CNRS Nantes University US2B US2B
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Should you encounter any unexpected behaviour,
please let us know.
elNémo has been hacked on november 27th.
It has been moved away and runs again.
**Still some additional cleaning from time to time**
Sorry for the inconvenience.


***    ***

elNémo ID: 260210125125448910

Job options:

ID        	=	 260210125125448910
JOBID     	=	 
USERID    	=	 unknown
PRIVAT    	=	 0

NMODES    	=	 5
DQMIN     	=	 -25
DQMAX     	=	 25
DQSTEP    	=	 20
DOGRAPHS  	=	 on

DOPROJMODS	=	 0
DORMSD    	=	 0

NRBL      	=	 0
CUTOFF    	=	 0
CAONLY    	=	 0


Input data for this run:


CRYST1   85.990   85.990   72.720  90.00  90.00 120.00 P 31          1
ATOM      1  N   ALA B   2      -6.833  62.197  92.011  1.00 60.07           N  
ANISOU    1  N   ALA B   2    10609   5094   7122   -633    148   -423       N  
ATOM      2  CA  ALA B   2      -6.834  60.964  92.858  1.00 58.16           C  
ANISOU    2  CA  ALA B   2    10123   5121   6852   -650    121   -493       C  
ATOM      3  C   ALA B   2      -5.679  60.044  92.483  1.00 56.93           C  
ANISOU    3  C   ALA B   2     9634   5222   6774   -899      7   -387       C  
ATOM      4  O   ALA B   2      -5.339  59.914  91.303  1.00 53.39           O  
ANISOU    4  O   ALA B   2     8997   4869   6421   -913      7   -251       O  
ATOM      5  CB  ALA B   2      -8.148  60.225  92.711  1.00 55.66           C  
ANISOU    5  CB  ALA B   2     9609   4989   6549   -304    253   -506       C  
ATOM      6  N   ALA B   3      -5.092  59.401  93.492  1.00 56.58           N  
ANISOU    6  N   ALA B   3     9521   5303   6674  -1067    -82   -444       N  
ATOM      7  CA  ALA B   3      -3.994  58.459  93.280  1.00 54.60           C  
ANISOU    7  CA  ALA B   3     8952   5319   6475  -1258   -183   -341       C  
ATOM      8  C   ALA B   3      -4.471  57.210  92.534  1.00 50.45           C  
ANISOU    8  C   ALA B   3     8094   5041   6032  -1041   -112   -280       C  
ATOM      9  O   ALA B   3      -5.618  56.788  92.673  1.00 44.28           O  
ANISOU    9  O   ALA B   3     7295   4283   5244   -804    -17   -343       O  
ATOM     10  CB  ALA B   3      -3.361  58.072  94.612  1.00 53.98           C  
ANISOU   10  CB  ALA B   3     8894   5319   6296  -1448   -293   -413       C  
ATOM     11  N   LYS B   4      -3.570  56.647  91.733  1.00 49.16           N  
ANISOU   11  N   LYS B   4     7676   5067   5934  -1131   -162   -150       N  
ATOM     12  CA  LYS B   4      -3.843  55.482  90.897  1.00 45.83           C  
ANISOU   12  CA  LYS B   4     6980   4856   5578   -950   -113    -93       C  
ATOM     13  C   LYS B   4      -4.114  54.254  91.767  1.00 39.20           C  
ANISOU   13  C   LYS B   4     6034   4152   4707   -884   -122   -159       C  
ATOM     14  O   LYS B   4      -3.241  53.849  92.535  1.00 44.29           O  
ANISOU   14  O   LYS B   4     6626   4893   5309  -1034   -210   -147       O  
ATOM     15  CB  LYS B   4      -2.622  55.237  89.999  1.00 49.51           C  
ANISOU   15  CB  LYS B   4     7234   5492   6085  -1066   -165     58       C  
ATOM     16  CG  LYS B   4      -2.784  54.183  88.919  1.00 49.61           C  
ANISOU   16  CG  LYS B   4     7014   5690   6145   -873   -113    118       C  
ATOM     17  CD  LYS B   4      -1.442  53.895  88.214  1.00 52.09           C  
ANISOU   17  CD  LYS B   4     7116   6210   6467   -968   -155    270       C  
ATOM     18  CE  LYS B   4      -1.004  55.044  87.298  1.00 55.93           C  
ANISOU   18  CE  LYS B   4     7641   6638   6972  -1076   -140    390       C  
ATOM     19  NZ  LYS B   4       0.247  54.744  86.536  1.00 53.75           N1+
ANISOU   19  NZ  LYS B   4     7121   6612   6690  -1144   -158    562       N1+
ATOM     20  N   LYS B   5      -5.314  53.678  91.673  1.00 27.08           N  
ANISOU   20  N   LYS B   5     4466   2637   3185   -676    -39   -211       N  
ATOM     21  CA  LYS B   5      -5.646  52.500  92.477  1.00 21.42           C  
ANISOU   21  CA  LYS B   5     3666   2034   2440   -631    -42   -255       C  
ATOM     22  C   LYS B   5      -5.156  51.275  91.718  1.00 17.43           C  
ANISOU   22  C   LYS B   5     2940   1696   1985   -593    -71   -177       C  
ATOM     23  O   LYS B   5      -5.257  51.222  90.495  1.00 17.18           O  
ANISOU   23  O   LYS B   5     2824   1696   2006   -507    -42   -127       O  
ATOM     24  CB  LYS B   5      -7.150  52.370  92.779  1.00 23.48           C  
ANISOU   24  CB  LYS B   5     3972   2268   2682   -458     55   -325       C  
ATOM     25  CG  LYS B   5      -7.691  53.389  93.801  1.00 33.04           C  
ANISOU   25  CG  LYS B   5     5420   3332   3803   -440    103   -418       C  
ATOM     26  CD  LYS B   5      -8.547  52.752  94.889  1.00 35.97           C  
ANISOU   26  CD  LYS B   5     5789   3776   4100   -365    156   -475       C  
ATOM     27  CE  LYS B   5      -8.769  53.708  96.060  1.00 42.39           C  
ANISOU   27  CE  LYS B   5     6863   4456   4785   -360    190   -577       C  
ATOM     28  NZ  LYS B   5      -9.321  53.006  97.256  1.00 42.82           N1+
ANISOU   28  NZ  LYS B   5     6907   4619   4744   -323    230   -615       N1+
ATOM     29  N   ASP B   6      -4.634  50.310  92.472  1.00 17.07           N  
ANISOU   29  N   ASP B   6     2827   1750   1907   -641   -125   -167       N  
ATOM     30  CA  ASP B   6      -4.134  49.060  91.903  1.00 14.43           C  
ANISOU   30  CA  ASP B   6     2332   1551   1600   -573   -148   -101       C  
ATOM     31  C   ASP B   6      -5.174  48.008  92.218  1.00 11.09           C  
ANISOU   31  C   ASP B   6     1913   1124   1176   -476   -113   -149       C  
ATOM     32  O   ASP B   6      -5.101  47.303  93.228  1.00 14.65           O  
ANISOU   32  O   ASP B   6     2382   1603   1583   -507   -140   -155       O  
ATOM     33  CB  ASP B   6      -2.798  48.682  92.523  1.00 14.62           C  
ANISOU   33  CB  ASP B   6     2281   1694   1580   -673   -234    -32       C  
ATOM     34  CG  ASP B   6      -2.204  47.424  91.930  1.00 12.26           C  
ANISOU   34  CG  ASP B   6     1841   1526   1293   -552   -245     44       C  
ATOM     35  OD1 ASP B   6      -2.924  46.698  91.232  1.00 13.49           O  
ANISOU   35  OD1 ASP B   6     1997   1647   1480   -415   -198     16       O  
ATOM     36  OD2 ASP B   6      -1.018  47.176  92.213  1.00 23.67           O1-
ANISOU   36  OD2 ASP B   6     3182   3110   2699   -594   -306    132       O1-
ATOM     37  N   TYR B   7      -6.145  47.897  91.328  1.00 11.92           N  
ANISOU   37  N   TYR B   7     2000   1207   1324   -374    -60   -170       N  
ATOM     38  CA  TYR B   7      -7.249  46.981  91.531  1.00 11.53           C  
ANISOU   38  CA  TYR B   7     1944   1164   1274   -324    -34   -203       C  
ATOM     39  C   TYR B   7      -6.802  45.520  91.474  1.00 14.02           C  
ANISOU   39  C   TYR B   7     2224   1517   1587   -308    -83   -171       C  
ATOM     40  O   TYR B   7      -7.380  44.671  92.140  1.00 11.58           O  
ANISOU   40  O   TYR B   7     1942   1198   1259   -331    -84   -178       O  
ATOM     41  CB  TYR B   7      -8.337  47.231  90.499  1.00 11.28           C  
ANISOU   41  CB  TYR B   7     1877   1133   1276   -238     12   -218       C  
ATOM     42  CG  TYR B   7      -9.059  48.546  90.634  1.00 11.96           C  
ANISOU   42  CG  TYR B   7     2019   1173   1354   -199     77   -243       C  
ATOM     43  CD1 TYR B   7      -9.331  49.323  89.519  1.00 14.26           C  
ANISOU   43  CD1 TYR B   7     2295   1451   1672   -116    105   -223       C  
ATOM     44  CD2 TYR B   7      -9.544  48.985  91.862  1.00 11.53           C  
ANISOU   44  CD2 TYR B   7     2047   1087   1248   -215    121   -284       C  
ATOM     45  CE1 TYR B   7     -10.022  50.515  89.635  1.00 14.97           C  
ANISOU   45  CE1 TYR B   7     2462   1480   1747    -41    173   -237       C  
ATOM     46  CE2 TYR B   7     -10.249  50.154  91.982  1.00 14.93           C  
ANISOU   46  CE2 TYR B   7     2559   1460   1652   -131    195   -312       C  
ATOM     47  CZ  TYR B   7     -10.475  50.937  90.860  1.00 13.82           C  
ANISOU   47  CZ  TYR B   7     2415   1288   1549    -38    221   -285       C  
ATOM     48  OH  TYR B   7     -11.202  52.109  90.996  1.00 17.00           O  
ANISOU   48  OH  TYR B   7     2927   1616   1917     84    303   -304       O  
ATOM     49  N   TYR B   8      -5.769  45.231  90.686  1.00 10.40           N  
ANISOU   49  N   TYR B   8     1716   1100   1137   -258   -115   -124       N  
ATOM     50  CA  TYR B   8      -5.234  43.872  90.628  1.00 10.69           C  
ANISOU   50  CA  TYR B   8     1755   1153   1154   -194   -152    -92       C  
ATOM     51  C   TYR B   8      -4.686  43.432  91.993  1.00  8.23           C  
ANISOU   51  C   TYR B   8     1469    860    797   -248   -188    -56       C  
ATOM     52  O   TYR B   8      -4.914  42.282  92.423  1.00 11.49           O  
ANISOU   52  O   TYR B   8     1944   1230   1192   -225   -204    -46       O  
ATOM     53  CB  TYR B   8      -4.158  43.771  89.541  1.00 11.17           C  
ANISOU   53  CB  TYR B   8     1747   1289   1208    -87   -159    -38       C  
ATOM     54  CG  TYR B   8      -4.717  43.971  88.145  1.00 11.41           C  
ANISOU   54  CG  TYR B   8     1770   1308   1257    -14   -129    -70       C  
ATOM     55  CD1 TYR B   8      -5.498  42.992  87.546  1.00 12.43           C  
ANISOU   55  CD1 TYR B   8     1971   1376   1377     44   -141   -125       C  
ATOM     56  CD2 TYR B   8      -4.445  45.118  87.421  1.00 11.18           C  
ANISOU   56  CD2 TYR B   8     1677   1330   1243    -18   -101    -38       C  
ATOM     57  CE1 TYR B   8      -6.024  43.176  86.264  1.00 12.64           C  
ANISOU   57  CE1 TYR B   8     1991   1414   1398    103   -130   -157       C  
ATOM     58  CE2 TYR B   8      -4.961  45.307  86.144  1.00 12.40           C  
ANISOU   58  CE2 TYR B   8     1824   1490   1397     60    -76    -55       C  
ATOM     59  CZ  TYR B   8      -5.739  44.323  85.570  1.00 12.35           C  
ANISOU   59  CZ  TYR B   8     1876   1446   1371    126    -94   -119       C  
ATOM     60  OH  TYR B   8      -6.242  44.515  84.313  1.00 12.18           O  
ANISOU   60  OH  TYR B   8     1847   1452   1328    195    -85   -137       O  
ATOM     61  N   ALA B   9      -3.995  44.339  92.684  1.00 12.01           N  
ANISOU   61  N   ALA B   9     1919   1396   1250   -335   -209    -33       N  
ATOM     62  CA  ALA B   9      -3.446  44.052  94.023  1.00  9.55           C  
ANISOU   62  CA  ALA B   9     1626   1131    872   -399   -257      2       C  
ATOM     63  C   ALA B   9      -4.553  43.891  95.077  1.00 12.75           C  
ANISOU   63  C   ALA B   9     2131   1468   1246   -457   -228    -51       C  
ATOM     64  O   ALA B   9      -4.433  43.098  96.011  1.00 12.34           O  
ANISOU   64  O   ALA B   9     2116   1433   1141   -466   -253    -13       O  
ATOM     65  CB  ALA B   9      -2.472  45.105  94.417  1.00 10.52           C  
ANISOU   65  CB  ALA B   9     1702   1337    960   -511   -306     32       C  
ATOM     66  N   ILE B  10      -5.657  44.605  94.897  1.00  9.79           N  
ANISOU   66  N   ILE B  10     1792   1033    896   -476   -165   -122       N  
ATOM     67  CA  ILE B  10      -6.797  44.453  95.795  1.00 10.99           C  
ANISOU   67  CA  ILE B  10     2004   1162   1009   -507   -114   -155       C  
ATOM     68  C   ILE B  10      -7.387  43.056  95.720  1.00  9.29           C  
ANISOU   68  C   ILE B  10     1790    928    811   -488   -112   -116       C  
ATOM     69  O   ILE B  10      -7.737  42.473  96.756  1.00 13.67           O  
ANISOU   69  O   ILE B  10     2390   1494   1310   -535   -103    -85       O  
ATOM     70  CB  ILE B  10      -7.827  45.559  95.554  1.00 13.52           C  
ANISOU   70  CB  ILE B  10     2343   1453   1341   -488    -37   -221       C  
ATOM     71  CG1 ILE B  10      -7.205  46.880  96.041  1.00 15.73           C  
ANISOU   71  CG1 ILE B  10     2703   1702   1570   -538    -49   -264       C  
ATOM     72  CG2 ILE B  10      -9.145  45.244  96.273  1.00 12.53           C  
ANISOU   72  CG2 ILE B  10     2229   1358   1175   -486     36   -229       C  
ATOM     73  CD1 ILE B  10      -7.841  48.163  95.517  1.00 16.52           C  
ANISOU   73  CD1 ILE B  10     2858   1729   1689   -486     16   -320       C  
ATOM     74  N   LEU B  11      -7.450  42.498  94.509  1.00  9.70           N  
ANISOU   74  N   LEU B  11     1813    944    926   -431   -127   -112       N  
ATOM     75  CA  LEU B  11      -7.920  41.117  94.306  1.00 12.91           C  
ANISOU   75  CA  LEU B  11     2269   1290   1345   -436   -147    -84       C  
ATOM     76  C   LEU B  11      -6.838  40.025  94.434  1.00 14.74           C  
ANISOU   76  C   LEU B  11     2569   1478   1552   -369   -204    -23       C  
ATOM     77  O   LEU B  11      -7.167  38.858  94.582  1.00 17.23           O  
ANISOU   77  O   LEU B  11     2982   1705   1859   -386   -224     10       O  
ATOM     78  CB  LEU B  11      -8.694  40.951  92.991  1.00 14.87           C  
ANISOU   78  CB  LEU B  11     2494   1508   1646   -420   -146   -124       C  
ATOM     79  CG  LEU B  11      -9.920  41.845  92.792  1.00 11.43           C  
ANISOU   79  CG  LEU B  11     1976   1139   1229   -455    -90   -159       C  
ATOM     80  CD1 LEU B  11     -10.643  41.458  91.492  1.00 11.50           C  
ANISOU   80  CD1 LEU B  11     1957   1142   1271   -454   -118   -183       C  
ATOM     81  CD2 LEU B  11     -10.869  41.776  93.999  1.00 13.98           C  
ANISOU   81  CD2 LEU B  11     2288   1513   1511   -544    -39   -130       C  
ATOM     82  N   GLY B  12      -5.566  40.395  94.369  1.00 12.26           N  
ANISOU   82  N   GLY B  12     2206   1231   1220   -293   -231      6       N  
ATOM     83  CA  GLY B  12      -4.471  39.439  94.507  1.00 11.11           C  
ANISOU   83  CA  GLY B  12     2095   1089   1036   -181   -275     84       C  
ATOM     84  C   GLY B  12      -4.188  38.623  93.257  1.00 10.93           C  
ANISOU   84  C   GLY B  12     2126    995   1032    -32   -281     79       C  
ATOM     85  O   GLY B  12      -3.808  37.449  93.342  1.00 16.16           O  
ANISOU   85  O   GLY B  12     2904   1577   1659     76   -303    127       O  
ATOM     86  N   VAL B  13      -4.343  39.262  92.098  1.00 10.45           N  
ANISOU   86  N   VAL B  13     2003    958   1010     -7   -258     21       N  
ATOM     87  CA  VAL B  13      -4.116  38.631  90.806  1.00 10.98           C  
ANISOU   87  CA  VAL B  13     2128    974   1070    142   -258     -2       C  
ATOM     88  C   VAL B  13      -3.154  39.458  89.955  1.00 12.29           C  
ANISOU   88  C   VAL B  13     2150   1290   1231    245   -233     25       C  
ATOM     89  O   VAL B  13      -3.021  40.648  90.171  1.00 12.07           O  
ANISOU   89  O   VAL B  13     1996   1361   1227    146   -222     38       O  
ATOM     90  CB  VAL B  13      -5.450  38.437  90.042  1.00 13.04           C  
ANISOU   90  CB  VAL B  13     2468   1125   1362     60   -261    -94       C  
ATOM     91  CG1 VAL B  13      -6.381  37.550  90.849  1.00 15.27           C  
ANISOU   91  CG1 VAL B  13     2877   1279   1646    -72   -287    -94       C  
ATOM     92  CG2 VAL B  13      -6.142  39.754  89.729  1.00 13.76           C  
ANISOU   92  CG2 VAL B  13     2429   1302   1499    -36   -230   -134       C  
ATOM     93  N   PRO B  14      -2.480  38.819  88.992  1.00 12.78           N  
ANISOU   93  N   PRO B  14     2247   1362   1247    444   -221     39       N  
ATOM     94  CA  PRO B  14      -1.615  39.580  88.105  1.00 13.17           C  
ANISOU   94  CA  PRO B  14     2142   1583   1280    539   -184     86       C  
ATOM     95  C   PRO B  14      -2.417  40.397  87.136  1.00 12.71           C  
ANISOU   95  C   PRO B  14     2060   1510   1258    466   -162     14       C  
ATOM     96  O   PRO B  14      -3.581  40.094  86.886  1.00 12.89           O  
ANISOU   96  O   PRO B  14     2196   1401   1301    401   -179    -77       O  
ATOM     97  CB  PRO B  14      -0.875  38.491  87.326  1.00 15.23           C  
ANISOU   97  CB  PRO B  14     2487   1844   1458    811   -161    108       C  
ATOM     98  CG  PRO B  14      -1.798  37.341  87.355  1.00 18.91           C  
ANISOU   98  CG  PRO B  14     3207   2063   1913    811   -195     14       C  
ATOM     99  CD  PRO B  14      -2.407  37.371  88.704  1.00 18.11           C  
ANISOU   99  CD  PRO B  14     3122   1892   1867    607   -234     24       C  
ATOM    100  N   ARG B  15      -1.773  41.386  86.535  1.00 11.97           N  
ANISOU  100  N   ARG B  15     1816   1568   1164    480   -128     73       N  
ATOM    101  CA  ARG B  15      -2.413  42.245  85.563  1.00 13.94           C  
ANISOU  101  CA  ARG B  15     2039   1819   1437    437   -102     33       C  
ATOM    102  C   ARG B  15      -2.906  41.506  84.322  1.00 10.99           C  
ANISOU  102  C   ARG B  15     1779   1388   1009    576    -96    -42       C  
ATOM    103  O   ARG B  15      -3.853  41.965  83.715  1.00 14.91           O  
ANISOU  103  O   ARG B  15     2293   1849   1524    516    -99   -100       O  
ATOM    104  CB  ARG B  15      -1.436  43.342  85.128  1.00 13.79           C  
ANISOU  104  CB  ARG B  15     1850   1975   1414    429    -65    143       C  
ATOM    105  CG  ARG B  15      -1.998  44.369  84.129  1.00 14.92           C  
ANISOU  105  CG  ARG B  15     1971   2121   1578    391    -31    133       C  
ATOM    106  CD  ARG B  15      -1.005  45.493  83.890  1.00 19.88           C  
ANISOU  106  CD  ARG B  15     2448   2898   2208    327     -2    265       C  
ATOM    107  NE  ARG B  15      -1.527  46.563  83.020  1.00 20.36           N  
ANISOU  107  NE  ARG B  15     2509   2938   2288    285     32    276       N  
ATOM    108  CZ  ARG B  15      -1.726  46.458  81.705  1.00 31.37           C  
ANISOU  108  CZ  ARG B  15     3908   4382   3629    423     72    278       C  
ATOM    109  NH1 ARG B  15      -2.211  47.501  81.035  1.00 32.66           N1+
ANISOU  109  NH1 ARG B  15     4075   4525   3809    380     98    307       N1+
ATOM    110  NH2 ARG B  15      -1.460  45.329  81.046  1.00 32.25           N  
ANISOU  110  NH2 ARG B  15     4045   4553   3654    618     86    250       N  
ATOM    111  N   ASN B  16      -2.275  40.378  83.989  1.00 14.47           N  
ANISOU  111  N   ASN B  16     2309   1819   1370    769    -90    -42       N  
ATOM    112  CA  ASN B  16      -2.697  39.561  82.846  1.00 17.13           C  
ANISOU  112  CA  ASN B  16     2813   2071   1625    904    -97   -136       C  
ATOM    113  C   ASN B  16      -3.742  38.480  83.167  1.00 18.97           C  
ANISOU  113  C   ASN B  16     3271   2076   1860    822   -171   -248       C  
ATOM    114  O   ASN B  16      -3.991  37.597  82.339  1.00 18.41           O  
ANISOU  114  O   ASN B  16     3395   1897   1703    923   -198   -336       O  
ATOM    115  CB  ASN B  16      -1.473  38.921  82.154  1.00 18.34           C  
ANISOU  115  CB  ASN B  16     2987   2322   1661   1196    -39    -86       C  
ATOM    116  CG  ASN B  16      -0.778  37.845  82.989  1.00 16.30           C  
ANISOU  116  CG  ASN B  16     2820   2002   1369   1331    -45    -49       C  
ATOM    117  ND2 ASN B  16       0.367  37.375  82.484  1.00 21.72           N  
ANISOU  117  ND2 ASN B  16     3490   2815   1946   1625     23     21       N  
ATOM    118  OD1 ASN B  16      -1.259  37.406  84.044  1.00 20.65           O  
ANISOU  118  OD1 ASN B  16     3461   2407   1980   1200   -100    -71       O  
ATOM    119  N   ALA B  17      -4.333  38.533  84.356  1.00 15.33           N  
ANISOU  119  N   ALA B  17     2799   1543   1482    631   -205   -242       N  
ATOM    120  CA  ALA B  17      -5.285  37.525  84.802  1.00 16.31           C  
ANISOU  120  CA  ALA B  17     3111   1472   1612    513   -272   -311       C  
ATOM    121  C   ALA B  17      -6.445  37.390  83.834  1.00 15.76           C  
ANISOU  121  C   ALA B  17     3123   1345   1519    420   -327   -412       C  
ATOM    122  O   ALA B  17      -6.893  38.363  83.238  1.00 15.91           O  
ANISOU  122  O   ALA B  17     3003   1485   1557    377   -313   -418       O  
ATOM    123  CB  ALA B  17      -5.805  37.875  86.211  1.00 15.24           C  
ANISOU  123  CB  ALA B  17     2895   1333   1562    313   -280   -267       C  
ATOM    124  N   THR B  18      -6.937  36.167  83.664  1.00 19.45           N  
ANISOU  124  N   THR B  18     3832   1623   1936    381   -399   -487       N  
ATOM    125  CA  THR B  18      -8.157  35.954  82.903  1.00 20.69           C  
ANISOU  125  CA  THR B  18     4062   1733   2064    224   -483   -578       C  
ATOM    126  C   THR B  18      -9.350  36.466  83.698  1.00 17.76           C  
ANISOU  126  C   THR B  18     3534   1427   1789    -38   -505   -540       C  
ATOM    127  O   THR B  18      -9.259  36.679  84.905  1.00 17.90           O  
ANISOU  127  O   THR B  18     3468   1458   1876    -99   -464   -467       O  
ATOM    128  CB  THR B  18      -8.406  34.458  82.626  1.00 21.99           C  
ANISOU  128  CB  THR B  18     4564   1645   2144    195   -575   -666       C  
ATOM    129  CG2 THR B  18      -7.205  33.805  81.903  1.00 25.46           C  
ANISOU  129  CG2 THR B  18     5211   2000   2464    512   -537   -708       C  
ATOM    130  OG1 THR B  18      -8.686  33.771  83.849  1.00 21.05           O  
ANISOU  130  OG1 THR B  18     4533   1382   2082     42   -600   -617       O  
ATOM    131  N   GLN B  19     -10.485  36.644  83.028  1.00 20.35           N  
ANISOU  131  N   GLN B  19     3815   1816   2101   -182   -571   -585       N  
ATOM    132  CA  GLN B  19     -11.707  37.034  83.734  1.00 20.71           C  
ANISOU  132  CA  GLN B  19     3696   1956   2216   -409   -586   -536       C  
ATOM    133  C   GLN B  19     -12.102  35.958  84.766  1.00 18.45           C  
ANISOU  133  C   GLN B  19     3542   1517   1950   -597   -631   -509       C  
ATOM    134  O   GLN B  19     -12.631  36.280  85.838  1.00 22.65           O  
ANISOU  134  O   GLN B  19     3935   2126   2545   -719   -591   -431       O  
ATOM    135  CB  GLN B  19     -12.864  37.322  82.769  1.00 22.49           C  
ANISOU  135  CB  GLN B  19     3828   2312   2404   -522   -662   -569       C  
ATOM    136  CG  GLN B  19     -12.625  38.457  81.766  1.00 21.64           C  
ANISOU  136  CG  GLN B  19     3583   2367   2272   -346   -616   -571       C  
ATOM    137  CD  GLN B  19     -12.281  39.799  82.411  1.00 19.94           C  
ANISOU  137  CD  GLN B  19     3168   2268   2141   -246   -491   -485       C  
ATOM    138  NE2 GLN B  19     -12.828  40.052  83.599  1.00 18.39           N  
ANISOU  138  NE2 GLN B  19     2870   2102   2015   -357   -454   -427       N  
ATOM    139  OE1 GLN B  19     -11.531  40.596  81.845  1.00 17.79           O  
ANISOU  139  OE1 GLN B  19     2849   2051   1858    -78   -430   -468       O  
ATOM    140  N   GLU B  20     -11.840  34.687  84.460  1.00 25.27           N  
ANISOU  140  N   GLU B  20     4694   2157   2749   -609   -708   -569       N  
ATOM    141  CA  GLU B  20     -12.132  33.613  85.408  1.00 27.30           C  
ANISOU  141  CA  GLU B  20     5121   2231   3020   -786   -752   -528       C  
ATOM    142  C   GLU B  20     -11.271  33.689  86.679  1.00 22.99           C  
ANISOU  142  C   GLU B  20     4550   1661   2523   -673   -656   -436       C  
ATOM    143  O   GLU B  20     -11.779  33.491  87.797  1.00 21.23           O  
ANISOU  143  O   GLU B  20     4287   1438   2343   -843   -646   -350       O  
ATOM    144  CB  GLU B  20     -11.988  32.248  84.729  1.00 37.24           C  
ANISOU  144  CB  GLU B  20     6758   3207   4186   -803   -858   -621       C  
ATOM    145  CG  GLU B  20     -13.140  31.914  83.780  1.00 47.87           C  
ANISOU  145  CG  GLU B  20     8163   4554   5473  -1049   -999   -699       C  
ATOM    146  CD  GLU B  20     -14.475  31.755  84.492  1.00 51.53           C  
ANISOU  146  CD  GLU B  20     8493   5096   5991  -1423  -1061   -610       C  
ATOM    147  OE1 GLU B  20     -15.525  31.910  83.826  1.00 53.91           O  
ANISOU  147  OE1 GLU B  20     8679   5542   6263  -1630  -1159   -632       O  
ATOM    148  OE2 GLU B  20     -14.475  31.479  85.713  1.00 48.89           O1-
ANISOU  148  OE2 GLU B  20     8150   4708   5717  -1505  -1012   -505       O1-
ATOM    149  N   GLU B  21      -9.987  34.005  86.534  1.00 23.46           N  
ANISOU  149  N   GLU B  21     4611   1737   2567   -395   -587   -438       N  
ATOM    150  CA  GLU B  21      -9.136  34.190  87.704  1.00 21.53           C  
ANISOU  150  CA  GLU B  21     4305   1520   2356   -296   -513   -344       C  
ATOM    151  C   GLU B  21      -9.624  35.353  88.570  1.00 16.15           C  
ANISOU  151  C   GLU B  21     3352   1042   1743   -408   -453   -283       C  
ATOM    152  O   GLU B  21      -9.609  35.266  89.792  1.00 20.10           O  
ANISOU  152  O   GLU B  21     3832   1545   2261   -473   -426   -207       O  
ATOM    153  CB  GLU B  21      -7.657  34.410  87.354  1.00 25.91           C  
ANISOU  153  CB  GLU B  21     4853   2119   2873      6   -456   -336       C  
ATOM    154  CG  GLU B  21      -6.809  34.448  88.640  1.00 32.18           C  
ANISOU  154  CG  GLU B  21     5591   2953   3684     76   -409   -227       C  
ATOM    155  CD  GLU B  21      -5.295  34.570  88.501  1.00 35.30           C  
ANISOU  155  CD  GLU B  21     5940   3436   4035    356   -361   -176       C  
ATOM    156  OE1 GLU B  21      -4.761  34.711  87.384  1.00 35.83           O  
ANISOU  156  OE1 GLU B  21     6002   3554   4057    531   -339   -217       O  
ATOM    157  OE2 GLU B  21      -4.640  34.521  89.571  1.00 35.76           O1-
ANISOU  157  OE2 GLU B  21     5951   3542   4093    396   -344    -80       O1-
ATOM    158  N   ILE B  22     -10.025  36.447  87.921  1.00 15.93           N  
ANISOU  158  N   ILE B  22     3138   1178   1738   -405   -429   -316       N  
ATOM    159  CA  ILE B  22     -10.559  37.628  88.626  1.00 13.52           C  
ANISOU  159  CA  ILE B  22     2612   1044   1481   -476   -364   -272       C  
ATOM    160  C   ILE B  22     -11.839  37.243  89.407  1.00 15.61           C  
ANISOU  160  C   ILE B  22     2847   1327   1758   -701   -378   -228       C  
ATOM    161  O   ILE B  22     -12.017  37.612  90.570  1.00 16.62           O  
ANISOU  161  O   ILE B  22     2894   1524   1898   -748   -319   -167       O  
ATOM    162  CB  ILE B  22     -10.841  38.786  87.614  1.00 18.07           C  
ANISOU  162  CB  ILE B  22     3036   1761   2068   -410   -340   -309       C  
ATOM    163  CG1 ILE B  22      -9.515  39.400  87.154  1.00 13.52           C  
ANISOU  163  CG1 ILE B  22     2441   1211   1484   -215   -300   -310       C  
ATOM    164  CG2 ILE B  22     -11.748  39.897  88.199  1.00 15.53           C  
ANISOU  164  CG2 ILE B  22     2529   1589   1781   -477   -279   -274       C  
ATOM    165  CD1 ILE B  22      -9.568  40.085  85.794  1.00 16.09           C  
ANISOU  165  CD1 ILE B  22     2703   1619   1793   -125   -296   -344       C  
ATOM    166  N   LYS B  23     -12.732  36.526  88.737  1.00 16.50           N  
ANISOU  166  N   LYS B  23     3018   1398   1854   -847   -459   -254       N  
ATOM    167  CA  LYS B  23     -13.976  36.089  89.361  1.00 20.67           C  
ANISOU  167  CA  LYS B  23     3492   1976   2387  -1095   -482   -188       C  
ATOM    168  C   LYS B  23     -13.698  35.206  90.573  1.00 19.58           C  
ANISOU  168  C   LYS B  23     3494   1703   2243  -1174   -473   -112       C  
ATOM    169  O   LYS B  23     -14.299  35.389  91.634  1.00 23.38           O  
ANISOU  169  O   LYS B  23     3860   2295   2728  -1284   -416    -24       O  
ATOM    170  CB  LYS B  23     -14.838  35.359  88.334  1.00 28.97           C  
ANISOU  170  CB  LYS B  23     4609   2991   3407  -1272   -604   -230       C  
ATOM    171  CG  LYS B  23     -16.204  34.983  88.839  1.00 31.67           C  
ANISOU  171  CG  LYS B  23     4838   3444   3751  -1565   -638   -139       C  
ATOM    172  CD  LYS B  23     -17.139  34.596  87.692  1.00 34.06           C  
ANISOU  172  CD  LYS B  23     5130   3796   4015  -1754   -772   -179       C  
ATOM    173  CE  LYS B  23     -16.644  33.366  86.958  1.00 41.62           C  
ANISOU  173  CE  LYS B  23     6444   4450   4922  -1811   -901   -276       C  
ATOM    174  NZ  LYS B  23     -17.711  32.774  86.097  1.00 44.39           N1+
ANISOU  174  NZ  LYS B  23     6819   4828   5217  -2099  -1062   -302       N1+
ATOM    175  N   ARG B  24     -12.759  34.279  90.420  1.00 23.95           N  
ANISOU  175  N   ARG B  24     4299   2029   2772  -1088   -518   -139       N  
ATOM    176  CA  ARG B  24     -12.381  33.347  91.482  1.00 24.18           C  
ANISOU  176  CA  ARG B  24     4502   1901   2785  -1128   -518    -56       C  
ATOM    177  C   ARG B  24     -11.808  34.094  92.678  1.00 20.55           C  
ANISOU  177  C   ARG B  24     3907   1572   2330  -1020   -420     12       C  
ATOM    178  O   ARG B  24     -12.142  33.808  93.828  1.00 21.43           O  
ANISOU  178  O   ARG B  24     4018   1700   2425  -1134   -390    110       O  
ATOM    179  CB  ARG B  24     -11.351  32.345  90.939  1.00 27.25           C  
ANISOU  179  CB  ARG B  24     5190   2031   3133   -966   -572   -103       C  
ATOM    180  CG  ARG B  24     -11.105  31.110  91.784  1.00 39.83           C  
ANISOU  180  CG  ARG B  24     7042   3394   4698  -1015   -598    -16       C  
ATOM    181  CD  ARG B  24     -10.269  30.089  91.007  1.00 44.77           C  
ANISOU  181  CD  ARG B  24     8002   3741   5266   -830   -654    -80       C  
ATOM    182  NE  ARG B  24      -8.950  30.626  90.659  1.00 48.57           N  
ANISOU  182  NE  ARG B  24     8415   4311   5727   -484   -594   -113       N  
ATOM    183  CZ  ARG B  24      -8.170  30.192  89.664  1.00 49.51           C  
ANISOU  183  CZ  ARG B  24     8719   4308   5787   -244   -608   -192       C  
ATOM    184  NH1 ARG B  24      -8.536  29.185  88.874  1.00 55.10           N1+
ANISOU  184  NH1 ARG B  24     9744   4753   6438   -294   -691   -277       N1+
ATOM    185  NH2 ARG B  24      -6.993  30.776  89.459  1.00 48.78           N  
ANISOU  185  NH2 ARG B  24     8495   4365   5674     49   -540   -184       N  
ATOM    186  N   ALA B  25     -10.934  35.061  92.403  1.00 16.72           N  
ANISOU  186  N   ALA B  25     3316   1185   1852   -813   -376    -37       N  
ATOM    187  CA  ALA B  25     -10.287  35.823  93.449  1.00 16.78           C  
ANISOU  187  CA  ALA B  25     3220   1308   1848   -727   -308      9       C  
ATOM    188  C   ALA B  25     -11.322  36.625  94.226  1.00 19.61           C  
ANISOU  188  C   ALA B  25     3408   1836   2207   -854   -241     39       C  
ATOM    189  O   ALA B  25     -11.296  36.645  95.454  1.00 17.86           O  
ANISOU  189  O   ALA B  25     3180   1660   1944   -889   -200    107       O  
ATOM    190  CB  ALA B  25      -9.266  36.768  92.853  1.00 17.81           C  
ANISOU  190  CB  ALA B  25     3262   1516   1988   -538   -288    -45       C  
ATOM    191  N   TYR B  26     -12.225  37.291  93.501  1.00 17.57           N  
ANISOU  191  N   TYR B  26     3013   1685   1977   -897   -226     -6       N  
ATOM    192  CA  TYR B  26     -13.294  38.077  94.130  1.00 17.51           C  
ANISOU  192  CA  TYR B  26     2834   1862   1957   -969   -147     28       C  
ATOM    193  C   TYR B  26     -14.158  37.208  95.022  1.00 17.81           C  
ANISOU  193  C   TYR B  26     2883   1921   1963  -1161   -138    133       C  
ATOM    194  O   TYR B  26     -14.471  37.584  96.149  1.00 20.16           O  
ANISOU  194  O   TYR B  26     3112   2336   2211  -1174    -55    191       O  
ATOM    195  CB  TYR B  26     -14.189  38.789  93.093  1.00 16.36           C  
ANISOU  195  CB  TYR B  26     2535   1841   1839   -964   -141    -14       C  
ATOM    196  CG  TYR B  26     -15.426  39.425  93.716  1.00 17.59           C  
ANISOU  196  CG  TYR B  26     2506   2209   1967  -1013    -51     45       C  
ATOM    197  CD1 TYR B  26     -15.317  40.570  94.496  1.00 16.85           C  
ANISOU  197  CD1 TYR B  26     2358   2206   1838   -880     55     35       C  
ATOM    198  CD2 TYR B  26     -16.694  38.861  93.559  1.00 21.13           C  
ANISOU  198  CD2 TYR B  26     2842   2777   2409  -1193    -73    118       C  
ATOM    199  CE1 TYR B  26     -16.432  41.152  95.094  1.00 17.27           C  
ANISOU  199  CE1 TYR B  26     2259   2460   1842   -871    158     89       C  
ATOM    200  CE2 TYR B  26     -17.829  39.434  94.158  1.00 20.06           C  
ANISOU  200  CE2 TYR B  26     2501   2888   2233  -1207     26    197       C  
ATOM    201  CZ  TYR B  26     -17.685  40.596  94.916  1.00 23.67           C  
ANISOU  201  CZ  TYR B  26     2917   3429   2647  -1017    153    179       C  
ATOM    202  OH  TYR B  26     -18.798  41.167  95.518  1.00 25.03           O  
ANISOU  202  OH  TYR B  26     2903   3850   2757   -978    271    256       O  
ATOM    203  N   LYS B  27     -14.555  36.040  94.519  1.00 16.61           N  
ANISOU  203  N   LYS B  27     2835   1651   1826  -1320   -226    159       N  
ATOM    204  CA  LYS B  27     -15.372  35.116  95.304  1.00 20.68           C  
ANISOU  204  CA  LYS B  27     3376   2167   2314  -1550   -230    283       C  
ATOM    205  C   LYS B  27     -14.702  34.723  96.620  1.00 19.62           C  
ANISOU  205  C   LYS B  27     3361   1964   2131  -1519   -188    363       C  
ATOM    206  O   LYS B  27     -15.333  34.750  97.681  1.00 21.17           O  
ANISOU  206  O   LYS B  27     3472   2296   2276  -1617   -115    469       O  
ATOM    207  CB  LYS B  27     -15.715  33.882  94.461  1.00 24.73           C  
ANISOU  207  CB  LYS B  27     4054   2495   2846  -1743   -358    282       C  
ATOM    208  CG  LYS B  27     -16.751  34.199  93.406  1.00 34.80           C  
ANISOU  208  CG  LYS B  27     5164   3917   4140  -1857   -406    245       C  
ATOM    209  CD  LYS B  27     -16.907  33.107  92.361  1.00 37.38           C  
ANISOU  209  CD  LYS B  27     5696   4037   4468  -2024   -558    196       C  
ATOM    210  CE  LYS B  27     -17.975  33.493  91.340  1.00 41.24           C  
ANISOU  210  CE  LYS B  27     5986   4724   4957  -2150   -620    169       C  
ATOM    211  NZ  LYS B  27     -19.342  33.550  91.917  1.00 43.57           N1+
ANISOU  211  NZ  LYS B  27     6023   5290   5240  -2397   -593    315       N1+
ATOM    212  N   ARG B  28     -13.422  34.382  96.545  1.00 20.51           N  
ANISOU  212  N   ARG B  28     3654   1896   2244  -1364   -231    324       N  
ATOM    213  CA  ARG B  28     -12.635  34.030  97.736  1.00 22.70           C  
ANISOU  213  CA  ARG B  28     4039   2123   2462  -1300   -208    405       C  
ATOM    214  C   ARG B  28     -12.681  35.157  98.768  1.00 18.71           C  
ANISOU  214  C   ARG B  28     3370   1841   1899  -1238   -108    415       C  
ATOM    215  O   ARG B  28     -12.981  34.924  99.941  1.00 22.31           O  
ANISOU  215  O   ARG B  28     3832   2365   2281  -1312    -57    519       O  
ATOM    216  CB  ARG B  28     -11.195  33.712  97.322  1.00 28.53           C  
ANISOU  216  CB  ARG B  28     4933   2702   3206  -1090   -265    358       C  
ATOM    217  CG  ARG B  28     -10.394  32.893  98.313  1.00 37.24           C  
ANISOU  217  CG  ARG B  28     6202   3701   4246  -1029   -279    467       C  
ATOM    218  CD  ARG B  28      -9.400  31.972  97.589  1.00 43.96           C  
ANISOU  218  CD  ARG B  28     7272   4325   5105   -863   -351    452       C  
ATOM    219  NE  ARG B  28      -8.411  32.719  96.801  1.00 47.27           N  
ANISOU  219  NE  ARG B  28     7598   4821   5543   -643   -353    355       N  
ATOM    220  CZ  ARG B  28      -8.400  32.873  95.472  1.00 47.85           C  
ANISOU  220  CZ  ARG B  28     7669   4850   5660   -583   -377    246       C  
ATOM    221  NH1 ARG B  28      -7.426  33.589  94.909  1.00 48.03           N1+
ANISOU  221  NH1 ARG B  28     7587   4977   5687   -387   -366    193       N1+
ATOM    222  NH2 ARG B  28      -9.327  32.334  94.685  1.00 49.65           N  
ANISOU  222  NH2 ARG B  28     7996   4951   5917   -728   -418    198       N  
ATOM    223  N   LEU B  29     -12.435  36.383  98.308  1.00 16.91           N  
ANISOU  223  N   LEU B  29     3018   1716   1691  -1106    -78    306       N  
ATOM    224  CA  LEU B  29     -12.386  37.547  99.185  1.00 17.24           C  
ANISOU  224  CA  LEU B  29     2962   1922   1666  -1030      6    283       C  
ATOM    225  C   LEU B  29     -13.782  37.916  99.693  1.00 17.28           C  
ANISOU  225  C   LEU B  29     2829   2109   1628  -1121    107    331       C  
ATOM    226  O   LEU B  29     -13.939  38.242 100.857  1.00 18.21           O  
ANISOU  226  O   LEU B  29     2935   2340   1645  -1109    184    373       O  
ATOM    227  CB  LEU B  29     -11.715  38.734  98.479  1.00 16.51           C  
ANISOU  227  CB  LEU B  29     2816   1848   1609   -882      1    162       C  
ATOM    228  CG  LEU B  29     -10.223  38.530  98.182  1.00 15.37           C  
ANISOU  228  CG  LEU B  29     2760   1600   1479   -775    -79    141       C  
ATOM    229  CD1 LEU B  29      -9.710  39.521  97.154  1.00 19.21           C  
ANISOU  229  CD1 LEU B  29     3180   2099   2020   -674    -90     47       C  
ATOM    230  CD2 LEU B  29      -9.430  38.652  99.470  1.00 17.25           C  
ANISOU  230  CD2 LEU B  29     3047   1889   1621   -750    -82    185       C  
ATOM    231  N   ALA B  30     -14.793  37.875  98.823  1.00 18.19           N  
ANISOU  231  N   ALA B  30     2828   2280   1801  -1201    108    332       N  
ATOM    232  CA  ALA B  30     -16.174  38.158  99.270  1.00 18.43           C  
ANISOU  232  CA  ALA B  30     2682   2538   1783  -1278    209    410       C  
ATOM    233  C   ALA B  30     -16.632  37.183 100.338  1.00 19.69           C  
ANISOU  233  C   ALA B  30     2868   2738   1873  -1449    238    565       C  
ATOM    234  O   ALA B  30     -17.358  37.552 101.260  1.00 24.33           O  
ANISOU  234  O   ALA B  30     3343   3535   2366  -1449    357    640       O  
ATOM    235  CB  ALA B  30     -17.135  38.181  98.084  1.00 19.87           C  
ANISOU  235  CB  ALA B  30     2713   2801   2035  -1352    178    405       C  
ATOM    236  N   ARG B  31     -16.231  35.913 100.220  1.00 20.85           N  
ANISOU  236  N   ARG B  31     3182   2682   2056  -1587    137    623       N  
ATOM    237  CA  ARG B  31     -16.536  34.894 101.233  1.00 25.91           C  
ANISOU  237  CA  ARG B  31     3898   3314   2633  -1761    153    790       C  
ATOM    238  C   ARG B  31     -15.895  35.162 102.606  1.00 22.98           C  
ANISOU  238  C   ARG B  31     3596   2993   2143  -1642    225    826       C  
ATOM    239  O   ARG B  31     -16.337  34.589 103.616  1.00 30.76           O  
ANISOU  239  O   ARG B  31     4593   4053   3041  -1762    279    980       O  
ATOM    240  CB  ARG B  31     -16.090  33.518 100.734  1.00 30.57           C  
ANISOU  240  CB  ARG B  31     4721   3610   3285  -1893     20    828       C  
ATOM    241  CG  ARG B  31     -17.008  32.882  99.700  1.00 39.28           C  
ANISOU  241  CG  ARG B  31     5798   4666   4461  -2125    -62    846       C  
ATOM    242  CD  ARG B  31     -16.336  31.656  99.081  1.00 44.82           C  
ANISOU  242  CD  ARG B  31     6810   5011   5209  -2185   -199    827       C  
ATOM    243  NE  ARG B  31     -17.281  30.619  98.665  1.00 50.27           N  
ANISOU  243  NE  ARG B  31     7570   5608   5922  -2516   -286    914       N  
ATOM    244  CZ  ARG B  31     -17.986  30.611  97.530  1.00 54.35           C  
ANISOU  244  CZ  ARG B  31     8011   6152   6486  -2660   -368    850       C  
ATOM    245  NH1 ARG B  31     -17.897  31.603  96.642  1.00 51.98           N1+
ANISOU  245  NH1 ARG B  31     7554   5976   6220  -2481   -363    703       N1+
ATOM    246  NH2 ARG B  31     -18.807  29.592  97.284  1.00 58.41           N  
ANISOU  246  NH2 ARG B  31     8615   6573   7005  -3009   -466    944       N  
ATOM    247  N   GLN B  32     -14.832  35.967 102.620  1.00 22.12           N  
ANISOU  247  N   GLN B  32     3540   2844   2022  -1431    211    697       N  
ATOM    248  CA  GLN B  32     -14.166  36.423 103.847  1.00 23.01           C  
ANISOU  248  CA  GLN B  32     3712   3027   2005  -1318    257    700       C  
ATOM    249  C   GLN B  32     -14.722  37.724 104.404  1.00 22.93           C  
ANISOU  249  C   GLN B  32     3580   3238   1896  -1214    383    636       C  
ATOM    250  O   GLN B  32     -14.748  37.902 105.626  1.00 26.12           O  
ANISOU  250  O   GLN B  32     4015   3760   2148  -1185    456    684       O  
ATOM    251  CB  GLN B  32     -12.674  36.666 103.607  1.00 32.39           C  
ANISOU  251  CB  GLN B  32     5013   4078   3213  -1169    160    602       C  
ATOM    252  CG  GLN B  32     -11.854  35.485 103.143  1.00 37.41           C  
ANISOU  252  CG  GLN B  32     5801   4496   3916  -1177     47    654       C  
ATOM    253  CD  GLN B  32     -10.483  35.919 102.642  1.00 40.57           C  
ANISOU  253  CD  GLN B  32     6234   4833   4347  -1007    -32    555       C  
ATOM    254  NE2 GLN B  32      -9.819  36.780 103.410  1.00 42.23           N  
ANISOU  254  NE2 GLN B  32     6420   5161   4463   -925    -24    515       N  
ATOM    255  OE1 GLN B  32     -10.036  35.503 101.570  1.00 45.32           O  
ANISOU  255  OE1 GLN B  32     6882   5294   5043   -957    -99    518       O  
ATOM    256  N   TYR B  33     -15.078  38.666 103.529  1.00 19.64           N  
ANISOU  256  N   TYR B  33     3053   2863   1545  -1130    408    522       N  
ATOM    257  CA  TYR B  33     -15.399  40.030 103.962  1.00 20.31           C  
ANISOU  257  CA  TYR B  33     3086   3097   1534   -973    520    431       C  
ATOM    258  C   TYR B  33     -16.837  40.531 103.836  1.00 22.18           C  
ANISOU  258  C   TYR B  33     3130   3552   1744   -940    655    469       C  
ATOM    259  O   TYR B  33     -17.143  41.597 104.345  1.00 21.75           O  
ANISOU  259  O   TYR B  33     3068   3616   1579   -775    769    405       O  
ATOM    260  CB  TYR B  33     -14.446  40.987 103.254  1.00 22.92           C  
ANISOU  260  CB  TYR B  33     3485   3297   1925   -845    453    267       C  
ATOM    261  CG  TYR B  33     -13.022  40.779 103.713  1.00 21.50           C  
ANISOU  261  CG  TYR B  33     3460   2996   1713   -842    348    241       C  
ATOM    262  CD1 TYR B  33     -12.672  41.024 105.036  1.00 30.92           C  
ANISOU  262  CD1 TYR B  33     4750   4259   2740   -818    375    246       C  
ATOM    263  CD2 TYR B  33     -12.048  40.311 102.863  1.00 27.60           C  
ANISOU  263  CD2 TYR B  33     4272   3615   2599   -854    224    224       C  
ATOM    264  CE1 TYR B  33     -11.386  40.823 105.486  1.00 31.70           C  
ANISOU  264  CE1 TYR B  33     4960   4291   2793   -823    266    242       C  
ATOM    265  CE2 TYR B  33     -10.745  40.122 103.302  1.00 30.73           C  
ANISOU  265  CE2 TYR B  33     4768   3954   2954   -833    132    227       C  
ATOM    266  CZ  TYR B  33     -10.428  40.375 104.618  1.00 28.63           C  
ANISOU  266  CZ  TYR B  33     4576   3774   2528   -828    146    241       C  
ATOM    267  OH  TYR B  33      -9.142  40.186 105.077  1.00 34.29           O  
ANISOU  267  OH  TYR B  33     5364   4475   3190   -814     40    260       O  
ATOM    268  N   HIS B  34     -17.719  39.770 103.187  1.00 19.90           N  
ANISOU  268  N   HIS B  34     2694   3329   1541  -1092    641    577       N  
ATOM    269  CA  HIS B  34     -19.143  40.122 103.087  1.00 22.30           C  
ANISOU  269  CA  HIS B  34     2758   3905   1811  -1080    763    656       C  
ATOM    270  C   HIS B  34     -19.788  40.298 104.479  1.00 26.04           C  
ANISOU  270  C   HIS B  34     3178   4621   2097  -1026    930    759       C  
ATOM    271  O   HIS B  34     -19.540  39.502 105.370  1.00 25.56           O  
ANISOU  271  O   HIS B  34     3204   4543   1966  -1147    926    858       O  
ATOM    272  CB  HIS B  34     -19.859  39.005 102.315  1.00 26.81           C  
ANISOU  272  CB  HIS B  34     3199   4501   2487  -1338    680    783       C  
ATOM    273  CG  HIS B  34     -21.235  39.355 101.865  1.00 27.01           C  
ANISOU  273  CG  HIS B  34     2935   4821   2507  -1345    759    866       C  
ATOM    274  CD2 HIS B  34     -21.724  39.604 100.627  1.00 27.77           C  
ANISOU  274  CD2 HIS B  34     2886   4969   2697  -1348    701    835       C  
ATOM    275  ND1 HIS B  34     -22.301  39.464 102.729  1.00 30.30           N  
ANISOU  275  ND1 HIS B  34     3153   5564   2796  -1341    918   1017       N  
ATOM    276  CE1 HIS B  34     -23.387  39.775 102.044  1.00 33.46           C  
ANISOU  276  CE1 HIS B  34     3279   6218   3217  -1334    954   1083       C  
ATOM    277  NE2 HIS B  34     -23.066  39.855 100.766  1.00 31.17           N  
ANISOU  277  NE2 HIS B  34     3021   5763   3060  -1347    816    973       N  
ATOM    278  N   PRO B  35     -20.595  41.360 104.679  1.00 29.34           N  
ANISOU  278  N   PRO B  35     3465   5266   2417   -815   1087    739       N  
ATOM    279  CA  PRO B  35     -21.054  41.667 106.049  1.00 32.78           C  
ANISOU  279  CA  PRO B  35     3895   5921   2638   -700   1262    804       C  
ATOM    280  C   PRO B  35     -21.942  40.652 106.765  1.00 39.36           C  
ANISOU  280  C   PRO B  35     4558   7003   3394   -896   1341   1046       C  
ATOM    281  O   PRO B  35     -22.061  40.721 107.992  1.00 41.87           O  
ANISOU  281  O   PRO B  35     4922   7464   3522   -824   1467   1105       O  
ATOM    282  CB  PRO B  35     -21.817  42.988 105.869  1.00 34.87           C  
ANISOU  282  CB  PRO B  35     4053   6367   2828   -400   1415    736       C  
ATOM    283  CG  PRO B  35     -22.225  43.000 104.471  1.00 33.21           C  
ANISOU  283  CG  PRO B  35     3670   6156   2792   -445   1336    741       C  
ATOM    284  CD  PRO B  35     -21.105  42.358 103.721  1.00 27.54           C  
ANISOU  284  CD  PRO B  35     3114   5107   2244   -635   1124    659       C  
ATOM    285  N   ASP B  36     -22.569  39.724 106.049  1.00 40.83           N  
ANISOU  285  N   ASP B  36     4561   7247   3707  -1155   1267   1191       N  
ATOM    286  CA  ASP B  36     -23.304  38.662 106.753  1.00 41.40           C  
ANISOU  286  CA  ASP B  36     4501   7518   3710  -1407   1319   1441       C  
ATOM    287  C   ASP B  36     -22.424  37.455 107.140  1.00 36.04           C  
ANISOU  287  C   ASP B  36     4064   6558   3070  -1644   1185   1497       C  
ATOM    288  O   ASP B  36     -22.892  36.568 107.858  1.00 36.22           O  
ANISOU  288  O   ASP B  36     4039   6700   3022  -1853   1227   1710       O  
ATOM    289  CB  ASP B  36     -24.622  38.266 106.047  1.00 47.45           C  
ANISOU  289  CB  ASP B  36     4924   8562   4542  -1602   1329   1619       C  
ATOM    290  CG  ASP B  36     -24.428  37.733 104.645  1.00 48.06           C  
ANISOU  290  CG  ASP B  36     5019   8415   4828  -1807   1118   1561       C  
ATOM    291  OD1 ASP B  36     -23.341  37.209 104.324  1.00 59.13           O  
ANISOU  291  OD1 ASP B  36     6698   9439   6329  -1886    962   1451       O  
ATOM    292  OD2 ASP B  36     -25.390  37.834 103.855  1.00 46.52           O1-
ANISOU  292  OD2 ASP B  36     4548   8445   4681  -1878   1111   1633       O1-
ATOM    293  N   VAL B  37     -21.163  37.433 106.694  1.00 35.36           N  
ANISOU  293  N   VAL B  37     4232   6120   3083  -1597   1034   1325       N  
ATOM    294  CA  VAL B  37     -20.170  36.467 107.199  1.00 38.23           C  
ANISOU  294  CA  VAL B  37     4850   6229   3449  -1717    927   1365       C  
ATOM    295  C   VAL B  37     -19.140  37.101 108.161  1.00 40.29           C  
ANISOU  295  C   VAL B  37     5307   6430   3570  -1495    955   1249       C  
ATOM    296  O   VAL B  37     -18.823  36.519 109.192  1.00 47.38           O  
ANISOU  296  O   VAL B  37     6323   7328   4351  -1547    969   1359       O  
ATOM    297  CB  VAL B  37     -19.446  35.685 106.048  1.00 39.98           C  
ANISOU  297  CB  VAL B  37     5219   6108   3865  -1851    723   1301       C  
ATOM    298  CG1 VAL B  37     -20.466  35.004 105.153  1.00 47.33           C  
ANISOU  298  CG1 VAL B  37     5990   7087   4904  -2111    673   1408       C  
ATOM    299  CG2 VAL B  37     -18.546  36.565 105.209  1.00 42.43           C  
ANISOU  299  CG2 VAL B  37     5606   6255   4261  -1638    649   1067       C  
ATOM    300  N   ASN B  38     -18.632  38.284 107.822  1.00 36.66           N  
ANISOU  300  N   ASN B  38     4892   5922   3116  -1266    952   1038       N  
ATOM    301  CA  ASN B  38     -17.606  38.970 108.624  1.00 35.99           C  
ANISOU  301  CA  ASN B  38     5004   5769   2901  -1092    945    907       C  
ATOM    302  C   ASN B  38     -18.258  40.096 109.406  1.00 37.79           C  
ANISOU  302  C   ASN B  38     5188   6236   2934   -887   1126    854       C  
ATOM    303  O   ASN B  38     -18.816  41.024 108.816  1.00 36.83           O  
ANISOU  303  O   ASN B  38     4966   6187   2842   -742   1198    761       O  
ATOM    304  CB  ASN B  38     -16.512  39.530 107.708  1.00 33.09           C  
ANISOU  304  CB  ASN B  38     4747   5162   2664  -1006    805    712       C  
ATOM    305  CG  ASN B  38     -15.195  39.811 108.437  1.00 29.36           C  
ANISOU  305  CG  ASN B  38     4483   4582   2090   -932    724    622       C  
ATOM    306  ND2 ASN B  38     -14.077  39.524 107.773  1.00 32.15           N  
ANISOU  306  ND2 ASN B  38     4918   4728   2568   -958    566    567       N  
ATOM    307  OD1 ASN B  38     -15.184  40.314 109.558  1.00 30.99           O  
ANISOU  307  OD1 ASN B  38     4768   4911   2097   -846    800    602       O  
ATOM    308  N   LYS B  39     -18.171  40.010 110.734  1.00 40.26           N  
ANISOU  308  N   LYS B  39     5597   6669   3033   -854   1202    915       N  
ATOM    309  CA  LYS B  39     -18.868  40.931 111.624  1.00 45.11           C  
ANISOU  309  CA  LYS B  39     6194   7529   3415   -647   1397    884       C  
ATOM    310  C   LYS B  39     -17.982  42.063 112.161  1.00 47.89           C  
ANISOU  310  C   LYS B  39     6802   7774   3618   -451   1373    655       C  
ATOM    311  O   LYS B  39     -18.427  42.841 113.009  1.00 50.38           O  
ANISOU  311  O   LYS B  39     7184   8256   3704   -258   1527    601       O  
ATOM    312  CB  LYS B  39     -19.476  40.148 112.793  1.00 46.29           C  
ANISOU  312  CB  LYS B  39     6286   7921   3381   -732   1520   1109       C  
ATOM    313  CG  LYS B  39     -20.343  38.951 112.382  1.00 46.88           C  
ANISOU  313  CG  LYS B  39     6130   8097   3584   -991   1530   1362       C  
ATOM    314  CD  LYS B  39     -21.503  39.367 111.485  1.00 45.71           C  
ANISOU  314  CD  LYS B  39     5703   8131   3535   -957   1621   1386       C  
ATOM    315  CE  LYS B  39     -22.513  38.242 111.321  1.00 54.25           C  
ANISOU  315  CE  LYS B  39     6538   9394   4682  -1245   1648   1664       C  
ATOM    316  NZ  LYS B  39     -21.894  36.997 110.780  1.00 56.84           N1+
ANISOU  316  NZ  LYS B  39     6981   9419   5196  -1547   1442   1731       N1+
ATOM    317  N   SER B  40     -16.743  42.156 111.681  1.00 44.12           N  
ANISOU  317  N   SER B  40     6475   7031   3256   -503   1182    526       N  
ATOM    318  CA  SER B  40     -15.871  43.269 112.035  1.00 43.11           C  
ANISOU  318  CA  SER B  40     6582   6788   3012   -375   1126    308       C  
ATOM    319  C   SER B  40     -16.303  44.474 111.206  1.00 44.23           C  
ANISOU  319  C   SER B  40     6713   6872   3220   -205   1189    152       C  
ATOM    320  O   SER B  40     -16.413  44.357 109.994  1.00 38.66           O  
ANISOU  320  O   SER B  40     5872   6076   2741   -253   1136    160       O  
ATOM    321  CB  SER B  40     -14.410  42.930 111.719  1.00 46.47           C  
ANISOU  321  CB  SER B  40     7117   6994   3547   -506    898    259       C  
ATOM    322  OG  SER B  40     -14.027  41.695 112.304  1.00 51.78           O  
ANISOU  322  OG  SER B  40     7786   7697   4189   -643    833    431       O  
ATOM    323  N   PRO B  41     -16.574  45.633 111.842  1.00 47.83           N  
ANISOU  323  N   PRO B  41     7333   7373   3467      7   1306     11       N  
ATOM    324  CA  PRO B  41     -16.802  46.851 111.048  1.00 45.77           C  
ANISOU  324  CA  PRO B  41     7130   6994   3268    184   1345   -148       C  
ATOM    325  C   PRO B  41     -15.650  47.185 110.089  1.00 42.25           C  
ANISOU  325  C   PRO B  41     6778   6262   3015     70   1142   -269       C  
ATOM    326  O   PRO B  41     -15.876  47.802 109.051  1.00 50.87           O  
ANISOU  326  O   PRO B  41     7826   7254   4248    150   1149   -327       O  
ATOM    327  CB  PRO B  41     -16.955  47.941 112.118  1.00 47.00           C  
ANISOU  327  CB  PRO B  41     7557   7178   3125    408   1466   -299       C  
ATOM    328  CG  PRO B  41     -17.424  47.230 113.303  1.00 50.40           C  
ANISOU  328  CG  PRO B  41     7937   7866   3348    407   1578   -162       C  
ATOM    329  CD  PRO B  41     -16.730  45.899 113.281  1.00 47.07           C  
ANISOU  329  CD  PRO B  41     7401   7425   3056    118   1415    -11       C  
ATOM    330  N   GLU B  42     -14.438  46.746 110.427  1.00 44.63           N  
ANISOU  330  N   GLU B  42     7183   6462   3313   -108    966   -283       N  
ATOM    331  CA  GLU B  42     -13.262  46.861 109.554  1.00 39.72           C  
ANISOU  331  CA  GLU B  42     6596   5627   2870   -239    770   -350       C  
ATOM    332  C   GLU B  42     -13.434  46.090 108.237  1.00 37.98           C  
ANISOU  332  C   GLU B  42     6136   5374   2920   -315    729   -240       C  
ATOM    333  O   GLU B  42     -12.808  46.415 107.229  1.00 32.74           O  
ANISOU  333  O   GLU B  42     5468   4557   2415   -353    626   -300       O  
ATOM    334  CB  GLU B  42     -12.008  46.347 110.274  1.00 45.45           C  
ANISOU  334  CB  GLU B  42     7419   6332   3517   -400    601   -334       C  
ATOM    335  CG  GLU B  42     -11.568  47.178 111.498  1.00 52.68           C  
ANISOU  335  CG  GLU B  42     8609   7253   4155   -373    580   -472       C  
ATOM    336  CD  GLU B  42     -12.303  46.822 112.795  1.00 58.08           C  
ANISOU  336  CD  GLU B  42     9335   8143   4590   -288    720   -406       C  
ATOM    337  OE1 GLU B  42     -11.820  47.207 113.882  1.00 60.51           O  
ANISOU  337  OE1 GLU B  42     9861   8479   4649   -296    674   -493       O  
ATOM    338  OE2 GLU B  42     -13.369  46.168 112.733  1.00 57.81           O1-
ANISOU  338  OE2 GLU B  42     9113   8257   4593   -226    872   -262       O1-
ATOM    339  N   ALA B  43     -14.270  45.058 108.257  1.00 36.10           N  
ANISOU  339  N   ALA B  43     5711   5284   2721   -354    805    -76       N  
ATOM    340  CA  ALA B  43     -14.608  44.315 107.051  1.00 31.86           C  
ANISOU  340  CA  ALA B  43     4975   4722   2409   -435    770     18       C  
ATOM    341  C   ALA B  43     -15.402  45.145 106.023  1.00 31.62           C  
ANISOU  341  C   ALA B  43     4846   4694   2474   -306    848    -40       C  
ATOM    342  O   ALA B  43     -15.330  44.864 104.831  1.00 23.85           O  
ANISOU  342  O   ALA B  43     3755   3631   1676   -363    774    -24       O  
ATOM    343  CB  ALA B  43     -15.374  43.058 107.418  1.00 31.54           C  
ANISOU  343  CB  ALA B  43     4788   4833   2361   -545    826    212       C  
ATOM    344  N   GLU B  44     -16.137  46.159 106.481  1.00 28.56           N  
ANISOU  344  N   GLU B  44     4510   4398   1946   -110    998   -104       N  
ATOM    345  CA  GLU B  44     -16.973  46.968 105.596  1.00 30.80           C  
ANISOU  345  CA  GLU B  44     4699   4709   2294     58   1088   -136       C  
ATOM    346  C   GLU B  44     -16.152  47.745 104.580  1.00 30.26           C  
ANISOU  346  C   GLU B  44     4742   4400   2356     72    976   -263       C  
ATOM    347  O   GLU B  44     -16.467  47.729 103.389  1.00 23.64           O  
ANISOU  347  O   GLU B  44     3758   3548   1675     80    954   -232       O  
ATOM    348  CB  GLU B  44     -17.825  47.955 106.385  1.00 36.42           C  
ANISOU  348  CB  GLU B  44     5491   5549   2797    320   1283   -185       C  
ATOM    349  CG  GLU B  44     -18.880  47.314 107.267  1.00 45.31           C  
ANISOU  349  CG  GLU B  44     6449   6984   3784    349   1439    -30       C  
ATOM    350  CD  GLU B  44     -19.852  48.331 107.840  1.00 49.93           C  
ANISOU  350  CD  GLU B  44     7074   7733   4164    674   1660    -66       C  
ATOM    351  OE1 GLU B  44     -20.914  47.914 108.346  1.00 59.39           O  
ANISOU  351  OE1 GLU B  44     8063   9244   5258    737   1819     89       O  
ATOM    352  OE2 GLU B  44     -19.560  49.547 107.779  1.00 55.78           O1-
ANISOU  352  OE2 GLU B  44     8063   8290   4842    870   1680   -240       O1-
ATOM    353  N   GLU B  45     -15.115  48.443 105.042  1.00 31.80           N  
ANISOU  353  N   GLU B  45     5192   4418   2474     60    901   -397       N  
ATOM    354  CA  GLU B  45     -14.253  49.176 104.101  1.00 35.33           C  
ANISOU  354  CA  GLU B  45     5740   4642   3041     33    788   -494       C  
ATOM    355  C   GLU B  45     -13.452  48.230 103.192  1.00 32.17           C  
ANISOU  355  C   GLU B  45     5199   4192   2832   -155    634   -423       C  
ATOM    356  O   GLU B  45     -13.263  48.533 102.018  1.00 26.91           O  
ANISOU  356  O   GLU B  45     4484   3434   2307   -148    588   -436       O  
ATOM    357  CB  GLU B  45     -13.345  50.197 104.814  1.00 41.51           C  
ANISOU  357  CB  GLU B  45     6834   5254   3686     23    730   -647       C  
ATOM    358  CG  GLU B  45     -12.206  49.621 105.632  1.00 44.87           C  
ANISOU  358  CG  GLU B  45     7333   5675   4042   -176    589   -646       C  
ATOM    359  CD  GLU B  45     -11.674  50.617 106.660  1.00 49.59           C  
ANISOU  359  CD  GLU B  45     8245   6169   4427   -177    559   -797       C  
ATOM    360  OE1 GLU B  45     -11.611  50.252 107.851  1.00 51.56           O  
ANISOU  360  OE1 GLU B  45     8568   6528   4496   -204    565   -794       O  
ATOM    361  OE2 GLU B  45     -11.342  51.768 106.284  1.00 53.45           O1-
ANISOU  361  OE2 GLU B  45     8929   6463   4917   -159    527   -916       O1-
ATOM    362  N   LYS B  46     -13.017  47.079 103.715  1.00 30.31           N  
ANISOU  362  N   LYS B  46     4911   4019   2588   -297    565   -340       N  
ATOM    363  CA  LYS B  46     -12.313  46.086 102.898  1.00 26.47           C  
ANISOU  363  CA  LYS B  46     4316   3483   2260   -429    437   -267       C  
ATOM    364  C   LYS B  46     -13.213  45.515 101.812  1.00 23.03           C  
ANISOU  364  C   LYS B  46     3690   3097   1962   -420    471   -192       C  
ATOM    365  O   LYS B  46     -12.789  45.330 100.660  1.00 21.66           O  
ANISOU  365  O   LYS B  46     3462   2840   1927   -450    390   -194       O  
ATOM    366  CB  LYS B  46     -11.791  44.933 103.746  1.00 32.55           C  
ANISOU  366  CB  LYS B  46     5094   4301   2975   -544    374   -177       C  
ATOM    367  CG  LYS B  46     -10.741  45.334 104.749  1.00 38.32           C  
ANISOU  367  CG  LYS B  46     5985   5008   3565   -584    298   -235       C  
ATOM    368  CD  LYS B  46     -10.121  44.113 105.394  1.00 39.80           C  
ANISOU  368  CD  LYS B  46     6161   5246   3717   -677    218   -119       C  
ATOM    369  CE  LYS B  46      -8.889  43.655 104.633  1.00 44.73           C  
ANISOU  369  CE  LYS B  46     6742   5792   4461   -730     72    -88       C  
ATOM    370  NZ  LYS B  46      -7.706  44.471 105.009  1.00 48.46           N1+
ANISOU  370  NZ  LYS B  46     7303   6256   4854   -775    -35   -161       N1+
ATOM    371  N   PHE B  47     -14.459  45.234 102.175  1.00 21.43           N  
ANISOU  371  N   PHE B  47     3380   3054   1708   -386    588   -119       N  
ATOM    372  CA  PHE B  47     -15.432  44.730 101.196  1.00 17.56           C  
ANISOU  372  CA  PHE B  47     2693   2651   1328   -407    609    -40       C  
ATOM    373  C   PHE B  47     -15.755  45.777 100.134  1.00 19.61           C  
ANISOU  373  C   PHE B  47     2912   2885   1654   -266    636   -107       C  
ATOM    374  O   PHE B  47     -15.876  45.447  98.958  1.00 16.44           O  
ANISOU  374  O   PHE B  47     2405   2466   1376   -306    573    -84       O  
ATOM    375  CB  PHE B  47     -16.699  44.286 101.917  1.00 20.00           C  
ANISOU  375  CB  PHE B  47     2866   3186   1546   -418    732     77       C  
ATOM    376  CG  PHE B  47     -17.655  43.502 101.072  1.00 21.55           C  
ANISOU  376  CG  PHE B  47     2847   3500   1841   -525    719    190       C  
ATOM    377  CD1 PHE B  47     -17.231  42.409 100.329  1.00 29.05           C  
ANISOU  377  CD1 PHE B  47     3796   4328   2913   -706    580    225       C  
ATOM    378  CD2 PHE B  47     -18.999  43.830 101.059  1.00 21.33           C  
ANISOU  378  CD2 PHE B  47     2620   3719   1765   -444    845    267       C  
ATOM    379  CE1 PHE B  47     -18.151  41.677  99.557  1.00 24.27           C  
ANISOU  379  CE1 PHE B  47     3020   3822   2380   -842    548    319       C  
ATOM    380  CE2 PHE B  47     -19.910  43.093 100.301  1.00 23.99           C  
ANISOU  380  CE2 PHE B  47     2736   4199   2179   -586    812    384       C  
ATOM    381  CZ  PHE B  47     -19.478  42.025  99.562  1.00 26.96           C  
ANISOU  381  CZ  PHE B  47     3142   4426   2675   -802    655    401       C  
ATOM    382  N   LYS B  48     -15.875  47.037 100.552  1.00 18.72           N  
ANISOU  382  N   LYS B  48     2913   2754   1445    -93    727   -191       N  
ATOM    383  CA  LYS B  48     -16.117  48.135  99.621  1.00 20.60           C  
ANISOU  383  CA  LYS B  48     3161   2934   1731     66    759   -248       C  
ATOM    384  C   LYS B  48     -15.001  48.222  98.577  1.00 18.23           C  
ANISOU  384  C   LYS B  48     2918   2447   1562    -17    620   -296       C  
ATOM    385  O   LYS B  48     -15.256  48.391  97.382  1.00 17.58           O  
ANISOU  385  O   LYS B  48     2740   2362   1578     27    600   -278       O  
ATOM    386  CB  LYS B  48     -16.217  49.462 100.378  1.00 21.70           C  
ANISOU  386  CB  LYS B  48     3505   3013   1727    260    866   -347       C  
ATOM    387  CG  LYS B  48     -16.598  50.657  99.507  1.00 33.19           C  
ANISOU  387  CG  LYS B  48     5004   4393   3213    463    922   -389       C  
ATOM    388  CD  LYS B  48     -16.202  52.008 100.131  1.00 38.29           C  
ANISOU  388  CD  LYS B  48     5974   4840   3733    602    972   -524       C  
ATOM    389  CE  LYS B  48     -17.224  52.503 101.134  1.00 42.78           C  
ANISOU  389  CE  LYS B  48     6605   5536   4113    843   1155   -537       C  
ATOM    390  NZ  LYS B  48     -17.046  53.959 101.439  1.00 48.57           N1+
ANISOU  390  NZ  LYS B  48     7689   6038   4728   1038   1215   -676       N1+
ATOM    391  N   GLU B  49     -13.760  48.102  99.032  1.00 16.40           N  
ANISOU  391  N   GLU B  49     2826   2089   1318   -132    526   -342       N  
ATOM    392  CA  GLU B  49     -12.609  48.187  98.125  1.00 20.64           C  
ANISOU  392  CA  GLU B  49     3395   2489   1960   -208    405   -366       C  
ATOM    393  C   GLU B  49     -12.588  47.007  97.156  1.00 20.02           C  
ANISOU  393  C   GLU B  49     3157   2451   1998   -286    334   -292       C  
ATOM    394  O   GLU B  49     -12.321  47.153  95.964  1.00 15.17           O  
ANISOU  394  O   GLU B  49     2498   1789   1475   -267    289   -293       O  
ATOM    395  CB  GLU B  49     -11.309  48.246  98.940  1.00 20.78           C  
ANISOU  395  CB  GLU B  49     3555   2424   1916   -321    316   -406       C  
ATOM    396  CG  GLU B  49     -11.139  49.509  99.756  1.00 26.57           C  
ANISOU  396  CG  GLU B  49     4503   3067   2524   -279    350   -506       C  
ATOM    397  CD  GLU B  49     -10.487  50.661  99.016  1.00 27.10           C  
ANISOU  397  CD  GLU B  49     4686   2972   2639   -284    305   -562       C  
ATOM    398  OE1 GLU B  49     -10.160  51.664  99.681  1.00 31.34           O  
ANISOU  398  OE1 GLU B  49     5446   3391   3070   -298    301   -652       O  
ATOM    399  OE2 GLU B  49     -10.284  50.584  97.794  1.00 24.97           O1-
ANISOU  399  OE2 GLU B  49     4307   2684   2498   -286    271   -517       O1-
ATOM    400  N   ILE B  50     -12.857  45.814  97.674  1.00 13.81           N  
ANISOU  400  N   ILE B  50     2311   1740   1197   -375    321   -226       N  
ATOM    401  CA  ILE B  50     -12.933  44.629  96.857  1.00 12.82           C  
ANISOU  401  CA  ILE B  50     2091   1620   1160   -457    252   -166       C  
ATOM    402  C   ILE B  50     -14.056  44.752  95.806  1.00 15.18           C  
ANISOU  402  C   ILE B  50     2250   2003   1514   -413    284   -146       C  
ATOM    403  O   ILE B  50     -13.881  44.357  94.661  1.00 14.90           O  
ANISOU  403  O   ILE B  50     2177   1929   1555   -434    212   -147       O  
ATOM    404  CB  ILE B  50     -13.085  43.390  97.782  1.00 21.87           C  
ANISOU  404  CB  ILE B  50     3244   2803   2261   -574    240    -88       C  
ATOM    405  CG1 ILE B  50     -11.748  43.132  98.495  1.00 19.39           C  
ANISOU  405  CG1 ILE B  50     3054   2407   1907   -604    171    -93       C  
ATOM    406  CG2 ILE B  50     -13.514  42.178  97.029  1.00 20.47           C  
ANISOU  406  CG2 ILE B  50     3004   2617   2156   -674    182    -26       C  
ATOM    407  CD1 ILE B  50     -11.898  42.381  99.821  1.00 24.05           C  
ANISOU  407  CD1 ILE B  50     3688   3050   2400   -675    192    -20       C  
ATOM    408  N   ASN B  51     -15.186  45.338  96.183  1.00 11.73           N  
ANISOU  408  N   ASN B  51     1735   1702   1020   -332    393   -126       N  
ATOM    409  CA  ASN B  51     -16.313  45.487  95.242  1.00 12.08           C  
ANISOU  409  CA  ASN B  51     1610   1881   1099   -279    419    -84       C  
ATOM    410  C   ASN B  51     -16.008  46.477  94.138  1.00 12.40           C  
ANISOU  410  C   ASN B  51     1675   1846   1190   -148    405   -138       C  
ATOM    411  O   ASN B  51     -16.383  46.257  92.981  1.00 15.00           O  
ANISOU  411  O   ASN B  51     1898   2227   1575   -154    354   -114       O  
ATOM    412  CB  ASN B  51     -17.586  45.881  95.970  1.00 16.33           C  
ANISOU  412  CB  ASN B  51     2028   2628   1547   -188    555    -24       C  
ATOM    413  CG  ASN B  51     -18.227  44.715  96.640  1.00 20.39           C  
ANISOU  413  CG  ASN B  51     2436   3283   2030   -358    559     79       C  
ATOM    414  ND2 ASN B  51     -18.844  44.947  97.781  1.00 23.24           N  
ANISOU  414  ND2 ASN B  51     2763   3791   2278   -297    686    127       N  
ATOM    415  OD1 ASN B  51     -18.159  43.600  96.134  1.00 24.57           O  
ANISOU  415  OD1 ASN B  51     2931   3778   2625   -546    451    119       O  
ATOM    416  N   GLU B  52     -15.349  47.573  94.507  1.00 12.36           N  
ANISOU  416  N   GLU B  52     1824   1718   1153    -44    445   -206       N  
ATOM    417  CA  GLU B  52     -14.907  48.544  93.512  1.00 15.17           C  
ANISOU  417  CA  GLU B  52     2239   1969   1555     55    429   -241       C  
ATOM    418  C   GLU B  52     -13.940  47.915  92.526  1.00 15.54           C  
ANISOU  418  C   GLU B  52     2281   1938   1686    -48    310   -243       C  
ATOM    419  O   GLU B  52     -14.115  48.047  91.312  1.00 14.46           O  
ANISOU  419  O   GLU B  52     2076   1823   1595      1    283   -225       O  
ATOM    420  CB  GLU B  52     -14.268  49.750  94.188  1.00 11.07           C  
ANISOU  420  CB  GLU B  52     1929   1296    980    126    473   -312       C  
ATOM    421  CG  GLU B  52     -13.783  50.820  93.196  1.00 14.67           C  
ANISOU  421  CG  GLU B  52     2473   1619   1482    203    458   -330       C  
ATOM    422  CD  GLU B  52     -13.183  52.045  93.869  1.00 16.04           C  
ANISOU  422  CD  GLU B  52     2896   1606   1593    233    487   -401       C  
ATOM    423  OE1 GLU B  52     -13.714  52.501  94.904  1.00 19.77           O  
ANISOU  423  OE1 GLU B  52     3478   2073   1962    324    573   -446       O  
ATOM    424  OE2 GLU B  52     -12.178  52.580  93.333  1.00 17.66           O1-
ANISOU  424  OE2 GLU B  52     3198   1669   1842    160    421   -409       O1-
ATOM    425  N   ALA B  53     -12.942  47.194  93.037  1.00 12.16           N  
ANISOU  425  N   ALA B  53     1919   1439   1261   -169    244   -255       N  
ATOM    426  CA  ALA B  53     -11.990  46.493  92.177  1.00 11.04           C  
ANISOU  426  CA  ALA B  53     1774   1244   1178   -228    148   -248       C  
ATOM    427  C   ALA B  53     -12.676  45.515  91.228  1.00 11.93           C  
ANISOU  427  C   ALA B  53     1786   1424   1324   -256    103   -222       C  
ATOM    428  O   ALA B  53     -12.326  45.424  90.043  1.00 13.42           O  
ANISOU  428  O   ALA B  53     1960   1593   1544   -224     54   -227       O  
ATOM    429  CB  ALA B  53     -10.896  45.785  93.015  1.00 11.13           C  
ANISOU  429  CB  ALA B  53     1858   1201   1168   -320     93   -245       C  
ATOM    430  N   TYR B  54     -13.651  44.773  91.749  1.00 11.78           N  
ANISOU  430  N   TYR B  54     1704   1488   1283   -331    115   -189       N  
ATOM    431  CA  TYR B  54     -14.365  43.789  90.968  1.00 12.56           C  
ANISOU  431  CA  TYR B  54     1727   1646   1400   -415     51   -164       C  
ATOM    432  C   TYR B  54     -15.289  44.451  89.947  1.00 13.19           C  
ANISOU  432  C   TYR B  54     1677   1849   1484   -335     64   -152       C  
ATOM    433  O   TYR B  54     -15.385  43.997  88.817  1.00 16.72           O  
ANISOU  433  O   TYR B  54     2102   2307   1944   -362    -16   -161       O  
ATOM    434  CB  TYR B  54     -15.138  42.877  91.894  1.00 14.14           C  
ANISOU  434  CB  TYR B  54     1890   1911   1571   -557     57   -107       C  
ATOM    435  CG  TYR B  54     -15.806  41.715  91.207  1.00 16.94           C  
ANISOU  435  CG  TYR B  54     2206   2292   1938   -712    -35    -79       C  
ATOM    436  CD1 TYR B  54     -15.049  40.753  90.532  1.00 20.33           C  
ANISOU  436  CD1 TYR B  54     2778   2560   2387   -764   -138   -120       C  
ATOM    437  CD2 TYR B  54     -17.184  41.550  91.265  1.00 20.92           C  
ANISOU  437  CD2 TYR B  54     2543   2986   2421   -812    -22     -6       C  
ATOM    438  CE1 TYR B  54     -15.660  39.664  89.927  1.00 22.70           C  
ANISOU  438  CE1 TYR B  54     3101   2842   2681   -928   -238   -111       C  
ATOM    439  CE2 TYR B  54     -17.802  40.479  90.654  1.00 22.25           C  
ANISOU  439  CE2 TYR B  54     2688   3174   2590  -1008   -130     22       C  
ATOM    440  CZ  TYR B  54     -17.026  39.535  89.991  1.00 22.50           C  
ANISOU  440  CZ  TYR B  54     2913   2997   2639  -1074   -244    -42       C  
ATOM    441  OH  TYR B  54     -17.635  38.459  89.390  1.00 27.91           O  
ANISOU  441  OH  TYR B  54     3632   3661   3311  -1287   -365    -32       O  
ATOM    442  N   ALA B  55     -15.927  45.552  90.333  1.00 14.64           N  
ANISOU  442  N   ALA B  55     1797   2126   1642   -213    164   -131       N  
ATOM    443  CA  ALA B  55     -16.791  46.299  89.414  1.00 15.87           C  
ANISOU  443  CA  ALA B  55     1827   2413   1790    -90    187    -99       C  
ATOM    444  C   ALA B  55     -16.048  46.709  88.159  1.00 15.72           C  
ANISOU  444  C   ALA B  55     1868   2303   1802    -17    135   -130       C  
ATOM    445  O   ALA B  55     -16.611  46.688  87.062  1.00 19.40           O  
ANISOU  445  O   ALA B  55     2236   2875   2261     12     89   -105       O  
ATOM    446  CB  ALA B  55     -17.341  47.522  90.090  1.00 16.51           C  
ANISOU  446  CB  ALA B  55     1895   2552   1827     90    320    -79       C  
ATOM    447  N   VAL B  56     -14.792  47.108  88.329  1.00 12.71           N  
ANISOU  447  N   VAL B  56     1636   1752   1443      5    141   -173       N  
ATOM    448  CA  VAL B  56     -13.938  47.524  87.213  1.00 13.68           C  
ANISOU  448  CA  VAL B  56     1811   1801   1587     65    106   -181       C  
ATOM    449  C   VAL B  56     -13.355  46.310  86.471  1.00 17.27           C  
ANISOU  449  C   VAL B  56     2281   2233   2046    -22      7   -205       C  
ATOM    450  O   VAL B  56     -13.461  46.218  85.248  1.00 17.17           O  
ANISOU  450  O   VAL B  56     2237   2269   2018     20    -39   -202       O  
ATOM    451  CB  VAL B  56     -12.809  48.470  87.691  1.00 15.53           C  
ANISOU  451  CB  VAL B  56     2178   1888   1833     93    147   -195       C  
ATOM    452  CG1 VAL B  56     -11.884  48.846  86.543  1.00 13.68           C  
ANISOU  452  CG1 VAL B  56     1973   1609   1617    130    117   -174       C  
ATOM    453  CG2 VAL B  56     -13.384  49.724  88.292  1.00 16.35           C  
ANISOU  453  CG2 VAL B  56     2333   1967   1913    202    243   -190       C  
ATOM    454  N   LEU B  57     -12.739  45.378  87.195  1.00 11.88           N  
ANISOU  454  N   LEU B  57     1668   1476   1369   -121    -25   -228       N  
ATOM    455  CA  LEU B  57     -12.012  44.287  86.536  1.00 10.54           C  
ANISOU  455  CA  LEU B  57     1566   1250   1191   -151   -104   -254       C  
ATOM    456  C   LEU B  57     -12.880  43.188  85.932  1.00 13.21           C  
ANISOU  456  C   LEU B  57     1895   1623   1501   -237   -185   -275       C  
ATOM    457  O   LEU B  57     -12.412  42.489  85.018  1.00 16.46           O  
ANISOU  457  O   LEU B  57     2388   1986   1881   -217   -249   -314       O  
ATOM    458  CB  LEU B  57     -10.953  43.685  87.465  1.00 13.14           C  
ANISOU  458  CB  LEU B  57     1986   1482   1524   -190   -111   -256       C  
ATOM    459  CG  LEU B  57      -9.849  44.626  87.954  1.00 11.24           C  
ANISOU  459  CG  LEU B  57     1761   1215   1295   -146    -68   -234       C  
ATOM    460  CD1 LEU B  57      -8.830  43.899  88.831  1.00 12.01           C  
ANISOU  460  CD1 LEU B  57     1920   1264   1380   -181    -94   -219       C  
ATOM    461  CD2 LEU B  57      -9.142  45.291  86.788  1.00 12.78           C  
ANISOU  461  CD2 LEU B  57     1935   1429   1491    -54    -62   -215       C  
ATOM    462  N   SER B  58     -14.108  43.018  86.435  1.00 14.87           N  
ANISOU  462  N   SER B  58     2016   1926   1710   -338   -185   -248       N  
ATOM    463  CA  SER B  58     -14.949  41.884  86.041  1.00 14.18           C  
ANISOU  463  CA  SER B  58     1924   1870   1593   -494   -283   -256       C  
ATOM    464  C   SER B  58     -15.675  42.121  84.721  1.00 15.47           C  
ANISOU  464  C   SER B  58     1997   2164   1717   -473   -344   -262       C  
ATOM    465  O   SER B  58     -16.159  41.182  84.099  1.00 18.62           O  
ANISOU  465  O   SER B  58     2432   2569   2073   -608   -456   -291       O  
ATOM    466  CB  SER B  58     -15.975  41.571  87.121  1.00 17.12           C  
ANISOU  466  CB  SER B  58     2202   2333   1970   -641   -261   -193       C  
ATOM    467  OG  SER B  58     -16.941  42.591  87.216  1.00 18.66           O  
ANISOU  467  OG  SER B  58     2205   2728   2159   -570   -189   -136       O  
ATOM    468  N   ASP B  59     -15.730  43.376  84.295  1.00 17.12           N  
ANISOU  468  N   ASP B  59     2110   2466   1929   -309   -278   -234       N  
ATOM    469  CA  ASP B  59     -16.312  43.715  83.013  1.00 18.45           C  
ANISOU  469  CA  ASP B  59     2193   2771   2048   -253   -331   -224       C  
ATOM    470  C   ASP B  59     -15.142  44.002  82.088  1.00 17.82           C  
ANISOU  470  C   ASP B  59     2231   2591   1949   -115   -327   -264       C  
ATOM    471  O   ASP B  59     -14.451  44.989  82.268  1.00 18.00           O  
ANISOU  471  O   ASP B  59     2266   2567   2006     14   -236   -234       O  
ATOM    472  CB  ASP B  59     -17.217  44.935  83.136  1.00 21.06           C  
ANISOU  472  CB  ASP B  59     2342   3278   2382   -132   -250   -140       C  
ATOM    473  CG  ASP B  59     -17.943  45.235  81.857  1.00 26.92           C  
ANISOU  473  CG  ASP B  59     2969   4200   3060    -73   -315   -106       C  
ATOM    474  OD1 ASP B  59     -17.276  45.541  80.851  1.00 27.77           O  
ANISOU  474  OD1 ASP B  59     3157   4258   3138     32   -333   -130       O  
ATOM    475  OD2 ASP B  59     -19.187  45.170  81.858  1.00 36.95           O1-
ANISOU  475  OD2 ASP B  59     4052   5690   4298   -132   -349    -42       O1-
ATOM    476  N   PRO B  60     -14.896  43.126  81.109  1.00 16.27           N  
ANISOU  476  N   PRO B  60     2137   2361   1685   -149   -426   -328       N  
ATOM    477  CA  PRO B  60     -13.725  43.304  80.257  1.00 17.77           C  
ANISOU  477  CA  PRO B  60     2432   2483   1837     -1   -406   -354       C  
ATOM    478  C   PRO B  60     -13.584  44.692  79.623  1.00 15.49           C  
ANISOU  478  C   PRO B  60     2052   2287   1546    163   -332   -281       C  
ATOM    479  O   PRO B  60     -12.456  45.186  79.476  1.00 15.40           O  
ANISOU  479  O   PRO B  60     2091   2214   1547    268   -264   -257       O  
ATOM    480  CB  PRO B  60     -13.950  42.283  79.162  1.00 19.69           C  
ANISOU  480  CB  PRO B  60     2780   2730   1971    -50   -530   -435       C  
ATOM    481  CG  PRO B  60     -14.784  41.244  79.749  1.00 23.44           C  
ANISOU  481  CG  PRO B  60     3285   3169   2451   -269   -621   -468       C  
ATOM    482  CD  PRO B  60     -15.659  41.919  80.743  1.00 17.89           C  
ANISOU  482  CD  PRO B  60     2383   2583   1829   -333   -563   -379       C  
ATOM    483  N   GLU B  61     -14.694  45.314  79.244  1.00 19.18           N  
ANISOU  483  N   GLU B  61     2385   2910   1994    185   -346   -230       N  
ATOM    484  CA  GLU B  61     -14.625  46.649  78.641  1.00 18.15           C  
ANISOU  484  CA  GLU B  61     2197   2844   1856    355   -274   -145       C  
ATOM    485  C   GLU B  61     -14.179  47.730  79.632  1.00 17.18           C  
ANISOU  485  C   GLU B  61     2087   2618   1825    416   -150    -90       C  
ATOM    486  O   GLU B  61     -13.358  48.586  79.299  1.00 21.47           O  
ANISOU  486  O   GLU B  61     2684   3097   2378    510    -87    -40       O  
ATOM    487  CB  GLU B  61     -15.959  47.035  78.010  1.00 22.44           C  
ANISOU  487  CB  GLU B  61     2589   3595   2342    395   -321    -87       C  
ATOM    488  CG  GLU B  61     -15.900  48.369  77.282  1.00 24.00           C  
ANISOU  488  CG  GLU B  61     2757   3845   2518    594   -252     14       C  
ATOM    489  CD  GLU B  61     -16.753  48.423  76.024  1.00 25.50           C  
ANISOU  489  CD  GLU B  61     2845   4251   2591    657   -340     58       C  
ATOM    490  OE1 GLU B  61     -17.912  47.932  76.020  1.00 26.60           O  
ANISOU  490  OE1 GLU B  61     2846   4570   2690    569   -431     58       O  
ATOM    491  OE2 GLU B  61     -16.258  48.970  75.014  1.00 23.79           O1-
ANISOU  491  OE2 GLU B  61     2677   4049   2312    785   -323    106       O1-
ATOM    492  N   LYS B  62     -14.723  47.690  80.844  1.00 16.28           N  
ANISOU  492  N   LYS B  62     1934   2486   1764    349   -119    -96       N  
ATOM    493  CA  LYS B  62     -14.297  48.595  81.907  1.00 16.14           C  
ANISOU  493  CA  LYS B  62     1973   2350   1810    388    -16    -73       C  
ATOM    494  C   LYS B  62     -12.825  48.347  82.261  1.00 15.13           C  
ANISOU  494  C   LYS B  62     1964   2070   1713    327     -8   -106       C  
ATOM    495  O   LYS B  62     -12.057  49.285  82.516  1.00 12.83           O  
ANISOU  495  O   LYS B  62     1741   1682   1451    360     53    -71       O  
ATOM    496  CB  LYS B  62     -15.173  48.405  83.164  1.00 14.98           C  
ANISOU  496  CB  LYS B  62     1766   2241   1684    330     16    -82       C  
ATOM    497  CG  LYS B  62     -16.686  48.521  82.966  1.00 21.76           C  
ANISOU  497  CG  LYS B  62     2453   3312   2504    381     11    -26       C  
ATOM    498  CD  LYS B  62     -17.081  49.850  82.350  1.00 22.57           C  
ANISOU  498  CD  LYS B  62     2527   3466   2583    597     76     53       C  
ATOM    499  CE  LYS B  62     -18.564  50.138  82.577  1.00 23.09           C  
ANISOU  499  CE  LYS B  62     2406   3758   2609    696    111    129       C  
ATOM    500  NZ  LYS B  62     -19.458  49.080  82.025  1.00 25.12           N1+
ANISOU  500  NZ  LYS B  62     2473   4251   2820    557    -10    145       N1+
ATOM    501  N   ARG B  63     -12.434  47.073  82.300  1.00 12.75           N  
ANISOU  501  N   ARG B  63     1694   1752   1400    233    -74   -164       N  
ATOM    502  CA  ARG B  63     -11.051  46.698  82.576  1.00 10.13           C  
ANISOU  502  CA  ARG B  63     1445   1323   1081    209    -70   -178       C  
ATOM    503  C   ARG B  63     -10.092  47.295  81.558  1.00 11.30           C  
ANISOU  503  C   ARG B  63     1604   1486   1203    302    -45   -126       C  
ATOM    504  O   ARG B  63      -9.036  47.781  81.917  1.00 13.48           O  
ANISOU  504  O   ARG B  63     1902   1715   1506    290     -6    -83       O  
ATOM    505  CB  ARG B  63     -10.908  45.177  82.580  1.00 11.70           C  
ANISOU  505  CB  ARG B  63     1701   1495   1249    144   -144   -243       C  
ATOM    506  CG  ARG B  63      -9.544  44.710  82.896  1.00 10.80           C  
ANISOU  506  CG  ARG B  63     1656   1311   1136    162   -135   -242       C  
ATOM    507  CD  ARG B  63      -9.452  43.225  82.749  1.00 13.61           C  
ANISOU  507  CD  ARG B  63     2114   1611   1446    145   -202   -304       C  
ATOM    508  NE  ARG B  63      -8.133  42.744  83.080  1.00 11.93           N  
ANISOU  508  NE  ARG B  63     1958   1352   1223    209   -185   -286       N  
ATOM    509  CZ  ARG B  63      -7.766  41.463  82.967  1.00 14.40           C  
ANISOU  509  CZ  ARG B  63     2399   1588   1484    252   -226   -329       C  
ATOM    510  NH1 ARG B  63      -6.546  41.100  83.302  1.00 14.39           N1+
ANISOU  510  NH1 ARG B  63     2424   1577   1467    349   -199   -290       N1+
ATOM    511  NH2 ARG B  63      -8.618  40.547  82.563  1.00 13.57           N  
ANISOU  511  NH2 ARG B  63     2405   1414   1338    196   -299   -405       N  
ATOM    512  N   ARG B  64     -10.482  47.264  80.283  1.00 12.00           N  
ANISOU  512  N   ARG B  64     1668   1664   1227    382    -72   -118       N  
ATOM    513  CA  ARG B  64      -9.679  47.886  79.228  1.00 13.14           C  
ANISOU  513  CA  ARG B  64     1813   1852   1329    480    -36    -47       C  
ATOM    514  C   ARG B  64      -9.466  49.390  79.465  1.00 15.15           C  
ANISOU  514  C   ARG B  64     2064   2056   1636    492     40     50       C  
ATOM    515  O   ARG B  64      -8.370  49.919  79.246  1.00 13.99           O  
ANISOU  515  O   ARG B  64     1929   1895   1492    489     81    127       O  
ATOM    516  CB  ARG B  64     -10.351  47.690  77.880  1.00 14.41           C  
ANISOU  516  CB  ARG B  64     1953   2129   1392    565    -83    -54       C  
ATOM    517  CG  ARG B  64      -9.616  48.367  76.734  1.00 15.12           C  
ANISOU  517  CG  ARG B  64     2039   2287   1418    679    -35     38       C  
ATOM    518  CD  ARG B  64     -10.282  48.109  75.397  1.00 15.37           C  
ANISOU  518  CD  ARG B  64     2063   2451   1326    768    -92     24       C  
ATOM    519  NE  ARG B  64     -11.671  48.542  75.355  1.00 17.60           N  
ANISOU  519  NE  ARG B  64     2278   2797   1614    768   -133     36       N  
ATOM    520  CZ  ARG B  64     -12.094  49.791  75.194  1.00 18.74           C  
ANISOU  520  CZ  ARG B  64     2377   2964   1780    848    -80    147       C  
ATOM    521  NH1 ARG B  64     -13.392  49.987  75.156  1.00 18.70           N1+
ANISOU  521  NH1 ARG B  64     2288   3056   1761    875   -121    158       N1+
ATOM    522  NH2 ARG B  64     -11.257  50.825  75.076  1.00 16.47           N  
ANISOU  522  NH2 ARG B  64     2128   2607   1522    898     11    256       N  
ATOM    523  N   ILE B  65     -10.515  50.078  79.884  1.00 15.94           N  
ANISOU  523  N   ILE B  65     2157   2132   1767    509     59     57       N  
ATOM    524  CA  ILE B  65     -10.449  51.520  80.176  1.00 16.90           C  
ANISOU  524  CA  ILE B  65     2340   2154   1929    538    130    134       C  
ATOM    525  C   ILE B  65      -9.463  51.782  81.302  1.00 12.06           C  
ANISOU  525  C   ILE B  65     1801   1409   1370    411    151    125       C  
ATOM    526  O   ILE B  65      -8.551  52.609  81.188  1.00 18.35           O  
ANISOU  526  O   ILE B  65     2655   2136   2181    364    179    201       O  
ATOM    527  CB  ILE B  65     -11.852  52.105  80.533  1.00 23.73           C  
ANISOU  527  CB  ILE B  65     3192   3025   2798    629    158    135       C  
ATOM    528  CG1 ILE B  65     -12.825  51.940  79.358  1.00 26.76           C  
ANISOU  528  CG1 ILE B  65     3472   3582   3114    747    121    169       C  
ATOM    529  CG2 ILE B  65     -11.743  53.582  80.917  1.00 21.01           C  
ANISOU  529  CG2 ILE B  65     2979   2521   2483    682    238    199       C  
ATOM    530  CD1 ILE B  65     -12.378  52.563  78.087  1.00 30.14           C  
ANISOU  530  CD1 ILE B  65     3922   4037   3493    837    133    265       C  
ATOM    531  N   TYR B  66      -9.617  51.028  82.380  1.00 13.23           N  
ANISOU  531  N   TYR B  66     1945   1540   1541    335    127     41       N  
ATOM    532  CA  TYR B  66      -8.683  51.085  83.503  1.00 13.01           C  
ANISOU  532  CA  TYR B  66     1975   1423   1544    207    125     25       C  
ATOM    533  C   TYR B  66      -7.246  50.785  83.089  1.00 11.69           C  
ANISOU  533  C   TYR B  66     1769   1304   1367    151    103     81       C  
ATOM    534  O   TYR B  66      -6.308  51.477  83.490  1.00 12.88           O  
ANISOU  534  O   TYR B  66     1956   1405   1535     47    108    136       O  
ATOM    535  CB  TYR B  66      -9.148  50.078  84.555  1.00 11.18           C  
ANISOU  535  CB  TYR B  66     1728   1203   1317    156     98    -60       C  
ATOM    536  CG  TYR B  66      -8.160  49.892  85.668  1.00 11.74           C  
ANISOU  536  CG  TYR B  66     1842   1221   1399     35     79    -74       C  
ATOM    537  CD1 TYR B  66      -7.502  48.685  85.834  1.00 10.56           C  
ANISOU  537  CD1 TYR B  66     1647   1125   1238      1     31    -86       C  
ATOM    538  CD2 TYR B  66      -7.885  50.923  86.566  1.00 14.19           C  
ANISOU  538  CD2 TYR B  66     2254   1423   1715    -39    100    -74       C  
ATOM    539  CE1 TYR B  66      -6.581  48.504  86.830  1.00 11.14           C  
ANISOU  539  CE1 TYR B  66     1738   1184   1309    -94      6    -79       C  
ATOM    540  CE2 TYR B  66      -6.957  50.753  87.595  1.00 14.27           C  
ANISOU  540  CE2 TYR B  66     2295   1412   1715   -169     61    -84       C  
ATOM    541  CZ  TYR B  66      -6.317  49.513  87.718  1.00 12.53           C  
ANISOU  541  CZ  TYR B  66     1988   1286   1487   -190     14    -78       C  
ATOM    542  OH  TYR B  66      -5.404  49.277  88.714  1.00 14.34           O  
ANISOU  542  OH  TYR B  66     2223   1530   1696   -298    -32    -69       O  
ATOM    543  N   ASP B  67      -7.068  49.732  82.299  1.00 13.16           N  
ANISOU  543  N   ASP B  67     1887   1600   1515    218     77     71       N  
ATOM    544  CA  ASP B  67      -5.755  49.318  81.881  1.00 13.73           C  
ANISOU  544  CA  ASP B  67     1903   1757   1556    221     74    130       C  
ATOM    545  C   ASP B  67      -5.070  50.409  81.043  1.00 14.94           C  
ANISOU  545  C   ASP B  67     2030   1950   1697    218    118    258       C  
ATOM    546  O   ASP B  67      -3.854  50.555  81.093  1.00 17.92           O  
ANISOU  546  O   ASP B  67     2346   2395   2067    152    125    347       O  
ATOM    547  CB  ASP B  67      -5.811  48.004  81.090  1.00 12.79           C  
ANISOU  547  CB  ASP B  67     1765   1723   1370    339     48     79       C  
ATOM    548  CG  ASP B  67      -5.966  46.776  81.974  1.00 16.23           C  
ANISOU  548  CG  ASP B  67     2242   2112   1812    311      1    -10       C  
ATOM    549  OD1 ASP B  67      -6.349  45.716  81.436  1.00 15.60           O  
ANISOU  549  OD1 ASP B  67     2208   2040   1681    381    -35    -78       O  
ATOM    550  OD2 ASP B  67      -5.651  46.840  83.186  1.00 13.39           O1-
ANISOU  550  OD2 ASP B  67     1888   1703   1498    213     -6     -9       O1-
ATOM    551  N   THR B  68      -5.867  51.147  80.272  1.00 16.11           N  
ANISOU  551  N   THR B  68     2213   2073   1836    287    144    284       N  
ATOM    552  CA  THR B  68      -5.348  52.241  79.443  1.00 19.55           C  
ANISOU  552  CA  THR B  68     2650   2522   2256    282    190    424       C  
ATOM    553  C   THR B  68      -4.887  53.411  80.322  1.00 22.00           C  
ANISOU  553  C   THR B  68     3048   2682   2628    111    198    480       C  
ATOM    554  O   THR B  68      -4.068  54.228  79.910  1.00 24.67           O  
ANISOU  554  O   THR B  68     3387   3024   2964     22    221    614       O  
ATOM    555  CB  THR B  68      -6.430  52.728  78.435  1.00 21.18           C  
ANISOU  555  CB  THR B  68     2887   2733   2426    423    211    444       C  
ATOM    556  CG2 THR B  68      -5.859  53.777  77.456  1.00 20.10           C  
ANISOU  556  CG2 THR B  68     2762   2617   2260    430    264    612       C  
ATOM    557  OG1 THR B  68      -6.922  51.617  77.671  1.00 29.73           O  
ANISOU  557  OG1 THR B  68     3912   3950   3436    546    178    373       O  
ATOM    558  N   TYR B  69      -5.429  53.516  81.530  1.00 25.41           N  
ANISOU  558  N   TYR B  69     3571   2980   3104     52    177    380       N  
ATOM    559  CA  TYR B  69      -5.113  54.646  82.409  1.00 29.50           C  
ANISOU  559  CA  TYR B  69     4232   3320   3657   -106    175    401       C  
ATOM    560  C   TYR B  69      -3.669  54.590  82.887  1.00 30.66           C  
ANISOU  560  C   TYR B  69     4315   3528   3806   -310    130    466       C  
ATOM    561  O   TYR B  69      -3.131  53.518  83.143  1.00 33.70           O  
ANISOU  561  O   TYR B  69     4567   4062   4177   -308     99    443       O  
ATOM    562  CB  TYR B  69      -6.065  54.670  83.609  1.00 32.63           C  
ANISOU  562  CB  TYR B  69     4742   3585   4068    -87    173    268       C  
ATOM    563  CG  TYR B  69      -6.115  56.013  84.298  1.00 36.86           C  
ANISOU  563  CG  TYR B  69     5502   3890   4611   -175    187    266       C  
ATOM    564  CD1 TYR B  69      -7.009  56.990  83.881  1.00 38.25           C  
ANISOU  564  CD1 TYR B  69     5823   3928   4783    -35    248    289       C  
ATOM    565  CD2 TYR B  69      -5.256  56.311  85.350  1.00 37.65           C  
ANISOU  565  CD2 TYR B  69     5690   3905   4709   -391    133    245       C  
ATOM    566  CE1 TYR B  69      -7.061  58.230  84.502  1.00 40.75           C  
ANISOU  566  CE1 TYR B  69     6404   3988   5091    -90    266    278       C  
ATOM    567  CE2 TYR B  69      -5.293  57.549  85.973  1.00 38.81           C  
ANISOU  567  CE2 TYR B  69     6098   3806   4843   -485    135    225       C  
ATOM    568  CZ  TYR B  69      -6.202  58.503  85.547  1.00 43.51           C  
ANISOU  568  CZ  TYR B  69     6871   4227   5433   -325    206    236       C  
ATOM    569  OH  TYR B  69      -6.256  59.736  86.159  1.00 45.35           O  
ANISOU  569  OH  TYR B  69     7419   4172   5639   -392    213    207       O  
ATOM    570  N   GLY B  70      -3.037  55.758  82.980  1.00 39.10           N  
ANISOU  570  N   GLY B  70     5483   4487   4886   -488    121    560       N  
ATOM    571  CA  GLY B  70      -1.633  55.840  83.360  1.00 40.35           C  
ANISOU  571  CA  GLY B  70     5552   4741   5038   -722     65    655       C  
ATOM    572  C   GLY B  70      -0.679  55.254  82.334  1.00 44.78           C  
ANISOU  572  C   GLY B  70     5870   5577   5565   -684     88    799       C  
ATOM    573  O   GLY B  70       0.402  54.783  82.694  1.00 51.84           O  
ANISOU  573  O   GLY B  70     6604   6654   6440   -791     47    863       O  
ATOM    574  N   THR B  71      -1.077  55.272  81.061  1.00 39.39           N  
ANISOU  574  N   THR B  71     5157   4950   4859   -510    158    856       N  
ATOM    575  CA  THR B  71      -0.217  54.814  79.972  1.00 32.19           C  
ANISOU  575  CA  THR B  71     4039   4303   3887   -438    202    998       C  
ATOM    576  C   THR B  71      -0.126  55.935  78.960  1.00 27.82           C  
ANISOU  576  C   THR B  71     3534   3716   3321   -485    254   1162       C  
ATOM    577  O   THR B  71      -0.787  56.963  79.109  1.00 27.78           O  
ANISOU  577  O   THR B  71     3737   3462   3356   -544    253   1151       O  
ATOM    578  CB  THR B  71      -0.737  53.507  79.320  1.00 28.49           C  
ANISOU  578  CB  THR B  71     3492   3968   3363   -155    233    901       C  
ATOM    579  CG2 THR B  71      -1.859  53.745  78.313  1.00 20.30           C  
ANISOU  579  CG2 THR B  71     2547   2866   2300     19    274    871       C  
ATOM    580  OG1 THR B  71       0.331  52.850  78.635  1.00 43.55           O  
ANISOU  580  OG1 THR B  71     5205   6149   5194    -77    271   1012       O  
ATOM    581  N   THR B  72       0.677  55.741  77.921  1.00 26.36           N  
ANISOU  581  N   THR B  72     3170   3779   3066   -435    310   1322       N  
ATOM    582  CA  THR B  72       0.824  56.762  76.895  1.00 28.60           C  
ANISOU  582  CA  THR B  72     3486   4058   3323   -482    368   1509       C  
ATOM    583  C   THR B  72      -0.326  56.795  75.879  1.00 18.53           C  
ANISOU  583  C   THR B  72     2311   2726   2005   -224    421   1465       C  
ATOM    584  O   THR B  72      -0.391  57.708  75.077  1.00 24.32           O  
ANISOU  584  O   THR B  72     3112   3413   2715   -240    467   1614       O  
ATOM    585  CB  THR B  72       2.160  56.625  76.121  1.00 32.05           C  
ANISOU  585  CB  THR B  72     3671   4827   3681   -530    424   1734       C  
ATOM    586  CG2 THR B  72       3.348  56.626  77.091  1.00 35.97           C  
ANISOU  586  CG2 THR B  72     4021   5439   4207   -800    361   1812       C  
ATOM    587  OG1 THR B  72       2.163  55.421  75.340  1.00 33.48           O  
ANISOU  587  OG1 THR B  72     3707   5254   3760   -228    484   1688       O  
ATOM    588  N   GLU B  73      -1.190  55.782  75.891  1.00 21.28           N  
ANISOU  588  N   GLU B  73     2661   3094   2333     -3    406   1279       N  
ATOM    589  CA  GLU B  73      -2.368  55.754  75.007  1.00 19.99           C  
ANISOU  589  CA  GLU B  73     2574   2902   2118    221    427   1227       C  
ATOM    590  C   GLU B  73      -3.441  56.720  75.497  1.00 18.42           C  
ANISOU  590  C   GLU B  73     2580   2426   1994    202    409   1181       C  
ATOM    591  O   GLU B  73      -3.789  56.714  76.692  1.00 19.88           O  
ANISOU  591  O   GLU B  73     2848   2449   2255    124    365   1054       O  
ATOM    592  CB  GLU B  73      -2.989  54.356  74.960  1.00 22.24           C  
ANISOU  592  CB  GLU B  73     2810   3284   2358    411    394   1039       C  
ATOM    593  CG  GLU B  73      -2.123  53.233  74.403  1.00 33.20           C  
ANISOU  593  CG  GLU B  73     4050   4921   3644    518    419   1046       C  
ATOM    594  CD  GLU B  73      -2.550  51.871  74.949  1.00 36.23           C  
ANISOU  594  CD  GLU B  73     4446   5296   4024    611    361    842       C  
ATOM    595  OE1 GLU B  73      -3.765  51.689  75.222  1.00 41.68           O  
ANISOU  595  OE1 GLU B  73     5231   5858   4747    643    308    705       O  
ATOM    596  OE2 GLU B  73      -1.675  50.991  75.130  1.00 38.32           O1-
ANISOU  596  OE2 GLU B  73     4623   5686   4249    650    370    833       O1-
ATOM    597  N   ALA B  74      -4.014  57.487  74.574  1.00 17.19           N  
ANISOU  597  N   ALA B  74     2505   2229   1797    311    449   1282       N  
ATOM    598  CA  ALA B  74      -5.093  58.418  74.931  1.00 20.59           C  
ANISOU  598  CA  ALA B  74     3136   2411   2278    364    449   1255       C  
ATOM    599  C   ALA B  74      -6.331  57.639  75.378  1.00 19.62           C  
ANISOU  599  C   ALA B  74     2993   2300   2161    528    409   1059       C  
ATOM    600  O   ALA B  74      -6.754  56.696  74.709  1.00 16.35           O  
ANISOU  600  O   ALA B  74     2454   2082   1675    670    389    999       O  
ATOM    601  CB  ALA B  74      -5.427  59.285  73.771  1.00 20.12           C  
ANISOU  601  CB  ALA B  74     3148   2342   2157    484    500   1423       C  
ATOM    602  N   PRO B  75      -6.934  58.028  76.509  1.00 20.44           N  
ANISOU  602  N   PRO B  75     3228   2202   2337    500    397    961       N  
ATOM    603  CA  PRO B  75      -8.170  57.387  76.891  1.00 18.27           C  
ANISOU  603  CA  PRO B  75     2912   1970   2060    651    372    814       C  
ATOM    604  C   PRO B  75      -9.338  57.859  76.024  1.00 16.52           C  
ANISOU  604  C   PRO B  75     2705   1790   1782    883    395    876       C  
ATOM    605  O   PRO B  75      -9.287  58.945  75.448  1.00 17.39           O  
ANISOU  605  O   PRO B  75     2935   1797   1874    936    442   1022       O  
ATOM    606  CB  PRO B  75      -8.353  57.845  78.340  1.00 18.65           C  
ANISOU  606  CB  PRO B  75     3108   1798   2180    563    375    723       C  
ATOM    607  CG  PRO B  75      -7.716  59.153  78.397  1.00 29.27           C  
ANISOU  607  CG  PRO B  75     4653   2920   3548    451    407    840       C  
ATOM    608  CD  PRO B  75      -6.525  59.055  77.484  1.00 27.70           C  
ANISOU  608  CD  PRO B  75     4347   2854   3325    327    404    981       C  
ATOM    609  N   PRO B  76     -10.378  57.018  75.917  1.00 16.67           N  
ANISOU  609  N   PRO B  76     2598   1973   1764   1009    354    778       N  
ATOM    610  CA  PRO B  76     -11.528  57.400  75.145  1.00 19.68           C  
ANISOU  610  CA  PRO B  76     2952   2447   2080   1227    359    844       C  
ATOM    611  C   PRO B  76     -12.368  58.361  75.938  1.00 20.58           C  
ANISOU  611  C   PRO B  76     3196   2390   2235   1344    414    853       C  
ATOM    612  O   PRO B  76     -12.258  58.404  77.165  1.00 18.62           O  
ANISOU  612  O   PRO B  76     3029   1990   2053   1253    431    758       O  
ATOM    613  CB  PRO B  76     -12.288  56.081  74.999  1.00 20.28           C  
ANISOU  613  CB  PRO B  76     2842   2756   2108   1253    277    722       C  
ATOM    614  CG  PRO B  76     -11.963  55.349  76.197  1.00 20.99           C  
ANISOU  614  CG  PRO B  76     2925   2777   2273   1095    259    585       C  
ATOM    615  CD  PRO B  76     -10.544  55.674  76.488  1.00 16.61           C  
ANISOU  615  CD  PRO B  76     2466   2078   1766    942    293    621       C  
ATOM    616  N   PRO B  77     -13.249  59.076  75.254  1.00 23.23           N  
ANISOU  616  N   PRO B  77     3547   2766   2512   1572    442    965       N  
ATOM    617  CA  PRO B  77     -14.235  59.870  75.974  1.00 24.82           C  
ANISOU  617  CA  PRO B  77     3852   2851   2728   1759    504    970       C  
ATOM    618  C   PRO B  77     -15.245  58.929  76.595  1.00 23.25           C  
ANISOU  618  C   PRO B  77     3452   2860   2523   1798    467    850       C  
ATOM    619  O   PRO B  77     -15.325  57.777  76.185  1.00 21.01           O  
ANISOU  619  O   PRO B  77     2967   2805   2210   1703    381    789       O  
ATOM    620  CB  PRO B  77     -14.897  60.674  74.869  1.00 27.53           C  
ANISOU  620  CB  PRO B  77     4211   3261   2989   2016    531   1144       C  
ATOM    621  CG  PRO B  77     -14.727  59.839  73.640  1.00 26.88           C  
ANISOU  621  CG  PRO B  77     3928   3456   2828   1973    449   1175       C  
ATOM    622  CD  PRO B  77     -13.417  59.156  73.795  1.00 25.92           C  
ANISOU  622  CD  PRO B  77     3810   3287   2753   1697    421   1095       C  
ATOM    623  N   PRO B  78     -16.062  59.420  77.545  1.00 23.00           N  
ANISOU  623  N   PRO B  78     3481   2755   2502   1945    535    823       N  
ATOM    624  CA  PRO B  78     -17.099  58.519  78.041  1.00 23.88           C  
ANISOU  624  CA  PRO B  78     3358   3120   2595   1977    504    747       C  
ATOM    625  C   PRO B  78     -18.073  58.227  76.903  1.00 18.91           C  
ANISOU  625  C   PRO B  78     2492   2817   1876   2128    443    844       C  
ATOM    626  O   PRO B  78     -18.186  59.032  75.983  1.00 23.34           O  
ANISOU  626  O   PRO B  78     3110   3374   2384   2307    464    982       O  
ATOM    627  CB  PRO B  78     -17.788  59.311  79.158  1.00 25.07           C  
ANISOU  627  CB  PRO B  78     3633   3147   2747   2168    617    735       C  
ATOM    628  CG  PRO B  78     -17.003  60.571  79.334  1.00 30.66           C  
ANISOU  628  CG  PRO B  78     4692   3476   3479   2199    691    771       C  
ATOM    629  CD  PRO B  78     -16.114  60.758  78.152  1.00 30.41           C  
ANISOU  629  CD  PRO B  78     4706   3395   3453   2095    642    867       C  
ATOM    630  N   PRO B  79     -18.723  57.048  76.938  1.00 21.50           N  
ANISOU  630  N   PRO B  79     2565   3424   2179   2028    354    779       N  
ATOM    631  CA  PRO B  79     -19.656  56.742  75.865  1.00 23.03           C  
ANISOU  631  CA  PRO B  79     2529   3949   2271   2131    268    867       C  
ATOM    632  C   PRO B  79     -20.943  57.533  76.042  1.00 23.89           C  
ANISOU  632  C   PRO B  79     2535   4216   2328   2441    340    992       C  
ATOM    633  O   PRO B  79     -21.147  58.180  77.090  1.00 25.75           O  
ANISOU  633  O   PRO B  79     2882   4299   2602   2573    463    985       O  
ATOM    634  CB  PRO B  79     -19.928  55.244  76.066  1.00 21.61           C  
ANISOU  634  CB  PRO B  79     2151   3971   2088   1880    147    748       C  
ATOM    635  CG  PRO B  79     -19.777  55.046  77.522  1.00 24.42           C  
ANISOU  635  CG  PRO B  79     2568   4177   2534   1782    217    650       C  
ATOM    636  CD  PRO B  79     -18.659  55.965  77.931  1.00 23.51           C  
ANISOU  636  CD  PRO B  79     2742   3705   2486   1806    318    636       C  
ATOM    637  N   PRO B  80     -21.826  57.501  75.032  1.00 26.33           N  
ANISOU  637  N   PRO B  80     2630   4843   2529   2579    266   1112       N  
ATOM    638  CA  PRO B  80     -23.118  58.188  75.161  1.00 30.70           C  
ANISOU  638  CA  PRO B  80     3030   5618   3016   2906    332   1257       C  
ATOM    639  C   PRO B  80     -23.891  57.747  76.416  1.00 22.17           C  
ANISOU  639  C   PRO B  80     1785   4675   1963   2886    381   1204       C  
ATOM    640  O   PRO B  80     -24.032  56.508  76.680  1.00 29.71           O  
ANISOU  640  O   PRO B  80     2555   5799   2934   2591    275   1107       O  
ATOM    641  CB  PRO B  80     -23.858  57.781  73.891  1.00 30.44           C  
ANISOU  641  CB  PRO B  80     2727   5981   2856   2935    187   1363       C  
ATOM    642  CG  PRO B  80     -22.784  57.401  72.915  1.00 29.05           C  
ANISOU  642  CG  PRO B  80     2689   5680   2668   2735     93   1304       C  
ATOM    643  CD  PRO B  80     -21.665  56.856  73.714  1.00 28.91           C  
ANISOU  643  CD  PRO B  80     2856   5358   2772   2460    118   1124       C  
ATOM    644  N   GLY B  81     -24.335  58.739  77.214  1.00 27.70           N  
ANISOU  644  N   GLY B  81     2585   5278   2662   3192    546   1265       N  
ATOM    645  CA  GLY B  81     -25.051  58.428  78.446  1.00 27.23           C  
ANISOU  645  CA  GLY B  81     2383   5356   2607   3215    623   1229       C  
ATOM    646  C   GLY B  81     -24.159  58.202  79.652  1.00 28.44           C  
ANISOU  646  C   GLY B  81     2776   5172   2857   3007    684   1051       C  
ATOM    647  O   GLY B  81     -24.651  58.147  80.771  1.00 32.36           O  
ANISOU  647  O   GLY B  81     3225   5724   3345   3070    781   1023       O  
ATOM    648  N   GLY B  82     -22.849  58.093  79.433  1.00 27.25           N  
ANISOU  648  N   GLY B  82     2873   4698   2783   2774    633    945       N  
ATOM    649  CA  GLY B  82     -21.906  57.796  80.509  1.00 24.10           C  
ANISOU  649  CA  GLY B  82     2678   4010   2468   2545    662    784       C  
ATOM    650  C   GLY B  82     -21.738  56.300  80.710  1.00 25.73           C  
ANISOU  650  C   GLY B  82     2698   4366   2712   2192    539    682       C  
ATOM    651  O   GLY B  82     -22.431  55.498  80.090  1.00 28.54           O  
ANISOU  651  O   GLY B  82     2778   5039   3026   2111    433    727       O  
ATOM    652  N   TYR B  83     -20.815  55.925  81.586  1.00 23.90           N  
ANISOU  652  N   TYR B  83     2633   3898   2551   1978    547    550       N  
ATOM    653  CA  TYR B  83     -20.560  54.508  81.877  1.00 25.26           C  
ANISOU  653  CA  TYR B  83     2684   4156   2759   1659    442    455       C  
ATOM    654  C   TYR B  83     -21.658  53.941  82.759  1.00 30.73           C  
ANISOU  654  C   TYR B  83     3155   5100   3419   1649    472    473       C  
ATOM    655  O   TYR B  83     -22.223  54.663  83.576  1.00 32.51           O  
ANISOU  655  O   TYR B  83     3403   5339   3610   1866    607    508       O  
ATOM    656  CB  TYR B  83     -19.202  54.329  82.557  1.00 22.77           C  
ANISOU  656  CB  TYR B  83     2605   3529   2517   1462    443    332       C  
ATOM    657  CG  TYR B  83     -18.030  54.557  81.640  1.00 17.20           C  
ANISOU  657  CG  TYR B  83     2050   2643   1841   1393    392    327       C  
ATOM    658  CD1 TYR B  83     -17.299  55.743  81.680  1.00 17.29           C  
ANISOU  658  CD1 TYR B  83     2308   2390   1872   1483    465    349       C  
ATOM    659  CD2 TYR B  83     -17.660  53.594  80.718  1.00 17.25           C  
ANISOU  659  CD2 TYR B  83     1963   2748   1843   1235    272    306       C  
ATOM    660  CE1 TYR B  83     -16.220  55.963  80.836  1.00 17.93           C  
ANISOU  660  CE1 TYR B  83     2497   2342   1975   1401    425    374       C  
ATOM    661  CE2 TYR B  83     -16.568  53.788  79.876  1.00 19.23           C  
ANISOU  661  CE2 TYR B  83     2332   2873   2102   1193    243    316       C  
ATOM    662  CZ  TYR B  83     -15.856  54.976  79.930  1.00 16.00           C  
ANISOU  662  CZ  TYR B  83     2124   2237   1719   1270    322    362       C  
ATOM    663  OH  TYR B  83     -14.805  55.170  79.082  1.00 21.71           O  
ANISOU  663  OH  TYR B  83     2929   2876   2443   1214    301    401       O  
ATOM    664  N   ASP B  84     -21.956  52.657  82.573  1.00 28.00           N  
ANISOU  664  N   ASP B  84     2612   4952   3075   1400    349    454       N  
ATOM    665  CA  ASP B  84     -22.936  51.927  83.384  1.00 29.06           C  
ANISOU  665  CA  ASP B  84     2517   5341   3182   1306    357    487       C  
ATOM    666  C   ASP B  84     -22.264  50.800  84.141  1.00 33.40           C  
ANISOU  666  C   ASP B  84     3151   5752   3789    996    303    376       C  
ATOM    667  O   ASP B  84     -21.542  50.013  83.540  1.00 26.90           O  
ANISOU  667  O   ASP B  84     2403   4820   2999    789    178    303       O  
ATOM    668  CB  ASP B  84     -24.007  51.300  82.493  1.00 35.35           C  
ANISOU  668  CB  ASP B  84     2998   6514   3917   1230    233    588       C  
ATOM    669  CG  ASP B  84     -24.890  52.318  81.833  1.00 39.24           C  
ANISOU  669  CG  ASP B  84     3340   7236   4334   1556    284    734       C  
ATOM    670  OD1 ASP B  84     -25.468  51.984  80.785  1.00 43.60           O  
ANISOU  670  OD1 ASP B  84     3690   8048   4828   1506    153    807       O  
ATOM    671  OD2 ASP B  84     -25.012  53.443  82.352  1.00 48.34           O1-
ANISOU  671  OD2 ASP B  84     4591   8306   5471   1868    449    776       O1-
ATOM    672  N   PHE B  85     -22.522  50.716  85.445  1.00 33.02           N  
ANISOU  672  N   PHE B  85     3094   5715   3735    988    402    370       N  
ATOM    673  CA  PHE B  85     -22.092  49.580  86.267  1.00 36.38           C  
ANISOU  673  CA  PHE B  85     3565   6060   4199    704    356    299       C  
ATOM    674  C   PHE B  85     -23.305  48.914  86.910  1.00 40.52           C  
ANISOU  674  C   PHE B  85     3820   6901   4675    606    373    397       C  
ATOM    675  O   PHE B  85     -23.659  49.209  88.057  1.00 45.36           O  
ANISOU  675  O   PHE B  85     4415   7570   5250    703    509    425       O  
ATOM    676  CB  PHE B  85     -21.117  50.040  87.343  1.00 33.56           C  
ANISOU  676  CB  PHE B  85     3471   5414   3867    746    453    206       C  
ATOM    677  CG  PHE B  85     -19.793  50.467  86.803  1.00 31.13           C  
ANISOU  677  CG  PHE B  85     3405   4809   3612    748    413    122       C  
ATOM    678  CD1 PHE B  85     -19.627  51.741  86.276  1.00 32.43           C  
ANISOU  678  CD1 PHE B  85     3681   4874   3768    978    474    143       C  
ATOM    679  CD2 PHE B  85     -18.709  49.600  86.807  1.00 26.82           C  
ANISOU  679  CD2 PHE B  85     2976   4096   3118    527    320     42       C  
ATOM    680  CE1 PHE B  85     -18.404  52.141  85.777  1.00 27.50           C  
ANISOU  680  CE1 PHE B  85     3259   4002   3189    948    439     93       C  
ATOM    681  CE2 PHE B  85     -17.482  49.995  86.304  1.00 26.03           C  
ANISOU  681  CE2 PHE B  85     3056   3778   3057    532    292     -9       C  
ATOM    682  CZ  PHE B  85     -17.330  51.264  85.777  1.00 26.89           C  
ANISOU  682  CZ  PHE B  85     3253   3805   3160    722    349     21       C  
ATOM    683  N   SER B  86     -23.929  48.008  86.163  1.00 44.63           N  
ANISOU  683  N   SER B  86     4138   7635   5183    398    231    452       N  
ATOM    684  CA  SER B  86     -25.159  47.355  86.605  1.00 50.16           C  
ANISOU  684  CA  SER B  86     4538   8686   5834    255    223    578       C  
ATOM    685  C   SER B  86     -24.891  46.452  87.806  1.00 51.35           C  
ANISOU  685  C   SER B  86     4766   8737   6009     21    244    550       C  
ATOM    686  O   SER B  86     -23.914  45.699  87.824  1.00 54.90           O  
ANISOU  686  O   SER B  86     5441   8902   6516   -177    156    439       O  
ATOM    687  CB  SER B  86     -25.780  46.546  85.458  1.00 53.26           C  
ANISOU  687  CB  SER B  86     4737   9296   6202     23     26    630       C  
ATOM    688  OG  SER B  86     -27.133  46.220  85.732  1.00 58.00           O  
ANISOU  688  OG  SER B  86     4980  10319   6738    -74     24    797       O  
ATOM    689  N   GLY B  87     -25.747  46.553  88.817  1.00 56.24           N  
ANISOU  689  N   GLY B  87     5198   9601   6570     73    372    662       N  
ATOM    690  CA  GLY B  87     -25.621  45.736  90.020  1.00 55.51           C  
ANISOU  690  CA  GLY B  87     5153   9458   6478   -135    408    668       C  
ATOM    691  C   GLY B  87     -24.529  46.149  90.995  1.00 56.05           C  
ANISOU  691  C   GLY B  87     5533   9201   6563    -15    515    545       C  
ATOM    692  O   GLY B  87     -24.210  45.388  91.912  1.00 56.92           O  
ANISOU  692  O   GLY B  87     5729   9220   6675   -201    519    536       O  
ATOM    693  N   PHE B  88     -23.951  47.338  90.808  1.00 50.50           N  
ANISOU  693  N   PHE B  88     5005   8320   5863    278    590    460       N  
ATOM    694  CA  PHE B  88     -23.031  47.906  91.788  1.00 45.64           C  
ANISOU  694  CA  PHE B  88     4669   7435   5236    397    691    353       C  
ATOM    695  C   PHE B  88     -23.532  49.250  92.280  1.00 48.46           C  
ANISOU  695  C   PHE B  88     5042   7869   5502    765    877    373       C  
ATOM    696  O   PHE B  88     -24.103  50.034  91.517  1.00 52.94           O  
ANISOU  696  O   PHE B  88     5509   8556   6050    992    910    427       O  
ATOM    697  CB  PHE B  88     -21.627  48.062  91.206  1.00 37.19           C  
ANISOU  697  CB  PHE B  88     3873   6008   4247    360    596    216       C  
ATOM    698  CG  PHE B  88     -20.912  46.766  91.033  1.00 33.93           C  
ANISOU  698  CG  PHE B  88     3528   5461   3901     57    449    174       C  
ATOM    699  CD1 PHE B  88     -20.933  46.108  89.810  1.00 32.82           C  
ANISOU  699  CD1 PHE B  88     3326   5339   3807    -82    303    176       C  
ATOM    700  CD2 PHE B  88     -20.240  46.183  92.099  1.00 28.11           C  
ANISOU  700  CD2 PHE B  88     2935   4582   3161    -73    456    134       C  
ATOM    701  CE1 PHE B  88     -20.281  44.899  89.649  1.00 34.30           C  
ANISOU  701  CE1 PHE B  88     3620   5375   4038   -326    177    130       C  
ATOM    702  CE2 PHE B  88     -19.590  44.976  91.945  1.00 34.01           C  
ANISOU  702  CE2 PHE B  88     3766   5196   3961   -312    330    107       C  
ATOM    703  CZ  PHE B  88     -19.613  44.332  90.716  1.00 32.54           C  
ANISOU  703  CZ  PHE B  88     3542   5001   3821   -430    194    101       C  
ATOM    704  N   ASP B  89     -23.307  49.496  93.566  1.00 45.11           N  
ANISOU  704  N   ASP B  89     4764   7368   5006    835    996    329       N  
ATOM    705  CA  ASP B  89     -23.576  50.778  94.177  1.00 49.38           C  
ANISOU  705  CA  ASP B  89     5429   7893   5440   1193   1175    305       C  
ATOM    706  C   ASP B  89     -22.308  51.608  94.014  1.00 42.37           C  
ANISOU  706  C   ASP B  89     4912   6594   4595   1250   1139    148       C  
ATOM    707  O   ASP B  89     -21.401  51.538  94.842  1.00 46.94           O  
ANISOU  707  O   ASP B  89     5723   6952   5159   1143   1127     44       O  
ATOM    708  CB  ASP B  89     -23.932  50.588  95.657  1.00 53.59           C  
ANISOU  708  CB  ASP B  89     5964   8550   5849   1222   1313    326       C  
ATOM    709  CG  ASP B  89     -25.104  49.635  95.863  1.00 61.14           C  
ANISOU  709  CG  ASP B  89     6537   9926   6769   1090   1338    508       C  
ATOM    710  OD1 ASP B  89     -25.105  48.910  96.881  1.00 65.15           O  
ANISOU  710  OD1 ASP B  89     7032  10497   7226    926   1371    537       O  
ATOM    711  OD2 ASP B  89     -26.018  49.606  95.007  1.00 64.61           O1-
ANISOU  711  OD2 ASP B  89     6683  10643   7223   1134   1318    634       O1-
ATOM    712  N   VAL B  90     -22.247  52.387  92.937  1.00 41.09           N  
ANISOU  712  N   VAL B  90     4791   6345   4476   1403   1113    149       N  
ATOM    713  CA  VAL B  90     -21.013  53.097  92.566  1.00 41.24           C  
ANISOU  713  CA  VAL B  90     5126   5990   4552   1395   1054     31       C  
ATOM    714  C   VAL B  90     -20.864  54.497  93.162  1.00 38.68           C  
ANISOU  714  C   VAL B  90     5114   5447   4136   1672   1184    -43       C  
ATOM    715  O   VAL B  90     -19.770  55.048  93.151  1.00 36.26           O  
ANISOU  715  O   VAL B  90     5098   4818   3860   1603   1132   -144       O  
ATOM    716  CB  VAL B  90     -20.829  53.200  91.021  1.00 43.39           C  
ANISOU  716  CB  VAL B  90     5330   6236   4919   1379    945     72       C  
ATOM    717  CG1 VAL B  90     -20.685  51.816  90.407  1.00 40.12           C  
ANISOU  717  CG1 VAL B  90     4717   5941   4587   1076    791     98       C  
ATOM    718  CG2 VAL B  90     -21.970  53.988  90.350  1.00 45.14           C  
ANISOU  718  CG2 VAL B  90     5405   6657   5088   1695   1031    185       C  
ATOM    719  N   GLU B  91     -21.946  55.083  93.671  1.00 40.47           N  
ANISOU  719  N   GLU B  91     5291   5846   4239   1984   1351     11       N  
ATOM    720  CA  GLU B  91     -21.889  56.467  94.140  1.00 44.43           C  
ANISOU  720  CA  GLU B  91     6137   6109   4634   2293   1480    -66       C  
ATOM    721  C   GLU B  91     -20.879  56.692  95.270  1.00 42.73           C  
ANISOU  721  C   GLU B  91     6281   5593   4362   2163   1472   -230       C  
ATOM    722  O   GLU B  91     -20.335  57.787  95.399  1.00 43.21           O  
ANISOU  722  O   GLU B  91     6714   5325   4378   2274   1494   -330       O  
ATOM    723  CB  GLU B  91     -23.281  56.962  94.566  1.00 47.26           C  
ANISOU  723  CB  GLU B  91     6366   6747   4844   2697   1683     28       C  
ATOM    724  CG  GLU B  91     -24.259  57.127  93.400  1.00 52.29           C  
ANISOU  724  CG  GLU B  91     6703   7655   5509   2905   1698    196       C  
ATOM    725  CD  GLU B  91     -25.497  57.950  93.753  1.00 57.94           C  
ANISOU  725  CD  GLU B  91     7359   8596   6062   3399   1916    292       C  
ATOM    726  OE1 GLU B  91     -25.865  58.021  94.947  1.00 63.17           O  
ANISOU  726  OE1 GLU B  91     8079   9343   6582   3544   2065    261       O  
ATOM    727  OE2 GLU B  91     -26.108  58.525  92.825  1.00 59.68           O1-
ANISOU  727  OE2 GLU B  91     7468   8926   6282   3665   1944    408       O1-
ATOM    728  N   ASP B  92     -20.627  55.662  96.077  1.00 43.77           N  
ANISOU  728  N   ASP B  92     6314   5833   4485   1916   1428   -252       N  
ATOM    729  CA  ASP B  92     -19.670  55.764  97.180  1.00 42.66           C  
ANISOU  729  CA  ASP B  92     6477   5458   4274   1772   1400   -395       C  
ATOM    730  C   ASP B  92     -18.305  55.115  96.864  1.00 35.76           C  
ANISOU  730  C   ASP B  92     5640   4413   3535   1392   1201   -442       C  
ATOM    731  O   ASP B  92     -17.504  54.888  97.763  1.00 34.33           O  
ANISOU  731  O   ASP B  92     5618   4121   3304   1217   1147   -528       O  
ATOM    732  CB  ASP B  92     -20.296  55.195  98.465  1.00 47.40           C  
ANISOU  732  CB  ASP B  92     6985   6294   4731   1808   1511   -379       C  
ATOM    733  CG  ASP B  92     -21.547  55.975  98.910  1.00 57.21           C  
ANISOU  733  CG  ASP B  92     8227   7707   5803   2234   1735   -340       C  
ATOM    734  OD1 ASP B  92     -21.567  57.225  98.812  1.00 58.67           O  
ANISOU  734  OD1 ASP B  92     8709   7667   5916   2512   1812   -413       O  
ATOM    735  OD2 ASP B  92     -22.518  55.338  99.371  1.00 57.85           O1-
ANISOU  735  OD2 ASP B  92     8017   8151   5812   2300   1840   -224       O1-
ATOM    736  N   PHE B  93     -18.022  54.861  95.586  1.00 30.56           N  
ANISOU  736  N   PHE B  93     4840   3745   3025   1288   1095   -381       N  
ATOM    737  CA  PHE B  93     -16.689  54.390  95.173  1.00 23.61           C  
ANISOU  737  CA  PHE B  93     4005   2708   2258    989    927   -416       C  
ATOM    738  C   PHE B  93     -15.692  55.542  95.214  1.00 22.82           C  
ANISOU  738  C   PHE B  93     4249   2279   2142    968    891   -509       C  
ATOM    739  O   PHE B  93     -16.070  56.705  95.375  1.00 27.85           O  
ANISOU  739  O   PHE B  93     5113   2771   2696   1191    988   -549       O  
ATOM    740  CB  PHE B  93     -16.723  53.721  93.788  1.00 23.12           C  
ANISOU  740  CB  PHE B  93     3693   2757   2333    903    836   -324       C  
ATOM    741  CG  PHE B  93     -17.297  52.309  93.782  1.00 21.73           C  
ANISOU  741  CG  PHE B  93     3223   2843   2188    776    802   -250       C  
ATOM    742  CD1 PHE B  93     -17.659  51.635  94.957  1.00 24.60           C  
ANISOU  742  CD1 PHE B  93     3536   3335   2477    716    849   -246       C  
ATOM    743  CD2 PHE B  93     -17.443  51.641  92.581  1.00 21.37           C  
ANISOU  743  CD2 PHE B  93     2979   2904   2238    696    714   -183       C  
ATOM    744  CE1 PHE B  93     -18.158  50.349  94.903  1.00 23.50           C  
ANISOU  744  CE1 PHE B  93     3156   3403   2371    564    807   -164       C  
ATOM    745  CE2 PHE B  93     -17.935  50.348  92.525  1.00 22.14           C  
ANISOU  745  CE2 PHE B  93     2855   3197   2360    543    662   -124       C  
ATOM    746  CZ  PHE B  93     -18.300  49.708  93.694  1.00 22.34           C  
ANISOU  746  CZ  PHE B  93     2837   3328   2323    469    709   -108       C  
ATOM    747  N   SER B  94     -14.415  55.203  95.114  1.00 23.55           N  
ANISOU  747  N   SER B  94     4388   2258   2303    699    751   -537       N  
ATOM    748  CA  SER B  94     -13.324  56.135  95.358  1.00 23.37           C  
ANISOU  748  CA  SER B  94     4671   1955   2254    583    687   -617       C  
ATOM    749  C   SER B  94     -13.291  57.307  94.388  1.00 26.91           C  
ANISOU  749  C   SER B  94     5277   2206   2742    693    705   -592       C  
ATOM    750  O   SER B  94     -13.864  57.245  93.310  1.00 21.84           O  
ANISOU  750  O   SER B  94     4462   1664   2174    822    736   -500       O  
ATOM    751  CB  SER B  94     -11.996  55.403  95.243  1.00 25.94           C  
ANISOU  751  CB  SER B  94     4915   2284   2656    279    531   -603       C  
ATOM    752  OG  SER B  94     -11.746  55.056  93.893  1.00 19.80           O  
ANISOU  752  OG  SER B  94     3950   1565   2009    242    479   -510       O  
ATOM    753  N   GLU B  95     -12.581  58.359  94.782  1.00 26.92           N  
ANISOU  753  N   GLU B  95     5621   1923   2685    617    674   -670       N  
ATOM    754  CA  GLU B  95     -12.308  59.509  93.920  1.00 27.69           C  
ANISOU  754  CA  GLU B  95     5926   1775   2821    653    669   -638       C  
ATOM    755  C   GLU B  95     -11.694  59.071  92.593  1.00 24.51           C  
ANISOU  755  C   GLU B  95     5284   1461   2566    510    581   -515       C  
ATOM    756  O   GLU B  95     -12.092  59.563  91.526  1.00 27.38           O  
ANISOU  756  O   GLU B  95     5630   1795   2979    661    625   -428       O  
ATOM    757  CB  GLU B  95     -11.347  60.474  94.624  1.00 36.63           C  
ANISOU  757  CB  GLU B  95     7456   2589   3874    458    594   -739       C  
ATOM    758  CG  GLU B  95     -11.241  61.850  93.993  1.00 42.07           C  
ANISOU  758  CG  GLU B  95     8468   2952   4563    518    612   -719       C  
ATOM    759  CD  GLU B  95     -10.142  62.704  94.620  1.00 48.10           C  
ANISOU  759  CD  GLU B  95     9618   3400   5259    225    497   -808       C  
ATOM    760  OE1 GLU B  95      -9.834  62.508  95.818  1.00 52.09           O  
ANISOU  760  OE1 GLU B  95    10238   3901   5654     97    448   -931       O  
ATOM    761  OE2 GLU B  95      -9.587  63.572  93.908  1.00 54.89           O1-
ANISOU  761  OE2 GLU B  95    10666   4021   6167    105    447   -746       O1-
ATOM    762  N   PHE B  96     -10.716  58.167  92.665  1.00 24.54           N  
ANISOU  762  N   PHE B  96     5117   1583   2624    243    464   -501       N  
ATOM    763  CA  PHE B  96     -10.079  57.614  91.483  1.00 23.01           C  
ANISOU  763  CA  PHE B  96     4690   1506   2545    128    392   -392       C  
ATOM    764  C   PHE B  96     -11.097  56.988  90.537  1.00 18.73           C  
ANISOU  764  C   PHE B  96     3893   1169   2055    333    452   -321       C  
ATOM    765  O   PHE B  96     -11.055  57.233  89.326  1.00 24.30           O  
ANISOU  765  O   PHE B  96     4533   1882   2816    380    448   -231       O  
ATOM    766  CB  PHE B  96      -9.026  56.550  91.856  1.00 20.44           C  
ANISOU  766  CB  PHE B  96     4200   1322   2246   -118    279   -390       C  
ATOM    767  CG  PHE B  96      -8.407  55.895  90.662  1.00 20.19           C  
ANISOU  767  CG  PHE B  96     3932   1430   2308   -185    225   -283       C  
ATOM    768  CD1 PHE B  96      -7.473  56.578  89.895  1.00 24.23           C  
ANISOU  768  CD1 PHE B  96     4493   1857   2858   -310    178   -202       C  
ATOM    769  CD2 PHE B  96      -8.786  54.631  90.268  1.00 20.79           C  
ANISOU  769  CD2 PHE B  96     3760   1718   2423   -118    225   -258       C  
ATOM    770  CE1 PHE B  96      -6.916  55.986  88.777  1.00 23.19           C  
ANISOU  770  CE1 PHE B  96     4144   1878   2788   -337    147    -99       C  
ATOM    771  CE2 PHE B  96      -8.233  54.042  89.147  1.00 21.26           C  
ANISOU  771  CE2 PHE B  96     3644   1892   2542   -147    182   -177       C  
ATOM    772  CZ  PHE B  96      -7.302  54.720  88.402  1.00 20.88           C  
ANISOU  772  CZ  PHE B  96     3628   1786   2519   -238    152    -97       C  
ATOM    773  N   PHE B  97     -11.991  56.160  91.083  1.00 17.43           N  
ANISOU  773  N   PHE B  97     3578   1185   1860    430    498   -351       N  
ATOM    774  CA  PHE B  97     -13.045  55.524  90.283  1.00 20.75           C  
ANISOU  774  CA  PHE B  97     3748   1824   2312    586    537   -284       C  
ATOM    775  C   PHE B  97     -13.909  56.596  89.611  1.00 19.91           C  
ANISOU  775  C   PHE B  97     3716   1665   2185    844    627   -231       C  
ATOM    776  O   PHE B  97     -14.148  56.546  88.404  1.00 22.47           O  
ANISOU  776  O   PHE B  97     3905   2079   2555    912    611   -145       O  
ATOM    777  CB  PHE B  97     -13.915  54.608  91.165  1.00 18.94           C  
ANISOU  777  CB  PHE B  97     3374   1787   2037    620    578   -311       C  
ATOM    778  CG  PHE B  97     -15.067  53.967  90.434  1.00 18.46           C  
ANISOU  778  CG  PHE B  97     3049   1970   1997    735    602   -235       C  
ATOM    779  CD1 PHE B  97     -14.931  52.708  89.871  1.00 17.18           C  
ANISOU  779  CD1 PHE B  97     2683   1952   1892    589    511   -205       C  
ATOM    780  CD2 PHE B  97     -16.286  54.620  90.312  1.00 21.31           C  
ANISOU  780  CD2 PHE B  97     3373   2420   2304    993    710   -190       C  
ATOM    781  CE1 PHE B  97     -15.987  52.119  89.209  1.00 17.50           C  
ANISOU  781  CE1 PHE B  97     2499   2213   1938    648    508   -141       C  
ATOM    782  CE2 PHE B  97     -17.342  54.036  89.620  1.00 22.06           C  
ANISOU  782  CE2 PHE B  97     3193   2781   2408   1070    712   -104       C  
ATOM    783  CZ  PHE B  97     -17.191  52.784  89.081  1.00 19.14           C  
ANISOU  783  CZ  PHE B  97     2632   2544   2095    872    601    -85       C  
ATOM    784  N   GLN B  98     -14.359  57.574  90.391  1.00 25.67           N  
ANISOU  784  N   GLN B  98     4679   2246   2829   1006    723   -282       N  
ATOM    785  CA  GLN B  98     -15.231  58.622  89.852  1.00 28.22           C  
ANISOU  785  CA  GLN B  98     5099   2508   3114   1308    825   -224       C  
ATOM    786  C   GLN B  98     -14.522  59.409  88.762  1.00 24.42           C  
ANISOU  786  C   GLN B  98     4752   1834   2691   1265    778   -154       C  
ATOM    787  O   GLN B  98     -15.157  59.848  87.809  1.00 25.98           O  
ANISOU  787  O   GLN B  98     4900   2078   2894   1474    822    -54       O  
ATOM    788  CB  GLN B  98     -15.710  59.592  90.934  1.00 27.76           C  
ANISOU  788  CB  GLN B  98     5342   2273   2934   1513    943   -305       C  
ATOM    789  CG  GLN B  98     -16.377  58.976  92.151  1.00 24.90           C  
ANISOU  789  CG  GLN B  98     4890   2091   2481   1574   1013   -370       C  
ATOM    790  CD  GLN B  98     -17.585  58.121  91.848  1.00 36.66           C  
ANISOU  790  CD  GLN B  98     5993   3961   3976   1716   1067   -273       C  
ATOM    791  NE2 GLN B  98     -17.871  57.171  92.743  1.00 35.10           N  
ANISOU  791  NE2 GLN B  98     5634   3962   3740   1624   1078   -299       N  
ATOM    792  OE1 GLN B  98     -18.269  58.315  90.842  1.00 41.24           O  
ANISOU  792  OE1 GLN B  98     6420   4666   4583   1893   1092   -165       O  
ATOM    793  N   GLU B  99     -13.208  59.574  88.899  1.00 27.08           N  
ANISOU  793  N   GLU B  99     5242   1984   3064    987    687   -187       N  
ATOM    794  CA  GLU B  99     -12.391  60.281  87.899  1.00 29.81           C  
ANISOU  794  CA  GLU B  99     5701   2163   3463    888    638    -99       C  
ATOM    795  C   GLU B  99     -12.277  59.493  86.597  1.00 30.96           C  
ANISOU  795  C   GLU B  99     5536   2545   3681    856    587      9       C  
ATOM    796  O   GLU B  99     -12.420  60.035  85.506  1.00 29.96           O  
ANISOU  796  O   GLU B  99     5418   2396   3569    966    605    118       O  
ATOM    797  CB  GLU B  99     -10.994  60.515  88.477  1.00 31.94           C  
ANISOU  797  CB  GLU B  99     6151   2244   3742    557    542   -148       C  
ATOM    798  CG  GLU B  99      -9.986  61.143  87.539  1.00 38.62           C  
ANISOU  798  CG  GLU B  99     7077   2956   4642    380    482    -36       C  
ATOM    799  CD  GLU B  99      -8.869  61.834  88.302  1.00 46.86           C  
ANISOU  799  CD  GLU B  99     8398   3746   5659     83    402    -83       C  
ATOM    800  OE1 GLU B  99      -8.479  61.323  89.380  1.00 50.18           O  
ANISOU  800  OE1 GLU B  99     8809   4214   6045    -71    346   -189       O  
ATOM    801  OE2 GLU B  99      -8.392  62.891  87.830  1.00 45.91           O1-
ANISOU  801  OE2 GLU B  99     8513   3385   5546    -10    388     -6       O1-
ATOM    802  N   LEU B 100     -11.994  58.206  86.737  1.00 23.97           N  
ANISOU  802  N   LEU B 100     4406   1873   2827    711    521    -24       N  
ATOM    803  CA  LEU B 100     -11.790  57.303  85.617  1.00 27.11           C  
ANISOU  803  CA  LEU B 100     4546   2482   3271    666    463     45       C  
ATOM    804  C   LEU B 100     -13.053  57.083  84.797  1.00 26.46           C  
ANISOU  804  C   LEU B 100     4290   2593   3170    897    501    101       C  
ATOM    805  O   LEU B 100     -12.966  56.969  83.571  1.00 30.10           O  
ANISOU  805  O   LEU B 100     4646   3150   3642    926    470    185       O  
ATOM    806  CB  LEU B 100     -11.286  55.951  86.142  1.00 23.54           C  
ANISOU  806  CB  LEU B 100     3929   2174   2840    487    391    -19       C  
ATOM    807  CG  LEU B 100     -10.866  54.820  85.199  1.00 25.70           C  
ANISOU  807  CG  LEU B 100     3986   2634   3144    418    322     18       C  
ATOM    808  CD1 LEU B 100      -9.747  55.244  84.308  1.00 29.36           C  
ANISOU  808  CD1 LEU B 100     4477   3051   3627    333    294    104       C  
ATOM    809  CD2 LEU B 100     -10.413  53.617  86.003  1.00 24.61           C  
ANISOU  809  CD2 LEU B 100     3765   2572   3014    274    267    -51       C  
ATOM    810  N   PHE B 101     -14.209  57.025  85.463  1.00 23.60           N  
ANISOU  810  N   PHE B 101     3886   2316   2766   1059    565     65       N  
ATOM    811  CA  PHE B 101     -15.447  56.546  84.840  1.00 28.63           C  
ANISOU  811  CA  PHE B 101     4282   3219   3378   1227    577    122       C  
ATOM    812  C   PHE B 101     -16.549  57.588  84.862  1.00 39.36           C  
ANISOU  812  C   PHE B 101     5706   4574   4675   1539    688    182       C  
ATOM    813  O   PHE B 101     -17.678  57.355  85.307  1.00 40.46           O  
ANISOU  813  O   PHE B 101     5700   4909   4766   1690    745    191       O  
ATOM    814  CB  PHE B 101     -15.910  55.243  85.488  1.00 26.62           C  
ANISOU  814  CB  PHE B 101     3823   3170   3121   1119    543     64       C  
ATOM    815  CG  PHE B 101     -15.052  54.070  85.132  1.00 18.63           C  
ANISOU  815  CG  PHE B 101     2718   2206   2157    882    431     30       C  
ATOM    816  CD1 PHE B 101     -14.285  53.427  86.090  1.00 20.13           C  
ANISOU  816  CD1 PHE B 101     2958   2324   2368    695    399    -48       C  
ATOM    817  CD2 PHE B 101     -14.993  53.609  83.822  1.00 17.84           C  
ANISOU  817  CD2 PHE B 101     2494   2223   2061    869    360     80       C  
ATOM    818  CE1 PHE B 101     -13.495  52.373  85.745  1.00 16.28           C  
ANISOU  818  CE1 PHE B 101     2401   1873   1911    529    309    -67       C  
ATOM    819  CE2 PHE B 101     -14.194  52.536  83.464  1.00 17.26           C  
ANISOU  819  CE2 PHE B 101     2369   2179   2009    696    270     43       C  
ATOM    820  CZ  PHE B 101     -13.441  51.912  84.442  1.00 16.96           C  
ANISOU  820  CZ  PHE B 101     2384   2060   1999    537    249    -28       C  
TER   
HETATM  821  C1  GOL B 201      -1.108  45.551  88.350  1.00 29.50           C  
HETATM  822  O1  GOL B 201      -0.334  46.579  87.798  1.00 40.40           O  
HETATM  823  C2  GOL B 201      -0.250  44.359  88.754  1.00 17.29           C  
HETATM  824  O2  GOL B 201       0.855  44.283  87.899  1.00 14.30           O  
HETATM  825  C3  GOL B 201       0.242  44.452  90.199  1.00 14.55           C  
HETATM  826  O3  GOL B 201      -0.834  44.582  91.090  1.00 11.22           O  
HETATM  827  O   HOH B 301      -1.482  42.045  92.008  1.00 12.77           O  
HETATM  828  O   HOH B 302     -10.322  43.764  78.834  1.00 14.87           O  
HETATM  829  O   HOH B 303      -5.722  55.302  72.589  1.00 14.46           O  
HETATM  830  O   HOH B 304     -10.671  40.869  79.274  1.00 16.29           O  
HETATM  831  O   HOH B 305       0.562  40.206  84.789  1.00 16.59           O  
HETATM  832  O   HOH B 306      -7.914  45.027  79.420  1.00 18.86           O  
HETATM  833  O   HOH B 307     -15.480  54.081  76.463  1.00 18.66           O  
HETATM  834  O   HOH B 308      -4.635  43.578  81.452  1.00 19.50           O  
HETATM  835  O   HOH B 309      -1.565  60.073  75.193  1.00 20.01           O  
HETATM  836  O   HOH B 310     -16.063  55.881  74.576  1.00 19.78           O  
HETATM  837  O   HOH B 311     -14.143  38.518  85.725  1.00 21.10           O  
HETATM  838  O   HOH B 312     -10.910  49.698  95.348  1.00 22.39           O  
HETATM  839  O   HOH B 313     -19.509  49.269  74.140  1.00 21.11           O  
HETATM  840  O   HOH B 314      -3.174  60.131  77.340  1.00 23.87           O  
HETATM  841  O   HOH B 315      -3.943  50.863  95.123  1.00 28.45           O  
HETATM  842  O   HOH B 316      -3.723  51.066  84.383  1.00 25.80           O  
HETATM  843  O   HOH B 317      -3.556  48.375  84.464  1.00 23.59           O  
HETATM  844  O   HOH B 318     -20.941  51.258  80.211  1.00 25.48           O  
HETATM  845  O   HOH B 319     -19.061  46.073  86.191  1.00 25.80           O  
HETATM  846  O   HOH B 320     -19.060  47.385 102.299  1.00 27.61           O  
HETATM  847  O   HOH B 321     -19.897  51.622  75.335  1.00 27.29           O  
HETATM  848  O   HOH B 322     -20.394  32.705 101.894  1.00 25.72           O  
HETATM  849  O   HOH B 323      -2.969  48.193  87.046  1.00 27.11           O  
HETATM  850  O   HOH B 324     -17.691  43.954  78.395  1.00 25.14           O  
HETATM  851  O   HOH B 325      -5.682  52.613  73.249  1.00 26.87           O  
HETATM  852  O   HOH B 326      -6.673  36.452  95.768  1.00 26.84           O  
HETATM  853  O   HOH B 327       1.728  35.326  83.899  1.00 25.79           O  
HETATM  854  O   HOH B 328     -18.540  43.840 105.396  1.00 28.94           O  
HETATM  855  O   HOH B 329      -3.630  57.095  79.296  1.00 28.66           O  
HETATM  856  O   HOH B 330      -9.227  57.625  95.182  1.00 27.07           O  
HETATM  857  O   HOH B 331     -18.110  32.519 103.543  1.00 31.13           O  
HETATM  858  O   HOH B 332     -18.687  45.469  76.444  1.00 28.02           O  
HETATM  859  O   HOH B 333     -18.517  50.445  79.221  1.00 27.62           O  
HETATM  860  O   HOH B 334      -6.197  48.775  77.597  1.00 25.70           O  
HETATM  861  O   HOH B 335      -1.634  34.815  84.733  1.00 30.24           O  
HETATM  862  O   HOH B 336     -17.245  52.100  76.763  1.00 28.17           O  
HETATM  863  O   HOH B 337      -8.098  50.834  74.917  1.00 27.39           O  
HETATM  864  O   HOH B 338     -11.496  58.415  97.537  1.00 31.94           O  
HETATM  865  O   HOH B 339     -19.855  46.961  83.810  1.00 30.51           O  
HETATM  866  O   HOH B 340      -3.338  35.124  91.875  1.00 32.86           O  
HETATM  867  O   HOH B 341      -3.771  52.860  86.350  1.00 47.18           O  
HETATM  868  O   HOH B 342      -7.784  33.597  91.201  1.00 35.45           O  
HETATM  869  O   HOH B 343      -0.447  42.424  81.719  1.00 30.83           O  
HETATM  870  O   HOH B 344     -23.651  54.481  75.209  1.00 31.94           O  
HETATM  871  O   HOH B 345     -18.366  58.895  73.084  1.00 31.73           O  
HETATM  872  O   HOH B 346     -14.346  51.623  97.340  1.00 32.92           O  
HETATM  873  O   HOH B 347      -3.754  48.205  95.970  1.00 35.21           O  
HETATM  874  O   HOH B 348     -13.410  57.328  79.294  1.00 31.89           O  
HETATM  875  O   HOH B 349     -20.153  45.751 104.009  1.00 35.03           O  
HETATM  876  O   HOH B 350     -22.482  53.037  78.761  1.00 33.64           O  
HETATM  877  O   HOH B 351     -12.766  32.602 101.261  1.00 36.70           O  
HETATM  878  O   HOH B 352     -17.243  38.129  86.665  1.00 38.64           O  
HETATM  879  O   HOH B 353      -5.363  29.948  96.613  1.00 44.97           O  
HETATM  880  O   HOH B 354     -19.826  58.207  83.045  1.00 36.86           O  
HETATM  881  O   HOH B 355     -20.902  61.148  77.623  1.00 34.04           O  
HETATM  882  O   HOH B 356     -14.115  30.634  96.754  1.00 38.29           O  
HETATM  883  O   HOH B 357      -5.084  32.758  97.727  1.00 39.94           O  
HETATM  884  O   HOH B 358     -18.186  41.314  77.852  1.00 45.34           O  
HETATM  885  O   HOH B 359     -19.328  43.237  85.650  1.00 36.88           O  
HETATM  886  O   HOH B 360     -19.419  47.134  79.862  1.00 41.31           O  
HETATM  887  O   HOH B 361     -11.078  60.556  78.863  1.00 45.77           O  
HETATM  888  O   HOH B 362      -7.865  35.187  98.346  1.00 45.11           O  
HETATM  889  O   HOH B 363     -19.809  48.151  98.002  1.00 39.88           O  
HETATM  890  O   HOH B 364     -14.471  36.259 107.589  1.00 48.81           O  
HETATM  891  O   HOH B 365     -11.683  60.293  82.821  1.00 49.74           O  
HETATM  892  O   HOH B 366      -9.553  37.122 105.688  1.00 39.76           O  
HETATM  893  O   HOH B 367     -24.689  34.455 103.974  1.00 31.67           O  
HETATM  894  O   HOH B 368     -22.116  48.511  80.504  1.00 37.52           O  
HETATM  895  O   HOH B 369      -9.609  51.081 103.994  1.00 45.46           O  
HETATM  896  O   HOH B 370      -8.812  55.194  80.292  1.00 30.74           O  
HETATM  897  O   HOH B 371     -24.698  59.623  83.254  1.00 31.24           O  
HETATM  898  O   HOH B 372      -6.324  51.020  97.362  1.00 38.94           O  
HETATM  899  O   HOH B 373     -13.093  31.216  94.472  1.00 27.49           O  
HETATM  900  O   HOH B 374     -21.371  47.477  74.210  1.00 33.18           O  
HETATM  901  O   HOH B 375     -10.935  57.024  81.321  1.00 28.60           O  
HETATM  902  O   HOH B 376      -7.721  38.156 102.665  1.00 41.94           O  
HETATM  903  O   HOH B 377      -5.335  36.374  80.370  1.00 29.22           O  
HETATM  904  O   HOH B 378     -20.517  32.165  98.999  1.00 31.67           O  
HETATM  905  O   HOH B 379     -11.704  52.806 101.821  1.00 47.26           O  
HETATM  906  O   HOH B 380       0.424  48.797  93.278  1.00 47.81           O  
HETATM  907  O   HOH B 381     -19.280  43.961 107.835  1.00 30.45           O  
HETATM  908  O   HOH B 382     -16.403  38.775  82.946  1.00 32.24           O  
HETATM  909  O   HOH B 383     -12.425  63.269  96.784  1.00 57.45           O  
CONECT  821  822  823
CONECT  822  821
CONECT  823  821  824  825
CONECT  824  823
CONECT  825  823  826
CONECT  826  825
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: december 26th, 2025.