longtext: 2HM7-pdb

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HEADER    HYDROLASE                               11-JUL-06   2HM7
TITLE     CRYSTAL STRUCTURE ANALYSIS OF THE G84S EST2 MUTANT
COMPND    MOL_ID: 1;
COMPND   2 MOLECULE: CARBOXYLESTERASE;
COMPND   3 CHAIN: A;
COMPND   4 EC: 3.1.1.1;
COMPND   5 ENGINEERED: YES;
COMPND   6 MUTATION: YES
SOURCE    MOL_ID: 1;
SOURCE   2 ORGANISM_SCIENTIFIC: ALICYCLOBACILLUS ACIDOCALDARIUS;
SOURCE   3 ORGANISM_COMMON: BACTERIA;
SOURCE   4 EXPRESSION_SYSTEM: ESCHERICHIA COLI;
SOURCE   5 EXPRESSION_SYSTEM_COMMON: BACTERIA;
SOURCE   6 EXPRESSION_SYSTEM_STRAIN: BL21 (DE3);
SOURCE   7 EXPRESSION_SYSTEM_VECTOR_TYPE: PLASMID;
SOURCE   8 EXPRESSION_SYSTEM_PLASMID: PT7-7SCII
KEYWDS    ALPHA/BETA HYDROLASE FOLD, X-RAY DIFFRACTION
EXPDTA    X-RAY DIFFRACTION
AUTHOR    V.MENCHISE,V.ALTERIO,G.DE SIMONE
REVDAT   1   26-JUN-07 2HM7    0
JRNL        AUTH   L.MANDRICH,V.MENCHISE,V.ALTERIO,G.DE SIMONE,
JRNL        AUTH 2 C.PEDONE,M.ROSSI,G.MANCO
JRNL        TITL   FUNCTIONAL AND STRUCTURAL CHARATERISTICS OF THE
JRNL        TITL 2 OXYANION HOLE IN A THERMOPHILIC ESTERASE FROM
JRNL        TITL 3 ALICYCLOBACILLUS ACIDOCALDARIUS
JRNL        REF    TO BE PUBLISHED
JRNL        REFN
REMARK   1
REMARK   1 REFERENCE 1
REMARK   1  AUTH   G.DE SIMONE,S.GALDIERO,G.MANCO,D.LANG,M.ROSSI,
REMARK   1  AUTH 2 C.PEDONE
REMARK   1  TITL   A SNAPSHOT OF THE TRANSITION STATE ANALOGUE OF A
REMARK   1  TITL 2 NOVEL THERMOPHILIC ESTERASE BELONGING TO THE
REMARK   1  TITL 3 SUBFAMILY OF MAMMALIAN HORMONE-SENSITIVE LIPASE
REMARK   1  REF    J.MOL.BIOL.                   V. 303   761 2000
REMARK   1  REFN   ASTM JMOBAK  UK ISSN 0022-2836
REMARK   2
REMARK   2 RESOLUTION. 2.00 ANGSTROMS.
REMARK   3
REMARK   3 REFINEMENT.
REMARK   3   PROGRAM     : CNS 1.1
REMARK   3   AUTHORS     : BRUNGER,ADAMS,CLORE,DELANO,GROS,GROSSE-
REMARK   3               : KUNSTLEVE,JIANG,KUSZEWSKI,NILGES, PANNU,
REMARK   3               : READ,RICE,SIMONSON,WARREN
REMARK   3
REMARK   3  REFINEMENT TARGET : ENGH & HUBER
REMARK   3
REMARK   3  DATA USED IN REFINEMENT.
REMARK   3   RESOLUTION RANGE HIGH (ANGSTROMS) : 2.00
REMARK   3   RESOLUTION RANGE LOW  (ANGSTROMS) : 20.00
REMARK   3   DATA CUTOFF            (SIGMA(F)) : 0.000
REMARK   3   DATA CUTOFF HIGH         (ABS(F)) : NULL
REMARK   3   DATA CUTOFF LOW          (ABS(F)) : NULL
REMARK   3   COMPLETENESS (WORKING+TEST)   (%) : NULL
REMARK   3   NUMBER OF REFLECTIONS             : 17482
REMARK   3
REMARK   3  FIT TO DATA USED IN REFINEMENT.
REMARK   3   CROSS-VALIDATION METHOD          : THROUGHOUT
REMARK   3   FREE R VALUE TEST SET SELECTION  : RANDOM
REMARK   3   R VALUE            (WORKING SET) : 0.196
REMARK   3   FREE R VALUE                     : 0.222
REMARK   3   FREE R VALUE TEST SET SIZE   (%) : NULL
REMARK   3   FREE R VALUE TEST SET COUNT      : 882
REMARK   3   ESTIMATED ERROR OF FREE R VALUE  : NULL
REMARK   3
REMARK   3  FIT IN THE HIGHEST RESOLUTION BIN.
REMARK   3   TOTAL NUMBER OF BINS USED           : NULL
REMARK   3   BIN RESOLUTION RANGE HIGH       (A) : NULL
REMARK   3   BIN RESOLUTION RANGE LOW        (A) : NULL
REMARK   3   BIN COMPLETENESS (WORKING+TEST) (%) : NULL
REMARK   3   REFLECTIONS IN BIN    (WORKING SET) : NULL
REMARK   3   BIN R VALUE           (WORKING SET) : NULL
REMARK   3   BIN FREE R VALUE                    : NULL
REMARK   3   BIN FREE R VALUE TEST SET SIZE  (%) : NULL
REMARK   3   BIN FREE R VALUE TEST SET COUNT     : NULL
REMARK   3   ESTIMATED ERROR OF BIN FREE R VALUE : NULL
REMARK   3
REMARK   3  NUMBER OF NON-HYDROGEN ATOMS USED IN REFINEMENT.
REMARK   3   PROTEIN ATOMS            : 2414
REMARK   3   NUCLEIC ACID ATOMS       : 0
REMARK   3   HETEROGEN ATOMS          : 4
REMARK   3   SOLVENT ATOMS            : 162
REMARK   3
REMARK   3  B VALUES.
REMARK   3   FROM WILSON PLOT           (A**2) : NULL
REMARK   3   MEAN B VALUE      (OVERALL, A**2) : NULL
REMARK   3   OVERALL ANISOTROPIC B VALUE.
REMARK   3    B11 (A**2) : NULL
REMARK   3    B22 (A**2) : NULL
REMARK   3    B33 (A**2) : NULL
REMARK   3    B12 (A**2) : NULL
REMARK   3    B13 (A**2) : NULL
REMARK   3    B23 (A**2) : NULL
REMARK   3
REMARK   3  ESTIMATED COORDINATE ERROR.
REMARK   3   ESD FROM LUZZATI PLOT        (A) : NULL
REMARK   3   ESD FROM SIGMAA              (A) : NULL
REMARK   3   LOW RESOLUTION CUTOFF        (A) : NULL
REMARK   3
REMARK   3  CROSS-VALIDATED ESTIMATED COORDINATE ERROR.
REMARK   3   ESD FROM C-V LUZZATI PLOT    (A) : NULL
REMARK   3   ESD FROM C-V SIGMAA          (A) : NULL
REMARK   3
REMARK   3  RMS DEVIATIONS FROM IDEAL VALUES.
REMARK   3   BOND LENGTHS                 (A) : 0.006
REMARK   3   BOND ANGLES            (DEGREES) : 1.30
REMARK   3   DIHEDRAL ANGLES        (DEGREES) : NULL
REMARK   3   IMPROPER ANGLES        (DEGREES) : NULL
REMARK   3
REMARK   3  ISOTROPIC THERMAL MODEL : NULL
REMARK   3
REMARK   3  ISOTROPIC THERMAL FACTOR RESTRAINTS.    RMS    SIGMA
REMARK   3   MAIN-CHAIN BOND              (A**2) : NULL  ; NULL
REMARK   3   MAIN-CHAIN ANGLE             (A**2) : NULL  ; NULL
REMARK   3   SIDE-CHAIN BOND              (A**2) : NULL  ; NULL
REMARK   3   SIDE-CHAIN ANGLE             (A**2) : NULL  ; NULL
REMARK   3
REMARK   3  BULK SOLVENT MODELING.
REMARK   3   METHOD USED : NULL
REMARK   3   KSOL        : NULL
REMARK   3   BSOL        : NULL
REMARK   3
REMARK   3  NCS MODEL : NULL
REMARK   3
REMARK   3  NCS RESTRAINTS.                         RMS   SIGMA/WEIGHT
REMARK   3   GROUP  1  POSITIONAL            (A) : NULL  ; NULL
REMARK   3   GROUP  1  B-FACTOR           (A**2) : NULL  ; NULL
REMARK   3
REMARK   3  PARAMETER FILE  1  : NULL
REMARK   3  TOPOLOGY FILE  1   : NULL
REMARK   3
REMARK   3  OTHER REFINEMENT REMARKS: NULL
REMARK   4
REMARK   4 2HM7 COMPLIES WITH FORMAT V. 3.0, 1-DEC-2006
REMARK   4
REMARK   4 THIS IS THE REMEDIATED VERSION OF THIS PDB ENTRY.
REMARK   4 REMEDIATED DATA FILE REVISION 3.100 (2007-06-18)
REMARK 100
REMARK 100 THIS ENTRY HAS BEEN PROCESSED BY RCSB.
REMARK 100 THE RCSB ID CODE IS RCSB038507.
REMARK 200
REMARK 200 EXPERIMENTAL DETAILS
REMARK 200  EXPERIMENT TYPE                : X-RAY DIFFRACTION
REMARK 200  DATE OF DATA COLLECTION        : NULL
REMARK 200  TEMPERATURE           (KELVIN) : 100.0
REMARK 200  PH                             : 8.00
REMARK 200  NUMBER OF CRYSTALS USED        : 1
REMARK 200
REMARK 200  SYNCHROTRON              (Y/N) : Y
REMARK 200  RADIATION SOURCE               : ESRF
REMARK 200  BEAMLINE                       : ID14-1
REMARK 200  X-RAY GENERATOR MODEL          : NULL
REMARK 200  MONOCHROMATIC OR LAUE    (M/L) : M
REMARK 200  WAVELENGTH OR RANGE        (A) : 0.934
REMARK 200  MONOCHROMATOR                  : NULL
REMARK 200  OPTICS                         : NULL
REMARK 200
REMARK 200  DETECTOR TYPE                  : CCD
REMARK 200  DETECTOR MANUFACTURER          : ADSC QUANTUM 210
REMARK 200  INTENSITY-INTEGRATION SOFTWARE : DENZO
REMARK 200  DATA SCALING SOFTWARE          : SCALEPACK
REMARK 200
REMARK 200  NUMBER OF UNIQUE REFLECTIONS   : 17662
REMARK 200  RESOLUTION RANGE HIGH      (A) : 2.000
REMARK 200  RESOLUTION RANGE LOW       (A) : 20.000
REMARK 200  REJECTION CRITERIA  (SIGMA(I)) : NULL
REMARK 200
REMARK 200 OVERALL.
REMARK 200  COMPLETENESS FOR RANGE     (%) : 97.8
REMARK 200  DATA REDUNDANCY                : NULL
REMARK 200  R MERGE                    (I) : NULL
REMARK 200  R SYM                      (I) : 0.05600
REMARK 200   FOR THE DATA SET  : 17.7000
REMARK 200
REMARK 200 IN THE HIGHEST RESOLUTION SHELL.
REMARK 200  HIGHEST RESOLUTION SHELL, RANGE HIGH (A) : NULL
REMARK 200  HIGHEST RESOLUTION SHELL, RANGE LOW  (A) : NULL
REMARK 200  COMPLETENESS FOR SHELL     (%) : 80.4
REMARK 200  DATA REDUNDANCY IN SHELL       : NULL
REMARK 200  R MERGE FOR SHELL          (I) : NULL
REMARK 200  R SYM FOR SHELL            (I) : 0.13700
REMARK 200   FOR SHELL         : 6.800
REMARK 200
REMARK 200 DIFFRACTION PROTOCOL: SINGLE WAVELENGTH
REMARK 200 METHOD USED TO DETERMINE THE STRUCTURE: MOLECULAR REPLACEMENT
REMARK 200 SOFTWARE USED: AMORE
REMARK 200 STARTING MODEL: PDB ENTRY 1EVQ
REMARK 200
REMARK 200 REMARK: NULL
REMARK 280
REMARK 280 CRYSTAL
REMARK 280 SOLVENT CONTENT, VS   (%): 32.54
REMARK 280 MATTHEWS COEFFICIENT, VM (ANGSTROMS**3/DA): 1.82
REMARK 280
REMARK 280 CRYSTALLIZATION CONDITIONS: 18% PEG 8000, 0.1M TRIS/HCL, 0.2M
REMARK 280  MAGNESIUM CHLORIDE, PH 8.0, VAPOR DIFFUSION, HANGING DROP,
REMARK 280  TEMPERATURE 298K
REMARK 290
REMARK 290 CRYSTALLOGRAPHIC SYMMETRY
REMARK 290 SYMMETRY OPERATORS FOR SPACE GROUP: P 21 21 2
REMARK 290
REMARK 290      SYMOP   SYMMETRY
REMARK 290     NNNMMM   OPERATOR
REMARK 290       1555   X,Y,Z
REMARK 290       2555   -X,-Y,Z
REMARK 290       3555   1/2-X,1/2+Y,-Z
REMARK 290       4555   1/2+X,1/2-Y,-Z
REMARK 290
REMARK 290     WHERE NNN -> OPERATOR NUMBER
REMARK 290           MMM -> TRANSLATION VECTOR
REMARK 290
REMARK 290 CRYSTALLOGRAPHIC SYMMETRY TRANSFORMATIONS
REMARK 290 THE FOLLOWING TRANSFORMATIONS OPERATE ON THE ATOM/HETATM
REMARK 290 RECORDS IN THIS ENTRY TO PRODUCE CRYSTALLOGRAPHICALLY
REMARK 290 RELATED MOLECULES.
REMARK 290   SMTRY1   1  1.000000  0.000000  0.000000        0.00000
REMARK 290   SMTRY2   1  0.000000  1.000000  0.000000        0.00000
REMARK 290   SMTRY3   1  0.000000  0.000000  1.000000        0.00000
REMARK 290   SMTRY1   2 -1.000000  0.000000  0.000000        0.00000
REMARK 290   SMTRY2   2  0.000000 -1.000000  0.000000        0.00000
REMARK 290   SMTRY3   2  0.000000  0.000000  1.000000        0.00000
REMARK 290   SMTRY1   3 -1.000000  0.000000  0.000000       31.83000
REMARK 290   SMTRY2   3  0.000000  1.000000  0.000000       41.08500
REMARK 290   SMTRY3   3  0.000000  0.000000 -1.000000        0.00000
REMARK 290   SMTRY1   4  1.000000  0.000000  0.000000       31.83000
REMARK 290   SMTRY2   4  0.000000 -1.000000  0.000000       41.08500
REMARK 290   SMTRY3   4  0.000000  0.000000 -1.000000        0.00000
REMARK 290
REMARK 290 REMARK: NULL
REMARK 300
REMARK 300 BIOMOLECULE: 1
REMARK 300 THIS ENTRY CONTAINS THE CRYSTALLOGRAPHIC ASYMMETRIC UNIT
REMARK 300 WHICH CONSISTS OF 1 CHAIN(S). SEE REMARK 350 FOR
REMARK 300 INFORMATION ON GENERATING THE BIOLOGICAL MOLECULE(S).
REMARK 350
REMARK 350 GENERATING THE BIOMOLECULE
REMARK 350 COORDINATES FOR A COMPLETE MULTIMER REPRESENTING THE KNOWN
REMARK 350 BIOLOGICALLY SIGNIFICANT OLIGOMERIZATION STATE OF THE
REMARK 350 MOLECULE CAN BE GENERATED BY APPLYING BIOMT TRANSFORMATIONS
REMARK 350 GIVEN BELOW.  BOTH NON-CRYSTALLOGRAPHIC AND
REMARK 350 CRYSTALLOGRAPHIC OPERATIONS ARE GIVEN.
REMARK 350
REMARK 350 BIOMOLECULE: 1
REMARK 350 APPLY THE FOLLOWING TO CHAINS: A
REMARK 350   BIOMT1   1  1.000000  0.000000  0.000000        0.00000
REMARK 350   BIOMT2   1  0.000000  1.000000  0.000000        0.00000
REMARK 350   BIOMT3   1  0.000000  0.000000  1.000000        0.00000
REMARK 465
REMARK 465 MISSING RESIDUES
REMARK 465 THE FOLLOWING RESIDUES WERE NOT LOCATED IN THE
REMARK 465 EXPERIMENT. (M=MODEL NUMBER; RES=RESIDUE NAME; C=CHAIN
REMARK 465 IDENTIFIER; SSSEQ=SEQUENCE NUMBER; I=INSERTION CODE.)
REMARK 465
REMARK 465   M RES C SSSEQI
REMARK 465     MET A     1
REMARK 465     PRO A     2
REMARK 500
REMARK 500 GEOMETRY AND STEREOCHEMISTRY
REMARK 500 SUBTOPIC: COVALENT BOND LENGTHS
REMARK 500
REMARK 500 THE STEREOCHEMICAL PARAMETERS OF THE FOLLOWING RESIDUES
REMARK 500 HAVE VALUES WHICH DEVIATE FROM EXPECTED VALUES BY MORE
REMARK 500 THAN 6*RMSD (M=MODEL NUMBER; RES=RESIDUE NAME; C=CHAIN
REMARK 500 IDENTIFIER; SSEQ=SEQUENCE NUMBER; I=INSERTION CODE).
REMARK 500
REMARK 500 STANDARD TABLE:
REMARK 500 FORMAT: (10X,I3,1X,2(A3,1X,A1,I4,A1,1X,A4,3X),F6.3)
REMARK 500
REMARK 500 EXPECTED VALUES: ENGH AND HUBER, 1991
REMARK 500
REMARK 500  M RES CSSEQI ATM1   RES CSSEQI ATM2   DEVIATION
REMARK 500    PRO A  38   CB    PRO A  38   CG     0.038
REMARK 500    PRO A 122   CG    PRO A 122   CD     0.034
REMARK 500    SER A 155   CB    SER A 155   OG     0.035
REMARK 500    MET A 211   SD    MET A 211   CE    -0.062
REMARK 500
REMARK 500 GEOMETRY AND STEREOCHEMISTRY
REMARK 500 SUBTOPIC: COVALENT BOND ANGLES
REMARK 500
REMARK 500 THE STEREOCHEMICAL PARAMETERS OF THE FOLLOWING RESIDUES
REMARK 500 HAVE VALUES WHICH DEVIATE FROM EXPECTED VALUES BY MORE
REMARK 500 THAN 6*RMSD (M=MODEL NUMBER; RES=RESIDUE NAME; C=CHAIN
REMARK 500 IDENTIFIER; SSEQ=SEQUENCE NUMBER; I=INSERTION CODE).
REMARK 500
REMARK 500 STANDARD TABLE:
REMARK 500 FORMAT: (10X,I3,1X,A3,1X,A1,I4,A1,3(1X,A4,2X),12X,F5.1)
REMARK 500
REMARK 500 EXPECTED VALUES: ENGH AND HUBER, 1991
REMARK 500
REMARK 500  M RES CSSEQI ATM1   ATM2   ATM3
REMARK 500    PRO A  75   N   -  CA  -  C   ANGL. DEV. =-12.5 DEGREES
REMARK 500    VAL A  78   N   -  CA  -  C   ANGL. DEV. = -9.1 DEGREES
REMARK 500    PRO A 122   C   -  N   -  CA  ANGL. DEV. =  8.0 DEGREES
REMARK 500    HIS A 227   N   -  CA  -  C   ANGL. DEV. = -8.3 DEGREES
REMARK 500    PRO A 236   N   -  CA  -  C   ANGL. DEV. =  7.9 DEGREES
REMARK 500
REMARK 500 GEOMETRY AND STEREOCHEMISTRY
REMARK 500 SUBTOPIC: TORSION ANGLES
REMARK 500
REMARK 500 TORSION ANGLES OUTSIDE THE EXPECTED RAMACHANDRAN REGIONS:
REMARK 500 (M=MODEL NUMBER; RES=RESIDUE NAME; C=CHAIN IDENTIFIER;
REMARK 500 SSEQ=SEQUENCE NUMBER; I=INSERTION CODE).
REMARK 500
REMARK 500 STANDARD TABLE:
REMARK 500 FORMAT:(10X,I3,1X,A3,1X,A1,I4,A1,4X,F7.2,3X,F7.2)
REMARK 500
REMARK 500  M RES CSSEQI        PSI       PHI
REMARK 500    LEU A 205      -67.31     73.57
REMARK 900
REMARK 900 RELATED ENTRIES
REMARK 900 RELATED ID: 1EVQ   RELATED DB: PDB
REMARK 900 THE CRYSTAL STRUCTURE OF THE CARBOXYLESTERASE EST2 FROM
REMARK 900 ALICYCLOBACILLUS ACIDOCALDARIUS
DBREF  2HM7 A    1   310  UNP    Q7SIG1   Q7SIG1_ALIAC     1    310
SEQADV 2HM7 SER A   84  UNP  Q7SIG1    GLY    84 ENGINEERED
SEQRES   1 A  310  MET PRO LEU ASP PRO VAL ILE GLN GLN VAL LEU ASP GLN
SEQRES   2 A  310  LEU ASN ARG MET PRO ALA PRO ASP TYR LYS HIS LEU SER
SEQRES   3 A  310  ALA GLN GLN PHE ARG SER GLN GLN SER LEU PHE PRO PRO
SEQRES   4 A  310  VAL LYS LYS GLU PRO VAL ALA GLU VAL ARG GLU PHE ASP
SEQRES   5 A  310  MET ASP LEU PRO GLY ARG THR LEU LYS VAL ARG MET TYR
SEQRES   6 A  310  ARG PRO GLU GLY VAL GLU PRO PRO TYR PRO ALA LEU VAL
SEQRES   7 A  310  TYR TYR HIS GLY GLY SER TRP VAL VAL GLY ASP LEU GLU
SEQRES   8 A  310  THR HIS ASP PRO VAL CYS ARG VAL LEU ALA LYS ASP GLY
SEQRES   9 A  310  ARG ALA VAL VAL PHE SER VAL ASP TYR ARG LEU ALA PRO
SEQRES  10 A  310  GLU HIS LYS PHE PRO ALA ALA VAL GLU ASP ALA TYR ASP
SEQRES  11 A  310  ALA LEU GLN TRP ILE ALA GLU ARG ALA ALA ASP PHE HIS
SEQRES  12 A  310  LEU ASP PRO ALA ARG ILE ALA VAL GLY GLY ASP SER ALA
SEQRES  13 A  310  GLY GLY ASN LEU ALA ALA VAL THR SER ILE LEU ALA LYS
SEQRES  14 A  310  GLU ARG GLY GLY PRO ALA LEU ALA PHE GLN LEU LEU ILE
SEQRES  15 A  310  TYR PRO SER THR GLY TYR ASP PRO ALA HIS PRO PRO ALA
SEQRES  16 A  310  SER ILE GLU GLU ASN ALA GLU GLY TYR LEU LEU THR GLY
SEQRES  17 A  310  GLY MET MET LEU TRP PHE ARG ASP GLN TYR LEU ASN SER
SEQRES  18 A  310  LEU GLU GLU LEU THR HIS PRO TRP PHE SER PRO VAL LEU
SEQRES  19 A  310  TYR PRO ASP LEU SER GLY LEU PRO PRO ALA TYR ILE ALA
SEQRES  20 A  310  THR ALA GLN TYR ASP PRO LEU ARG ASP VAL GLY LYS LEU
SEQRES  21 A  310  TYR ALA GLU ALA LEU ASN LYS ALA GLY VAL LYS VAL GLU
SEQRES  22 A  310  ILE GLU ASN PHE GLU ASP LEU ILE HIS GLY PHE ALA GLN
SEQRES  23 A  310  PHE TYR SER LEU SER PRO GLY ALA THR LYS ALA LEU VAL
SEQRES  24 A  310  ARG ILE ALA GLU LYS LEU ARG ASP ALA LEU ALA
HET    SO4  A 455       4
HETNAM     SO4 SULFATE ION
FORMUL   2  SO4    O4 S 2-
FORMUL   3  HOH   *162(H2 O)
HELIX    1   1 ASP A    4  ARG A   16  1                                  13
HELIX    2   2 ASP A   21  LEU A   25  5                                   5
HELIX    3   3 SER A   26  GLN A   34  1                                   9
HELIX    4   4 HIS A   93  ARG A  105  1                                  13
HELIX    5   5 PRO A  122  ARG A  138  1                                  17
HELIX    6   6 ALA A  139  PHE A  142  5                                   4
HELIX    7   7 SER A  155  ARG A  171  1                                  17
HELIX    8   8 PRO A  194  ASN A  200  1                                   7
HELIX    9   9 THR A  207  LEU A  219  1                                  13
HELIX   10  10 SER A  221  HIS A  227  5                                   7
HELIX   11  11 SER A  231  TYR A  235  5                                   5
HELIX   12  12 LEU A  254  ALA A  268  1                                  15
HELIX   13  13 GLY A  283  TYR A  288  5                                   6
HELIX   14  14 SER A  291  ALA A  310  1                                  20
SHEET    1   A 8 GLU A  47  LEU A  55  0
SHEET    2   A 8 ARG A  58  ARG A  66 -1  O  MET A  64   N  ARG A  49
SHEET    3   A 8 VAL A 107  VAL A 111 -1  O  VAL A 108   N  TYR A  65
SHEET    4   A 8 TYR A  74  TYR A  80  1  N  TYR A  79   O  PHE A 109
SHEET    5   A 8 LEU A 144  ASP A 154  1  O  ARG A 148   N  ALA A  76
SHEET    6   A 8 GLN A 179  ILE A 182  1  O  LEU A 180   N  VAL A 151
SHEET    7   A 8 ALA A 244  TYR A 251  1  O  TYR A 245   N  LEU A 181
SHEET    8   A 8 VAL A 272  ILE A 281  1  O  GLU A 273   N  ILE A 246
LINK         OG  SER A 155                 S   SO4 A 455
CISPEP   1 PHE A   37    PRO A   38          0        -0.07
CISPEP   2 PRO A   72    PRO A   73          0        -0.27
CISPEP   3 ALA A  116    PRO A  117          0         0.10
CISPEP   4 PHE A  121    PRO A  122          0         0.31
CISPEP   5 GLY A  173    PRO A  174          0         0.05
CRYST1   63.660   82.170   47.960  90.00  90.00  90.00 P 21 21 2     4
ORIGX1      1.000000  0.000000  0.000000        0.00000
ORIGX2      0.000000  1.000000  0.000000        0.00000
ORIGX3      0.000000  0.000000  1.000000        0.00000
SCALE1      0.015708  0.000000  0.000000        0.00000
SCALE2      0.000000  0.012170  0.000000        0.00000
SCALE3      0.000000  0.000000  0.020851        0.00000
TER    2415      ALA A 310
MASTER      286    0    1   14    8    0    0    6 2580    1    5   24
END