.00 31.16           N  
ANISOU 2102  N   SER B  70     4564   3446   3830    113   -554    -29
ATOM   2103  CA  SER B  70     -31.194   6.737 -46.250  1.00 30.75           C  
ANISOU 2103  CA  SER B  70     4605   3304   3775     97   -542    -48
ATOM   2104  C   SER B  70     -31.535   5.827 -47.440  1.00 31.23           C  
ANISOU 2104  C   SER B  70     4749   3303   3813     43   -598    -23
ATOM   2105  O   SER B  70     -32.635   5.276 -47.487  1.00 32.04           O  
ANISOU 2105  O   SER B  70     4828   3443   3902    -20   -653     24
ATOM   2106  CB  SER B  70     -30.633   5.946 -45.048  1.00 31.92           C  
ANISOU 2106  CB  SER B  70     4737   3469   3923     84   -521    -43
ATOM   2107  OG  SER B  70     -29.576   5.055 -45.371  1.00 31.52           O  
ANISOU 2107  OG  SER B  70     4776   3346   3854     92   -512    -61
ATOM   2108  H   SER B  70     -32.717   7.307 -44.899  1.00 31.16           H  
ATOM   2109  HA  SER B  70     -30.452   7.458 -46.560  1.00 30.75           H  
ATOM   2110  HB3 SER B  70     -31.430   5.379 -44.567  1.00 31.92           H  
ATOM   2111  HB2 SER B  70     -30.246   6.644 -44.305  1.00 31.92           H  
ATOM   2112  HG  SER B  70     -28.724   5.499 -45.193  1.00 31.52           H  
ATOM   2113  N   THR B  71     -30.550   5.600 -48.317  1.00 30.43           N  
ANISOU 2113  N   THR B  71     4746   3120   3697     65   -589    -50
ATOM   2114  CA  THR B  71     -30.595   4.538 -49.321  1.00 31.04           C  
ANISOU 2114  CA  THR B  71     4932   3122   3739     27   -644    -32
ATOM   2115  C   THR B  71     -30.583   3.139 -48.663  1.00 31.15           C  
ANISOU 2115  C   THR B  71     4997   3113   3725    -13   -677     -7
ATOM   2116  O   THR B  71     -30.990   2.168 -49.288  1.00 32.20           O  
ANISOU 2116  O   THR B  71     5239   3178   3817    -61   -743     17
ATOM   2117  CB  THR B  71     -29.377   4.630 -50.274  1.00 32.77           C  
ANISOU 2117  CB  THR B  71     5241   3276   3935     79   -622    -68
ATOM   2118  OG1 THR B  71     -28.146   4.496 -49.572  1.00 33.64           O  
ANISOU 2118  OG1 THR B  71     5360   3393   4029    134   -570    -96
ATOM   2119  CG2 THR B  71     -29.331   5.951 -51.046  1.00 33.66           C  
ANISOU 2119  CG2 THR B  71     5324   3399   4065    102   -599    -88
ATOM   2120  H   THR B  71     -29.669   6.107 -48.241  1.00 30.43           H  
ATOM   2121  HA  THR B  71     -31.514   4.642 -49.899  1.00 31.04           H  
ATOM   2122  HB  THR B  71     -29.446   3.821 -51.006  1.00 32.77           H  
ATOM   2123  HG1 THR B  71     -28.102   3.616 -49.189  1.00 33.64           H  
ATOM   2124 HG21 THR B  71     -28.498   5.964 -51.750  1.00 33.66           H  
ATOM   2125 HG22 THR B  71     -30.245   6.095 -51.624  1.00 33.66           H  
ATOM   2126 HG23 THR B  71     -29.215   6.806 -50.382  1.00 33.66           H  
ATOM   2127  N   SER B  72     -30.152   3.045 -47.403  1.00 30.67           N  
ANISOU 2127  N   SER B  72     4879   3098   3678      8   -636    -15
ATOM   2128  CA  SER B  72     -30.146   1.837 -46.587  1.00 29.71           C  
ANISOU 2128  CA  SER B  72     4805   2957   3528    -30   -669      9
ATOM   2129  C   SER B  72     -30.937   2.094 -45.289  1.00 30.14           C  
ANISOU 2129  C   SER B  72     4726   3117   3611    -76   -659     40
ATOM   2130  O   SER B  72     -30.310   2.207 -44.234  1.00 31.85           O  
ANISOU 2130  O   SER B  72     4889   3369   3842    -40   -611     23
ATOM   2131  CB  SER B  72     -28.674   1.447 -46.337  1.00 30.08           C  
ANISOU 2131  CB  SER B  72     4903   2971   3554     56   -623    -32
ATOM   2132  OG  SER B  72     -27.915   2.579 -45.926  1.00 31.37           O  
ANISOU 2132  OG  SER B  72     4958   3205   3755    110   -544    -63
ATOM   2133  H   SER B  72     -29.875   3.891 -46.908  1.00 30.67           H  
ATOM   2134  HA  SER B  72     -30.629   1.008 -47.100  1.00 29.71           H  
ATOM   2135  HB3 SER B  72     -28.245   1.020 -47.242  1.00 30.08           H  
ATOM   2136  HB2 SER B  72     -28.604   0.667 -45.578  1.00 30.08           H  
ATOM   2137  HG  SER B  72     -28.445   3.050 -45.267  1.00 31.37           H  
ATOM   2138  N   PRO B  73     -32.276   2.279 -45.382  1.00 31.75           N  
ANISOU 2138  N   PRO B  73     4866   3385   3814   -150   -704     87
ATOM   2139  CA  PRO B  73     -33.081   2.695 -44.224  1.00 32.28           C  
ANISOU 2139  CA  PRO B  73     4788   3582   3894   -173   -688    117
ATOM   2140  C   PRO B  73     -33.150   1.617 -43.128  1.00 32.25           C  
ANISOU 2140  C   PRO B  73     4790   3598   3864   -244   -713    154
ATOM   2141  O   PRO B  73     -32.960   0.428 -43.400  1.00 32.09           O  
ANISOU 2141  O   PRO B  73     4903   3485   3804   -303   -770    174
ATOM   2142  CB  PRO B  73     -34.449   3.020 -44.839  1.00 34.31           C  
ANISOU 2142  CB  PRO B  73     4982   3919   4136   -230   -738    164
ATOM   2143  CG  PRO B  73     -34.554   2.113 -46.051  1.00 35.57           C  
ANISOU 2143  CG  PRO B  73     5285   3969   4260   -302   -812    186
ATOM   2144  CD  PRO B  73     -33.119   2.050 -46.560  1.00 32.93           C  
ANISOU 2144  CD  PRO B  73     5063   3508   3940   -208   -768    118
ATOM   2145  HA  PRO B  73     -32.650   3.595 -43.784  1.00 32.28           H  
ATOM   2146  HB3 PRO B  73     -34.457   4.064 -45.161  1.00 34.31           H  
ATOM   2147  HB2 PRO B  73     -35.279   2.888 -44.147  1.00 34.31           H  
ATOM   2148  HG3 PRO B  73     -35.262   2.467 -46.801  1.00 35.57           H  
ATOM   2149  HG2 PRO B  73     -34.874   1.126 -45.726  1.00 35.57           H  
ATOM   2150  HD2 PRO B  73     -32.910   1.100 -47.053  1.00 32.93           H  
ATOM   2151  HD3 PRO B  73     -32.964   2.841 -47.288  1.00 32.93           H  
ATOM   2152  N   TRP B  74     -33.398   2.052 -41.893  1.00 32.63           N  
ANISOU 2152  N   TRP B  74     4711   3761   3926   -237   -678    166
ATOM   2153  CA  TRP B  74     -33.382   1.183 -40.720  1.00 32.67           C  
ANISOU 2153  CA  TRP B  74     4713   3797   3905   -309   -699    205
ATOM   2154  C   TRP B  74     -34.539   1.528 -39.785  1.00 35.22           C  
ANISOU 2154  C   TRP B  74     4875   4294   4213   -356   -698    257
ATOM   2155  O   TRP B  74     -35.236   2.521 -39.994  1.00 36.83           O  
ANISOU 2155  O   TRP B  74     4967   4600   4427   -302   -673    253
ATOM   2156  CB  TRP B  74     -32.001   1.245 -40.025  1.00 31.68           C  
ANISOU 2156  CB  TRP B  74     4626   3610   3802   -226   -640    151
ATOM   2157  CG  TRP B  74     -31.564   2.515 -39.351  1.00 31.61           C  
ANISOU 2157  CG  TRP B  74     4506   3668   3836   -127   -557    105
ATOM   2158  CD1 TRP B  74     -31.781   2.831 -38.054  1.00 32.66           C  
ANISOU 2158  CD1 TRP B  74     4532   3904   3975   -116   -523    113
ATOM   2159  CD2 TRP B  74     -30.817   3.636 -39.912  1.00 30.15           C  
ANISOU 2159  CD2 TRP B  74     4333   3440   3682    -29   -505     44
ATOM   2160  NE1 TRP B  74     -31.162   4.029 -37.755  1.00 32.15           N  
ANISOU 2160  NE1 TRP B  74     4421   3852   3942    -15   -458     59
ATOM   2161  CE2 TRP B  74     -30.565   4.578 -38.867  1.00 30.48           C  
ANISOU 2161  CE2 TRP B  74     4283   3552   3745     30   -449     19
ATOM   2162  CE3 TRP B  74     -30.304   3.946 -41.191  1.00 29.52           C  
ANISOU 2162  CE3 TRP B  74     4331   3278   3606      5   -506     14
ATOM   2163  CZ2 TRP B  74     -29.840   5.760 -39.080  1.00 29.69           C  
ANISOU 2163  CZ2 TRP B  74     4187   3427   3665    107   -402    -32
ATOM   2164  CZ3 TRP B  74     -29.576   5.131 -41.420  1.00 30.01           C  
ANISOU 2164  CZ3 TRP B  74     4383   3330   3690     80   -453    -35
ATOM   2165  CH2 TRP B  74     -29.347   6.038 -40.365  1.00 29.82           C  
ANISOU 2165  CH2 TRP B  74     4282   3365   3682    122   -406    -55
ATOM   2166  H   TRP B  74     -33.670   3.020 -41.749  1.00 32.63           H  
ATOM   2167  HA  TRP B  74     -33.559   0.154 -41.035  1.00 32.67           H  
ATOM   2168  HB3 TRP B  74     -31.235   0.988 -40.756  1.00 31.68           H  
ATOM   2169  HB2 TRP B  74     -31.940   0.465 -39.268  1.00 31.68           H  
ATOM   2170  HD1 TRP B  74     -32.308   2.198 -37.354  1.00 32.66           H  
ATOM   2171  HE1 TRP B  74     -31.095   4.411 -36.814  1.00 32.15           H  
ATOM   2172  HE3 TRP B  74     -30.475   3.261 -42.007  1.00 29.52           H  
ATOM   2173  HZ2 TRP B  74     -29.658   6.442 -38.261  1.00 29.69           H  
ATOM   2174  HZ3 TRP B  74     -29.191   5.336 -42.409  1.00 30.01           H  
ATOM   2175  HH2 TRP B  74     -28.791   6.949 -40.531  1.00 29.82           H  
ATOM   2176  N   ASN B  75     -34.747   0.671 -38.787  1.00 35.07           N  
ANISOU 2176  N   ASN B  75     4850   4321   4156   -458   -734    312
ATOM   2177  CA  ASN B  75     -35.754   0.829 -37.742  1.00 36.56           C  
ANISOU 2177  CA  ASN B  75     4871   4701   4319   -497   -724    364
ATOM   2178  C   ASN B  75     -35.052   0.517 -36.422  1.00 36.68           C  
ANISOU 2178  C   ASN B  75     4881   4712   4345   -473   -682    345
ATOM   2179  O   ASN B  75     -34.328  -0.478 -36.337  1.00 36.20           O  
ANISOU 2179  O   ASN B  75     4956   4504   4293   -465   -687    314
ATOM   2180  CB  ASN B  75     -36.953  -0.117 -37.986  1.00 39.09           C  
ANISOU 2180  CB  ASN B  75     5166   5120   4568   -673   -814    467
ATOM   2181  CG  ASN B  75     -37.806   0.301 -39.187  1.00 45.16           C  
ANISOU 2181  CG  ASN B  75     5913   5919   5327   -684   -849    485
ATOM   2182  OD1 ASN B  75     -37.456   0.041 -40.334  1.00 48.10           O  
ANISOU 2182  OD1 ASN B  75     6431   6152   5692   -734   -905    484
ATOM   2183  ND2 ASN B  75     -38.927   0.980 -38.965  1.00 46.16           N  
ANISOU 2183  ND2 ASN B  75     5871   6214   5454   -603   -810    486
ATOM   2184  H   ASN B  75     -34.155  -0.155 -38.707  1.00 35.07           H  
ATOM   2185  HA  ASN B  75     -36.105   1.863 -37.737  1.00 36.56           H  
ATOM   2186  HB3 ASN B  75     -37.589  -0.142 -37.098  1.00 39.09           H  
ATOM   2187  HB2 ASN B  75     -36.603  -1.139 -38.134  1.00 39.09           H  
ATOM   2188 HD22 ASN B  75     -39.493   1.264 -39.749  1.00 46.16           H  
ATOM   2189 HD21 ASN B  75     -39.244   1.183 -38.028  1.00 46.16           H  
ATOM   2190  N   LEU B  76     -35.256   1.381 -35.423  1.00 37.51           N  
ANISOU 2190  N   LEU B  76     4831   4974   4445   -435   -636    355
ATOM   2191  CA  LEU B  76     -34.660   1.230 -34.100  1.00 38.83           C  
ANISOU 2191  CA  LEU B  76     4985   5146   4622   -409   -594    337
ATOM   2192  C   LEU B  76     -35.516   0.290 -33.243  1.00 39.18           C  
ANISOU 2192  C   LEU B  76     4978   5304   4603   -554   -643    425
ATOM   2193  O   LEU B  76     -36.735   0.451 -33.197  1.00 40.86           O  
ANISOU 2193  O   LEU B  76     5076   5687   4764   -634   -676    497
ATOM   2194  CB  LEU B  76     -34.535   2.603 -33.410  1.00 40.32           C  
ANISOU 2194  CB  LEU B  76     5060   5420   4840   -262   -510    284
ATOM   2195  CG  LEU B  76     -33.524   3.574 -34.053  1.00 43.28           C  
ANISOU 2195  CG  LEU B  76     5499   5674   5271   -129   -459    195
ATOM   2196  CD1 LEU B  76     -33.622   4.951 -33.379  1.00 45.77           C  
ANISOU 2196  CD1 LEU B  76     5728   6070   5593     -9   -395    154
ATOM   2197  CD2 LEU B  76     -32.077   3.045 -33.998  1.00 42.93           C  
ANISOU 2197  CD2 LEU B  76     5582   5474   5255   -124   -448    155
ATOM   2198  H   LEU B  76     -35.905   2.145 -35.527  1.00 37.51           H  
ATOM   2199  HA  LEU B  76     -33.664   0.800 -34.205  1.00 38.83           H  
ATOM   2200  HB3 LEU B  76     -34.216   2.448 -32.380  1.00 40.32           H  
ATOM   2201  HB2 LEU B  76     -35.519   3.070 -33.350  1.00 40.32           H  
ATOM   2202  HG  LEU B  76     -33.796   3.713 -35.101  1.00 43.28           H  
ATOM   2203 HD11 LEU B  76     -33.067   5.702 -33.943  1.00 45.77           H  
ATOM   2204 HD12 LEU B  76     -34.654   5.296 -33.309  1.00 45.77           H  
ATOM   2205 HD13 LEU B  76     -33.212   4.930 -32.368  1.00 45.77           H  
ATOM   2206 HD21 LEU B  76     -31.379   3.792 -33.614  1.00 42.93           H  
ATOM   2207 HD22 LEU B  76     -31.972   2.170 -33.356  1.00 42.93           H  
ATOM   2208 HD23 LEU B  76     -31.727   2.766 -34.990  1.00 42.93           H  
ATOM   2209  N   HIS B  77     -34.852  -0.657 -32.582  1.00 38.79           N  
ANISOU 2209  N   HIS B  77     5016   5173   4548   -596   -653    425
ATOM   2210  CA  HIS B  77     -35.426  -1.596 -31.632  1.00 39.44           C  
ANISOU 2210  CA  HIS B  77     5076   5343   4566   -744   -702    508
ATOM   2211  C   HIS B  77     -34.942  -1.177 -30.237  1.00 37.89           C  
ANISOU 2211  C   HIS B  77     4802   5202   4392   -659   -627    473
ATOM   2212  O   HIS B  77     -33.751  -0.920 -30.067  1.00 38.25           O  
ANISOU 2212  O   HIS B  77     4917   5127   4491   -545   -577    396
ATOM   2213  CB  HIS B  77     -34.944  -3.020 -31.981  1.00 42.05           C  
ANISOU 2213  CB  HIS B  77     5622   5495   4861   -857   -791    533
ATOM   2214  CG  HIS B  77     -35.493  -3.579 -33.274  1.00 48.79           C  
ANISOU 2214  CG  HIS B  77     6570   6294   5674   -967   -881    579
ATOM   2215  ND1 HIS B  77     -35.401  -2.921 -34.492  1.00 52.76           N  
ANISOU 2215  ND1 HIS B  77     7077   6753   6218   -880   -862    534
ATOM   2216  CD2 HIS B  77     -36.173  -4.747 -33.541  1.00 51.05           C  
ANISOU 2216  CD2 HIS B  77     6970   6550   5877  -1161   -996    666
ATOM   2217  CE1 HIS B  77     -36.024  -3.670 -35.401  1.00 53.23           C  
ANISOU 2217  CE1 HIS B  77     7225   6780   6220  -1021   -960    597
ATOM   2218  NE2 HIS B  77     -36.493  -4.805 -34.898  1.00 53.67           N  
ANISOU 2218  NE2 HIS B  77     7360   6834   6197  -1196  -1047    678
ATOM   2219  H   HIS B  77     -33.839  -0.741 -32.697  1.00 38.79           H  
ATOM   2220  HA  HIS B  77     -36.517  -1.568 -31.668  1.00 39.44           H  
ATOM   2221  HB3 HIS B  77     -35.221  -3.702 -31.175  1.00 42.05           H  
ATOM   2222  HB2 HIS B  77     -33.854  -3.048 -32.028  1.00 42.05           H  
ATOM   2223  HD1 HIS B  77     -34.954  -2.029 -34.666  1.00 52.76           H  
ATOM   2224  HD2 HIS B  77     -36.457  -5.544 -32.868  1.00 51.05           H  
ATOM   2225  HE1 HIS B  77     -36.122  -3.388 -36.439  1.00 53.23           H  
ATOM   2226  N   ARG B  78     -35.863  -1.087 -29.273  1.00 37.58           N  
ANISOU 2226  N   ARG B  78     4613   5360   4305   -710   -618    531
ATOM   2227  CA  ARG B  78     -35.562  -0.691 -27.899  1.00 37.95           C  
ANISOU 2227  CA  ARG B  78     4581   5476   4364   -632   -550    503
ATOM   2228  C   ARG B  78     -35.140  -1.934 -27.096  1.00 39.34           C  
ANISOU 2228  C   ARG B  78     4850   5593   4503   -757   -597    546
ATOM   2229  O   ARG B  78     -35.999  -2.725 -26.712  1.00 41.05           O  
ANISOU 2229  O   ARG B  78     5065   5887   4647   -931   -671    640
ATOM   2230  CB  ARG B  78     -36.807  -0.001 -27.301  1.00 38.99           C  
ANISOU 2230  CB  ARG B  78     4499   5869   4445   -609   -516    546
ATOM   2231  CG  ARG B  78     -36.561   0.688 -25.948  1.00 42.06           C  
ANISOU 2231  CG  ARG B  78     4799   6345   4836   -503   -442    511
ATOM   2232  CD  ARG B  78     -37.826   1.392 -25.428  1.00 43.09           C  
ANISOU 2232  CD  ARG B  78     4727   6751   4893   -476   -420    563
ATOM   2233  NE  ARG B  78     -37.696   1.866 -24.037  1.00 41.67           N  
ANISOU 2233  NE  ARG B  78     4453   6682   4697   -359   -350    533
ATOM   2234  CZ  ARG B  78     -37.867   1.138 -22.920  1.00 43.16           C  
ANISOU 2234  CZ  ARG B  78     4573   6997   4831   -440   -350    589
ATOM   2235  NH1 ARG B  78     -37.715   1.698 -21.720  1.00 43.74           N  
ANISOU 2235  NH1 ARG B  78     4552   7187   4879   -315   -284    560
ATOM   2236  NH2 ARG B  78     -38.179  -0.156 -22.975  1.00 45.59           N1+
ANISOU 2236  NH2 ARG B  78     4909   7320   5095   -652   -421    680
ATOM   2237  H   ARG B  78     -36.809  -1.379 -29.463  1.00 37.58           H  
ATOM   2238  HA  ARG B  78     -34.740   0.031 -27.900  1.00 37.95           H  
ATOM   2239  HB3 ARG B  78     -37.615  -0.727 -27.195  1.00 38.99           H  
ATOM   2240  HB2 ARG B  78     -37.175   0.746 -28.002  1.00 38.99           H  
ATOM   2241  HG3 ARG B  78     -35.817   1.458 -26.155  1.00 42.06           H  
ATOM   2242  HG2 ARG B  78     -36.115   0.025 -25.203  1.00 42.06           H  
ATOM   2243  HD3 ARG B  78     -38.740   0.827 -25.612  1.00 43.09           H  
ATOM   2244  HD2 ARG B  78     -37.940   2.317 -25.990  1.00 43.09           H  
ATOM   2245 HH22 ARG B  78     -38.166  -0.703 -22.085  1.00 45.59           H  
ATOM   2246 HH21 ARG B  78     -38.380  -0.668 -23.818  1.00 45.59           H  
ATOM   2247 HH12 ARG B  78     -37.540   1.088 -20.894  1.00 43.74           H  
ATOM   2248 HH11 ARG B  78     -37.611   2.682 -21.545  1.00 43.74           H  
ATOM   2249  HE  ARG B  78     -37.381   2.822 -23.952  1.00 41.67           H  
ATOM   2250  N   ASN B  79     -33.835  -2.084 -26.868  1.00 38.28           N  
ANISOU 2250  N   ASN B  79     4806   5326   4413   -676   -561    482
ATOM   2251  CA  ASN B  79     -33.224  -3.150 -26.075  1.00 39.26           C  
ANISOU 2251  CA  ASN B  79     5039   5372   4504   -763   -605    510
ATOM   2252  C   ASN B  79     -33.167  -2.636 -24.627  1.00 38.56           C  
ANISOU 2252  C   ASN B  79     4824   5407   4419   -708   -535    499
ATOM   2253  O   ASN B  79     -32.418  -1.690 -24.380  1.00 37.55           O  
ANISOU 2253  O   ASN B  79     4657   5261   4349   -556   -457    421
ATOM   2254  CB  ASN B  79     -31.836  -3.420 -26.723  1.00 42.71           C  
ANISOU 2254  CB  ASN B  79     5661   5584   4983   -677   -609    437
ATOM   2255  CG  ASN B  79     -30.905  -4.435 -26.053  1.00 49.28           C  
ANISOU 2255  CG  ASN B  79     6632   6305   5788   -702   -643    438
ATOM   2256  OD1 ASN B  79     -30.781  -4.506 -24.831  1.00 49.70           O  
ANISOU 2256  OD1 ASN B  79     6627   6425   5833   -707   -615    447
ATOM   2257  ND2 ASN B  79     -30.155  -5.179 -26.860  1.00 51.15           N  
ANISOU 2257  ND2 ASN B  79     7067   6362   6007   -692   -702    420
ATOM   2258  H   ASN B  79     -33.187  -1.350 -27.155  1.00 38.28           H  
ATOM   2259  HA  ASN B  79     -33.830  -4.057 -26.132  1.00 39.26           H  
ATOM   2260  HB3 ASN B  79     -31.267  -2.495 -26.786  1.00 42.71           H  
ATOM   2261  HB2 ASN B  79     -31.999  -3.736 -27.755  1.00 42.71           H  
ATOM   2262 HD22 ASN B  79     -29.511  -5.852 -26.477  1.00 51.15           H  
ATOM   2263 HD21 ASN B  79     -30.190  -5.070 -27.871  1.00 51.15           H  
ATOM   2264  N   GLU B  80     -33.968  -3.203 -23.711  1.00 37.74           N  
ANISOU 2264  N   GLU B  80     4655   5440   4246   -840   -567    582
ATOM   2265  CA  GLU B  80     -33.969  -2.828 -22.295  1.00 39.18           C  
ANISOU 2265  CA  GLU B  80     4716   5752   4419   -793   -505    578
ATOM   2266  C   GLU B  80     -33.428  -3.975 -21.429  1.00 39.20           C  
ANISOU 2266  C   GLU B  80     4825   5678   4390   -886   -546    607
ATOM   2267  O   GLU B  80     -33.616  -5.141 -21.772  1.00 39.41           O  
ANISOU 2267  O   GLU B  80     4953   5669   4351  -1061   -641    685
ATOM   2268  CB  GLU B  80     -35.354  -2.333 -21.838  1.00 42.40           C  
ANISOU 2268  CB  GLU B  80     4914   6436   4759   -838   -489    649
ATOM   2269  CG  GLU B  80     -35.382  -1.887 -20.353  1.00 49.96           C  
ANISOU 2269  CG  GLU B  80     5746   7533   5704   -751   -415    633
ATOM   2270  CD  GLU B  80     -36.562  -0.992 -20.013  1.00 63.21           C  
ANISOU 2270  CD  GLU B  80     7209   9511   7297   -764   -391    699
ATOM   2271  OE1 GLU B  80     -37.696  -1.330 -20.408  1.00 65.24           O  
ANISOU 2271  OE1 GLU B  80     7385   9897   7506   -831   -427    760
ATOM   2272  OE2 GLU B  80     -36.312   0.127 -19.514  1.00 67.10           O1-
ANISOU 2272  OE2 GLU B  80     7609  10123   7764   -699   -337    692
ATOM   2273  H   GLU B  80     -34.505  -4.030 -23.932  1.00 37.74           H  
ATOM   2274  HA  GLU B  80     -33.311  -1.979 -22.162  1.00 39.18           H  
ATOM   2275  HB3 GLU B  80     -36.105  -3.109 -21.996  1.00 42.40           H  
ATOM   2276  HB2 GLU B  80     -35.644  -1.493 -22.470  1.00 42.40           H  
ATOM   2277  HG3 GLU B  80     -34.462  -1.355 -20.107  1.00 49.96           H  
ATOM   2278  HG2 GLU B  80     -35.429  -2.753 -19.693  1.00 49.96           H  
ATOM   2279  N   ASP B  81     -32.756  -3.603 -20.335  1.00 36.97           N  
ANISOU 2279  N   ASP B  81     4533   5367   4146   -774   -481    547
ATOM   2280  CA  ASP B  81     -31.999  -4.485 -19.450  1.00 35.83           C  
ANISOU 2280  CA  ASP B  81     4489   5151   3974   -839   -515    566
ATOM   2281  C   ASP B  81     -31.887  -3.755 -18.091  1.00 37.49           C  
ANISOU 2281  C   ASP B  81     4568   5487   4191   -762   -436    545
ATOM   2282  O   ASP B  81     -31.162  -2.759 -18.019  1.00 36.72           O  
ANISOU 2282  O   ASP B  81     4454   5342   4157   -603   -364    459
ATOM   2283  CB  ASP B  81     -30.630  -4.751 -20.111  1.00 35.23           C  
ANISOU 2283  CB  ASP B  81     4600   4842   3944   -753   -529    496
ATOM   2284  CG  ASP B  81     -29.588  -5.619 -19.412  1.00 38.62           C  
ANISOU 2284  CG  ASP B  81     5160   5174   4339   -794   -571    507
ATOM   2285  OD1 ASP B  81     -29.698  -5.942 -18.212  1.00 40.98           O  
ANISOU 2285  OD1 ASP B  81     5394   5582   4596   -872   -571    557
ATOM   2286  OD2 ASP B  81     -28.557  -5.851 -20.086  1.00 40.00           O1-
ANISOU 2286  OD2 ASP B  81     5501   5173   4522   -735   -602    467
ATOM   2287  H   ASP B  81     -32.607  -2.613 -20.164  1.00 36.97           H  
ATOM   2288  HA  ASP B  81     -32.514  -5.441 -19.363  1.00 35.83           H  
ATOM   2289  HB3 ASP B  81     -30.167  -3.785 -20.294  1.00 35.23           H  
ATOM   2290  HB2 ASP B  81     -30.801  -5.187 -21.095  1.00 35.23           H  
ATOM   2291  N   PRO B  82     -32.635  -4.184 -17.046  1.00 39.17           N  
ANISOU 2291  N   PRO B  82     4698   5857   4329   -881   -453    624
ATOM   2292  CA  PRO B  82     -32.641  -3.473 -15.749  1.00 40.25           C  
ANISOU 2292  CA  PRO B  82     4710   6121   4460   -802   -378    605
ATOM   2293  C   PRO B  82     -31.340  -3.613 -14.932  1.00 39.96           C  
ANISOU 2293  C   PRO B  82     4779   5939   4463   -735   -359    547
ATOM   2294  O   PRO B  82     -31.074  -2.776 -14.062  1.00 41.13           O  
ANISOU 2294  O   PRO B  82     4846   6160   4622   -645   -293    512
ATOM   2295  CB  PRO B  82     -33.853  -4.071 -15.018  1.00 42.19           C  
ANISOU 2295  CB  PRO B  82     4852   6579   4601   -973   -415    720
ATOM   2296  CG  PRO B  82     -33.979  -5.481 -15.573  1.00 42.85           C  
ANISOU 2296  CG  PRO B  82     5077   6567   4636  -1170   -529    797
ATOM   2297  CD  PRO B  82     -33.546  -5.332 -17.030  1.00 40.33           C  
ANISOU 2297  CD  PRO B  82     4855   6087   4379  -1103   -545    743
ATOM   2298  HA  PRO B  82     -32.806  -2.405 -15.910  1.00 40.25           H  
ATOM   2299  HB3 PRO B  82     -34.744  -3.497 -15.274  1.00 42.19           H  
ATOM   2300  HB2 PRO B  82     -33.762  -4.061 -13.931  1.00 42.19           H  
ATOM   2301  HG3 PRO B  82     -34.977  -5.906 -15.457  1.00 42.85           H  
ATOM   2302  HG2 PRO B  82     -33.282  -6.138 -15.051  1.00 42.85           H  
ATOM   2303  HD2 PRO B  82     -33.074  -6.251 -17.383  1.00 40.33           H  
ATOM   2304  HD3 PRO B  82     -34.403  -5.114 -17.669  1.00 40.33           H  
ATOM   2305  N   GLU B  83     -30.540  -4.638 -15.253  1.00 38.17           N  
ANISOU 2305  N   GLU B  83     4737   5517   4250   -773   -421    538
ATOM   2306  CA  GLU B  83     -29.235  -4.913 -14.662  1.00 36.22           C  
ANISOU 2306  CA  GLU B  83     4589   5141   4032   -695   -407    484
ATOM   2307  C   GLU B  83     -28.107  -4.085 -15.302  1.00 34.42           C  
ANISOU 2307  C   GLU B  83     4390   4802   3886   -523   -352    385
ATOM   2308  O   GLU B  83     -26.942  -4.288 -14.956  1.00 33.27           O  
ANISOU 2308  O   GLU B  83     4325   4554   3763   -450   -343    339
ATOM   2309  CB  GLU B  83     -28.961  -6.432 -14.746  1.00 37.97           C  
ANISOU 2309  CB  GLU B  83     5004   5220   4202   -804   -506    527
ATOM   2310  CG  GLU B  83     -29.906  -7.283 -13.877  1.00 41.53           C  
ANISOU 2310  CG  GLU B  83     5443   5776   4561   -994   -566    631
ATOM   2311  CD  GLU B  83     -29.730  -6.990 -12.391  1.00 44.08           C  
ANISOU 2311  CD  GLU B  83     5671   6199   4878   -965   -509    626
ATOM   2312  OE1 GLU B  83     -28.584  -7.091 -11.906  1.00 40.28           O  
ANISOU 2312  OE1 GLU B  83     5268   5605   4433   -860   -489    565
ATOM   2313  OE2 GLU B  83     -30.725  -6.605 -11.743  1.00 48.44           O1-
ANISOU 2313  OE2 GLU B  83     6067   6955   5384  -1037   -485    683
ATOM   2314  H   GLU B  83     -30.791  -5.256 -16.017  1.00 38.17           H  
ATOM   2315  HA  GLU B  83     -29.249  -4.620 -13.616  1.00 36.22           H  
ATOM   2316  HB3 GLU B  83     -27.927  -6.652 -14.475  1.00 37.97           H  
ATOM   2317  HB2 GLU B  83     -29.076  -6.768 -15.773  1.00 37.97           H  
ATOM   2318  HG3 GLU B  83     -29.692  -8.339 -14.037  1.00 41.53           H  
ATOM   2319  HG2 GLU B  83     -30.944  -7.138 -14.177  1.00 41.53           H  
ATOM   2320  N   ARG B  84     -28.454  -3.179 -16.221  1.00 32.91           N  
ANISOU 2320  N   ARG B  84     4132   4641   3731   -464   -320    356
ATOM   2321  CA  ARG B  84     -27.523  -2.369 -16.982  1.00 32.03           C  
ANISOU 2321  CA  ARG B  84     4053   4432   3685   -328   -278    274
ATOM   2322  C   ARG B  84     -27.820  -0.880 -16.768  1.00 32.58           C  
ANISOU 2322  C   ARG B  84     3993   4602   3783   -234   -205    233
ATOM   2323  O   ARG B  84     -28.979  -0.485 -16.633  1.00 34.66           O  
ANISOU 2323  O   ARG B  84     4151   5001   4018   -257   -195    266
ATOM   2324  CB  ARG B  84     -27.667  -2.773 -18.460  1.00 32.43           C  
ANISOU 2324  CB  ARG B  84     4196   4383   3742   -349   -328    277
ATOM   2325  CG  ARG B  84     -26.625  -2.183 -19.423  1.00 32.30           C  
ANISOU 2325  CG  ARG B  84     4205   4285   3782   -225   -289    202
ATOM   2326  CD  ARG B  84     -26.826  -2.641 -20.877  1.00 31.93           C  
ANISOU 2326  CD  ARG B  84     4246   4155   3731   -252   -339    212
ATOM   2327  NE  ARG B  84     -28.129  -2.227 -21.433  1.00 33.19           N  
ANISOU 2327  NE  ARG B  84     4320   4409   3881   -315   -349    252
ATOM   2328  CZ  ARG B  84     -28.903  -2.891 -22.307  1.00 35.49           C  
ANISOU 2328  CZ  ARG B  84     4674   4667   4145   -402   -415    295
ATOM   2329  NH1 ARG B  84     -29.999  -2.309 -22.766  1.00 35.42           N  
ANISOU 2329  NH1 ARG B  84     4567   4769   4123   -453   -420    333
ATOM   2330  NH2 ARG B  84     -28.631  -4.120 -22.739  1.00 35.09           N1+
ANISOU 2330  NH2 ARG B  84     4792   4473   4068   -431   -480    301
ATOM   2331  H   ARG B  84     -29.435  -3.043 -16.434  1.00 32.91           H  
ATOM   2332  HA  ARG B  84     -26.507  -2.583 -16.658  1.00 32.03           H  
ATOM   2333  HB3 ARG B  84     -28.673  -2.524 -18.796  1.00 32.43           H  
ATOM   2334  HB2 ARG B  84     -27.583  -3.857 -18.520  1.00 32.43           H  
ATOM   2335  HG3 ARG B  84     -25.659  -2.562 -19.088  1.00 32.30           H  
ATOM   2336  HG2 ARG B  84     -26.541  -1.099 -19.367  1.00 32.30           H  
ATOM   2337  HD3 ARG B  84     -26.610  -3.704 -20.986  1.00 31.93           H  
ATOM   2338  HD2 ARG B  84     -26.098  -2.122 -21.493  1.00 31.93           H  
ATOM   2339 HH22 ARG B  84     -29.230  -4.547 -23.444  1.00 35.09           H  
ATOM   2340 HH21 ARG B  84     -28.213  -4.758 -22.063  1.00 35.09           H  
ATOM   2341 HH12 ARG B  84     -30.576  -2.739 -23.485  1.00 35.42           H  
ATOM   2342 HH11 ARG B  84     -30.434  -1.529 -22.276  1.00 35.42           H  
ATOM   2343  HE  ARG B  84     -28.403  -1.289 -21.121  1.00 33.19           H  
ATOM   2344  N   TYR B  85     -26.764  -0.065 -16.807  1.00 32.46           N  
ANISOU 2344  N   TYR B  85     3995   4524   3813   -125   -160    163
ATOM   2345  CA  TYR B  85     -26.841   1.375 -16.993  1.00 32.19           C  
ANISOU 2345  CA  TYR B  85     3892   4539   3800    -33   -108    118
ATOM   2346  C   TYR B  85     -25.966   1.706 -18.228  1.00 30.57           C  
ANISOU 2346  C   TYR B  85     3755   4220   3638     21   -107     70
ATOM   2347  O   TYR B  85     -24.781   1.354 -18.213  1.00 29.06           O  
ANISOU 2347  O   TYR B  85     3631   3946   3464     41   -108     45
ATOM   2348  CB  TYR B  85     -26.351   2.077 -15.711  1.00 34.53           C  
ANISOU 2348  CB  TYR B  85     4160   4865   4095     27    -64     84
ATOM   2349  CG  TYR B  85     -26.454   3.591 -15.778  1.00 38.73           C  
ANISOU 2349  CG  TYR B  85     4658   5426   4631    122    -25     37
ATOM   2350  CD1 TYR B  85     -25.472   4.349 -16.451  1.00 41.30           C  
ANISOU 2350  CD1 TYR B  85     5043   5659   4991    174    -15    -14
ATOM   2351  CD2 TYR B  85     -27.561   4.245 -15.200  1.00 42.72           C  
ANISOU 2351  CD2 TYR B  85     5079   6059   5093    163     -4     48
ATOM   2352  CE1 TYR B  85     -25.620   5.741 -16.575  1.00 44.06           C  
ANISOU 2352  CE1 TYR B  85     5393   6014   5333    251      5    -54
ATOM   2353  CE2 TYR B  85     -27.688   5.644 -15.293  1.00 44.75           C  
ANISOU 2353  CE2 TYR B  85     5337   6328   5340    268     20      2
ATOM   2354  CZ  TYR B  85     -26.721   6.391 -15.990  1.00 46.61           C  
ANISOU 2354  CZ  TYR B  85     5656   6443   5612    306     20    -49
ATOM   2355  OH  TYR B  85     -26.837   7.743 -16.099  1.00 49.85           O  
ANISOU 2355  OH  TYR B  85     6097   6844   5999    402     31    -94
ATOM   2356  H   TYR B  85     -25.827  -0.468 -16.869  1.00 32.46           H  
ATOM   2357  HA  TYR B  85     -27.873   1.688 -17.123  1.00 32.19           H  
ATOM   2358  HB3 TYR B  85     -25.329   1.808 -15.471  1.00 34.53           H  
ATOM   2359  HB2 TYR B  85     -26.941   1.727 -14.862  1.00 34.53           H  
ATOM   2360  HD1 TYR B  85     -24.609   3.871 -16.894  1.00 41.30           H  
ATOM   2361  HD2 TYR B  85     -28.322   3.679 -14.684  1.00 42.72           H  
ATOM   2362  HE1 TYR B  85     -24.880   6.311 -17.114  1.00 44.06           H  
ATOM   2363  HE2 TYR B  85     -28.540   6.129 -14.839  1.00 44.75           H  
ATOM   2364  HH  TYR B  85     -27.457   8.156 -15.491  1.00 49.85           H  
ATOM   2365  N   PRO B  86     -26.509   2.379 -19.272  1.00 30.53           N  
ANISOU 2365  N   PRO B  86     3731   4224   3646     50   -103     58
ATOM   2366  CA  PRO B  86     -27.931   2.726 -19.489  1.00 31.59           C  
ANISOU 2366  CA  PRO B  86     3781   4472   3752     43   -105     88
ATOM   2367  C   PRO B  86     -28.836   1.491 -19.579  1.00 31.67           C  
ANISOU 2367  C   PRO B  86     3782   4524   3728    -75   -157    162
ATOM   2368  O   PRO B  86     -28.435   0.497 -20.186  1.00 32.12           O  
ANISOU 2368  O   PRO B  86     3932   4479   3793   -135   -202    177
ATOM   2369  CB  PRO B  86     -27.923   3.478 -20.834  1.00 32.98           C  
ANISOU 2369  CB  PRO B  86     3981   4598   3953     96   -104     55
ATOM   2370  CG  PRO B  86     -26.503   3.973 -21.000  1.00 33.67           C  
ANISOU 2370  CG  PRO B  86     4157   4558   4079    121    -99     10
ATOM   2371  CD  PRO B  86     -25.689   2.846 -20.390  1.00 30.87           C  
ANISOU 2371  CD  PRO B  86     3838   4168   3723     90   -103     17
ATOM   2372  HA  PRO B  86     -28.247   3.398 -18.689  1.00 31.59           H  
ATOM   2373  HB3 PRO B  86     -28.648   4.291 -20.869  1.00 32.98           H  
ATOM   2374  HB2 PRO B  86     -28.154   2.803 -21.661  1.00 32.98           H  
ATOM   2375  HG3 PRO B  86     -26.367   4.880 -20.412  1.00 33.67           H  
ATOM   2376  HG2 PRO B  86     -26.242   4.191 -22.033  1.00 33.67           H  
ATOM   2377  HD2 PRO B  86     -25.570   2.029 -21.104  1.00 30.87           H  
ATOM   2378  HD3 PRO B  86     -24.694   3.185 -20.095  1.00 30.87           H  
ATOM   2379  N   SER B  87     -30.036   1.561 -18.991  1.00 31.90           N  
ANISOU 2379  N   SER B  87     3704   4710   3707   -108   -156    211
ATOM   2380  CA  SER B  87     -30.978   0.447 -19.027  1.00 33.63           C  
ANISOU 2380  CA  SER B  87     3907   4993   3877   -253   -214    297
ATOM   2381  C   SER B  87     -31.501   0.193 -20.447  1.00 33.52           C  
ANISOU 2381  C   SER B  87     3925   4943   3869   -297   -258    317
ATOM   2382  O   SER B  87     -31.661  -0.959 -20.831  1.00 34.04           O  
ANISOU 2382  O   SER B  87     4064   4961   3910   -422   -326    371
ATOM   2383  CB  SER B  87     -32.108   0.705 -18.015  1.00 37.89           C  
ANISOU 2383  CB  SER B  87     4300   5751   4347   -285   -200    355
ATOM   2384  OG  SER B  87     -32.796   1.914 -18.314  1.00 41.47           O  
ANISOU 2384  OG  SER B  87     4648   6327   4782   -188   -168    342
ATOM   2385  H   SER B  87     -30.394   2.393 -18.544  1.00 31.90           H  
ATOM   2386  HA  SER B  87     -30.446  -0.453 -18.721  1.00 33.63           H  
ATOM   2387  HB3 SER B  87     -31.703   0.755 -17.004  1.00 37.89           H  
ATOM   2388  HB2 SER B  87     -32.815  -0.127 -18.025  1.00 37.89           H  
ATOM   2389  HG  SER B  87     -33.742   1.711 -18.352  1.00 41.47           H  
ATOM   2390  N   VAL B  88     -31.681   1.267 -21.219  1.00 33.28           N  
ANISOU 2390  N   VAL B  88     3862   4917   3865   -194   -228    272
ATOM   2391  CA  VAL B  88     -32.166   1.248 -22.589  1.00 34.44           C  
ANISOU 2391  CA  VAL B  88     4033   5034   4017   -227   -266    288
ATOM   2392  C   VAL B  88     -30.995   1.525 -23.544  1.00 33.73           C  
ANISOU 2392  C   VAL B  88     4062   4765   3990   -161   -261    221
ATOM   2393  O   VAL B  88     -30.241   2.475 -23.330  1.00 33.72           O  
ANISOU 2393  O   VAL B  88     4064   4726   4023    -48   -212    155
ATOM   2394  CB  VAL B  88     -33.237   2.351 -22.803  1.00 37.22           C  
ANISOU 2394  CB  VAL B  88     4252   5553   4337   -161   -243    298
ATOM   2395  CG1 VAL B  88     -33.765   2.430 -24.251  1.00 37.98           C  
ANISOU 2395  CG1 VAL B  88     4369   5621   4440   -185   -282    311
ATOM   2396  CG2 VAL B  88     -34.413   2.152 -21.836  1.00 37.93           C  
ANISOU 2396  CG2 VAL B  88     4201   5863   4347   -221   -246    373
ATOM   2397  H   VAL B  88     -31.440   2.169 -20.845  1.00 33.28           H  
ATOM   2398  HA  VAL B  88     -32.617   0.282 -22.816  1.00 34.44           H  
ATOM   2399  HB  VAL B  88     -32.790   3.321 -22.571  1.00 37.22           H  
ATOM   2400 HG11 VAL B  88     -34.618   3.103 -24.332  1.00 37.98           H  
ATOM   2401 HG12 VAL B  88     -33.010   2.804 -24.945  1.00 37.98           H  
ATOM   2402 HG13 VAL B  88     -34.073   1.447 -24.604  1.00 37.98           H  
ATOM   2403 HG21 VAL B  88     -35.164   2.928 -21.971  1.00 37.93           H  
ATOM   2404 HG22 VAL B  88     -34.885   1.179 -21.990  1.00 37.93           H  
ATOM   2405 HG23 VAL B  88     -34.100   2.197 -20.793  1.00 37.93           H  
ATOM   2406  N   ILE B  89     -30.907   0.703 -24.588  1.00 33.07           N  
ANISOU 2406  N   ILE B  89     4079   4578   3908   -237   -318    243
ATOM   2407  CA  ILE B  89     -30.049   0.892 -25.750  1.00 33.64           C  
ANISOU 2407  CA  ILE B  89     4256   4502   4024   -179   -318    189
ATOM   2408  C   ILE B  89     -30.982   0.789 -26.973  1.00 35.18           C  
ANISOU 2408  C   ILE B  89     4458   4703   4205   -233   -365    222
ATOM   2409  O   ILE B  89     -31.866  -0.073 -26.992  1.00 36.10           O  
ANISOU 2409  O   ILE B  89     4582   4858   4275   -356   -427    293
ATOM   2410  CB  ILE B  89     -28.942  -0.210 -25.795  1.00 35.43           C  
ANISOU 2410  CB  ILE B  89     4618   4594   4249   -198   -347    180
ATOM   2411  CG1 ILE B  89     -27.930  -0.066 -24.627  1.00 36.46           C  
ANISOU 2411  CG1 ILE B  89     4730   4729   4393   -137   -298    145
ATOM   2412  CG2 ILE B  89     -28.193  -0.348 -27.135  1.00 37.42           C  
ANISOU 2412  CG2 ILE B  89     4975   4719   4524   -145   -356    138
ATOM   2413  CD1 ILE B  89     -27.081   1.214 -24.629  1.00 39.69           C  
ANISOU 2413  CD1 ILE B  89     5100   5138   4843    -29   -234     81
ATOM   2414  H   ILE B  89     -31.594  -0.041 -24.704  1.00 33.07           H  
ATOM   2415  HA  ILE B  89     -29.594   1.883 -25.741  1.00 33.64           H  
ATOM   2416  HB  ILE B  89     -29.440  -1.169 -25.647  1.00 35.43           H  
ATOM   2417 HG13 ILE B  89     -27.264  -0.931 -24.611  1.00 36.46           H  
ATOM   2418 HG12 ILE B  89     -28.463  -0.097 -23.677  1.00 36.46           H  
ATOM   2419 HG21 ILE B  89     -27.430  -1.123 -27.069  1.00 37.42           H  
ATOM   2420 HG22 ILE B  89     -28.851  -0.636 -27.955  1.00 37.42           H  
ATOM   2421 HG23 ILE B  89     -27.700   0.579 -27.418  1.00 37.42           H  
ATOM   2422 HD11 ILE B  89     -26.288   1.150 -23.884  1.00 39.69           H  
ATOM   2423 HD12 ILE B  89     -26.605   1.395 -25.592  1.00 39.69           H  
ATOM   2424 HD13 ILE B  89     -27.686   2.084 -24.378  1.00 39.69           H  
ATOM   2425  N   TRP B  90     -30.818   1.682 -27.952  1.00 35.42           N  
ANISOU 2425  N   TRP B  90     4490   4699   4268   -153   -342    178
ATOM   2426  CA  TRP B  90     -31.590   1.684 -29.189  1.00 37.36           C  
ANISOU 2426  CA  TRP B  90     4744   4948   4504   -193   -384    204
ATOM   2427  C   TRP B  90     -30.748   1.039 -30.287  1.00 39.58           C  
ANISOU 2427  C   TRP B  90     5172   5065   4802   -198   -415    180
ATOM   2428  O   TRP B  90     -29.724   1.596 -30.662  1.00 42.13           O  
ANISOU 2428  O   TRP B  90     5538   5310   5159   -108   -374    119
ATOM   2429  CB  TRP B  90     -31.975   3.123 -29.558  1.00 38.58           C  
ANISOU 2429  CB  TRP B  90     4823   5158   4677    -88   -342    166
ATOM   2430  CG  TRP B  90     -33.025   3.732 -28.682  1.00 41.51           C  
ANISOU 2430  CG  TRP B  90     5052   5710   5009    -62   -321    194
ATOM   2431  CD1 TRP B  90     -32.812   4.533 -27.613  1.00 43.04           C  
ANISOU 2431  CD1 TRP B  90     5187   5969   5198     24   -269    164
ATOM   2432  CD2 TRP B  90     -34.468   3.543 -28.760  1.00 43.64           C  
ANISOU 2432  CD2 TRP B  90     5218   6139   5226   -122   -356    263
ATOM   2433  NE1 TRP B  90     -34.027   4.906 -27.068  1.00 44.70           N  
ANISOU 2433  NE1 TRP B  90     5262   6371   5350     40   -264    206
ATOM   2434  CE2 TRP B  90     -35.084   4.328 -27.740  1.00 45.30           C  
ANISOU 2434  CE2 TRP B  90     5297   6520   5395    -49   -315    270
ATOM   2435  CE3 TRP B  90     -35.324   2.805 -29.608  1.00 45.31           C  
ANISOU 2435  CE3 TRP B  90     5433   6372   5411   -228   -419    322
ATOM   2436  CZ2 TRP B  90     -36.480   4.401 -27.593  1.00 47.02           C  
ANISOU 2436  CZ2 TRP B  90     5370   6954   5542    -70   -331    336
ATOM   2437  CZ3 TRP B  90     -36.724   2.890 -29.491  1.00 47.46           C  
ANISOU 2437  CZ3 TRP B  90     5564   6851   5619   -266   -439    390
ATOM   2438  CH2 TRP B  90     -37.302   3.686 -28.483  1.00 47.73           C  
ANISOU 2438  CH2 TRP B  90     5451   7076   5607   -185   -393    399
ATOM   2439  H   TRP B  90     -30.055   2.366 -27.916  1.00 35.42           H  
ATOM   2440  HA  TRP B  90     -32.515   1.115 -29.083  1.00 37.36           H  
ATOM   2441  HB3 TRP B  90     -32.365   3.147 -30.576  1.00 38.58           H  
ATOM   2442  HB2 TRP B  90     -31.096   3.769 -29.563  1.00 38.58           H  
ATOM   2443  HD1 TRP B  90     -31.832   4.847 -27.280  1.00 43.04           H  
ATOM   2444  HE1 TRP B  90     -34.092   5.569 -26.307  1.00 44.70           H  
ATOM   2445  HE3 TRP B  90     -34.890   2.175 -30.368  1.00 45.31           H  
ATOM   2446  HZ2 TRP B  90     -36.918   5.019 -26.824  1.00 47.02           H  
ATOM   2447  HZ3 TRP B  90     -37.352   2.341 -30.178  1.00 47.46           H  
ATOM   2448  HH2 TRP B  90     -38.378   3.756 -28.401  1.00 47.73           H  
ATOM   2449  N   GLU B  91     -31.173  -0.125 -30.773  1.00 37.13           N  
ANISOU 2449  N   GLU B  91     4944   4709   4456   -302   -490    230
ATOM   2450  CA  GLU B  91     -30.427  -0.886 -31.756  1.00 37.76           C  
ANISOU 2450  CA  GLU B  91     5186   4629   4531   -295   -527    208
ATOM   2451  C   GLU B  91     -31.094  -0.777 -33.134  1.00 37.26           C  
ANISOU 2451  C   GLU B  91     5152   4541   4465   -320   -564    220
ATOM   2452  O   GLU B  91     -32.269  -1.118 -33.269  1.00 38.82           O  
ANISOU 2452  O   GLU B  91     5298   4822   4631   -420   -611    282
ATOM   2453  CB  GLU B  91     -30.276  -2.327 -31.253  1.00 41.73           C  
ANISOU 2453  CB  GLU B  91     5813   5067   4976   -399   -605    258
ATOM   2454  CG  GLU B  91     -29.664  -3.241 -32.316  1.00 51.70           C  
ANISOU 2454  CG  GLU B  91     7265   6160   6217   -350   -640    225
ATOM   2455  CD  GLU B  91     -29.129  -4.545 -31.767  1.00 61.13           C  
ANISOU 2455  CD  GLU B  91     8528   7296   7401   -276   -621    191
ATOM   2456  OE1 GLU B  91     -29.800  -5.160 -30.919  1.00 66.70           O  
ANISOU 2456  OE1 GLU B  91     9163   8073   8108   -306   -602    210
ATOM   2457  OE2 GLU B  91     -28.177  -5.040 -32.413  1.00 58.23           O1-
ANISOU 2457  OE2 GLU B  91     8286   6822   7017   -183   -626    148
ATOM   2458  H   GLU B  91     -32.075  -0.506 -30.493  1.00 37.13           H  
ATOM   2459  HA  GLU B  91     -29.410  -0.500 -31.847  1.00 37.76           H  
ATOM   2460  HB3 GLU B  91     -31.223  -2.724 -30.880  1.00 41.73           H  
ATOM   2461  HB2 GLU B  91     -29.593  -2.314 -30.403  1.00 41.73           H  
ATOM   2462  HG3 GLU B  91     -28.849  -2.703 -32.794  1.00 51.70           H  
ATOM   2463  HG2 GLU B  91     -30.387  -3.469 -33.101  1.00 51.70           H  
ATOM   2464  N   ALA B  92     -30.336  -0.317 -34.131  1.00 35.46           N  
ANISOU 2464  N   ALA B  92     5002   4210   4259   -238   -548    167
ATOM   2465  CA  ALA B  92     -30.749  -0.253 -35.526  1.00 34.70           C  
ANISOU 2465  CA  ALA B  92     4945   4078   4160   -256   -583    173
ATOM   2466  C   ALA B  92     -30.759  -1.647 -36.167  1.00 35.27           C  
ANISOU 2466  C   ALA B  92     5187   4036   4177   -336   -673    206
ATOM   2467  O   ALA B  92     -29.746  -2.344 -36.109  1.00 37.09           O  
ANISOU 2467  O   ALA B  92     5544   4166   4380   -305   -690    188
ATOM   2468  CB  ALA B  92     -29.774   0.654 -36.291  1.00 34.02           C  
ANISOU 2468  CB  ALA B  92     4874   3940   4114   -139   -528    105
ATOM   2469  H   ALA B  92     -29.365  -0.072 -33.934  1.00 35.46           H  
ATOM   2470  HA  ALA B  92     -31.748   0.181 -35.578  1.00 34.70           H  
ATOM   2471  HB1 ALA B  92     -30.029   0.709 -37.350  1.00 34.02           H  
ATOM   2472  HB2 ALA B  92     -29.779   1.669 -35.892  1.00 34.02           H  
ATOM   2473  HB3 ALA B  92     -28.748   0.288 -36.233  1.00 34.02           H  
ATOM   2474  N   LYS B  93     -31.862  -2.010 -36.821  1.00 34.49           N  
ANISOU 2474  N   LYS B  93     5099   3955   4050   -436   -738    258
ATOM   2475  CA  LYS B  93     -31.913  -3.145 -37.739  1.00 36.30           C  
ANISOU 2475  CA  LYS B  93     5513   4059   4218   -517   -835    290
ATOM   2476  C   LYS B  93     -32.279  -2.573 -39.115  1.00 36.14           C  
ANISOU 2476  C   LYS B  93     5507   4013   4213   -495   -843    275
ATOM   2477  O   LYS B  93     -33.208  -1.764 -39.200  1.00 36.23           O  
ANISOU 2477  O   LYS B  93     5382   4140   4243   -529   -834    302
ATOM   2478  CB  LYS B  93     -32.962  -4.172 -37.264  1.00 39.93           C  
ANISOU 2478  CB  LYS B  93     5985   4574   4612   -707   -928    387
ATOM   2479  CG  LYS B  93     -32.732  -4.761 -35.852  1.00 50.58           C  
ANISOU 2479  CG  LYS B  93     7301   5975   5943   -750   -922    413
ATOM   2480  CD  LYS B  93     -31.363  -5.433 -35.633  1.00 58.54           C  
ANISOU 2480  CD  LYS B  93     8486   6828   6927   -681   -934    372
ATOM   2481  CE  LYS B  93     -31.334  -6.275 -34.344  1.00 64.61           C  
ANISOU 2481  CE  LYS B  93     9338   7588   7624   -821  -1014    440
ATOM   2482  NZ  LYS B  93     -29.975  -6.719 -33.981  1.00 69.36           N1+
ANISOU 2482  NZ  LYS B  93    10080   8067   8208   -720  -1008    393
ATOM   2483  H   LYS B  93     -32.674  -1.401 -36.834  1.00 34.49           H  
ATOM   2484  HA  LYS B  93     -30.944  -3.641 -37.821  1.00 36.30           H  
ATOM   2485  HB3 LYS B  93     -33.002  -4.992 -37.983  1.00 39.93           H  
ATOM   2486  HB2 LYS B  93     -33.948  -3.710 -37.291  1.00 39.93           H  
ATOM   2487  HG3 LYS B  93     -33.526  -5.484 -35.655  1.00 50.58           H  
ATOM   2488  HG2 LYS B  93     -32.858  -3.979 -35.101  1.00 50.58           H  
ATOM   2489  HD3 LYS B  93     -30.596  -4.661 -35.574  1.00 58.54           H  
ATOM   2490  HD2 LYS B  93     -31.115  -6.047 -36.501  1.00 58.54           H  
ATOM   2491  HE3 LYS B  93     -31.982  -7.146 -34.461  1.00 64.61           H  
ATOM   2492  HE2 LYS B  93     -31.722  -5.698 -33.502  1.00 64.61           H  
ATOM   2493  HZ1 LYS B  93     -29.422  -5.933 -33.610  1.00 69.36           H  
ATOM   2494  HZ2 LYS B  93     -30.006  -7.346 -33.190  1.00 69.36           H  
ATOM   2495  HZ3 LYS B  93     -29.462  -7.126 -34.744  1.00 69.36           H  
ATOM   2496  N   CYS B  94     -31.530  -2.960 -40.155  1.00 35.54           N  
ANISOU 2496  N   CYS B  94     5591   3794   4121   -425   -859    232
ATOM   2497  CA  CYS B  94     -31.741  -2.490 -41.529  1.00 36.71           C  
ANISOU 2497  CA  CYS B  94     5767   3904   4276   -404   -869    217
ATOM   2498  C   CYS B  94     -33.062  -3.031 -42.098  1.00 37.73           C  
ANISOU 2498  C   CYS B  94     5919   4056   4361   -565   -966    295
ATOM   2499  O   CYS B  94     -33.415  -4.177 -41.828  1.00 38.56           O  
ANISOU 2499  O   CYS B  94     6134   4119   4399   -692  -1057    354
ATOM   2500  CB  CYS B  94     -30.555  -2.883 -42.430  1.00 37.21           C  
ANISOU 2500  CB  CYS B  94     6004   3823   4312   -298   -872    161
ATOM   2501  SG  CYS B  94     -28.900  -2.593 -41.725  1.00 39.14           S  
ANISOU 2501  SG  CYS B  94     6213   4073   4586   -121   -766     82
ATOM   2502  H   CYS B  94     -30.756  -3.594 -40.020  1.00 35.54           H  
ATOM   2503  HA  CYS B  94     -31.795  -1.400 -41.505  1.00 36.71           H  
ATOM   2504  HB3 CYS B  94     -30.631  -2.336 -43.368  1.00 37.21           H  
ATOM   2505  HB2 CYS B  94     -30.616  -3.940 -42.700  1.00 37.21           H  
ATOM   2506  N   ARG B  95     -33.773  -2.189 -42.852  1.00 37.39           N  
ANISOU 2506  N   ARG B  95     5777   4083   4346   -568   -955    301
ATOM   2507  CA  ARG B  95     -35.135  -2.466 -43.304  1.00 38.27           C  
ANISOU 2507  CA  ARG B  95     5875   4254   4414   -722  -1042    383
ATOM   2508  C   ARG B  95     -35.196  -3.362 -44.553  1.00 39.71           C  
ANISOU 2508  C   ARG B  95     6277   4277   4536   -782  -1137    395
ATOM   2509  O   ARG B  95     -36.237  -3.962 -44.813  1.00 41.11           O  
ANISOU 2509  O   ARG B  95     6513   4462   4646   -950  -1242    476
ATOM   2510  CB  ARG B  95     -35.808  -1.102 -43.536  1.00 40.33           C  
ANISOU 2510  CB  ARG B  95     5965   4641   4718   -678   -997    378
ATOM   2511  CG  ARG B  95     -37.325  -1.133 -43.802  1.00 45.93           C  
ANISOU 2511  CG  ARG B  95     6533   5532   5388   -813  -1049    470
ATOM   2512  CD  ARG B  95     -37.933   0.254 -44.063  1.00 47.13           C  
ANISOU 2512  CD  ARG B  95     6511   5817   5580   -713   -989    449
ATOM   2513  NE  ARG B  95     -37.666   1.210 -42.968  1.00 44.61           N  
ANISOU 2513  NE  ARG B  95     6054   5591   5306   -587   -893    405
ATOM   2514  CZ  ARG B  95     -37.780   2.543 -42.976  1.00 46.22           C  
ANISOU 2514  CZ  ARG B  95     6150   5869   5543   -459   -833    364
ATOM   2515  NH1 ARG B  95     -38.250   3.203 -44.037  1.00 45.14           N  
ANISOU 2515  NH1 ARG B  95     6018   5727   5406   -437   -855    361
ATOM   2516  NH2 ARG B  95     -37.407   3.228 -41.902  1.00 45.34           N1+
ANISOU 2516  NH2 ARG B  95     5938   5832   5456   -353   -760    328
ATOM   2517  H   ARG B  95     -33.409  -1.260 -43.065  1.00 37.39           H  
ATOM   2518  HA  ARG B  95     -35.669  -2.984 -42.505  1.00 38.27           H  
ATOM   2519  HB3 ARG B  95     -35.314  -0.598 -44.366  1.00 40.33           H  
ATOM   2520  HB2 ARG B  95     -35.618  -0.491 -42.653  1.00 40.33           H  
ATOM   2521  HG3 ARG B  95     -37.881  -1.684 -43.042  1.00 45.93           H  
ATOM   2522  HG2 ARG B  95     -37.467  -1.695 -44.726  1.00 45.93           H  
ATOM   2523  HD3 ARG B  95     -39.018   0.137 -44.065  1.00 47.13           H  
ATOM   2524  HD2 ARG B  95     -37.659   0.622 -45.053  1.00 47.13           H  
ATOM   2525 HH22 ARG B  95     -37.577   4.234 -41.841  1.00 45.34           H  
ATOM   2526 HH21 ARG B  95     -36.793   2.832 -41.189  1.00 45.34           H  
ATOM   2527 HH12 ARG B  95     -38.360   4.210 -44.032  1.00 45.14           H  
ATOM   2528 HH11 ARG B  95     -38.445   2.716 -44.899  1.00 45.14           H  
ATOM   2529  HE  ARG B  95     -37.452   0.755 -42.071  1.00 44.61           H  
ATOM   2530  N   HIS B  96     -34.102  -3.415 -45.316  1.00 39.49           N  
ANISOU 2530  N   HIS B  96     6366   4117   4522   -648  -1105    320
ATOM   2531  CA  HIS B  96     -33.984  -4.165 -46.560  1.00 40.02           C  
ANISOU 2531  CA  HIS B  96     6651   4028   4526   -671  -1189    321
ATOM   2532  C   HIS B  96     -32.623  -4.862 -46.577  1.00 40.63           C  
ANISOU 2532  C   HIS B  96     6921   3952   4565   -547  -1183    260
ATOM   2533  O   HIS B  96     -31.727  -4.480 -45.823  1.00 39.38           O  
ANISOU 2533  O   HIS B  96     6700   3817   4444   -418  -1094    205
ATOM   2534  CB  HIS B  96     -34.119  -3.207 -47.767  1.00 40.41           C  
ANISOU 2534  CB  HIS B  96     6654   4085   4614   -605  -1155    287
ATOM   2535  CG  HIS B  96     -35.365  -2.356 -47.775  1.00 41.67           C  
ANISOU 2535  CG  HIS B  96     6625   4401   4805   -688  -1156    338
ATOM   2536  ND1 HIS B  96     -36.645  -2.871 -47.898  1.00 44.68           N  
ANISOU 2536  ND1 HIS B  96     7029   4817   5129   -859  -1261    423
ATOM   2537  CD2 HIS B  96     -35.524  -0.997 -47.641  1.00 42.91           C  
ANISOU 2537  CD2 HIS B  96     6583   4692   5031   -612  -1070    315
ATOM   2538  CE1 HIS B  96     -37.493  -1.844 -47.801  1.00 44.86           C  
ANISOU 2538  CE1 HIS B  96     6844   5012   5188   -869  -1229    449
ATOM   2539  NE2 HIS B  96     -36.884  -0.679 -47.614  1.00 43.62           N  
ANISOU 2539  NE2 HIS B  96     6561   4908   5106   -713  -1116    382
ATOM   2540  H   HIS B  96     -33.236  -3.017 -44.983  1.00 39.49           H  
ATOM   2541  HA  HIS B  96     -34.760  -4.930 -46.611  1.00 40.02           H  
ATOM   2542  HB3 HIS B  96     -34.086  -3.766 -48.703  1.00 40.41           H  
ATOM   2543  HB2 HIS B  96     -33.259  -2.533 -47.798  1.00 40.41           H  
ATOM   2544  HD1 HIS B  96     -36.910  -3.840 -47.984  1.00 44.68           H  
ATOM   2545  HD2 HIS B  96     -34.765  -0.239 -47.541  1.00 42.91           H  
ATOM   2546  HE1 HIS B  96     -38.566  -1.954 -47.847  1.00 44.86           H  
ATOM   2547  N   LEU B  97     -32.503  -5.857 -47.464  1.00 41.04           N  
ANISOU 2547  N   LEU B  97     7213   3849   4531   -575  -1281    269
ATOM   2548  CA  LEU B  97     -31.231  -6.500 -47.792  1.00 41.19           C  
ANISOU 2548  CA  LEU B  97     7435   3724   4491   -424  -1283    206
ATOM   2549  C   LEU B  97     -30.450  -5.633 -48.792  1.00 40.39           C  
ANISOU 2549  C   LEU B  97     7283   3633   4429   -263  -1194    134
ATOM   2550  O   LEU B  97     -29.264  -5.389 -48.591  1.00 40.93           O  
ANISOU 2550  O   LEU B  97     7357   3698   4496    -97  -1120     71
ATOM   2551  CB  LEU B  97     -31.491  -7.901 -48.394  1.00 41.86           C  
ANISOU 2551  CB  LEU B  97     7821   3632   4454   -511  -1434    243
ATOM   2552  CG  LEU B  97     -32.184  -8.897 -47.440  1.00 46.43           C  
ANISOU 2552  CG  LEU B  97     8490   4181   4969   -684  -1537    319
ATOM   2553  CD1 LEU B  97     -32.594 -10.174 -48.190  1.00 49.14           C  
ANISOU 2553  CD1 LEU B  97     9152   4340   5181   -797  -1703    363
ATOM   2554  CD2 LEU B  97     -31.319  -9.231 -46.209  1.00 49.17           C  
ANISOU 2554  CD2 LEU B  97     8854   4517   5310   -575  -1492    282
ATOM   2555  H   LEU B  97     -33.301  -6.128 -48.013  1.00 41.04           H  
ATOM   2556  HA  LEU B  97     -30.624  -6.595 -46.890  1.00 41.19           H  
ATOM   2557  HB3 LEU B  97     -30.540  -8.327 -48.718  1.00 41.86           H  
ATOM   2558  HB2 LEU B  97     -32.086  -7.797 -49.303  1.00 41.86           H  
ATOM   2559  HG  LEU B  97     -33.108  -8.443 -47.077  1.00 46.43           H  
ATOM   2560 HD11 LEU B  97     -33.139 -10.855 -47.536  1.00 49.14           H  
ATOM   2561 HD12 LEU B  97     -33.244  -9.948 -49.035  1.00 49.14           H  
ATOM   2562 HD13 LEU B  97     -31.724 -10.711 -48.573  1.00 49.14           H  
ATOM   2563 HD21 LEU B  97     -31.211 -10.307 -46.062  1.00 49.17           H  
ATOM   2564 HD22 LEU B  97     -30.310  -8.824 -46.285  1.00 49.17           H  
ATOM   2565 HD23 LEU B  97     -31.765  -8.826 -45.300  1.00 49.17           H  
ATOM   2566  N   GLY B  98     -31.151  -5.173 -49.837  1.00 39.12           N  
ANISOU 2566  N   GLY B  98     7078   3492   4292   -318  -1207    150
ATOM   2567  CA  GLY B  98     -30.614  -4.300 -50.878  1.00 37.36           C  
ANISOU 2567  CA  GLY B  98     6807   3284   4103   -188  -1129     90
ATOM   2568  C   GLY B  98     -30.680  -2.835 -50.428  1.00 37.51           C  
ANISOU 2568  C   GLY B  98     6571   3455   4227   -165  -1023     76
ATOM   2569  O   GLY B  98     -30.994  -2.551 -49.269  1.00 37.57           O  
ANISOU 2569  O   GLY B  98     6440   3556   4279   -204   -990     95
ATOM   2570  H   GLY B  98     -32.136  -5.359 -49.881  1.00 39.12           H  
ATOM   2571  HA3 GLY B  98     -31.206  -4.438 -51.782  1.00 37.36           H  
ATOM   2572  HA2 GLY B  98     -29.590  -4.573 -51.115  1.00 37.36           H  
ATOM   2573  N   CYS B  99     -30.403  -1.904 -51.346  1.00 36.39           N  
ANISOU 2573  N   CYS B  99     6383   3330   4113    -96   -972     40
ATOM   2574  CA  CYS B  99     -30.465  -0.457 -51.104  1.00 36.92           C  
ANISOU 2574  CA  CYS B  99     6247   3517   4264    -74   -886     24
ATOM   2575  C   CYS B  99     -31.547   0.170 -51.988  1.00 40.23           C  
ANISOU 2575  C   CYS B  99     6624   3957   4706   -143   -920     51
ATOM   2576  O   CYS B  99     -31.790  -0.321 -53.084  1.00 41.40           O  
ANISOU 2576  O   CYS B  99     6903   4020   4808   -170   -983     61
ATOM   2577  CB  CYS B  99     -29.121   0.203 -51.445  1.00 37.95           C  
ANISOU 2577  CB  CYS B  99     6352   3667   4403     62   -795    -38
ATOM   2578  SG  CYS B  99     -27.690  -0.388 -50.508  1.00 37.59           S  
ANISOU 2578  SG  CYS B  99     6337   3626   4320    165   -749    -70
ATOM   2579  H   CYS B  99     -30.276  -2.188 -52.319  1.00 36.39           H  
ATOM   2580  HA  CYS B  99     -30.703  -0.249 -50.061  1.00 36.92           H  
ATOM   2581  HB3 CYS B  99     -29.199   1.277 -51.272  1.00 37.95           H  
ATOM   2582  HB2 CYS B  99     -28.899   0.091 -52.508  1.00 37.95           H  
ATOM   2583  N   ILE B 100     -32.157   1.258 -51.519  1.00 39.24           N  
ANISOU 2583  N   ILE B 100     6329   3940   4643   -152   -876     57
ATOM   2584  CA  ILE B 100     -33.147   2.032 -52.255  1.00 41.82           C  
ANISOU 2584  CA  ILE B 100     6604   4301   4985   -196   -906     80
ATOM   2585  C   ILE B 100     -32.444   2.902 -53.314  1.00 44.92           C  
ANISOU 2585  C   ILE B 100     7026   4653   5389   -111   -862     30
ATOM   2586  O   ILE B 100     -31.514   3.637 -52.970  1.00 44.65           O  
ANISOU 2586  O   ILE B 100     6940   4646   5381    -31   -785    -13
ATOM   2587  CB  ILE B 100     -33.979   2.937 -51.299  1.00 44.56           C  
ANISOU 2587  CB  ILE B 100     6768   4787   5375   -217   -884    106
ATOM   2588  CG1 ILE B 100     -34.658   2.125 -50.173  1.00 46.68           C  
ANISOU 2588  CG1 ILE B 100     6990   5121   5625   -307   -921    160
ATOM   2589  CG2 ILE B 100     -35.021   3.809 -52.026  1.00 45.96           C  
ANISOU 2589  CG2 ILE B 100     6888   5018   5558   -241   -917    130
ATOM   2590  CD1 ILE B 100     -35.542   0.974 -50.671  1.00 49.81           C  
ANISOU 2590  CD1 ILE B 100     7479   5486   5962   -446  -1029    227
ATOM   2591  H   ILE B 100     -31.837   1.663 -50.641  1.00 39.24           H  
ATOM   2592  HA  ILE B 100     -33.822   1.337 -52.751  1.00 41.82           H  
ATOM   2593  HB  ILE B 100     -33.292   3.629 -50.812  1.00 44.56           H  
ATOM   2594 HG13 ILE B 100     -35.242   2.792 -49.538  1.00 46.68           H  
ATOM   2595 HG12 ILE B 100     -33.890   1.709 -49.520  1.00 46.68           H  
ATOM   2596 HG21 ILE B 100     -35.661   4.340 -51.321  1.00 45.96           H  
ATOM   2597 HG22 ILE B 100     -34.549   4.571 -52.646  1.00 45.96           H  
ATOM   2598 HG23 ILE B 100     -35.659   3.209 -52.674  1.00 45.96           H  
ATOM   2599 HD11 ILE B 100     -36.274   0.688 -49.917  1.00 49.81           H  
ATOM   2600 HD12 ILE B 100     -36.094   1.229 -51.575  1.00 49.81           H  
ATOM   2601 HD13 ILE B 100     -34.929   0.102 -50.893  1.00 49.81           H  
ATOM   2602  N   ASN B 101     -32.894   2.768 -54.564  1.00 46.86           N  
ANISOU 2602  N   ASN B 101     7357   4840   5607   -143   -917     43
ATOM   2603  CA  ASN B 101     -32.409   3.507 -55.730  1.00 50.65           C  
ANISOU 2603  CA  ASN B 101     7877   5281   6087    -78   -887      4
ATOM   2604  C   ASN B 101     -33.160   4.853 -55.901  1.00 54.24           C  
ANISOU 2604  C   ASN B 101     8222   5803   6584    -79   -876      9
ATOM   2605  O   ASN B 101     -34.056   5.161 -55.112  1.00 54.64           O  
ANISOU 2605  O   ASN B 101     8159   5942   6658   -113   -889     40
ATOM   2606  CB  ASN B 101     -32.440   2.582 -56.988  1.00 52.63           C  
ANISOU 2606  CB  ASN B 101     8301   5422   6276    -94   -950      7
ATOM   2607  CG  ASN B 101     -33.766   2.476 -57.763  1.00 56.78           C  
ANISOU 2607  CG  ASN B 101     8855   5934   6785   -205  -1046     63
ATOM   2608  OD1 ASN B 101     -34.833   2.794 -57.246  1.00 57.81           O  
ANISOU 2608  OD1 ASN B 101     8857   6158   6950   -256  -1059     97
ATOM   2609  ND2 ASN B 101     -33.712   2.057 -59.022  1.00 57.04           N  
ANISOU 2609  ND2 ASN B 101     9062   5859   6751   -243  -1122     76
ATOM   2610  H   ASN B 101     -33.683   2.144 -54.739  1.00 46.86           H  
ATOM   2611  HA  ASN B 101     -31.374   3.818 -55.577  1.00 50.65           H  
ATOM   2612  HB3 ASN B 101     -32.107   1.578 -56.722  1.00 52.63           H  
ATOM   2613  HB2 ASN B 101     -31.696   2.957 -57.691  1.00 52.63           H  
ATOM   2614 HD22 ASN B 101     -34.530   2.165 -59.642  1.00 57.04           H  
ATOM   2615 HD21 ASN B 101     -32.847   1.787 -59.458  1.00 57.04           H  
ATOM   2616  N   ALA B 102     -32.817   5.623 -56.945  1.00 56.91           N  
ANISOU 2616  N   ALA B 102     8596   6107   6921    -35   -855    -21
ATOM   2617  CA  ALA B 102     -33.440   6.917 -57.268  1.00 59.68           C  
ANISOU 2617  CA  ALA B 102     8877   6500   7299    -19   -851    -23
ATOM   2618  C   ALA B 102     -34.951   6.848 -57.577  1.00 62.04           C  
ANISOU 2618  C   ALA B 102     9131   6845   7596    -78   -924     26
ATOM   2619  O   ALA B 102     -35.672   7.803 -57.289  1.00 63.03           O  
ANISOU 2619  O   ALA B 102     9155   7052   7740    -52   -921     35
ATOM   2620  CB  ALA B 102     -32.687   7.553 -58.445  1.00 60.22           C  
ANISOU 2620  CB  ALA B 102     9022   6507   7350     18   -831    -56
ATOM   2621  H   ALA B 102     -32.104   5.300 -57.578  1.00 56.91           H  
ATOM   2622  HA  ALA B 102     -33.325   7.566 -56.398  1.00 59.68           H  
ATOM   2623  HB1 ALA B 102     -33.100   8.535 -58.680  1.00 60.22           H  
ATOM   2624  HB2 ALA B 102     -31.630   7.687 -58.214  1.00 60.22           H  
ATOM   2625  HB3 ALA B 102     -32.768   6.945 -59.347  1.00 60.22           H  
ATOM   2626  N   ASP B 103     -35.399   5.710 -58.119  1.00 62.58           N  
ANISOU 2626  N   ASP B 103     9277   6870   7629   -155   -993     62
ATOM   2627  CA  ASP B 103     -36.800   5.408 -58.445  1.00 63.46           C  
ANISOU 2627  CA  ASP B 103     9345   7043   7724   -237  -1072    123
ATOM   2628  C   ASP B 103     -37.631   5.117 -57.180  1.00 63.09           C  
ANISOU 2628  C   ASP B 103     9176   7119   7677   -298  -1092    175
ATOM   2629  O   ASP B 103     -38.861   5.089 -57.244  1.00 64.05           O  
ANISOU 2629  O   ASP B 103     9223   7338   7776   -367  -1153    235
ATOM   2630  CB  ASP B 103     -36.969   4.211 -59.428  1.00 66.59           C  
ANISOU 2630  CB  ASP B 103     9890   7341   8069   -320  -1152    150
ATOM   2631  CG  ASP B 103     -35.992   4.135 -60.608  1.00 73.61           C  
ANISOU 2631  CG  ASP B 103    10898   8125   8946   -266  -1142    107
ATOM   2632  OD1 ASP B 103     -35.601   5.195 -61.138  1.00 75.35           O  
ANISOU 2632  OD1 ASP B 103    11067   8368   9194   -200  -1101     78
ATOM   2633  OD2 ASP B 103     -35.692   2.991 -61.022  1.00 76.80           O1-
ANISOU 2633  OD2 ASP B 103    11457   8421   9302   -288  -1179    103
ATOM   2634  H   ASP B 103     -34.745   4.986 -58.374  1.00 62.58           H  
ATOM   2635  HA  ASP B 103     -37.224   6.295 -58.920  1.00 63.46           H  
ATOM   2636  HB3 ASP B 103     -37.965   4.264 -59.868  1.00 66.59           H  
ATOM   2637  HB2 ASP B 103     -36.922   3.268 -58.880  1.00 66.59           H  
ATOM   2638  N   GLY B 104     -36.956   4.857 -56.052  1.00 61.20           N  
ANISOU 2638  N   GLY B 104     8913   6887   7452   -278  -1045    159
ATOM   2639  CA  GLY B 104     -37.572   4.454 -54.793  1.00 59.46           C  
ANISOU 2639  CA  GLY B 104     8584   6783   7225   -342  -1063    210
ATOM   2640  C   GLY B 104     -37.766   2.931 -54.737  1.00 57.69           C  
ANISOU 2640  C   GLY B 104     8461   6508   6951   -470  -1137    260
ATOM   2641  O   GLY B 104     -38.544   2.451 -53.914  1.00 59.12           O  
ANISOU 2641  O   GLY B 104     8564   6789   7110   -560  -1171    319
ATOM   2642  H   GLY B 104     -35.944   4.908 -56.077  1.00 61.20           H  
ATOM   2643  HA3 GLY B 104     -38.530   4.957 -54.646  1.00 59.46           H  
ATOM   2644  HA2 GLY B 104     -36.925   4.760 -53.973  1.00 59.46           H  
ATOM   2645  N   ASN B 105     -37.106   2.164 -55.615  1.00 55.14           N  
ANISOU 2645  N   ASN B 105     8322   6031   6598   -480  -1169    239
ATOM   2646  CA  ASN B 105     -37.160   0.700 -55.683  1.00 54.25           C  
ANISOU 2646  CA  ASN B 105     8359   5833   6421   -589  -1254    280
ATOM   2647  C   ASN B 105     -35.900   0.129 -55.018  1.00 51.84           C  
ANISOU 2647  C   ASN B 105     8150   5438   6110   -518  -1211    232
ATOM   2648  O   ASN B 105     -34.893   0.827 -54.908  1.00 50.16           O  
ANISOU 2648  O   ASN B 105     7909   5212   5936   -386  -1118    165
ATOM   2649  CB  ASN B 105     -37.250   0.258 -57.165  1.00 56.54           C  
ANISOU 2649  CB  ASN B 105     8822   6002   6659   -633  -1331    287
ATOM   2650  CG  ASN B 105     -38.613   0.455 -57.837  1.00 61.07           C  
ANISOU 2650  CG  ASN B 105     9309   6666   7228   -713  -1386    341
ATOM   2651  OD1 ASN B 105     -38.936  -0.234 -58.795  1.00 62.79           O  
ANISOU 2651  OD1 ASN B 105     9563   6840   7455   -662  -1381    313
ATOM   2652  ND2 ASN B 105     -39.455   1.368 -57.369  1.00 61.28           N  
ANISOU 2652  ND2 ASN B 105     9208   6839   7237   -833  -1435    420
ATOM   2653  H   ASN B 105     -36.394   2.592 -56.208  1.00 55.14           H  
ATOM   2654  HA  ASN B 105     -38.050   0.353 -55.153  1.00 54.25           H  
ATOM   2655  HB3 ASN B 105     -37.040  -0.810 -57.233  1.00 56.54           H  
ATOM   2656  HB2 ASN B 105     -36.482   0.743 -57.769  1.00 56.54           H  
ATOM   2657 HD22 ASN B 105     -40.311   1.529 -57.870  1.00 61.28           H  
ATOM   2658 HD21 ASN B 105     -39.179   1.997 -56.626  1.00 61.28           H  
ATOM   2659  N   VAL B 106     -35.963  -1.132 -54.567  1.00 50.79           N  
ANISOU 2659  N   VAL B 106     8137   5244   5916   -610  -1284    271
ATOM   2660  CA  VAL B 106     -34.809  -1.801 -53.967  1.00 50.52           C  
ANISOU 2660  CA  VAL B 106     8208   5124   5864   -532  -1254    228
ATOM   2661  C   VAL B 106     -33.888  -2.333 -55.084  1.00 49.97           C  
ANISOU 2661  C   VAL B 106     8343   4900   5742   -431  -1261    173
ATOM   2662  O   VAL B 106     -34.321  -3.182 -55.865  1.00 50.48           O  
ANISOU 2662  O   VAL B 106     8572   4866   5744   -493  -1353    196
ATOM   2663  CB  VAL B 106     -35.222  -2.999 -53.058  1.00 51.67           C  
ANISOU 2663  CB  VAL B 106     8417   5260   5956   -656  -1331    288
ATOM   2664  CG1 VAL B 106     -34.011  -3.690 -52.392  1.00 52.22           C  
ANISOU 2664  CG1 VAL B 106     8603   5237   6001   -551  -1299    237
ATOM   2665  CG2 VAL B 106     -36.227  -2.592 -51.967  1.00 52.23           C  
ANISOU 2665  CG2 VAL B 106     8263   5514   6068   -743  -1312    343
ATOM   2666  H   VAL B 106     -36.766  -1.707 -54.760  1.00 50.79           H  
ATOM   2667  HA  VAL B 106     -34.264  -1.086 -53.348  1.00 50.52           H  
ATOM   2668  HB  VAL B 106     -35.718  -3.747 -53.681  1.00 51.67           H  
ATOM   2669 HG11 VAL B 106     -34.332  -4.461 -51.691  1.00 52.22           H  
ATOM   2670 HG12 VAL B 106     -33.367  -4.181 -53.123  1.00 52.22           H  
ATOM   2671 HG13 VAL B 106     -33.402  -2.969 -51.844  1.00 52.22           H  
ATOM   2672 HG21 VAL B 106     -36.563  -3.464 -51.405  1.00 52.23           H  
ATOM   2673 HG22 VAL B 106     -35.782  -1.899 -51.256  1.00 52.23           H  
ATOM   2674 HG23 VAL B 106     -37.115  -2.117 -52.384  1.00 52.23           H  
ATOM   2675  N   ASP B 107     -32.643  -1.854 -55.110  1.00 47.60           N  
ANISOU 2675  N   ASP B 107     8029   4594   5462   -275  -1166    104
ATOM   2676  CA  ASP B 107     -31.546  -2.427 -55.881  1.00 48.19           C  
ANISOU 2676  CA  ASP B 107     8270   4563   5477   -147  -1154     48
ATOM   2677  C   ASP B 107     -30.885  -3.508 -55.010  1.00 47.91           C  
ANISOU 2677  C   ASP B 107     8368   4460   5378    -98  -1177     37
ATOM   2678  O   ASP B 107     -30.464  -3.218 -53.888  1.00 45.59           O  
ANISOU 2678  O   ASP B 107     7970   4235   5117    -36  -1104     16
ATOM   2679  CB  ASP B 107     -30.498  -1.373 -56.315  1.00 50.71           C  
ANISOU 2679  CB  ASP B 107     8468   4955   5844    -14  -1035    -11
ATOM   2680  CG  ASP B 107     -29.283  -1.954 -57.054  1.00 56.94           C  
ANISOU 2680  CG  ASP B 107     9388   5686   6560    135  -1004    -66
ATOM   2681  OD1 ASP B 107     -29.429  -3.012 -57.706  1.00 57.92           O  
ANISOU 2681  OD1 ASP B 107     9721   5694   6592    160  -1078    -68
ATOM   2682  OD2 ASP B 107     -28.225  -1.300 -57.028  1.00 59.42           O1-
ANISOU 2682  OD2 ASP B 107     9601   6078   6897    227   -911   -105
ATOM   2683  H   ASP B 107     -32.356  -1.182 -54.397  1.00 47.60           H  
ATOM   2684  HA  ASP B 107     -31.957  -2.884 -56.784  1.00 48.19           H  
ATOM   2685  HB3 ASP B 107     -30.157  -0.807 -55.447  1.00 50.71           H  
ATOM   2686  HB2 ASP B 107     -30.968  -0.646 -56.977  1.00 50.71           H  
ATOM   2687  N   TYR B 108     -30.801  -4.725 -55.546  1.00 49.46           N  
ANISOU 2687  N   TYR B 108     8808   4511   5472   -124  -1284     52
ATOM   2688  CA  TYR B 108     -30.230  -5.883 -54.864  1.00 51.49           C  
ANISOU 2688  CA  TYR B 108     9236   4680   5649    -69  -1324     41
ATOM   2689  C   TYR B 108     -28.747  -6.115 -55.182  1.00 50.12           C  
ANISOU 2689  C   TYR B 108     9149   4479   5417    158  -1260    -35
ATOM   2690  O   TYR B 108     -28.154  -6.975 -54.530  1.00 50.90           O  
ANISOU 2690  O   TYR B 108     9376   4518   5445    236  -1284    -51
ATOM   2691  CB  TYR B 108     -31.080  -7.129 -55.179  1.00 54.50           C  
ANISOU 2691  CB  TYR B 108     9872   4908   5929   -198  -1483     93
ATOM   2692  CG  TYR B 108     -32.451  -7.094 -54.527  1.00 58.91           C  
ANISOU 2692  CG  TYR B 108    10323   5535   6527   -431  -1546    182
ATOM   2693  CD1 TYR B 108     -32.616  -7.575 -53.211  1.00 61.06           C  
ANISOU 2693  CD1 TYR B 108    10502   5874   6823   -495  -1537    214
ATOM   2694  CD2 TYR B 108     -33.555  -6.551 -55.215  1.00 61.32           C  
ANISOU 2694  CD2 TYR B 108    10579   5871   6849   -577  -1600    235
ATOM   2695  CE1 TYR B 108     -33.878  -7.516 -52.590  1.00 62.73           C  
ANISOU 2695  CE1 TYR B 108    10592   6182   7059   -704  -1589    300
ATOM   2696  CE2 TYR B 108     -34.814  -6.485 -54.590  1.00 62.93           C  
ANISOU 2696  CE2 TYR B 108    10651   6182   7078   -781  -1651    323
ATOM   2697  CZ  TYR B 108     -34.977  -6.964 -53.277  1.00 64.17           C  
ANISOU 2697  CZ  TYR B 108    10723   6410   7247   -844  -1645    356
ATOM   2698  OH  TYR B 108     -36.198  -6.885 -52.673  1.00 67.02           O  
ANISOU 2698  OH  TYR B 108    10937   6908   7621  -1041  -1690    448
ATOM   2699  H   TYR B 108     -31.046  -4.824 -56.520  1.00 49.46           H  
ATOM   2700  HA  TYR B 108     -30.270  -5.724 -53.784  1.00 51.49           H  
ATOM   2701  HB3 TYR B 108     -30.570  -8.025 -54.822  1.00 54.50           H  
ATOM   2702  HB2 TYR B 108     -31.181  -7.260 -56.257  1.00 54.50           H  
ATOM   2703  HD1 TYR B 108     -31.772  -7.989 -52.677  1.00 61.06           H  
ATOM   2704  HD2 TYR B 108     -33.442  -6.157 -56.214  1.00 61.32           H  
ATOM   2705  HE1 TYR B 108     -33.988  -7.892 -51.584  1.00 62.73           H  
ATOM   2706  HE2 TYR B 108     -35.648  -6.049 -55.121  1.00 62.93           H  
ATOM   2707  HH  TYR B 108     -36.267  -7.421 -51.883  1.00 67.02           H  
ATOM   2708  N   HIS B 109     -28.155  -5.372 -56.132  1.00 49.66           N  
ANISOU 2708  N   HIS B 109     9011   4480   5379    265  -1178    -79
ATOM   2709  CA  HIS B 109     -26.720  -5.466 -56.428  1.00 51.00           C  
ANISOU 2709  CA  HIS B 109     9220   4675   5484    481  -1105   -144
ATOM   2710  C   HIS B 109     -25.855  -4.823 -55.331  1.00 50.90           C  
ANISOU 2710  C   HIS B 109     9001   4809   5530    551   -991   -165
ATOM   2711  O   HIS B 109     -24.708  -5.226 -55.158  1.00 52.54           O  
ANISOU 2711  O   HIS B 109     9223   5066   5673    724   -933   -209
ATOM   2712  CB  HIS B 109     -26.405  -4.851 -57.804  1.00 52.88           C  
ANISOU 2712  CB  HIS B 109     9446   4936   5708    548  -1065   -172
ATOM   2713  CG  HIS B 109     -27.176  -5.468 -58.941  1.00 57.56           C  
ANISOU 2713  CG  HIS B 109    10245   5385   6240    483  -1176   -153
ATOM   2714  ND1 HIS B 109     -28.341  -4.907 -59.424  1.00 60.39           N  
ANISOU 2714  ND1 HIS B 109    10890   5596   6460    574  -1263   -171
ATOM   2715  CD2 HIS B 109     -26.962  -6.595 -59.700  1.00 59.42           C  
ANISOU 2715  CD2 HIS B 109    10444   5604   6528    339  -1216   -117
ATOM   2716  CE1 HIS B 109     -28.787  -5.690 -60.406  1.00 60.74           C  
ANISOU 2716  CE1 HIS B 109    11065   5534   6479    470  -1356   -144
ATOM   2717  NE2 HIS B 109     -28.000  -6.740 -60.624  1.00 60.63           N  
ANISOU 2717  NE2 HIS B 109    10855   5601   6579    326  -1329   -109
ATOM   2718  H   HIS B 109     -28.666  -4.648 -56.639  1.00 49.66           H  
ATOM   2719  HA  HIS B 109     -26.450  -6.524 -56.472  1.00 51.00           H  
ATOM   2720  HB3 HIS B 109     -25.341  -4.956 -58.020  1.00 52.88           H  
ATOM   2721  HB2 HIS B 109     -26.603  -3.777 -57.786  1.00 52.88           H  
ATOM   2722  HD1 HIS B 109     -28.794  -4.074 -59.019  1.00 60.39           H  
ATOM   2723  HD2 HIS B 109     -26.160  -7.315 -59.645  1.00 59.42           H  
ATOM   2724  HE1 HIS B 109     -29.698  -5.496 -60.953  1.00 60.74           H  
ATOM   2725  N   MET B 110     -26.433  -3.870 -54.596  1.00 48.11           N  
ANISOU 2725  N   MET B 110     8457   4536   5287    421   -963   -131
ATOM   2726  CA  MET B 110     -25.855  -3.249 -53.411  1.00 45.35           C  
ANISOU 2726  CA  MET B 110     7922   4313   4995    459   -870   -144
ATOM   2727  C   MET B 110     -26.473  -3.876 -52.152  1.00 43.19           C  
ANISOU 2727  C   MET B 110     7643   4019   4748    355   -917   -105
ATOM   2728  O   MET B 110     -27.457  -4.613 -52.244  1.00 43.42           O  
ANISOU 2728  O   MET B 110     7762   3967   4768    221  -1014    -59
ATOM   2729  CB  MET B 110     -26.110  -1.735 -53.490  1.00 45.69           C  
ANISOU 2729  CB  MET B 110     7751   4472   5137    409   -791   -143
ATOM   2730  CG  MET B 110     -25.433  -1.080 -54.706  1.00 48.71           C  
ANISOU 2730  CG  MET B 110     8138   4880   5491    486   -749   -173
ATOM   2731  SD  MET B 110     -23.617  -1.152 -54.662  1.00 55.74           S  
ANISOU 2731  SD  MET B 110     9005   5871   6301    676   -661   -220
ATOM   2732  CE  MET B 110     -23.309   0.182 -53.482  1.00 46.06           C  
ANISOU 2732  CE  MET B 110     7527   4797   5178    616   -567   -212
ATOM   2733  H   MET B 110     -27.386  -3.613 -54.808  1.00 48.11           H  
ATOM   2734  HA  MET B 110     -24.780  -3.432 -53.371  1.00 45.35           H  
ATOM   2735  HB3 MET B 110     -25.742  -1.263 -52.582  1.00 45.69           H  
ATOM   2736  HB2 MET B 110     -27.182  -1.534 -53.524  1.00 45.69           H  
ATOM   2737  HG3 MET B 110     -25.745  -0.039 -54.790  1.00 48.71           H  
ATOM   2738  HG2 MET B 110     -25.768  -1.552 -55.631  1.00 48.71           H  
ATOM   2739  HE1 MET B 110     -22.239   0.340 -53.354  1.00 46.06           H  
ATOM   2740  HE2 MET B 110     -23.753   1.102 -53.860  1.00 46.06           H  
ATOM   2741  HE3 MET B 110     -23.747  -0.043 -52.510  1.00 46.06           H  
ATOM   2742  N   ASN B 111     -25.862  -3.641 -50.987  1.00 40.80           N  
ANISOU 2742  N   ASN B 111     7239   3795   4468    406   -856   -119
ATOM   2743  CA  ASN B 111     -26.287  -4.233 -49.716  1.00 38.53           C  
ANISOU 2743  CA  ASN B 111     6948   3494   4197    314   -898    -82
ATOM   2744  C   ASN B 111     -26.413  -3.142 -48.655  1.00 36.75           C  
ANISOU 2744  C   ASN B 111     6485   3403   4076    260   -819    -72
ATOM   2745  O   ASN B 111     -25.470  -2.373 -48.461  1.00 36.29           O  
ANISOU 2745  O   ASN B 111     6311   3437   4043    351   -728   -108
ATOM   2746  CB  ASN B 111     -25.254  -5.267 -49.212  1.00 40.13           C  
ANISOU 2746  CB  ASN B 111     7284   3650   4315    437   -911   -107
ATOM   2747  CG  ASN B 111     -25.089  -6.563 -50.011  1.00 45.72           C  
ANISOU 2747  CG  ASN B 111     8280   4196   4896    495  -1014   -114
ATOM   2748  OD1 ASN B 111     -24.189  -7.338 -49.700  1.00 44.53           O  
ANISOU 2748  OD1 ASN B 111     8237   3961   4723    424  -1083    -95
ATOM   2749  ND2 ASN B 111     -25.910  -6.839 -51.020  1.00 51.37           N  
ANISOU 2749  ND2 ASN B 111     9136   4861   5520    625  -1035   -139
ATOM   2750  H   ASN B 111     -25.039  -3.041 -50.949  1.00 40.80           H  
ATOM   2751  HA  ASN B 111     -27.251  -4.725 -49.831  1.00 38.53           H  
ATOM   2752  HB3 ASN B 111     -25.529  -5.579 -48.202  1.00 40.13           H  
ATOM   2753  HB2 ASN B 111     -24.275  -4.796 -49.122  1.00 40.13           H  
ATOM   2754 HD22 ASN B 111     -25.792  -7.693 -51.539  1.00 51.37           H  
ATOM   2755 HD21 ASN B 111     -26.608  -6.175 -51.353  1.00 51.37           H  
ATOM   2756  N   SER B 112     -27.527  -3.159 -47.920  1.00 35.41           N  
ANISOU 2756  N   SER B 112     6257   3251   3948    117   -860    -22
ATOM   2757  CA  SER B 112     -27.680  -2.452 -46.656  1.00 35.47           C  
ANISOU 2757  CA  SER B 112     6061   3380   4034     86   -792    -15
ATOM   2758  C   SER B 112     -26.964  -3.261 -45.562  1.00 35.74           C  
ANISOU 2758  C   SER B 112     6147   3401   4032    133   -792    -21
ATOM   2759  O   SER B 112     -27.288  -4.436 -45.392  1.00 35.70           O  
ANISOU 2759  O   SER B 112     6306   3300   3960     92   -879      5
ATOM   2760  CB  SER B 112     -29.177  -2.361 -46.313  1.00 36.67           C  
ANISOU 2760  CB  SER B 112     6135   3576   4221    -71   -840     47
ATOM   2761  OG  SER B 112     -29.843  -1.407 -47.114  1.00 36.14           O  
ANISOU 2761  OG  SER B 112     5991   3546   4192   -102   -833     53
ATOM   2762  H   SER B 112     -28.222  -3.879 -48.106  1.00 35.41           H  
ATOM   2763  HA  SER B 112     -27.252  -1.450 -46.722  1.00 35.47           H  
ATOM   2764  HB3 SER B 112     -29.310  -2.075 -45.270  1.00 36.67           H  
ATOM   2765  HB2 SER B 112     -29.649  -3.334 -46.440  1.00 36.67           H  
ATOM   2766  HG  SER B 112     -30.170  -1.862 -47.915  1.00 36.14           H  
ATOM   2767  N   VAL B 113     -26.022  -2.649 -44.839  1.00 34.94           N  
ANISOU 2767  N   VAL B 113     5919   3390   3966    214   -702    -54
ATOM   2768  CA  VAL B 113     -25.306  -3.305 -43.744  1.00 36.08           C  
ANISOU 2768  CA  VAL B 113     6094   3537   4080    267   -695    -61
ATOM   2769  C   VAL B 113     -25.321  -2.408 -42.486  1.00 34.85           C  
ANISOU 2769  C   VAL B 113     5747   3495   3998    234   -627    -57
ATOM   2770  O   VAL B 113     -25.270  -1.181 -42.633  1.00 33.33           O  
ANISOU 2770  O   VAL B 113     5416   3384   3864    239   -562    -72
ATOM   2771  CB  VAL B 113     -23.836  -3.602 -44.143  1.00 40.40           C  
ANISOU 2771  CB  VAL B 113     6713   4078   4557    442   -658   -112
ATOM   2772  CG1 VAL B 113     -23.760  -4.699 -45.220  1.00 42.65           C  
ANISOU 2772  CG1 VAL B 113     7225   4236   4744    504   -735   -121
ATOM   2773  CG2 VAL B 113     -23.032  -2.360 -44.564  1.00 41.88           C  
ANISOU 2773  CG2 VAL B 113     6748   4382   4782    507   -560   -144
ATOM   2774  H   VAL B 113     -25.749  -1.689 -45.049  1.00 34.94           H  
ATOM   2775  HA  VAL B 113     -25.798  -4.250 -43.521  1.00 36.08           H  
ATOM   2776  HB  VAL B 113     -23.339  -4.006 -43.260  1.00 40.40           H  
ATOM   2777 HG11 VAL B 113     -22.729  -4.964 -45.446  1.00 42.65           H  
ATOM   2778 HG12 VAL B 113     -24.271  -5.605 -44.888  1.00 42.65           H  
ATOM   2779 HG13 VAL B 113     -24.236  -4.380 -46.148  1.00 42.65           H  
ATOM   2780 HG21 VAL B 113     -22.033  -2.633 -44.888  1.00 41.88           H  
ATOM   2781 HG22 VAL B 113     -23.506  -1.838 -45.394  1.00 41.88           H  
ATOM   2782 HG23 VAL B 113     -22.911  -1.655 -43.743  1.00 41.88           H  
ATOM   2783  N   PRO B 114     -25.427  -3.021 -41.284  1.00 35.45           N  
ANISOU 2783  N   PRO B 114     5829   3574   4066    199   -647    -35
ATOM   2784  CA  PRO B 114     -25.391  -2.275 -40.017  1.00 35.73           C  
ANISOU 2784  CA  PRO B 114     5694   3718   4165    177   -583    -34
ATOM   2785  C   PRO B 114     -23.985  -1.735 -39.702  1.00 36.92           C  
ANISOU 2785  C   PRO B 114     5782   3931   4316    301   -502    -81
ATOM   2786  O   PRO B 114     -23.001  -2.465 -39.831  1.00 39.37           O  
ANISOU 2786  O   PRO B 114     6190   4209   4560    406   -506   -104
ATOM   2787  CB  PRO B 114     -25.848  -3.314 -38.981  1.00 37.22           C  
ANISOU 2787  CB  PRO B 114     5935   3882   4327    104   -639      6
ATOM   2788  CG  PRO B 114     -25.428  -4.656 -39.555  1.00 38.31           C  
ANISOU 2788  CG  PRO B 114     6305   3882   4370    135   -725      9
ATOM   2789  CD  PRO B 114     -25.601  -4.462 -41.054  1.00 35.64           C  
ANISOU 2789  CD  PRO B 114     6039   3490   4013    171   -740     -9
ATOM   2790  HA  PRO B 114     -26.101  -1.448 -40.039  1.00 35.73           H  
ATOM   2791  HB3 PRO B 114     -26.934  -3.269 -38.886  1.00 37.22           H  
ATOM   2792  HB2 PRO B 114     -25.425  -3.147 -37.988  1.00 37.22           H  
ATOM   2793  HG3 PRO B 114     -25.992  -5.500 -39.157  1.00 38.31           H  
ATOM   2794  HG2 PRO B 114     -24.373  -4.824 -39.328  1.00 38.31           H  
ATOM   2795  HD2 PRO B 114     -24.884  -5.071 -41.606  1.00 35.64           H  
ATOM   2796  HD3 PRO B 114     -26.609  -4.747 -41.360  1.00 35.64           H  
ATOM   2797  N   ILE B 115     -23.914  -0.472 -39.275  1.00 34.93           N  
ANISOU 2797  N   ILE B 115     5375   3774   4123    291   -434    -91
ATOM   2798  CA  ILE B 115     -22.707   0.121 -38.718  1.00 34.20           C  
ANISOU 2798  CA  ILE B 115     5209   3758   4027    370   -365   -121
ATOM   2799  C   ILE B 115     -22.756  -0.160 -37.208  1.00 33.71           C  
ANISOU 2799  C   ILE B 115     5103   3727   3978    347   -360   -108
ATOM   2800  O   ILE B 115     -23.612   0.396 -36.515  1.00 34.65           O  
ANISOU 2800  O   ILE B 115     5144   3876   4145    269   -358    -88
ATOM   2801  CB  ILE B 115     -22.639   1.660 -38.944  1.00 36.30           C  
ANISOU 2801  CB  ILE B 115     5357   4093   4343    347   -311   -133
ATOM   2802  CG1 ILE B 115     -22.721   1.996 -40.449  1.00 38.10           C  
ANISOU 2802  CG1 ILE B 115     5630   4289   4558    358   -319   -143
ATOM   2803  CG2 ILE B 115     -21.368   2.284 -38.317  1.00 37.46           C  
ANISOU 2803  CG2 ILE B 115     5428   4331   4474    400   -249   -153
ATOM   2804  CD1 ILE B 115     -22.882   3.489 -40.752  1.00 39.99           C  
ANISOU 2804  CD1 ILE B 115     5790   4565   4838    320   -289   -149
ATOM   2805  H   ILE B 115     -24.775   0.053 -39.114  1.00 34.93           H  
ATOM   2806  HA  ILE B 115     -21.817  -0.336 -39.157  1.00 34.20           H  
ATOM   2807  HB  ILE B 115     -23.505   2.119 -38.461  1.00 36.30           H  
ATOM   2808 HG13 ILE B 115     -23.573   1.482 -40.895  1.00 38.10           H  
ATOM   2809 HG12 ILE B 115     -21.843   1.602 -40.961  1.00 38.10           H  
ATOM   2810 HG21 ILE B 115     -21.325   3.364 -38.447  1.00 37.46           H  
ATOM   2811 HG22 ILE B 115     -21.315   2.114 -37.241  1.00 37.46           H  
ATOM   2812 HG23 ILE B 115     -20.463   1.866 -38.756  1.00 37.46           H  
ATOM   2813 HD11 ILE B 115     -22.091   3.854 -41.406  1.00 39.99           H  
ATOM   2814 HD12 ILE B 115     -23.832   3.663 -41.255  1.00 39.99           H  
ATOM   2815 HD13 ILE B 115     -22.885   4.108 -39.855  1.00 39.99           H  
ATOM   2816  N   GLN B 116     -21.875  -1.052 -36.751  1.00 34.01           N  
ANISOU 2816  N   GLN B 116     5195   3763   3965    425   -360   -119
ATOM   2817  CA  GLN B 116     -21.774  -1.421 -35.345  1.00 35.56           C  
ANISOU 2817  CA  GLN B 116     5360   3985   4167    408   -358   -107
ATOM   2818  C   GLN B 116     -20.674  -0.597 -34.669  1.00 35.76           C  
ANISOU 2818  C   GLN B 116     5263   4119   4207    454   -284   -128
ATOM   2819  O   GLN B 116     -19.549  -0.574 -35.170  1.00 38.15           O  
ANISOU 2819  O   GLN B 116     5550   4473   4471    537   -249   -150
ATOM   2820  CB  GLN B 116     -21.505  -2.929 -35.216  1.00 39.16           C  
ANISOU 2820  CB  GLN B 116     5972   4359   4548    460   -418   -101
ATOM   2821  CG  GLN B 116     -22.628  -3.783 -35.832  1.00 44.99           C  
ANISOU 2821  CG  GLN B 116     6854   4981   5261    387   -506    -72
ATOM   2822  CD  GLN B 116     -22.515  -5.244 -35.424  1.00 54.60           C  
ANISOU 2822  CD  GLN B 116     8235   6106   6405    396   -582    -55
ATOM   2823  OE1 GLN B 116     -23.294  -5.723 -34.610  1.00 56.98           O  
ANISOU 2823  OE1 GLN B 116     8531   6401   6716    294   -615    -18
ATOM   2824  NE2 GLN B 116     -21.546  -5.966 -35.973  1.00 57.66           N  
ANISOU 2824  NE2 GLN B 116     8774   6427   6706    528   -610    -83
ATOM   2825  H   GLN B 116     -21.191  -1.463 -37.364  1.00 34.01           H  
ATOM   2826  HA  GLN B 116     -22.715  -1.221 -34.844  1.00 35.56           H  
ATOM   2827  HB3 GLN B 116     -21.413  -3.173 -34.157  1.00 39.16           H  
ATOM   2828  HB2 GLN B 116     -20.547  -3.187 -35.669  1.00 39.16           H  
ATOM   2829  HG3 GLN B 116     -22.647  -3.699 -36.919  1.00 44.99           H  
ATOM   2830  HG2 GLN B 116     -23.595  -3.420 -35.482  1.00 44.99           H  
ATOM   2831 HE22 GLN B 116     -21.444  -6.947 -35.697  1.00 57.66           H  
ATOM   2832 HE21 GLN B 116     -20.909  -5.588 -36.651  1.00 57.66           H  
ATOM   2833  N   GLN B 117     -21.015   0.033 -33.544  1.00 33.40           N  
ANISOU 2833  N   GLN B 117     4879   3861   3950    396   -266   -116
ATOM   2834  CA AGLN B 117     -20.094   0.727 -32.651  0.50 32.45           C  
ANISOU 2834  CA AGLN B 117     4650   3835   3844    412   -207   -129
ATOM   2835  CA BGLN B 117     -19.986   0.576 -32.619  0.50 32.76           C  
ANISOU 2835  CA BGLN B 117     4697   3874   3877    421   -208   -130
ATOM   2836  C   GLN B 117     -19.729  -0.248 -31.518  1.00 33.25           C  
ANISOU 2836  C   GLN B 117     4767   3943   3924    432   -218   -121
ATOM   2837  O   GLN B 117     -20.632  -0.927 -31.021  1.00 33.10           O  
ANISOU 2837  O   GLN B 117     4782   3877   3917    371   -257    -96
ATOM   2838  CB AGLN B 117     -20.839   1.951 -32.064  0.50 32.39           C  
ANISOU 2838  CB AGLN B 117     4548   3861   3898    334   -183   -126
ATOM   2839  CB BGLN B 117     -20.493   1.982 -32.337  0.50 33.38           C  
ANISOU 2839  CB BGLN B 117     4677   3993   4012    353   -177   -132
ATOM   2840  CG AGLN B 117     -19.911   2.998 -31.412  0.50 32.43           C  
ANISOU 2840  CG AGLN B 117     4461   3950   3911    333   -132   -139
ATOM   2841  CG BGLN B 117     -19.612   2.815 -31.366  0.50 34.46           C  
ANISOU 2841  CG BGLN B 117     4727   4214   4152    354   -130   -141
ATOM   2842  CD AGLN B 117     -20.659   4.184 -30.802  0.50 31.76           C  
ANISOU 2842  CD AGLN B 117     4318   3881   3866    279   -117   -142
ATOM   2843  CD BGLN B 117     -18.192   3.155 -31.830  0.50 34.10           C  
ANISOU 2843  CD BGLN B 117     4652   4244   4061    400    -96   -153
ATOM   2844  OE1AGLN B 117     -21.845   4.114 -30.506  0.50 32.67           O  
ANISOU 2844  OE1AGLN B 117     4433   3973   4009    249   -138   -131
ATOM   2845  OE1BGLN B 117     -17.968   3.644 -32.946  0.50 32.48           O  
ANISOU 2845  OE1BGLN B 117     4452   4046   3841    402    -90   -158
ATOM   2846  NE2AGLN B 117     -19.964   5.291 -30.569  0.50 32.68           N  
ANISOU 2846  NE2AGLN B 117     4393   4049   3975    267    -86   -154
ATOM   2847  NE2BGLN B 117     -17.183   2.893 -30.963  0.50 31.51           N  
ANISOU 2847  NE2BGLN B 117     4284   3989   3701    435    -76   -151
ATOM   2848  H   GLN B 117     -21.955  -0.100 -33.167  1.00 33.40           H  
ATOM   2849  HA AGLN B 117     -19.202   1.048 -33.192  0.50 32.45           H  
ATOM   2850  HA BGLN B 117     -19.040   0.647 -33.155  0.50 32.76           H  
ATOM   2851  HB3AGLN B 117     -21.574   1.614 -31.330  0.50 32.39           H  
ATOM   2852  HB3BGLN B 117     -21.509   1.927 -31.945  0.50 33.38           H  
ATOM   2853  HB2AGLN B 117     -21.426   2.439 -32.839  0.50 32.39           H  
ATOM   2854  HB2BGLN B 117     -20.602   2.521 -33.278  0.50 33.38           H  
ATOM   2855  HG3AGLN B 117     -19.195   3.364 -32.146  0.50 32.43           H  
ATOM   2856  HG3BGLN B 117     -19.562   2.308 -30.403  0.50 34.46           H  
ATOM   2857  HG2AGLN B 117     -19.334   2.539 -30.614  0.50 32.43           H  
ATOM   2858  HG2BGLN B 117     -20.135   3.736 -31.108  0.50 34.46           H  
ATOM   2859 HE22AGLN B 117     -20.458   6.071 -30.167  0.50 32.68           H  
ATOM   2860 HE22BGLN B 117     -16.229   3.099 -31.222  0.50 31.51           H  
ATOM   2861 HE21AGLN B 117     -18.988   5.367 -30.804  0.50 32.68           H  
ATOM   2862 HE21BGLN B 117     -17.386   2.492 -30.059  0.50 31.51           H  
ATOM   2863  N   GLU B 118     -18.464  -0.257 -31.066  1.00 32.20           N  
ANISOU 2863  N   GLU B 118     4602   3880   3754    506   -185   -135
ATOM   2864  CA  GLU B 118     -18.123  -0.782 -29.740  1.00 32.32           C  
ANISOU 2864  CA  GLU B 118     4620   3908   3751    525   -191   -128
ATOM   2865  C   GLU B 118     -18.494   0.282 -28.705  1.00 30.64           C  
ANISOU 2865  C   GLU B 118     4294   3752   3596    446   -155   -122
ATOM   2866  O   GLU B 118     -17.989   1.404 -28.810  1.00 30.99           O  
ANISOU 2866  O   GLU B 118     4257   3863   3656    432   -113   -133
ATOM   2867  CB  GLU B 118     -16.612  -1.065 -29.599  1.00 38.68           C  
ANISOU 2867  CB  GLU B 118     5412   4796   4489    642   -166   -143
ATOM   2868  CG  GLU B 118     -16.083  -2.287 -30.375  1.00 50.75           C  
ANISOU 2868  CG  GLU B 118     7065   6281   5935    766   -202   -155
ATOM   2869  CD  GLU B 118     -14.683  -2.725 -29.938  1.00 62.64           C  
ANISOU 2869  CD  GLU B 118     8547   7897   7357    908   -177   -168
ATOM   2870  OE1 GLU B 118     -13.936  -1.922 -29.330  1.00 65.56           O  
ANISOU 2870  OE1 GLU B 118     8792   8381   7736    892   -133   -162
ATOM   2871  OE2 GLU B 118     -14.390  -3.934 -30.027  1.00 67.59           O1-
ANISOU 2871  OE2 GLU B 118     9282   8499   7898   1041   -205   -182
ATOM   2872  H   GLU B 118     -17.778   0.359 -31.475  1.00 32.20           H  
ATOM   2873  HA  GLU B 118     -18.679  -1.699 -29.539  1.00 32.32           H  
ATOM   2874  HB3 GLU B 118     -16.388  -1.208 -28.538  1.00 38.68           H  
ATOM   2875  HB2 GLU B 118     -16.040  -0.183 -29.895  1.00 38.68           H  
ATOM   2876  HG3 GLU B 118     -16.077  -2.092 -31.447  1.00 50.75           H  
ATOM   2877  HG2 GLU B 118     -16.743  -3.135 -30.202  1.00 50.75           H  
ATOM   2878  N   ILE B 119     -19.315  -0.077 -27.717  1.00 28.03           N  
ANISOU 2878  N   ILE B 119     3970   3396   3284    394   -176   -104
ATOM   2879  CA  ILE B 119     -19.593   0.789 -26.576  1.00 27.94           C  
ANISOU 2879  CA  ILE B 119     3862   3440   3316    335   -144   -101
ATOM   2880  C   ILE B 119     -19.321   0.031 -25.271  1.00 26.65           C  
ANISOU 2880  C   ILE B 119     3698   3290   3137    335   -151    -88
ATOM   2881  O   ILE B 119     -19.368  -1.201 -25.241  1.00 27.73           O  
ANISOU 2881  O   ILE B 119     3924   3372   3238    351   -195    -74
ATOM   2882  CB  ILE B 119     -21.050   1.343 -26.557  1.00 30.20           C  
ANISOU 2882  CB  ILE B 119     4119   3712   3644    262   -153    -87
ATOM   2883  CG1 ILE B 119     -22.167   0.321 -26.253  1.00 33.50           C  
ANISOU 2883  CG1 ILE B 119     4577   4097   4054    207   -200    -52
ATOM   2884  CG2 ILE B 119     -21.357   2.125 -27.845  1.00 30.98           C  
ANISOU 2884  CG2 ILE B 119     4226   3788   3757    262   -152    -99
ATOM   2885  CD1 ILE B 119     -23.525   0.964 -25.940  1.00 36.46           C  
ANISOU 2885  CD1 ILE B 119     4877   4520   4456    145   -195    -32
ATOM   2886  H   ILE B 119     -19.649  -1.038 -27.654  1.00 28.03           H  
ATOM   2887  HA  ILE B 119     -18.910   1.639 -26.580  1.00 27.94           H  
ATOM   2888  HB  ILE B 119     -21.071   2.077 -25.750  1.00 30.20           H  
ATOM   2889 HG13 ILE B 119     -21.916  -0.305 -25.400  1.00 33.50           H  
ATOM   2890 HG12 ILE B 119     -22.264  -0.348 -27.106  1.00 33.50           H  
ATOM   2891 HG21 ILE B 119     -22.248   2.736 -27.726  1.00 30.98           H  
ATOM   2892 HG22 ILE B 119     -20.546   2.800 -28.106  1.00 30.98           H  
ATOM   2893 HG23 ILE B 119     -21.513   1.459 -28.694  1.00 30.98           H  
ATOM   2894 HD11 ILE B 119     -24.165   0.279 -25.385  1.00 36.46           H  
ATOM   2895 HD12 ILE B 119     -23.418   1.866 -25.344  1.00 36.46           H  
ATOM   2896 HD13 ILE B 119     -24.050   1.236 -26.853  1.00 36.46           H  
ATOM   2897  N   LEU B 120     -19.071   0.796 -24.208  1.00 26.58           N  
ANISOU 2897  N   LEU B 120     3608   3342   3148    313   -116    -93
ATOM   2898  CA  LEU B 120     -19.052   0.287 -22.846  1.00 26.28           C  
ANISOU 2898  CA  LEU B 120     3567   3321   3099    304   -122    -79
ATOM   2899  C   LEU B 120     -20.450   0.461 -22.232  1.00 27.17           C  
ANISOU 2899  C   LEU B 120     3644   3439   3238    228   -128    -57
ATOM   2900  O   LEU B 120     -21.152   1.407 -22.568  1.00 28.97           O  
ANISOU 2900  O   LEU B 120     3822   3691   3495    205   -109    -64
ATOM   2901  CB  LEU B 120     -18.001   1.070 -22.031  1.00 27.12           C  
ANISOU 2901  CB  LEU B 120     3602   3502   3200    326    -80    -96
ATOM   2902  CG  LEU B 120     -16.540   0.881 -22.500  1.00 29.10           C  
ANISOU 2902  CG  LEU B 120     3849   3799   3410    397    -67   -109
ATOM   2903  CD1 LEU B 120     -15.579   1.784 -21.694  1.00 30.71           C  
ANISOU 2903  CD1 LEU B 120     3971   4094   3602    386    -32   -113
ATOM   2904  CD2 LEU B 120     -16.105  -0.600 -22.485  1.00 31.58           C  
ANISOU 2904  CD2 LEU B 120     4244   4086   3670    481    -99   -104
ATOM   2905  H   LEU B 120     -19.102   1.808 -24.324  1.00 26.58           H  
ATOM   2906  HA  LEU B 120     -18.801  -0.768 -22.850  1.00 26.28           H  
ATOM   2907  HB3 LEU B 120     -18.080   0.780 -20.983  1.00 27.12           H  
ATOM   2908  HB2 LEU B 120     -18.250   2.130 -22.074  1.00 27.12           H  
ATOM   2909  HG  LEU B 120     -16.483   1.224 -23.535  1.00 29.10           H  
ATOM   2910 HD11 LEU B 120     -14.956   2.380 -22.363  1.00 30.71           H  
ATOM   2911 HD12 LEU B 120     -16.115   2.487 -21.055  1.00 30.71           H  
ATOM   2912 HD13 LEU B 120     -14.909   1.213 -21.051  1.00 30.71           H  
ATOM   2913 HD21 LEU B 120     -15.072  -0.730 -22.167  1.00 31.58           H  
ATOM   2914 HD22 LEU B 120     -16.726  -1.207 -21.825  1.00 31.58           H  
ATOM   2915 HD23 LEU B 120     -16.182  -1.026 -23.486  1.00 31.58           H  
ATOM   2916  N   VAL B 121     -20.843  -0.405 -21.307  1.00 25.80           N  
ANISOU 2916  N   VAL B 121     3500   3258   3047    193   -157    -28
ATOM   2917  CA  VAL B 121     -22.027  -0.239 -20.475  1.00 27.35           C  
ANISOU 2917  CA  VAL B 121     3641   3499   3252    123   -158      0
ATOM   2918  C   VAL B 121     -21.661  -0.698 -19.058  1.00 27.62           C  
ANISOU 2918  C   VAL B 121     3663   3564   3269    116   -152      9
ATOM   2919  O   VAL B 121     -20.777  -1.539 -18.899  1.00 28.01           O  
ANISOU 2919  O   VAL B 121     3762   3584   3295    162   -160     -1
ATOM   2920  CB  VAL B 121     -23.237  -1.056 -21.010  1.00 27.45           C  
ANISOU 2920  CB  VAL B 121     3692   3489   3248     45   -210     45
ATOM   2921  CG1 VAL B 121     -23.730  -0.503 -22.361  1.00 27.08           C  
ANISOU 2921  CG1 VAL B 121     3651   3418   3220     53   -215     35
ATOM   2922  CG2 VAL B 121     -22.997  -2.580 -21.096  1.00 28.61           C  
ANISOU 2922  CG2 VAL B 121     3967   3557   3348     23   -274     71
ATOM   2923  H   VAL B 121     -20.278  -1.232 -21.104  1.00 25.80           H  
ATOM   2924  HA  VAL B 121     -22.303   0.816 -20.415  1.00 27.35           H  
ATOM   2925  HB  VAL B 121     -24.054  -0.906 -20.303  1.00 27.45           H  
ATOM   2926 HG11 VAL B 121     -24.647  -0.984 -22.695  1.00 27.08           H  
ATOM   2927 HG12 VAL B 121     -23.930   0.568 -22.299  1.00 27.08           H  
ATOM   2928 HG13 VAL B 121     -22.991  -0.652 -23.149  1.00 27.08           H  
ATOM   2929 HG21 VAL B 121     -23.862  -3.096 -21.509  1.00 28.61           H  
ATOM   2930 HG22 VAL B 121     -22.148  -2.817 -21.738  1.00 28.61           H  
ATOM   2931 HG23 VAL B 121     -22.801  -3.020 -20.118  1.00 28.61           H  
ATOM   2932  N   LEU B 122     -22.320  -0.128 -18.050  1.00 27.04           N  
ANISOU 2932  N   LEU B 122     3518   3560   3197     74   -135     26
ATOM   2933  CA  LEU B 122     -22.175  -0.554 -16.668  1.00 28.04           C  
ANISOU 2933  CA  LEU B 122     3633   3718   3303     58   -133     40
ATOM   2934  C   LEU B 122     -23.170  -1.693 -16.439  1.00 30.62           C  
ANISOU 2934  C   LEU B 122     4001   4041   3593    -30   -186     98
ATOM   2935  O   LEU B 122     -24.358  -1.473 -16.676  1.00 32.84           O  
ANISOU 2935  O   LEU B 122     4237   4375   3867    -92   -196    131
ATOM   2936  CB  LEU B 122     -22.513   0.639 -15.748  1.00 27.83           C  
ANISOU 2936  CB  LEU B 122     3510   3778   3286     69    -84     26
ATOM   2937  CG  LEU B 122     -21.557   1.838 -15.828  1.00 29.85           C  
ANISOU 2937  CG  LEU B 122     3745   4032   3563    133    -44    -24
ATOM   2938  CD1 LEU B 122     -22.069   3.017 -14.976  1.00 33.14           C  
ANISOU 2938  CD1 LEU B 122     4104   4517   3972    149    -11    -37
ATOM   2939  CD2 LEU B 122     -20.141   1.439 -15.418  1.00 31.69           C  
ANISOU 2939  CD2 LEU B 122     4009   4241   3792    163    -41    -40
ATOM   2940  H   LEU B 122     -23.095   0.505 -18.226  1.00 27.04           H  
ATOM   2941  HA  LEU B 122     -21.163  -0.906 -16.465  1.00 28.04           H  
ATOM   2942  HB3 LEU B 122     -22.556   0.305 -14.716  1.00 27.83           H  
ATOM   2943  HB2 LEU B 122     -23.513   0.975 -15.989  1.00 27.83           H  
ATOM   2944  HG  LEU B 122     -21.528   2.174 -16.864  1.00 29.85           H  
ATOM   2945 HD11 LEU B 122     -21.832   3.973 -15.445  1.00 33.14           H  
ATOM   2946 HD12 LEU B 122     -23.151   2.987 -14.835  1.00 33.14           H  
ATOM   2947 HD13 LEU B 122     -21.622   3.021 -13.981  1.00 33.14           H  
ATOM   2948 HD21 LEU B 122     -19.518   2.322 -15.283  1.00 31.69           H  
ATOM   2949 HD22 LEU B 122     -20.142   0.875 -14.485  1.00 31.69           H  
ATOM   2950 HD23 LEU B 122     -19.672   0.815 -16.176  1.00 31.69           H  
ATOM   2951  N   ARG B 123     -22.701  -2.856 -15.983  1.00 30.01           N  
ANISOU 2951  N   ARG B 123     4013   3909   3481    -43   -226    115
ATOM   2952  CA  ARG B 123     -23.563  -3.918 -15.472  1.00 30.67           C  
ANISOU 2952  CA  ARG B 123     4156   3984   3515   -154   -290    179
ATOM   2953  C   ARG B 123     -23.411  -3.960 -13.953  1.00 29.47           C  
ANISOU 2953  C   ARG B 123     3958   3897   3343   -183   -274    196
ATOM   2954  O   ARG B 123     -22.285  -3.811 -13.482  1.00 28.83           O  
ANISOU 2954  O   ARG B 123     3894   3792   3267   -111   -255    164
ATOM   2955  CB  ARG B 123     -23.187  -5.269 -16.100  1.00 33.15           C  
ANISOU 2955  CB  ARG B 123     4644   4166   3784   -153   -366    190
ATOM   2956  CG  ARG B 123     -24.068  -6.422 -15.552  1.00 36.36           C  
ANISOU 2956  CG  ARG B 123     5130   4559   4125   -303   -447    267
ATOM   2957  CD  ARG B 123     -24.151  -7.681 -16.419  1.00 40.14           C  
ANISOU 2957  CD  ARG B 123     5787   4912   4551   -351   -541    295
ATOM   2958  NE  ARG B 123     -24.574  -7.374 -17.793  1.00 38.59           N  
ANISOU 2958  NE  ARG B 123     5572   4703   4386   -332   -533    279
ATOM   2959  CZ  ARG B 123     -25.763  -6.989 -18.271  1.00 39.19           C  
ANISOU 2959  CZ  ARG B 123     5585   4843   4461   -443   -548    325
ATOM   2960  NH1 ARG B 123     -26.850  -6.859 -17.507  1.00 38.46           N  
ANISOU 2960  NH1 ARG B 123     5433   4850   4330   -586   -573    396
ATOM   2961  NH2 ARG B 123     -25.855  -6.719 -19.565  1.00 40.25           N1+
ANISOU 2961  NH2 ARG B 123     5717   4954   4622   -413   -544    305
ATOM   2962  H   ARG B 123     -21.704  -2.970 -15.796  1.00 30.01           H  
ATOM   2963  HA  ARG B 123     -24.605  -3.713 -15.713  1.00 30.67           H  
ATOM   2964  HB3 ARG B 123     -22.135  -5.498 -15.913  1.00 33.15           H  
ATOM   2965  HB2 ARG B 123     -23.281  -5.168 -17.180  1.00 33.15           H  
ATOM   2966  HG3 ARG B 123     -25.069  -6.093 -15.270  1.00 36.36           H  
ATOM   2967  HG2 ARG B 123     -23.606  -6.731 -14.613  1.00 36.36           H  
ATOM   2968  HD3 ARG B 123     -24.921  -8.336 -16.011  1.00 40.14           H  
ATOM   2969  HD2 ARG B 123     -23.219  -8.249 -16.389  1.00 40.14           H  
ATOM   2970 HH22 ARG B 123     -26.786  -6.440 -19.921  1.00 40.25           H  
ATOM   2971 HH21 ARG B 123     -25.062  -6.776 -20.189  1.00 40.25           H  
ATOM   2972 HH12 ARG B 123     -27.769  -6.582 -17.900  1.00 38.46           H  
ATOM   2973 HH11 ARG B 123     -26.827  -6.988 -16.508  1.00 38.46           H  
ATOM   2974  HE  ARG B 123     -23.758  -7.380 -18.428  1.00 38.59           H  
ATOM   2975  N   ARG B 124     -24.515  -4.167 -13.226  1.00 29.12           N  
ANISOU 2975  N   ARG B 124     3853   3944   3267   -288   -285    253
ATOM   2976  CA  ARG B 124     -24.527  -4.356 -11.771  1.00 30.23           C  
ANISOU 2976  CA  ARG B 124     3947   4158   3381   -320   -270    274
ATOM   2977  C   ARG B 124     -23.660  -5.559 -11.364  1.00 30.93           C  
ANISOU 2977  C   ARG B 124     4177   4144   3432   -334   -326    286
ATOM   2978  O   ARG B 124     -23.823  -6.638 -11.935  1.00 32.27           O  
ANISOU 2978  O   ARG B 124     4483   4219   3560   -395   -406    321
ATOM   2979  CB  ARG B 124     -25.980  -4.544 -11.280  1.00 31.02           C  
ANISOU 2979  CB  ARG B 124     3962   4395   3431   -447   -284    349
ATOM   2980  CG  ARG B 124     -26.889  -3.351 -11.607  1.00 33.42           C  
ANISOU 2980  CG  ARG B 124     4119   4825   3755   -407   -226    336
ATOM   2981  CD  ARG B 124     -28.345  -3.532 -11.134  1.00 36.12           C  
ANISOU 2981  CD  ARG B 124     4352   5342   4031   -518   -237    415
ATOM   2982  NE  ARG B 124     -29.228  -2.481 -11.678  1.00 39.05           N  
ANISOU 2982  NE  ARG B 124     4605   5824   4408   -468   -198    407
ATOM   2983  CZ  ARG B 124     -29.269  -1.176 -11.386  1.00 42.17           C  
ANISOU 2983  CZ  ARG B 124     4905   6297   4820   -339   -126    355
ATOM   2984  NH1 ARG B 124     -28.496  -0.646 -10.434  1.00 39.06           N  
ANISOU 2984  NH1 ARG B 124     4514   5888   4440   -263    -84    310
ATOM   2985  NH2 ARG B 124     -30.093  -0.401 -12.090  1.00 43.13           N1+
ANISOU 2985  NH2 ARG B 124     4942   6508   4937   -283   -103    348
ATOM   2986  H   ARG B 124     -25.400  -4.315 -13.702  1.00 29.12           H  
ATOM   2987  HA  ARG B 124     -24.118  -3.454 -11.313  1.00 30.23           H  
ATOM   2988  HB3 ARG B 124     -25.981  -4.708 -10.202  1.00 31.02           H  
ATOM   2989  HB2 ARG B 124     -26.396  -5.452 -11.719  1.00 31.02           H  
ATOM   2990  HG3 ARG B 124     -26.851  -3.068 -12.657  1.00 33.42           H  
ATOM   2991  HG2 ARG B 124     -26.449  -2.513 -11.065  1.00 33.42           H  
ATOM   2992  HD3 ARG B 124     -28.401  -3.435 -10.053  1.00 36.12           H  
ATOM   2993  HD2 ARG B 124     -28.722  -4.531 -11.336  1.00 36.12           H  
ATOM   2994 HH22 ARG B 124     -30.197   0.589 -11.940  1.00 43.13           H  
ATOM   2995 HH21 ARG B 124     -30.637  -0.825 -12.839  1.00 43.13           H  
ATOM   2996 HH12 ARG B 124     -28.440   0.335 -10.201  1.00 39.06           H  
ATOM   2997 HH11 ARG B 124     -27.893  -1.265  -9.879  1.00 39.06           H  
ATOM   2998  HE  ARG B 124     -29.885  -2.858 -12.367  1.00 39.05           H  
ATOM   2999  N   GLU B 125     -22.754  -5.349 -10.405  1.00 30.14           N  
ANISOU 2999  N   GLU B 125     4058   4052   3342   -266   -291    254
ATOM   3000  CA  GLU B 125     -21.895  -6.384  -9.842  1.00 31.01           C  
ANISOU 3000  CA  GLU B 125     4298   4073   3411   -258   -343    262
ATOM   3001  C   GLU B 125     -21.786  -6.105  -8.330  1.00 33.47           C  
ANISOU 3001  C   GLU B 125     4536   4462   3717   -258   -305    262
ATOM   3002  O   GLU B 125     -21.181  -5.087  -7.982  1.00 32.35           O  
ANISOU 3002  O   GLU B 125     4303   4371   3618   -175   -238    214
ATOM   3003  CB  GLU B 125     -20.521  -6.368 -10.549  1.00 35.36           C  
ANISOU 3003  CB  GLU B 125     4926   4532   3978   -122   -344    205
ATOM   3004  CG  GLU B 125     -19.498  -7.348  -9.924  1.00 41.13           C  
ANISOU 3004  CG  GLU B 125     5801   5176   4651    -84   -402    210
ATOM   3005  CD  GLU B 125     -18.218  -7.487 -10.738  1.00 44.50           C  
ANISOU 3005  CD  GLU B 125     6316   5527   5065     64   -415    163
ATOM   3006  OE1 GLU B 125     -18.295  -7.960 -11.887  1.00 46.36           O  
ANISOU 3006  OE1 GLU B 125     6595   5715   5305     95   -429    150
ATOM   3007  OE2 GLU B 125     -17.118  -7.159 -10.232  1.00 47.68           O1-
ANISOU 3007  OE2 GLU B 125     6746   5927   5442    153   -415    142
ATOM   3008  H   GLU B 125     -22.717  -4.447  -9.934  1.00 30.14           H  
ATOM   3009  HA  GLU B 125     -22.326  -7.363 -10.038  1.00 31.01           H  
ATOM   3010  HB3 GLU B 125     -20.103  -5.361 -10.537  1.00 35.36           H  
ATOM   3011  HB2 GLU B 125     -20.669  -6.617 -11.602  1.00 35.36           H  
ATOM   3012  HG3 GLU B 125     -19.942  -8.341  -9.839  1.00 41.13           H  
ATOM   3013  HG2 GLU B 125     -19.234  -7.040  -8.913  1.00 41.13           H  
ATOM   3014  N   PRO B 126     -22.343  -6.965  -7.445  1.00 35.62           N  
ANISOU 3014  N   PRO B 126     4859   4743   3932   -359   -352    319
ATOM   3015  CA  PRO B 126     -23.140  -8.171  -7.759  1.00 36.81           C  
ANISOU 3015  CA  PRO B 126     5138   4834   4013   -493   -448    390
ATOM   3016  C   PRO B 126     -24.495  -7.847  -8.433  1.00 38.69           C  
ANISOU 3016  C   PRO B 126     5298   5159   4243   -605   -452    439
ATOM   3017  O   PRO B 126     -24.891  -6.675  -8.435  1.00 38.29           O  
ANISOU 3017  O   PRO B 126     5083   5231   4235   -573   -377    420
ATOM   3018  CB  PRO B 126     -23.327  -8.835  -6.377  1.00 38.76           C  
ANISOU 3018  CB  PRO B 126     5416   5108   4201   -575   -477    436
ATOM   3019  CG  PRO B 126     -23.263  -7.693  -5.380  1.00 39.49           C  
ANISOU 3019  CG  PRO B 126     5335   5334   4335   -521   -382    406
ATOM   3020  CD  PRO B 126     -22.230  -6.761  -5.998  1.00 36.49           C  
ANISOU 3020  CD  PRO B 126     4903   4930   4031   -363   -317    322
ATOM   3021  HA  PRO B 126     -22.555  -8.830  -8.400  1.00 36.81           H  
ATOM   3022  HB3 PRO B 126     -22.506  -9.530  -6.193  1.00 38.76           H  
ATOM   3023  HB2 PRO B 126     -24.258  -9.396  -6.273  1.00 38.76           H  
ATOM   3024  HG3 PRO B 126     -23.015  -8.011  -4.367  1.00 39.49           H  
ATOM   3025  HG2 PRO B 126     -24.233  -7.193  -5.343  1.00 39.49           H  
ATOM   3026  HD2 PRO B 126     -22.410  -5.730  -5.691  1.00 36.49           H  
ATOM   3027  HD3 PRO B 126     -21.221  -7.035  -5.685  1.00 36.49           H  
ATOM   3028  N   PRO B 127     -25.193  -8.881  -8.963  1.00 40.56           N  
ANISOU 3028  N   PRO B 127     5660   5333   4419   -735   -547    503
ATOM   3029  CA  PRO B 127     -26.565  -8.731  -9.484  1.00 40.20           C  
ANISOU 3029  CA  PRO B 127     5528   5390   4357   -851   -556    558
ATOM   3030  C   PRO B 127     -27.507  -7.989  -8.524  1.00 39.14           C  
ANISOU 3030  C   PRO B 127     5188   5475   4210   -909   -494    597
ATOM   3031  O   PRO B 127     -27.438  -8.204  -7.312  1.00 40.09           O  
ANISOU 3031  O   PRO B 127     5287   5652   4293   -949   -488    622
ATOM   3032  CB  PRO B 127     -27.027 -10.177  -9.726  1.00 42.82           C  
ANISOU 3032  CB  PRO B 127     6048   5626   4594  -1025   -687    641
ATOM   3033  CG  PRO B 127     -25.745 -10.942 -10.002  1.00 44.03           C  
ANISOU 3033  CG  PRO B 127     6419   5574   4736   -926   -740    595
ATOM   3034  CD  PRO B 127     -24.741 -10.273  -9.072  1.00 42.02           C  
ANISOU 3034  CD  PRO B 127     6081   5353   4531   -786   -658    533
ATOM   3035  HA  PRO B 127     -26.493  -8.197 -10.434  1.00 40.20           H  
ATOM   3036  HB3 PRO B 127     -27.742 -10.248 -10.547  1.00 42.82           H  
ATOM   3037  HB2 PRO B 127     -27.512 -10.577  -8.833  1.00 42.82           H  
ATOM   3038  HG3 PRO B 127     -25.447 -10.780 -11.039  1.00 44.03           H  
ATOM   3039  HG2 PRO B 127     -25.840 -12.017  -9.842  1.00 44.03           H  
ATOM   3040  HD2 PRO B 127     -24.779 -10.739  -8.087  1.00 42.02           H  
ATOM   3041  HD3 PRO B 127     -23.730 -10.376  -9.467  1.00 42.02           H  
ATOM   3042  N   HIS B 128     -28.320  -7.093  -9.087  1.00 38.20           N  
ANISOU 3042  N   HIS B 128     4921   5481   4115   -894   -445    596
ATOM   3043  CA  HIS B 128     -29.328  -6.268  -8.422  1.00 39.18           C  
ANISOU 3043  CA  HIS B 128     4840   5833   4212   -912   -382    627
ATOM   3044  C   HIS B 128     -28.749  -5.122  -7.566  1.00 39.09           C  
ANISOU 3044  C   HIS B 128     4729   5875   4247   -753   -285    553
ATOM   3045  O   HIS B 128     -29.537  -4.356  -7.009  1.00 40.75           O  
ANISOU 3045  O   HIS B 128     4783   6274   4427   -735   -230    568
ATOM   3046  CB  HIS B 128     -30.342  -7.128  -7.624  1.00 41.28           C  
ANISOU 3046  CB  HIS B 128     5080   6234   4372  -1110   -437    740
ATOM   3047  CG  HIS B 128     -30.823  -8.396  -8.296  1.00 46.75           C  
ANISOU 3047  CG  HIS B 128     5915   6849   5000  -1299   -555    823
ATOM   3048  ND1 HIS B 128     -31.137  -8.474  -9.644  1.00 49.50           N  
ANISOU 3048  ND1 HIS B 128     6263   7194   5353  -1336   -585    840
ATOM   3049  CD2 HIS B 128     -30.993  -9.672  -7.806  1.00 48.86           C  
ANISOU 3049  CD2 HIS B 128     6345   7032   5189  -1460   -656    892
ATOM   3050  CE1 HIS B 128     -31.479  -9.737  -9.897  1.00 49.98           C  
ANISOU 3050  CE1 HIS B 128     6486   7167   5336  -1523   -705    920
ATOM   3051  NE2 HIS B 128     -31.426 -10.522  -8.827  1.00 50.16           N  
ANISOU 3051  NE2 HIS B 128     6623   7131   5306  -1603   -755    953
ATOM   3052  H   HIS B 128     -28.357  -7.054 -10.115  1.00 38.20           H  
ATOM   3053  HA  HIS B 128     -29.876  -5.787  -9.232  1.00 39.18           H  
ATOM   3054  HB3 HIS B 128     -31.216  -6.523  -7.384  1.00 41.28           H  
ATOM   3055  HB2 HIS B 128     -29.902  -7.410  -6.667  1.00 41.28           H  
ATOM   3056  HD1 HIS B 128     -31.039  -7.734 -10.355  1.00 49.50           H  
ATOM   3057  HD2 HIS B 128     -30.835 -10.042  -6.803  1.00 48.86           H  
ATOM   3058  HE1 HIS B 128     -31.753 -10.089 -10.881  1.00 49.98           H  
ATOM   3059  N   SER B 129     -27.413  -4.974  -7.487  1.00 36.43           N  
ANISOU 3059  N   SER B 129     4483   5386   3974   -634   -266    474
ATOM   3060  CA  SER B 129     -26.762  -3.894  -6.742  1.00 34.96           C  
ANISOU 3060  CA  SER B 129     4217   5243   3822   -503   -186    409
ATOM   3061  C   SER B 129     -27.184  -2.505  -7.272  1.00 35.19           C  
ANISOU 3061  C   SER B 129     4134   5353   3882   -399   -121    365
ATOM   3062  O   SER B 129     -26.981  -2.230  -8.462  1.00 35.15           O  
ANISOU 3062  O   SER B 129     4160   5272   3922   -354   -125    332
ATOM   3063  CB  SER B 129     -25.228  -4.028  -6.806  1.00 34.31           C  
ANISOU 3063  CB  SER B 129     4242   5004   3790   -411   -185    344
ATOM   3064  OG  SER B 129     -24.623  -2.975  -6.069  1.00 36.31           O  
ANISOU 3064  OG  SER B 129     4424   5301   4069   -307   -116    289
ATOM   3065  H   SER B 129     -26.820  -5.672  -7.922  1.00 36.43           H  
ATOM   3066  HA  SER B 129     -27.041  -4.036  -5.701  1.00 34.96           H  
ATOM   3067  HB3 SER B 129     -24.869  -3.994  -7.836  1.00 34.31           H  
ATOM   3068  HB2 SER B 129     -24.908  -4.979  -6.380  1.00 34.31           H  
ATOM   3069  HG  SER B 129     -23.652  -3.113  -6.054  1.00 36.31           H  
ATOM   3070  N   PRO B 130     -27.742  -1.632  -6.405  1.00 34.98           N  
ANISOU 3070  N   PRO B 130     3989   5475   3825   -346    -64    359
ATOM   3071  CA  PRO B 130     -27.994  -0.235  -6.781  1.00 35.63           C  
ANISOU 3071  CA  PRO B 130     3995   5619   3924   -222    -11    309
ATOM   3072  C   PRO B 130     -26.746   0.551  -7.228  1.00 34.80           C  
ANISOU 3072  C   PRO B 130     3955   5384   3885    -98     20    219
ATOM   3073  O   PRO B 130     -26.881   1.396  -8.114  1.00 36.16           O  
ANISOU 3073  O   PRO B 130     4111   5550   4077    -12     43    177
ATOM   3074  CB  PRO B 130     -28.621   0.385  -5.519  1.00 38.20           C  
ANISOU 3074  CB  PRO B 130     4198   6142   4176   -186     35    330
ATOM   3075  CG  PRO B 130     -29.182  -0.790  -4.741  1.00 38.39           C  
ANISOU 3075  CG  PRO B 130     4219   6220   4147   -318      4    401
ATOM   3076  CD  PRO B 130     -28.193  -1.905  -5.040  1.00 36.62           C  
ANISOU 3076  CD  PRO B 130     4141   5801   3973   -382    -48    395
ATOM   3077  HA  PRO B 130     -28.734  -0.243  -7.581  1.00 35.63           H  
ATOM   3078  HB3 PRO B 130     -29.388   1.124  -5.751  1.00 38.20           H  
ATOM   3079  HB2 PRO B 130     -27.861   0.880  -4.910  1.00 38.20           H  
ATOM   3080  HG3 PRO B 130     -30.157  -1.060  -5.149  1.00 38.39           H  
ATOM   3081  HG2 PRO B 130     -29.306  -0.594  -3.675  1.00 38.39           H  
ATOM   3082  HD2 PRO B 130     -27.335  -1.866  -4.367  1.00 36.62           H  
ATOM   3083  HD3 PRO B 130     -28.684  -2.873  -4.924  1.00 36.62           H  
ATOM   3084  N   ASN B 131     -25.591   0.296  -6.592  1.00 31.64           N  
ANISOU 3084  N   ASN B 131     3628   4886   3509    -94     15    195
ATOM   3085  CA  ASN B 131     -24.484   1.251  -6.519  1.00 30.43           C  
ANISOU 3085  CA  ASN B 131     3516   4649   3396      5     44    121
ATOM   3086  C   ASN B 131     -23.094   0.660  -6.810  1.00 29.21           C  
ANISOU 3086  C   ASN B 131     3452   4362   3283     -4     19    101
ATOM   3087  O   ASN B 131     -22.112   1.388  -6.628  1.00 30.90           O  
ANISOU 3087  O   ASN B 131     3691   4536   3515     51     38     57
ATOM   3088  CB  ASN B 131     -24.515   1.986  -5.149  1.00 31.53           C  
ANISOU 3088  CB  ASN B 131     3620   4867   3495     47     80    108
ATOM   3089  CG  ASN B 131     -24.143   1.116  -3.938  1.00 33.09           C  
ANISOU 3089  CG  ASN B 131     3836   5066   3671    -28     59    147
ATOM   3090  OD1 ASN B 131     -24.275  -0.102  -3.970  1.00 34.02           O  
ANISOU 3090  OD1 ASN B 131     4005   5125   3796   -110     13    185
ATOM   3091  ND2 ASN B 131     -23.697   1.721  -2.844  1.00 34.24           N  
ANISOU 3091  ND2 ASN B 131     3961   5267   3782     -1     85    138
ATOM   3092  H   ASN B 131     -25.527  -0.474  -5.931  1.00 31.64           H  
ATOM   3093  HA  ASN B 131     -24.599   1.998  -7.302  1.00 30.43           H  
ATOM   3094  HB3 ASN B 131     -25.504   2.414  -4.981  1.00 31.53           H  
ATOM   3095  HB2 ASN B 131     -23.824   2.829  -5.180  1.00 31.53           H  
ATOM   3096 HD22 ASN B 131     -23.470   1.148  -2.044  1.00 34.24           H  
ATOM   3097 HD21 ASN B 131     -23.571   2.722  -2.800  1.00 34.24           H  
ATOM   3098  N   SER B 132     -22.995  -0.591  -7.267  1.00 28.02           N  
ANISOU 3098  N   SER B 132     3361   4146   3139    -65    -30    134
ATOM   3099  CA  SER B 132     -21.720  -1.189  -7.646  1.00 27.44           C  
ANISOU 3099  CA  SER B 132     3374   3961   3091    -39    -53    111
ATOM   3100  C   SER B 132     -21.862  -1.874  -9.008  1.00 28.36           C  
ANISOU 3100  C   SER B 132     3555   4005   3216    -62    -96    126
ATOM   3101  O   SER B 132     -22.763  -2.693  -9.197  1.00 29.45           O  
ANISOU 3101  O   SER B 132     3710   4154   3327   -143   -135    176
ATOM   3102  CB  SER B 132     -21.189  -2.076  -6.502  1.00 30.51           C  
ANISOU 3102  CB  SER B 132     3808   4333   3450    -63    -76    130
ATOM   3103  OG  SER B 132     -21.974  -3.226  -6.266  1.00 34.47           O  
ANISOU 3103  OG  SER B 132     4329   4860   3908   -161   -116    193
ATOM   3104  H   SER B 132     -23.808  -1.183  -7.388  1.00 28.02           H  
ATOM   3105  HA  SER B 132     -20.975  -0.408  -7.767  1.00 27.44           H  
ATOM   3106  HB3 SER B 132     -21.136  -1.498  -5.579  1.00 30.51           H  
ATOM   3107  HB2 SER B 132     -20.172  -2.401  -6.730  1.00 30.51           H  
ATOM   3108  HG  SER B 132     -21.728  -3.887  -6.945  1.00 34.47           H  
ATOM   3109  N   PHE B 133     -20.986  -1.498  -9.942  1.00 27.49           N  
ANISOU 3109  N   PHE B 133     3481   3827   3136      5    -92     86
ATOM   3110  CA  PHE B 133     -21.031  -1.946 -11.327  1.00 27.65           C  
ANISOU 3110  CA  PHE B 133     3564   3777   3163      6   -127     89
ATOM   3111  C   PHE B 133     -19.639  -2.412 -11.778  1.00 27.05           C  
ANISOU 3111  C   PHE B 133     3559   3633   3087     82   -140     60
ATOM   3112  O   PHE B 133     -18.632  -2.001 -11.197  1.00 27.94           O  
ANISOU 3112  O   PHE B 133     3642   3771   3202    135   -112     33
ATOM   3113  CB  PHE B 133     -21.477  -0.771 -12.230  1.00 27.94           C  
ANISOU 3113  CB  PHE B 133     3540   3839   3236     30    -93     64
ATOM   3114  CG  PHE B 133     -22.847  -0.164 -11.960  1.00 28.44           C  
ANISOU 3114  CG  PHE B 133     3520   3994   3291     -5    -72     83
ATOM   3115  CD1 PHE B 133     -23.015   0.783 -10.928  1.00 30.01           C  
ANISOU 3115  CD1 PHE B 133     3652   4265   3484     31    -27     62
ATOM   3116  CD2 PHE B 133     -23.987  -0.616 -12.658  1.00 28.62           C  
ANISOU 3116  CD2 PHE B 133     3533   4041   3301    -66   -100    123
ATOM   3117  CE1 PHE B 133     -24.277   1.280 -10.641  1.00 31.47           C  
ANISOU 3117  CE1 PHE B 133     3760   4554   3643     25     -8     80
ATOM   3118  CE2 PHE B 133     -25.238  -0.088 -12.375  1.00 29.88           C  
ANISOU 3118  CE2 PHE B 133     3598   4318   3439    -84    -79    146
ATOM   3119  CZ  PHE B 133     -25.378   0.860 -11.370  1.00 30.77           C  
ANISOU 3119  CZ  PHE B 133     3641   4511   3538    -27    -31    122
ATOM   3120  H   PHE B 133     -20.290  -0.788  -9.734  1.00 27.49           H  
ATOM   3121  HA  PHE B 133     -21.722  -2.779 -11.417  1.00 27.65           H  
ATOM   3122  HB3 PHE B 133     -21.457  -1.101 -13.270  1.00 27.94           H  
ATOM   3123  HB2 PHE B 133     -20.742   0.032 -12.161  1.00 27.94           H  
ATOM   3124  HD1 PHE B 133     -22.165   1.114 -10.349  1.00 30.01           H  
ATOM   3125  HD2 PHE B 133     -23.894  -1.355 -13.436  1.00 28.62           H  
ATOM   3126  HE1 PHE B 133     -24.409   1.993  -9.844  1.00 31.47           H  
ATOM   3127  HE2 PHE B 133     -26.100  -0.425 -12.932  1.00 29.88           H  
ATOM   3128  HZ  PHE B 133     -26.351   1.263 -11.138  1.00 30.77           H  
ATOM   3129  N   ARG B 134     -19.592  -3.175 -12.872  1.00 26.36           N  
ANISOU 3129  N   ARG B 134     3558   3471   2988     96   -181     65
ATOM   3130  CA  ARG B 134     -18.403  -3.333 -13.704  1.00 27.28           C  
ANISOU 3130  CA  ARG B 134     3723   3548   3092    195   -185     33
ATOM   3131  C   ARG B 134     -18.738  -2.814 -15.108  1.00 26.35           C  
ANISOU 3131  C   ARG B 134     3600   3410   3000    210   -177     17
ATOM   3132  O   ARG B 134     -19.885  -2.932 -15.544  1.00 28.35           O  
ANISOU 3132  O   ARG B 134     3874   3636   3260    146   -202     41
ATOM   3133  CB  ARG B 134     -17.969  -4.815 -13.740  1.00 29.27           C  
ANISOU 3133  CB  ARG B 134     4121   3714   3285    225   -254     51
ATOM   3134  CG  ARG B 134     -16.631  -5.075 -14.482  1.00 30.58           C  
ANISOU 3134  CG  ARG B 134     4335   3864   3420    360   -256     17
ATOM   3135  CD  ARG B 134     -16.337  -6.557 -14.753  1.00 33.00           C  
ANISOU 3135  CD  ARG B 134     4821   4068   3650    414   -335     29
ATOM   3136  NE  ARG B 134     -16.055  -7.303 -13.521  1.00 31.73           N  
ANISOU 3136  NE  ARG B 134     4699   3902   3455    397   -361     49
ATOM   3137  CZ  ARG B 134     -14.910  -7.786 -13.039  1.00 34.60           C  
ANISOU 3137  CZ  ARG B 134     5053   4307   3785    500   -350     30
ATOM   3138  NH1 ARG B 134     -13.743  -7.538 -13.634  1.00 31.71           N  
ANISOU 3138  NH1 ARG B 134     4630   4010   3408    625   -313     -4
ATOM   3139  NH2 ARG B 134     -14.944  -8.508 -11.922  1.00 35.54           N1+
ANISOU 3139  NH2 ARG B 134     5219   4411   3873    478   -379     51
ATOM   3140  H   ARG B 134     -20.469  -3.483 -13.294  1.00 26.36           H  
ATOM   3141  HA  ARG B 134     -17.590  -2.722 -13.317  1.00 27.28           H  
ATOM   3142  HB3 ARG B 134     -18.763  -5.408 -14.198  1.00 29.27           H  
ATOM   3143  HB2 ARG B 134     -17.879  -5.183 -12.718  1.00 29.27           H  
ATOM   3144  HG3 ARG B 134     -15.846  -4.675 -13.839  1.00 30.58           H  
ATOM   3145  HG2 ARG B 134     -16.523  -4.531 -15.415  1.00 30.58           H  
ATOM   3146  HD3 ARG B 134     -15.612  -6.704 -15.552  1.00 33.00           H  
ATOM   3147  HD2 ARG B 134     -17.254  -7.022 -15.117  1.00 33.00           H  
ATOM   3148 HH22 ARG B 134     -14.285  -9.227 -11.681  1.00 35.54           H  
ATOM   3149 HH21 ARG B 134     -15.834  -8.470 -11.397  1.00 35.54           H  
ATOM   3150 HH12 ARG B 134     -12.886  -7.998 -13.389  1.00 31.71           H  
ATOM   3151 HH11 ARG B 134     -13.737  -6.918 -14.454  1.00 31.71           H  
ATOM   3152  HE  ARG B 134     -16.931  -7.530 -12.994  1.00 31.73           H  
ATOM   3153  N   LEU B 135     -17.729  -2.280 -15.805  1.00 25.69           N  
ANISOU 3153  N   LEU B 135     3486   3352   2924    287   -146    -17
ATOM   3154  CA  LEU B 135     -17.812  -2.036 -17.244  1.00 27.11           C  
ANISOU 3154  CA  LEU B 135     3671   3509   3119    305   -142    -32
ATOM   3155  C   LEU B 135     -17.862  -3.363 -18.025  1.00 26.92           C  
ANISOU 3155  C   LEU B 135     3777   3397   3054    340   -200    -22
ATOM   3156  O   LEU B 135     -16.950  -4.182 -17.885  1.00 27.91           O  
ANISOU 3156  O   LEU B 135     3983   3494   3126    408   -231    -22
ATOM   3157  CB  LEU B 135     -16.581  -1.232 -17.712  1.00 28.24           C  
ANISOU 3157  CB  LEU B 135     3752   3716   3262    367   -101    -62
ATOM   3158  CG  LEU B 135     -16.548   0.247 -17.285  1.00 29.93           C  
ANISOU 3158  CG  LEU B 135     3871   3991   3510    319    -56    -74
ATOM   3159  CD1 LEU B 135     -15.143   0.823 -17.475  1.00 32.30           C  
ANISOU 3159  CD1 LEU B 135     4121   4362   3788    355    -31    -88
ATOM   3160  CD2 LEU B 135     -17.591   1.110 -18.026  1.00 31.90           C  
ANISOU 3160  CD2 LEU B 135     4108   4216   3798    273    -49    -78
ATOM   3161  H   LEU B 135     -16.817  -2.188 -15.371  1.00 25.69           H  
ATOM   3162  HA  LEU B 135     -18.718  -1.467 -17.446  1.00 27.11           H  
ATOM   3163  HB3 LEU B 135     -16.524  -1.262 -18.802  1.00 28.24           H  
ATOM   3164  HB2 LEU B 135     -15.684  -1.744 -17.359  1.00 28.24           H  
ATOM   3165  HG  LEU B 135     -16.769   0.281 -16.218  1.00 29.93           H  
ATOM   3166 HD11 LEU B 135     -15.022   1.734 -16.891  1.00 32.30           H  
ATOM   3167 HD12 LEU B 135     -14.366   0.122 -17.168  1.00 32.30           H  
ATOM   3168 HD13 LEU B 135     -14.965   1.060 -18.522  1.00 32.30           H  
ATOM   3169 HD21 LEU B 135     -18.054   1.821 -17.344  1.00 31.90           H  
ATOM   3170 HD22 LEU B 135     -17.147   1.700 -18.828  1.00 31.90           H  
ATOM   3171 HD23 LEU B 135     -18.387   0.515 -18.476  1.00 31.90           H  
ATOM   3172  N   GLU B 136     -18.862  -3.516 -18.891  1.00 27.02           N  
ANISOU 3172  N   GLU B 136     3822   3363   3080    300   -220    -13
ATOM   3173  CA AGLU B 136     -18.845  -4.485 -19.977  0.50 27.07           C  
ANISOU 3173  CA AGLU B 136     3972   3272   3040    330   -282     -5
ATOM   3174  CA BGLU B 136     -18.790  -4.328 -19.972  0.50 27.56           C  
ANISOU 3174  CA BGLU B 136     4031   3335   3105    320   -283     -3
ATOM   3175  C   GLU B 136     -18.704  -3.732 -21.300  1.00 28.20           C  
ANISOU 3175  C   GLU B 136     4098   3414   3204    361   -263    -27
ATOM   3176  O   GLU B 136     -19.313  -2.676 -21.446  1.00 29.22           O  
ANISOU 3176  O   GLU B 136     4129   3586   3385    310   -225    -31
ATOM   3177  CB AGLU B 136     -20.122  -5.339 -19.983  0.50 29.07           C  
ANISOU 3177  CB AGLU B 136     4319   3454   3274    217   -352     43
ATOM   3178  CB BGLU B 136     -20.219  -4.813 -19.717  0.50 31.07           C  
ANISOU 3178  CB BGLU B 136     4517   3741   3550    189   -333     46
ATOM   3179  CG AGLU B 136     -20.210  -6.280 -18.767  0.50 31.78           C  
ANISOU 3179  CG AGLU B 136     4736   3769   3570    189   -396     71
ATOM   3180  CG BGLU B 136     -20.708  -5.898 -20.622  0.50 34.03           C  
ANISOU 3180  CG BGLU B 136     5052   4004   3875    162   -414     70
ATOM   3181  CD AGLU B 136     -21.256  -7.386 -18.898  0.50 38.26           C  
ANISOU 3181  CD AGLU B 136     5710   4494   4335     84   -491    123
ATOM   3182  CD BGLU B 136     -22.066  -6.431 -20.204  0.50 36.33           C  
ANISOU 3182  CD BGLU B 136     5374   4282   4148      4   -471    133
ATOM   3183  OE1AGLU B 136     -22.251  -7.254 -19.648  0.50 42.24           O  
ANISOU 3183  OE1AGLU B 136     6225   4977   4846      3   -518    148
ATOM   3184  OE1BGLU B 136     -22.090  -7.268 -19.274  0.50 40.23           O  
ANISOU 3184  OE1BGLU B 136     5942   4748   4595    -41   -517    164
ATOM   3185  OE2AGLU B 136     -21.096  -8.422 -18.225  0.50 38.80           O1-
ANISOU 3185  OE2AGLU B 136     5890   4507   4344     74   -546    144
ATOM   3186  OE2BGLU B 136     -23.090  -6.016 -20.793  0.50 37.99           O1-
ANISOU 3186  OE2BGLU B 136     5531   4520   4381    -79   -474    156
ATOM   3187  H   GLU B 136     -19.595  -2.808 -18.953  1.00 27.02           H  
ATOM   3188  HA AGLU B 136     -18.001  -5.149 -19.850  0.50 27.07           H  
ATOM   3189  HA BGLU B 136     -18.061  -5.118 -19.790  0.50 27.56           H  
ATOM   3190  HB3AGLU B 136     -20.151  -5.928 -20.902  0.50 29.07           H  
ATOM   3191  HB3BGLU B 136     -20.902  -3.965 -19.770  0.50 31.07           H  
ATOM   3192  HB2AGLU B 136     -21.001  -4.693 -20.012  0.50 29.07           H  
ATOM   3193  HB2BGLU B 136     -20.308  -5.141 -18.681  0.50 31.07           H  
ATOM   3194  HG3AGLU B 136     -20.426  -5.706 -17.865  0.50 31.78           H  
ATOM   3195  HG3BGLU B 136     -19.986  -6.714 -20.632  0.50 34.03           H  
ATOM   3196  HG2AGLU B 136     -19.241  -6.751 -18.602  0.50 31.78           H  
ATOM   3197  HG2BGLU B 136     -20.766  -5.520 -21.643  0.50 34.03           H  
ATOM   3198  N   LYS B 137     -17.932  -4.277 -22.244  1.00 27.69           N  
ANISOU 3198  N   LYS B 137     4134   3298   3088    456   -291    -43
ATOM   3199  CA  LYS B 137     -17.922  -3.832 -23.635  1.00 28.76           C  
ANISOU 3199  CA  LYS B 137     4260   3436   3233    494   -273    -64
ATOM   3200  C   LYS B 137     -18.944  -4.676 -24.416  1.00 29.65           C  
ANISOU 3200  C   LYS B 137     4506   3435   3324    451   -341    -45
ATOM   3201  O   LYS B 137     -18.904  -5.901 -24.283  1.00 30.69           O  
ANISOU 3201  O   LYS B 137     4794   3475   3390    476   -410    -32
ATOM   3202  CB  LYS B 137     -16.501  -3.992 -24.226  1.00 29.67           C  
ANISOU 3202  CB  LYS B 137     4380   3603   3292    641   -251    -94
ATOM   3203  CG  LYS B 137     -16.384  -3.449 -25.668  1.00 34.35           C  
ANISOU 3203  CG  LYS B 137     4939   4223   3889    674   -223   -113
ATOM   3204  CD  LYS B 137     -15.217  -4.019 -26.484  1.00 42.72           C  
ANISOU 3204  CD  LYS B 137     6004   5358   4869    830   -205   -135
ATOM   3205  CE  LYS B 137     -13.844  -3.384 -26.231  1.00 50.73           C  
ANISOU 3205  CE  LYS B 137     6913   6502   5859    879   -165   -137
ATOM   3206  NZ  LYS B 137     -12.910  -3.745 -27.313  1.00 54.51           N1+
ANISOU 3206  NZ  LYS B 137     7381   7088   6242   1041   -149   -152
ATOM   3207  H   LYS B 137     -17.478  -5.162 -22.035  1.00 27.69           H  
ATOM   3208  HA  LYS B 137     -18.199  -2.781 -23.695  1.00 28.76           H  
ATOM   3209  HB3 LYS B 137     -16.236  -5.050 -24.208  1.00 29.67           H  
ATOM   3210  HB2 LYS B 137     -15.774  -3.486 -23.593  1.00 29.67           H  
ATOM   3211  HG3 LYS B 137     -16.347  -2.359 -25.655  1.00 34.35           H  
ATOM   3212  HG2 LYS B 137     -17.285  -3.678 -26.236  1.00 34.35           H  
ATOM   3213  HD3 LYS B 137     -15.497  -3.935 -27.535  1.00 42.72           H  
ATOM   3214  HD2 LYS B 137     -15.142  -5.088 -26.293  1.00 42.72           H  
ATOM   3215  HE3 LYS B 137     -13.449  -3.696 -25.264  1.00 50.73           H  
ATOM   3216  HE2 LYS B 137     -13.939  -2.297 -26.211  1.00 50.73           H  
ATOM   3217  HZ1 LYS B 137     -13.313  -3.335 -28.176  1.00 54.51           H  
ATOM   3218  HZ2 LYS B 137     -11.998  -3.334 -27.222  1.00 54.51           H  
ATOM   3219  HZ3 LYS B 137     -12.870  -4.737 -27.487  1.00 54.51           H  
ATOM   3220  N   ILE B 138     -19.774  -4.030 -25.239  1.00 28.85           N  
ANISOU 3220  N   ILE B 138     4355   3334   3271    378   -331    -38
ATOM   3221  CA  ILE B 138     -20.705  -4.665 -26.172  1.00 29.25           C  
ANISOU 3221  CA  ILE B 138     4518   3292   3303    315   -398    -13
ATOM   3222  C   ILE B 138     -20.585  -3.995 -27.556  1.00 29.28           C  
ANISOU 3222  C   ILE B 138     4505   3295   3324    355   -375    -37
ATOM   3223  O   ILE B 138     -20.039  -2.894 -27.653  1.00 29.22           O  
ANISOU 3223  O   ILE B 138     4386   3367   3348    401   -309    -66
ATOM   3224  CB  ILE B 138     -22.185  -4.538 -25.689  1.00 30.26           C  
ANISOU 3224  CB  ILE B 138     4595   3439   3464    162   -419     35
ATOM   3225  CG1 ILE B 138     -22.674  -3.086 -25.482  1.00 30.07           C  
ANISOU 3225  CG1 ILE B 138     4394   3518   3511    133   -348     25
ATOM   3226  CG2 ILE B 138     -22.436  -5.386 -24.432  1.00 30.95           C  
ANISOU 3226  CG2 ILE B 138     4704   3531   3524    107   -447     68
ATOM   3227  CD1 ILE B 138     -24.182  -2.975 -25.202  1.00 32.17           C  
ANISOU 3227  CD1 ILE B 138     4598   3832   3793      6   -369     74
ATOM   3228  H   ILE B 138     -19.683  -3.019 -25.353  1.00 28.85           H  
ATOM   3229  HA  ILE B 138     -20.449  -5.718 -26.301  1.00 29.25           H  
ATOM   3230  HB  ILE B 138     -22.814  -4.970 -26.471  1.00 30.26           H  
ATOM   3231 HG13 ILE B 138     -22.460  -2.491 -26.367  1.00 30.07           H  
ATOM   3232 HG12 ILE B 138     -22.115  -2.627 -24.666  1.00 30.07           H  
ATOM   3233 HG21 ILE B 138     -23.484  -5.387 -24.138  1.00 30.95           H  
ATOM   3234 HG22 ILE B 138     -22.166  -6.419 -24.634  1.00 30.95           H  
ATOM   3235 HG23 ILE B 138     -21.849  -5.034 -23.584  1.00 30.95           H  
ATOM   3236 HD11 ILE B 138     -24.565  -2.001 -25.503  1.00 32.17           H  
ATOM   3237 HD12 ILE B 138     -24.747  -3.726 -25.755  1.00 32.17           H  
ATOM   3238 HD13 ILE B 138     -24.397  -3.100 -24.142  1.00 32.17           H  
ATOM   3239  N   LEU B 139     -21.115  -4.656 -28.588  1.00 30.53           N  
ANISOU 3239  N   LEU B 139     4776   3365   3457    319   -436    -21
ATOM   3240  CA  LEU B 139     -21.371  -4.058 -29.896  1.00 32.97           C  
ANISOU 3240  CA  LEU B 139     5078   3668   3782    342   -421    -39
ATOM   3241  C   LEU B 139     -22.833  -3.590 -29.920  1.00 34.35           C  
ANISOU 3241  C   LEU B 139     5206   3844   4001    208   -443     -3
ATOM   3242  O   LEU B 139     -23.686  -4.274 -29.350  1.00 35.91           O  
ANISOU 3242  O   LEU B 139     5474   3998   4173    107   -510     43
ATOM   3243  CB  LEU B 139     -21.141  -5.118 -30.997  1.00 35.98           C  
ANISOU 3243  CB  LEU B 139     5651   3939   4083    417   -487    -48
ATOM   3244  CG  LEU B 139     -19.655  -5.393 -31.298  1.00 40.50           C  
ANISOU 3244  CG  LEU B 139     6251   4538   4598    592   -455    -91
ATOM   3245  CD1 LEU B 139     -19.493  -6.649 -32.171  1.00 41.37           C  
ANISOU 3245  CD1 LEU B 139     6589   4522   4608    680   -535    -99
ATOM   3246  CD2 LEU B 139     -18.982  -4.179 -31.964  1.00 42.56           C  
ANISOU 3246  CD2 LEU B 139     6368   4903   4900    630   -375   -118
ATOM   3247  H   LEU B 139     -21.639  -5.502 -28.423  1.00 30.53           H  
ATOM   3248  HA  LEU B 139     -20.718  -3.204 -30.061  1.00 32.97           H  
ATOM   3249  HB3 LEU B 139     -21.627  -4.805 -31.923  1.00 35.98           H  
ATOM   3250  HB2 LEU B 139     -21.644  -6.043 -30.711  1.00 35.98           H  
ATOM   3251  HG  LEU B 139     -19.140  -5.594 -30.356  1.00 40.50           H  
ATOM   3252 HD11 LEU B 139     -18.442  -6.920 -32.277  1.00 41.37           H  
ATOM   3253 HD12 LEU B 139     -20.006  -7.510 -31.739  1.00 41.37           H  
ATOM   3254 HD13 LEU B 139     -19.904  -6.495 -33.170  1.00 41.37           H  
ATOM   3255 HD21 LEU B 139     -18.103  -4.463 -32.544  1.00 42.56           H  
ATOM   3256 HD22 LEU B 139     -19.660  -3.652 -32.633  1.00 42.56           H  
ATOM   3257 HD23 LEU B 139     -18.657  -3.458 -31.217  1.00 42.56           H  
ATOM   3258  N   VAL B 140     -23.099  -2.466 -30.592  1.00 33.73           N  
ANISOU 3258  N   VAL B 140     5016   3823   3976    204   -393    -19
ATOM   3259  CA  VAL B 140     -24.445  -1.971 -30.864  1.00 34.24           C  
ANISOU 3259  CA  VAL B 140     5024   3913   4075    103   -408     12
ATOM   3260  C   VAL B 140     -24.484  -1.421 -32.299  1.00 33.87           C  
ANISOU 3260  C   VAL B 140     4993   3837   4038    126   -406     -6
ATOM   3261  O   VAL B 140     -23.621  -0.620 -32.664  1.00 33.97           O  
ANISOU 3261  O   VAL B 140     4965   3876   4068    202   -353    -45
ATOM   3262  CB  VAL B 140     -24.863  -0.829 -29.890  1.00 34.44           C  
ANISOU 3262  CB  VAL B 140     4891   4045   4151     83   -349      9
ATOM   3263  CG1 VAL B 140     -26.237  -0.202 -30.212  1.00 35.47           C  
ANISOU 3263  CG1 VAL B 140     4952   4224   4302      9   -362     40
ATOM   3264  CG2 VAL B 140     -24.858  -1.301 -28.426  1.00 35.04           C  
ANISOU 3264  CG2 VAL B 140     4940   4159   4216     58   -346     28
ATOM   3265  H   VAL B 140     -22.337  -1.915 -30.977  1.00 33.73           H  
ATOM   3266  HA  VAL B 140     -25.166  -2.789 -30.790  1.00 34.24           H  
ATOM   3267  HB  VAL B 140     -24.127  -0.026 -29.968  1.00 34.44           H  
ATOM   3268 HG11 VAL B 140     -26.521   0.519 -29.449  1.00 35.47           H  
ATOM   3269 HG12 VAL B 140     -26.235   0.348 -31.153  1.00 35.47           H  
ATOM   3270 HG13 VAL B 140     -27.024  -0.954 -30.260  1.00 35.47           H  
ATOM   3271 HG21 VAL B 140     -25.198  -0.514 -27.755  1.00 35.04           H  
ATOM   3272 HG22 VAL B 140     -25.504  -2.167 -28.284  1.00 35.04           H  
ATOM   3273 HG23 VAL B 140     -23.859  -1.586 -28.101  1.00 35.04           H  
ATOM   3274  N   SER B 141     -25.493  -1.840 -33.071  1.00 33.35           N  
ANISOU 3274  N   SER B 141     4978   3732   3961     47   -465     29
ATOM   3275  CA ASER B 141     -25.817  -1.282 -34.381  0.50 33.27           C  
ANISOU 3275  CA ASER B 141     4978   3698   3964     63   -464     14
ATOM   3276  CA BSER B 141     -25.760  -1.291 -34.426  0.50 32.83           C  
ANISOU 3276  CA BSER B 141     4922   3643   3908     64   -464     14
ATOM   3277  C   SER B 141     -26.514   0.079 -34.191  1.00 32.26           C  
ANISOU 3277  C   SER B 141     4702   3663   3891     46   -416     10
ATOM   3278  O   SER B 141     -27.589   0.117 -33.587  1.00 32.25           O  
ANISOU 3278  O   SER B 141     4626   3727   3898    -24   -428     47
ATOM   3279  CB ASER B 141     -26.684  -2.308 -35.135  0.50 35.76           C  
ANISOU 3279  CB ASER B 141     5410   3940   4239    -22   -553     56
ATOM   3280  CB BSER B 141     -26.640  -2.216 -35.255  0.50 34.11           C  
ANISOU 3280  CB BSER B 141     5203   3728   4029    -16   -551     54
ATOM   3281  OG ASER B 141     -27.104  -1.866 -36.412  0.50 38.93           O  
ANISOU 3281  OG ASER B 141     5797   4336   4659    -23   -552     49
ATOM   3282  OG BSER B 141     -26.054  -3.506 -35.325  0.50 35.38           O  
ANISOU 3282  OG BSER B 141     5535   3784   4122     11   -607     54
ATOM   3283  H   SER B 141     -26.171  -2.479 -32.682  1.00 33.35           H  
ATOM   3284  HA ASER B 141     -24.903  -1.142 -34.951  0.50 33.27           H  
ATOM   3285  HA BSER B 141     -24.792  -1.190 -34.918  0.50 32.83           H  
ATOM   3286  HB3ASER B 141     -27.573  -2.551 -34.555  0.50 35.76           H  
ATOM   3287  HB3BSER B 141     -26.746  -1.810 -36.261  0.50 34.11           H  
ATOM   3288  HB2ASER B 141     -26.135  -3.242 -35.255  0.50 35.76           H  
ATOM   3289  HB2BSER B 141     -27.625  -2.289 -34.794  0.50 34.11           H  
ATOM   3290  HG ASER B 141     -28.053  -2.082 -36.454  0.50 38.93           H  
ATOM   3291  HG BSER B 141     -26.613  -4.084 -35.849  0.50 35.38           H  
ATOM   3292  N   VAL B 142     -25.888   1.159 -34.675  1.00 33.03           N  
ANISOU 3292  N   VAL B 142     4761   3775   4016    115   -363    -32
ATOM   3293  CA  VAL B 142     -26.374   2.532 -34.496  1.00 33.38           C  
ANISOU 3293  CA  VAL B 142     4699   3885   4098    117   -325    -43
ATOM   3294  C   VAL B 142     -27.120   3.068 -35.740  1.00 33.68           C  
ANISOU 3294  C   VAL B 142     4744   3908   4147    107   -343    -42
ATOM   3295  O   VAL B 142     -27.941   3.977 -35.629  1.00 35.64           O  
ANISOU 3295  O   VAL B 142     4922   4206   4414    114   -327    -46
ATOM   3296  CB  VAL B 142     -25.200   3.492 -34.165  1.00 37.27           C  
ANISOU 3296  CB  VAL B 142     5154   4405   4603    178   -264    -84
ATOM   3297  CG1 VAL B 142     -24.569   3.144 -32.804  1.00 37.38           C  
ANISOU 3297  CG1 VAL B 142     5142   4451   4609    186   -245    -82
ATOM   3298  CG2 VAL B 142     -24.112   3.589 -35.255  1.00 39.94           C  
ANISOU 3298  CG2 VAL B 142     5554   4703   4920    225   -254   -109
ATOM   3299  H   VAL B 142     -25.015   1.034 -35.179  1.00 33.03           H  
ATOM   3300  HA  VAL B 142     -27.080   2.574 -33.661  1.00 33.38           H  
ATOM   3301  HB  VAL B 142     -25.626   4.493 -34.057  1.00 37.27           H  
ATOM   3302 HG11 VAL B 142     -23.803   3.864 -32.519  1.00 37.38           H  
ATOM   3303 HG12 VAL B 142     -25.321   3.153 -32.013  1.00 37.38           H  
ATOM   3304 HG13 VAL B 142     -24.108   2.156 -32.806  1.00 37.38           H  
ATOM   3305 HG21 VAL B 142     -23.418   4.383 -34.996  1.00 39.94           H  
ATOM   3306 HG22 VAL B 142     -23.542   2.665 -35.337  1.00 39.94           H  
ATOM   3307 HG23 VAL B 142     -24.510   3.833 -36.239  1.00 39.94           H  
ATOM   3308  N   GLY B 143     -26.858   2.479 -36.908  1.00 31.77           N  
ANISOU 3308  N   GLY B 143     4594   3595   3883     99   -381    -37
ATOM   3309  CA  GLY B 143     -27.516   2.857 -38.148  1.00 32.15           C  
ANISOU 3309  CA  GLY B 143     4661   3620   3936     84   -406    -33
ATOM   3310  C   GLY B 143     -27.002   1.919 -39.235  1.00 32.60           C  
ANISOU 3310  C   GLY B 143     4845   3584   3956     95   -442    -37
ATOM   3311  O   GLY B 143     -26.164   1.055 -38.973  1.00 32.94           O  
ANISOU 3311  O   GLY B 143     4967   3584   3964    115   -457    -38
ATOM   3312  H   GLY B 143     -26.204   1.707 -36.965  1.00 31.77           H  
ATOM   3313  HA3 GLY B 143     -27.292   3.894 -38.399  1.00 32.15           H  
ATOM   3314  HA2 GLY B 143     -28.596   2.749 -38.049  1.00 32.15           H  
ATOM   3315  N   CYS B 144     -27.500   2.089 -40.463  1.00 31.22           N  
ANISOU 3315  N   CYS B 144     4705   3374   3781     89   -463    -38
ATOM   3316  CA  CYS B 144     -27.110   1.271 -41.608  1.00 31.96           C  
ANISOU 3316  CA  CYS B 144     4933   3379   3832    109   -500    -45
ATOM   3317  C   CYS B 144     -26.536   2.166 -42.711  1.00 32.21           C  
ANISOU 3317  C   CYS B 144     4969   3402   3867    167   -465    -80
ATOM   3318  O   CYS B 144     -26.905   3.339 -42.820  1.00 31.13           O  
ANISOU 3318  O   CYS B 144     4755   3307   3766    161   -437    -88
ATOM   3319  CB  CYS B 144     -28.318   0.449 -42.100  1.00 34.22           C  
ANISOU 3319  CB  CYS B 144     5292   3616   4094     19   -585      2
ATOM   3320  SG  CYS B 144     -28.954  -0.730 -40.869  1.00 37.38           S  
ANISOU 3320  SG  CYS B 144     5717   4023   4464    -80   -645     57
ATOM   3321  H   CYS B 144     -28.121   2.861 -40.666  1.00 31.22           H  
ATOM   3322  HA  CYS B 144     -26.326   0.575 -41.316  1.00 31.96           H  
ATOM   3323  HB3 CYS B 144     -28.049  -0.100 -43.003  1.00 34.22           H  
ATOM   3324  HB2 CYS B 144     -29.135   1.114 -42.370  1.00 34.22           H  
ATOM   3325  N   THR B 145     -25.631   1.587 -43.500  1.00 31.59           N  
ANISOU 3325  N   THR B 145     4988   3273   3740    229   -467   -100
ATOM   3326  CA  THR B 145     -25.003   2.210 -44.649  1.00 31.57           C  
ANISOU 3326  CA  THR B 145     4998   3274   3725    278   -438   -127
ATOM   3327  C   THR B 145     -25.116   1.215 -45.825  1.00 32.24           C  
ANISOU 3327  C   THR B 145     5225   3269   3758    294   -495   -123
ATOM   3328  O   THR B 145     -25.305   0.014 -45.601  1.00 32.05           O  
ANISOU 3328  O   THR B 145     5302   3177   3700    272   -556   -103
ATOM   3329  CB  THR B 145     -23.524   2.554 -44.314  1.00 33.02           C  
ANISOU 3329  CB  THR B 145     5137   3527   3882    355   -371   -154
ATOM   3330  OG1 THR B 145     -22.918   3.390 -45.283  1.00 32.79           O  
ANISOU 3330  OG1 THR B 145     5078   3533   3847    366   -337   -169
ATOM   3331  CG2 THR B 145     -22.604   1.348 -44.078  1.00 34.85           C  
ANISOU 3331  CG2 THR B 145     5460   3742   4041    447   -380   -166
ATOM   3332  H   THR B 145     -25.415   0.596 -43.397  1.00 31.59           H  
ATOM   3333  HA  THR B 145     -25.529   3.128 -44.922  1.00 31.57           H  
ATOM   3334  HB  THR B 145     -23.536   3.139 -43.398  1.00 33.02           H  
ATOM   3335  HG1 THR B 145     -23.009   4.304 -44.962  1.00 32.79           H  
ATOM   3336 HG21 THR B 145     -21.607   1.677 -43.799  1.00 34.85           H  
ATOM   3337 HG22 THR B 145     -22.977   0.717 -43.270  1.00 34.85           H  
ATOM   3338 HG23 THR B 145     -22.506   0.724 -44.962  1.00 34.85           H  
ATOM   3339  N   CYS B 146     -25.058   1.746 -47.047  1.00 31.86           N  
ANISOU 3339  N   CYS B 146     5200   3211   3695    319   -484   -139
ATOM   3340  CA  CYS B 146     -25.204   1.009 -48.294  1.00 34.27           C  
ANISOU 3340  CA  CYS B 146     5651   3427   3945    340   -540   -139
ATOM   3341  C   CYS B 146     -23.799   0.775 -48.852  1.00 36.53           C  
ANISOU 3341  C   CYS B 146     5991   3733   4154    467   -503   -172
ATOM   3342  O   CYS B 146     -23.115   1.763 -49.143  1.00 36.25           O  
ANISOU 3342  O   CYS B 146     5869   3785   4119    500   -439   -188
ATOM   3343  CB  CYS B 146     -26.072   1.823 -49.273  1.00 34.84           C  
ANISOU 3343  CB  CYS B 146     5714   3478   4046    284   -558   -130
ATOM   3344  SG  CYS B 146     -26.304   1.041 -50.888  1.00 37.54           S  
ANISOU 3344  SG  CYS B 146     6242   3706   4316    303   -630   -129
ATOM   3345  H   CYS B 146     -24.822   2.724 -47.132  1.00 31.86           H  
ATOM   3346  HA  CYS B 146     -25.702   0.057 -48.117  1.00 34.27           H  
ATOM   3347  HB3 CYS B 146     -25.643   2.807 -49.444  1.00 34.84           H  
ATOM   3348  HB2 CYS B 146     -27.053   1.999 -48.839  1.00 34.84           H  
ATOM   3349  N   VAL B 147     -23.403  -0.497 -48.964  1.00 37.52           N  
ANISOU 3349  N   VAL B 147     6268   3788   4199    542   -548   -179
ATOM   3350  CA  VAL B 147     -22.090  -0.935 -49.429  1.00 40.47           C  
ANISOU 3350  CA  VAL B 147     6685   4209   4482    695   -510   -212
ATOM   3351  C   VAL B 147     -22.209  -1.861 -50.650  1.00 44.15           C  
ANISOU 3351  C   VAL B 147     7342   4574   4859    767   -569   -225
ATOM   3352  O   VAL B 147     -23.250  -2.487 -50.866  1.00 43.85           O  
ANISOU 3352  O   VAL B 147     7432   4408   4822    692   -655   -205
ATOM   3353  CB  VAL B 147     -21.327  -1.731 -48.322  1.00 41.24           C  
ANISOU 3353  CB  VAL B 147     6797   4336   4538    779   -500   -221
ATOM   3354  CG1 VAL B 147     -21.008  -0.863 -47.096  1.00 40.79           C  
ANISOU 3354  CG1 VAL B 147     6553   4393   4553    728   -434   -213
ATOM   3355  CG2 VAL B 147     -22.010  -3.043 -47.885  1.00 42.55           C  
ANISOU 3355  CG2 VAL B 147     7133   4360   4676    749   -596   -205
ATOM   3356  H   VAL B 147     -24.076  -1.243 -48.779  1.00 37.52           H  
ATOM   3357  HA  VAL B 147     -21.512  -0.069 -49.739  1.00 40.47           H  
ATOM   3358  HB  VAL B 147     -20.357  -2.016 -48.734  1.00 41.24           H  
ATOM   3359 HG11 VAL B 147     -20.510  -1.433 -46.315  1.00 40.79           H  
ATOM   3360 HG12 VAL B 147     -20.349  -0.038 -47.351  1.00 40.79           H  
ATOM   3361 HG13 VAL B 147     -21.920  -0.447 -46.677  1.00 40.79           H  
ATOM   3362 HG21 VAL B 147     -21.465  -3.517 -47.071  1.00 42.55           H  
ATOM   3363 HG22 VAL B 147     -23.025  -2.857 -47.537  1.00 42.55           H  
ATOM   3364 HG23 VAL B 147     -22.069  -3.771 -48.695  1.00 42.55           H  
ATOM   3365  N   THR B 148     -21.101  -1.992 -51.382  1.00 47.73           N  
ANISOU 3365  N   THR B 148     7814   5098   5225    912   -526   -254
ATOM   3366  CA  THR B 148     -20.908  -3.020 -52.396  1.00 51.92           C  
ANISOU 3366  CA  THR B 148     8546   5538   5645   1023   -579   -274
ATOM   3367  C   THR B 148     -20.685  -4.395 -51.697  1.00 54.38           C  
ANISOU 3367  C   THR B 148     9020   5768   5873   1124   -636   -286
ATOM   3368  O   THR B 148     -20.014  -4.445 -50.651  1.00 55.36           O  
ANISOU 3368  O   THR B 148     9069   5977   5986   1190   -594   -293
ATOM   3369  CB  THR B 148     -19.642  -2.646 -53.214  1.00 55.54           C  
ANISOU 3369  CB  THR B 148     8949   6129   6024   1157   -507   -299
ATOM   3370  OG1 THR B 148     -18.478  -2.562 -52.400  1.00 57.85           O  
ANISOU 3370  OG1 THR B 148     9143   6570   6266   1274   -441   -311
ATOM   3371  CG2 THR B 148     -19.778  -1.305 -53.952  1.00 55.66           C  
ANISOU 3371  CG2 THR B 148     8819   6216   6112   1047   -459   -285
ATOM   3372  H   THR B 148     -20.279  -1.428 -51.191  1.00 47.73           H  
ATOM   3373  HA  THR B 148     -21.785  -3.025 -53.044  1.00 51.92           H  
ATOM   3374  HB  THR B 148     -19.471  -3.424 -53.962  1.00 55.54           H  
ATOM   3375  HG1 THR B 148     -18.103  -3.444 -52.331  1.00 57.85           H  
ATOM   3376 HG21 THR B 148     -18.894  -1.099 -54.556  1.00 55.66           H  
ATOM   3377 HG22 THR B 148     -20.633  -1.313 -54.627  1.00 55.66           H  
ATOM   3378 HG23 THR B 148     -19.903  -0.465 -53.268  1.00 55.66           H  
ATOM   3379  N   PRO B 149     -21.260  -5.491 -52.242  1.00 56.10           N  
ANISOU 3379  N   PRO B 149     9476   5813   6026   1127   -741   -284
ATOM   3380  CA  PRO B 149     -21.059  -6.847 -51.691  1.00 57.23           C  
ANISOU 3380  CA  PRO B 149     9815   5851   6080   1210   -814   -292
ATOM   3381  C   PRO B 149     -19.606  -7.346 -51.816  1.00 58.81           C  
ANISOU 3381  C   PRO B 149    10095   6113   6135   1473   -783   -339
ATOM   3382  O   PRO B 149     -18.838  -6.818 -52.620  1.00 58.76           O  
ANISOU 3382  O   PRO B 149    10065   6197   6066   1599   -731   -366
ATOM   3383  CB  PRO B 149     -22.027  -7.718 -52.513  1.00 57.92           C  
ANISOU 3383  CB  PRO B 149    10154   5732   6123   1124   -945   -272
ATOM   3384  CG  PRO B 149     -22.169  -6.995 -53.838  1.00 57.52           C  
ANISOU 3384  CG  PRO B 149    10074   5698   6082   1114   -923   -279
ATOM   3385  CD  PRO B 149     -22.108  -5.527 -53.435  1.00 55.31           C  
ANISOU 3385  CD  PRO B 149     9494   5595   5927   1041   -809   -271
ATOM   3386  HA  PRO B 149     -21.352  -6.870 -50.639  1.00 57.23           H  
ATOM   3387  HB3 PRO B 149     -22.998  -7.747 -52.018  1.00 57.92           H  
ATOM   3388  HB2 PRO B 149     -21.698  -8.750 -52.644  1.00 57.92           H  
ATOM   3389  HG3 PRO B 149     -23.080  -7.255 -54.377  1.00 57.52           H  
ATOM   3390  HG2 PRO B 149     -21.320  -7.237 -54.479  1.00 57.52           H  
ATOM   3391  HD2 PRO B 149     -21.742  -4.918 -54.262  1.00 55.31           H  
ATOM   3392  HD3 PRO B 149     -23.099  -5.169 -53.153  1.00 55.31           H  
ATOM   3393  N   ILE B 150     -19.256  -8.370 -51.026  1.00 59.61           N  
ANISOU 3393  N   ILE B 150    10302   6173   6173   1562   -819   -348
ATOM   3394  CA  ILE B 150     -18.029  -9.144 -51.208  1.00 61.67           C  
ANISOU 3394  CA  ILE B 150    10675   6483   6273   1839   -807   -394
ATOM   3395  C   ILE B 150     -18.430 -10.393 -52.011  1.00 63.02           C  
ANISOU 3395  C   ILE B 150    11199   6433   6314   1914   -936   -411
ATOM   3396  O   ILE B 150     -19.112 -11.266 -51.472  1.00 62.32           O  
ANISOU 3396  O   ILE B 150    11299   6152   6229   1789  -1050   -385
ATOM   3397  CB  ILE B 150     -17.396  -9.591 -49.853  1.00 62.84           C  
ANISOU 3397  CB  ILE B 150    10806   6671   6398   1914   -800   -398
ATOM   3398  CG1 ILE B 150     -16.951  -8.374 -49.011  1.00 63.54           C  
ANISOU 3398  CG1 ILE B 150    10563   6973   6606   1836   -681   -380
ATOM   3399  CG2 ILE B 150     -16.206 -10.569 -50.022  1.00 63.75           C  
ANISOU 3399  CG2 ILE B 150    11099   6805   6320   2225   -816   -447
ATOM   3400  CD1 ILE B 150     -16.566  -8.724 -47.565  1.00 65.13           C  
ANISOU 3400  CD1 ILE B 150    10749   7191   6806   1865   -685   -376
ATOM   3401  H   ILE B 150     -19.964  -8.827 -50.471  1.00 59.61           H  
ATOM   3402  HA  ILE B 150     -17.280  -8.577 -51.767  1.00 61.67           H  
ATOM   3403  HB  ILE B 150     -18.163 -10.122 -49.286  1.00 62.84           H  
ATOM   3404 HG13 ILE B 150     -17.746  -7.631 -48.982  1.00 63.54           H  
ATOM   3405 HG12 ILE B 150     -16.108  -7.880 -49.498  1.00 63.54           H  
ATOM   3406 HG21 ILE B 150     -15.800 -10.884 -49.062  1.00 63.75           H  
ATOM   3407 HG22 ILE B 150     -16.484 -11.488 -50.535  1.00 63.75           H  
ATOM   3408 HG23 ILE B 150     -15.394 -10.112 -50.588  1.00 63.75           H  
ATOM   3409 HD11 ILE B 150     -16.483  -7.827 -46.956  1.00 65.13           H  
ATOM   3410 HD12 ILE B 150     -17.304  -9.380 -47.101  1.00 65.13           H  
ATOM   3411 HD13 ILE B 150     -15.597  -9.224 -47.522  1.00 65.13           H  
ATOM   3412  N   VAL B 151     -18.027 -10.443 -53.280  1.00 64.38           N  
ANISOU 3412  N   VAL B 151    11469   6634   6360   2113   -924   -451
ATOM   3413  CA  VAL B 151     -18.320 -11.546 -54.183  1.00 67.11           C  
ANISOU 3413  CA  VAL B 151    12169   6767   6562   2210  -1047   -473
ATOM   3414  C   VAL B 151     -17.081 -12.457 -54.247  1.00 69.71           C  
ANISOU 3414  C   VAL B 151    12687   7116   6683   2551  -1060   -530
ATOM   3415  O   VAL B 151     -15.964 -11.953 -54.357  1.00 70.37           O  
ANISOU 3415  O   VAL B 151    12606   7426   6705   2750   -950   -559
ATOM   3416  CB  VAL B 151     -18.642 -11.010 -55.606  1.00 68.07           C  
ANISOU 3416  CB  VAL B 151    12283   6882   6699   2155  -1038   -473
ATOM   3417  CG1 VAL B 151     -18.964 -12.123 -56.623  1.00 68.63           C  
ANISOU 3417  CG1 VAL B 151    12739   6717   6621   2235  -1176   -493
ATOM   3418  CG2 VAL B 151     -19.801  -9.992 -55.571  1.00 68.32           C  
ANISOU 3418  CG2 VAL B 151    12113   6918   6928   1844  -1020   -419
ATOM   3419  H   VAL B 151     -17.427  -9.723 -53.652  1.00 64.38           H  
ATOM   3420  HA  VAL B 151     -19.177 -12.122 -53.826  1.00 67.11           H  
ATOM   3421  HB  VAL B 151     -17.765 -10.482 -55.985  1.00 68.07           H  
ATOM   3422 HG11 VAL B 151     -19.256 -11.702 -57.586  1.00 68.63           H  
ATOM   3423 HG12 VAL B 151     -18.108 -12.770 -56.813  1.00 68.63           H  
ATOM   3424 HG13 VAL B 151     -19.787 -12.750 -56.279  1.00 68.63           H  
ATOM   3425 HG21 VAL B 151     -20.059  -9.646 -56.572  1.00 68.32           H  
ATOM   3426 HG22 VAL B 151     -20.699 -10.426 -55.130  1.00 68.32           H  
ATOM   3427 HG23 VAL B 151     -19.546  -9.106 -54.989  1.00 68.32           H  
ATOM   3428  N   HIS B 152     -17.297 -13.772 -54.168  1.00 70.49           N  
ANISOU 3428  N   HIS B 152    13137   6987   6661   2622  -1198   -542
ATOM   3429  CA  HIS B 152     -16.277 -14.804 -54.294  1.00 71.90           C  
ANISOU 3429  CA  HIS B 152    13556   7146   6618   2969  -1235   -601
ATOM   3430  C   HIS B 152     -17.011 -16.113 -54.618  1.00 73.53           C  
ANISOU 3430  C   HIS B 152    14231   7021   6687   2980  -1425   -609
ATOM   3431  O   HIS B 152     -18.190 -16.243 -54.290  1.00 73.88           O  
ANISOU 3431  O   HIS B 152    14383   6880   6807   2722  -1527   -560
ATOM   3432  CB  HIS B 152     -15.401 -14.902 -53.019  1.00 73.19           C  
ANISOU 3432  CB  HIS B 152    13595   7450   6764   3100  -1178   -611
ATOM   3433  CG  HIS B 152     -16.102 -15.228 -51.718  1.00 77.25           C  
ANISOU 3433  CG  HIS B 152    14141   7829   7382   2874  -1246   -567
ATOM   3434  ND1 HIS B 152     -17.041 -14.399 -51.121  1.00 79.59           N  
ANISOU 3434  ND1 HIS B 152    14745   7946   7551   2980  -1365   -581
ATOM   3435  CD2 HIS B 152     -15.980 -16.312 -50.875  1.00 78.64           C  
ANISOU 3435  CD2 HIS B 152    14084   8032   7762   2560  -1213   -510
ATOM   3436  CE1 HIS B 152     -17.435 -14.992 -49.992  1.00 80.37           C  
ANISOU 3436  CE1 HIS B 152    14772   7980   7784   2715  -1396   -528
ATOM   3437  NE2 HIS B 152     -16.826 -16.152 -49.779  1.00 80.06           N  
ANISOU 3437  NE2 HIS B 152    14409   8066   7944   2465  -1305   -485
ATOM   3438  H   HIS B 152     -18.233 -14.155 -54.102  1.00 70.49           H  
ATOM   3439  HA  HIS B 152     -15.641 -14.552 -55.145  1.00 71.90           H  
ATOM   3440  HB3 HIS B 152     -14.855 -13.968 -52.883  1.00 73.19           H  
ATOM   3441  HB2 HIS B 152     -14.630 -15.657 -53.178  1.00 73.19           H  
ATOM   3442  HD1 HIS B 152     -17.387 -13.519 -51.474  1.00 79.59           H  
ATOM   3443  HD2 HIS B 152     -15.351 -17.185 -50.966  1.00 78.64           H  
ATOM   3444  HE1 HIS B 152     -18.169 -14.572 -49.320  1.00 80.37           H  
ATOM   3445  N   HIS B 153     -16.318 -17.061 -55.266  1.00 74.06           N  
ANISOU 3445  N   HIS B 153    14583   7016   6540   3274  -1479   -667
ATOM   3446  CA  HIS B 153     -16.875 -18.350 -55.724  1.00 74.78           C  
ANISOU 3446  CA  HIS B 153    15165   6777   6472   3305  -1673   -679
ATOM   3447  C   HIS B 153     -16.903 -19.303 -54.525  1.00 75.06           C  
ANISOU 3447  C   HIS B 153    15456   6644   6420   3347  -1788   -678
ATOM   3448  O   HIS B 153     -16.965 -20.530 -54.630  1.00 74.94           O  
ANISOU 3448  O   HIS B 153    15795   6332   6346   3199  -1964   -651
ATOM   3449  CB  HIS B 153     -16.033 -18.854 -56.930  1.00 76.27           C  
ANISOU 3449  CB  HIS B 153    15572   6964   6441   3652  -1684   -749
ATOM   3450  CG  HIS B 153     -16.657 -19.930 -57.792  1.00 79.27           C  
ANISOU 3450  CG  HIS B 153    16477   7000   6641   3698  -1884   -767
ATOM   3451  ND1 HIS B 153     -16.867 -21.228 -57.358  1.00 81.26           N  
ANISOU 3451  ND1 HIS B 153    16861   7138   6877   3610  -1936   -763
ATOM   3452  CD2 HIS B 153     -17.103 -19.905 -59.096  1.00 80.63           C  
ANISOU 3452  CD2 HIS B 153    17082   6930   6624   3847  -2042   -792
ATOM   3453  CE1 HIS B 153     -17.410 -21.910 -58.368  1.00 81.96           C  
ANISOU 3453  CE1 HIS B 153    17453   6915   6772   3688  -2127   -782
ATOM   3454  NE2 HIS B 153     -17.577 -21.166 -59.455  1.00 82.15           N  
ANISOU 3454  NE2 HIS B 153    17685   6845   6682   3833  -2201   -801
ATOM   3455  H   HIS B 153     -15.360 -16.873 -55.521  1.00 74.06           H  
ATOM   3456  HA  HIS B 153     -17.902 -18.194 -56.065  1.00 74.78           H  
ATOM   3457  HXT HIS B 153     -16.870 -18.828 -53.543  1.00 75.06           H  
ATOM   3458  HB3 HIS B 153     -15.057 -19.212 -56.598  1.00 76.27           H  
ATOM   3459  HB2 HIS B 153     -15.824 -18.019 -57.602  1.00 76.27           H  
ATOM   3460  HD1 HIS B 153     -16.706 -21.572 -56.418  1.00 81.26           H  
ATOM   3461  HD2 HIS B 153     -17.119 -19.087 -59.801  1.00 80.63           H  
ATOM   3462  HE1 HIS B 153     -17.695 -22.950 -58.306  1.00 81.96           H  
TER    3463      HIS B 153
HETATM 3464  C1  UNK A 201     -23.737   5.104 -23.573  1.00 31.78           C  
ANISOU 3464  C1  UNK A 201     4076   4101   3900    206    -80    -93
HETATM 3465  C3  UNK A 201     -24.920   5.913 -23.997  1.00 32.89           C  
ANISOU 3465  C3  UNK A 201     4191   4269   4037    226    -85    -94
HETATM 3466  O2  UNK A 201     -19.281   3.575 -24.968  1.00 32.98           O  
ANISOU 3466  O2  UNK A 201     4317   4217   3996    277    -56   -126
HETATM 3467  C13 UNK A 201     -25.370   4.512 -26.122  1.00 33.32           C  
ANISOU 3467  C13 UNK A 201     4307   4245   4106    173   -139    -63
HETATM 3468  C14 UNK A 201     -18.036   4.397 -27.635  1.00 36.88           C  
ANISOU 3468  C14 UNK A 201     4839   4716   4457    300    -46   -146
HETATM 3469  C15 UNK A 201     -17.650   5.437 -26.626  1.00 36.62           C  
ANISOU 3469  C15 UNK A 201     4764   4723   4426    256    -29   -148
HETATM 3470  C19 UNK A 201     -18.086   5.586 -25.271  1.00 34.06           C  
ANISOU 3470  C19 UNK A 201     4420   4402   4118    242    -27   -147
HETATM 3471  C20 UNK A 201     -19.019   4.687 -24.548  1.00 32.60           C  
ANISOU 3471  C20 UNK A 201     4240   4192   3955    252    -38   -138
HETATM 3472  C22 UNK A 201     -20.408   4.480 -22.471  1.00 29.71           C  
ANISOU 3472  C22 UNK A 201     3842   3833   3612    226    -44   -121
HETATM 3473  C23 UNK A 201     -20.181   5.043 -21.040  1.00 31.11           C  
ANISOU 3473  C23 UNK A 201     3986   4054   3782    221    -27   -124
HETATM 3474  C24 UNK A 201     -21.036   4.331 -19.964  1.00 29.68           C  
ANISOU 3474  C24 UNK A 201     3796   3902   3578    224    -13   -131
HETATM 3475  C25 UNK A 201     -20.802   4.919 -18.563  1.00 30.83           C  
ANISOU 3475  C25 UNK A 201     3916   4084   3713    215     -1   -131
HETATM 3476  C26 UNK A 201     -19.317   4.875 -18.178  1.00 31.83           C  
ANISOU 3476  C26 UNK A 201     4027   4219   3847    211     -7   -113
HETATM 3477  C27 UNK A 201     -18.463   5.594 -19.231  1.00 32.97           C  
ANISOU 3477  C27 UNK A 201     4165   4360   4003    211    -13   -108
HETATM 3478  C28 UNK A 201     -18.688   5.004 -20.630  1.00 31.36           C  
ANISOU 3478  C28 UNK A 201     3991   4110   3813    206    -34   -100
HETATM 3479  C29 UNK A 201     -21.843   4.563 -22.928  1.00 29.58           C  
ANISOU 3479  C29 UNK A 201     3824   3803   3611    214    -61   -110
HETATM 3480  C4  UNK A 201     -25.952   5.111 -24.819  1.00 34.14           C  
ANISOU 3480  C4  UNK A 201     4341   4437   4195    182   -120    -54
HETATM 3481  C5  UNK A 201     -27.230   5.927 -25.092  1.00 34.20           C  
ANISOU 3481  C5  UNK A 201     4291   4516   4186    211   -123    -45
HETATM 3482  C6  UNK A 201     -28.299   5.051 -25.767  1.00 34.86           C  
ANISOU 3482  C6  UNK A 201     4350   4635   4258    142   -164      9
HETATM 3483  C7  UNK A 201     -27.736   4.269 -26.910  1.00 34.38           C  
ANISOU 3483  C7  UNK A 201     4380   4464   4219    107   -192      6
HETATM 3484  N8  UNK A 201     -28.450   3.774 -27.919  1.00 34.64           N  
ANISOU 3484  N8  UNK A 201     4437   4480   4245     56   -234     37
HETATM 3485  C9  UNK A 201     -27.515   3.175 -28.759  1.00 34.92           C  
ANISOU 3485  C9  UNK A 201     4574   4399   4294     59   -248     16
HETATM 3486  C10 UNK A 201     -26.278   3.322 -28.190  1.00 34.48           C  
ANISOU 3486  C10 UNK A 201     4529   4323   4250    109   -210    -21
HETATM 3487 BR11 UNK A 201     -24.631   2.775 -28.968  0.80 34.04          Br  
ANISOU 3487 BR11 UNK A 201     4562   4177   4195    156   -198    -59
HETATM 3488  N12 UNK A 201     -26.414   4.029 -27.009  1.00 33.53           N  
ANISOU 3488  N12 UNK A 201     4339   4274   4129    131   -178    -28
HETATM 3489  N16 UNK A 201     -16.813   6.397 -26.927  1.00 37.55           N  
ANISOU 3489  N16 UNK A 201     4867   4884   4518    220    -19   -149
HETATM 3490  O17 UNK A 201     -16.715   7.175 -25.768  1.00 37.31           O  
ANISOU 3490  O17 UNK A 201     4822   4866   4488    182    -16   -151
HETATM 3491  N18 UNK A 201     -17.515   6.646 -24.751  1.00 36.01           N  
ANISOU 3491  N18 UNK A 201     4653   4679   4353    207    -17   -152
HETATM 3492  N21 UNK A 201     -19.561   5.175 -23.428  1.00 30.24           N  
ANISOU 3492  N21 UNK A 201     3921   3898   3670    232    -34   -140
HETATM 3493  N30 UNK A 201     -22.452   5.575 -23.540  1.00 30.53           N  
ANISOU 3493  N30 UNK A 201     3937   3925   3738    223    -59   -121
HETATM 3494  N31 UNK A 201     -23.915   3.889 -23.072  1.00 31.30           N  
ANISOU 3494  N31 UNK A 201     4030   4030   3832    173   -100    -66
HETATM 3495  N32 UNK A 201     -22.690   3.575 -22.662  1.00 31.26           N  
ANISOU 3495  N32 UNK A 201     4048   4009   3822    190    -87    -80
HETATM 3496 H3_1 UNK A 201     -24.583   6.776 -24.568  1.00 32.89           H  
HETATM 3497 H3_2 UNK A 201     -25.393   6.312 -23.099  1.00 32.89           H  
HETATM 3498 H131 UNK A 201     -24.688   3.689 -25.906  1.00 33.32           H  
HETATM 3499 H132 UNK A 201     -24.803   5.268 -26.666  1.00 33.32           H  
HETATM 3500 H141 UNK A 201     -17.720   3.404 -27.316  1.00 36.88           H  
HETATM 3501 H142 UNK A 201     -19.115   4.375 -27.779  1.00 36.88           H  
HETATM 3502 H143 UNK A 201     -17.581   4.584 -28.607  1.00 36.88           H  
HETATM 3503 HC22 UNK A 201     -20.102   3.437 -22.466  1.00 29.71           H  
HETATM 3504 HC23 UNK A 201     -20.491   6.087 -21.043  1.00 31.11           H  
HETATM 3505 H241 UNK A 201     -22.097   4.423 -20.194  1.00 29.68           H  
HETATM 3506 H242 UNK A 201     -20.810   3.263 -19.958  1.00 29.68           H  
HETATM 3507 H251 UNK A 201     -21.154   5.951 -18.541  1.00 30.83           H  
HETATM 3508 H252 UNK A 201     -21.395   4.375 -17.826  1.00 30.83           H  
HETATM 3509 H261 UNK A 201     -19.171   5.336 -17.200  1.00 31.83           H  
HETATM 3510 H262 UNK A 201     -18.993   3.838 -18.084  1.00 31.83           H  
HETATM 3511 H271 UNK A 201     -18.715   6.655 -19.241  1.00 32.97           H  
HETATM 3512 H272 UNK A 201     -17.407   5.526 -18.968  1.00 32.97           H  
HETATM 3513 H281 UNK A 201     -18.326   3.975 -20.655  1.00 31.36           H  
HETATM 3514 H282 UNK A 201     -18.075   5.562 -21.338  1.00 31.36           H  
HETATM 3515  HC4 UNK A 201     -26.274   4.269 -24.204  1.00 34.14           H  
HETATM 3516 H5_1 UNK A 201     -27.630   6.349 -24.170  1.00 34.20           H  
HETATM 3517 H5_2 UNK A 201     -26.986   6.770 -25.741  1.00 34.20           H  
HETATM 3518 H6_1 UNK A 201     -29.126   5.667 -26.121  1.00 34.86           H  
HETATM 3519 H6_2 UNK A 201     -28.715   4.345 -25.046  1.00 34.86           H  
HETATM 3520  HC9 UNK A 201     -27.791   2.744 -29.707  1.00 34.92           H  
HETATM 3521 HN21 UNK A 201     -19.382   6.151 -23.207  1.00 30.24           H  
HETATM 3522 HN32 UNK A 201     -22.442   2.667 -22.282  1.00 31.26           H  
CONECT  296  302
CONECT  808 1596
CONECT  885 1620
CONECT 1596  808
CONECT 1620  885
CONECT 1723 1733
CONECT 1985 1993
CONECT 2501 3320
CONECT 2578 3344
CONECT 3320 2501
CONECT 3344 2578
CONECT 3447 3457
CONECT  302  296
CONECT 1733 1723
CONECT 1993 1985
CONECT 3457 3447
CONECT 3464 3465 3493 3494
CONECT 3464 3494
CONECT 3465 3464 3480 3496 3497
CONECT 3466 3471
CONECT 3466 3471
CONECT 3467 3480 3488 3498 3499
CONECT 3468 3469 3500 3501 3502
CONECT 3469 3468 3470 3489
CONECT 3469 3489
CONECT 3470 3469 3471 3491
CONECT 3470 3491
CONECT 3471 3466 3470 3492
CONECT 3471 3466
CONECT 3472 3473 3479 3492 3503
CONECT 3473 3472 3474 3478 3504
CONECT 3474 3473 3475 3505 3506
CONECT 3475 3474 3476 3507 3508
CONECT 3476 3475 3477 3509 3510
CONECT 3477 3476 3478 3511 3512
CONECT 3478 3473 3477 3513 3514
CONECT 3479 3472 3493 3495
CONECT 3479 3493
CONECT 3480 3465 3467 3481 3515
CONECT 3481 3480 3482 3516 3517
CONECT 3482 3481 3483 3518 3519
CONECT 3483 3482 3484 3488
CONECT 3483 3484
CONECT 3484 3483 3485
CONECT 3484 3483
CONECT 3485 3484 3486 3520
CONECT 3485 3486
CONECT 3486 3485 3487 3488
CONECT 3486 3485
CONECT 3487 3486
CONECT 3488 3467 3483 3486
CONECT 3489 3469 3490
CONECT 3489 3469
CONECT 3490 3489 3491
CONECT 3491 3470 3490
CONECT 3491 3470
CONECT 3492 3471 3472 3521
CONECT 3493 3464 3479
CONECT 3493 3479
CONECT 3494 3464 3495
CONECT 3494 3464
CONECT 3495 3479 3494 3522
CONECT 3496 3465
CONECT 3497 3465
CONECT 3498 3467
CONECT 3499 3467
CONECT 3500 3468
CONECT 3501 3468
CONECT 3502 3468
CONECT 3503 3472
CONECT 3504 3473
CONECT 3505 3474
CONECT 3506 3474
CONECT 3507 3475
CONECT 3508 3475
CONECT 3509 3476
CONECT 3510 3476
CONECT 3511 3477
CONECT 3512 3477
CONECT 3513 3478
CONECT 3514 3478
CONECT 3515 3480
CONECT 3516 3481
CONECT 3517 3481
CONECT 3518 3482
CONECT 3519 3482
CONECT 3520 3485
CONECT 3521 3492
CONECT 3522 3495
END   



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elNémo is maintained by Yves-Henri Sanejouand.
It was developed by Karsten Suhre.
Between 2003 and 2014, it was hosted by IGS (Marseille).
Between 2015 and 2025, it was hosted by US2B (Nantes).
Last modification: april 24th, 2026.