longtext: 9UM6-pdb

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HEADER    HYDROLASE                               21-APR-25   9UM6
TITLE     CAPETASEM9 SEC LOOP OF 10CL+E289P VARIANT
COMPND    MOL_ID: 1;
COMPND   2 MOLECULE: CUTINASE;
COMPND   3 CHAIN: A, B;
COMPND   4 ENGINEERED: YES;
COMPND   5 OTHER_DETAILS: CAPETASEM9 SEC LOOP OF 10CL+E289P VARIANT
SOURCE    MOL_ID: 1;
SOURCE   2 ORGANISM_SCIENTIFIC: CRYPTOSPORANGIUM AURANTIACUM;
SOURCE   3 ORGANISM_TAXID: 134849;
SOURCE   4 GENE: SAMN05443668_101498;
SOURCE   5 EXPRESSION_SYSTEM: ESCHERICHIA COLI;
SOURCE   6 EXPRESSION_SYSTEM_TAXID: 562
KEYWDS    PETASE, CRYPTOSPORANGIUM, AURANTIACUM, CAPETASE, HYDROLASE
EXPDTA    X-RAY DIFFRACTION
AUTHOR    K.KIM,D.KI,J.PARK
REVDAT   1   29-APR-26 9UM6    0
JRNL        AUTH   K.KIM,D.KI,J.PARK
JRNL        TITL   MECHANISTIC INSIGHTS INTO MODULATION OF PRODUCTIVE SUBSTRATE
JRNL        TITL 2 ACCESSIBILITY FOR EFFICIENT PET DEPOLYMERIZATION
JRNL        REF    TO BE PUBLISHED
JRNL        REFN
REMARK   2
REMARK   2 RESOLUTION.    1.66 ANGSTROMS.
REMARK   3
REMARK   3 REFINEMENT.
REMARK   3   PROGRAM     : REFMAC 5.8.0425
REMARK   3   AUTHORS     : MURSHUDOV,SKUBAK,LEBEDEV,PANNU,STEINER,
REMARK   3               : NICHOLLS,WINN,LONG,VAGIN
REMARK   3
REMARK   3    REFINEMENT TARGET : MAXIMUM LIKELIHOOD
REMARK   3
REMARK   3  DATA USED IN REFINEMENT.
REMARK   3   RESOLUTION RANGE HIGH (ANGSTROMS) : 1.66
REMARK   3   RESOLUTION RANGE LOW  (ANGSTROMS) : 34.08
REMARK   3   DATA CUTOFF            (SIGMA(F)) : NULL
REMARK   3   COMPLETENESS FOR RANGE        (%) : 99.8
REMARK   3   NUMBER OF REFLECTIONS             : 77432
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 + TEST SET) : 0.186
REMARK   3   R VALUE            (WORKING SET) : 0.185
REMARK   3   FREE R VALUE                     : 0.209
REMARK   3   FREE R VALUE TEST SET SIZE   (%) : 5.000
REMARK   3   FREE R VALUE TEST SET COUNT      : 4060
REMARK   3
REMARK   3  FIT IN THE HIGHEST RESOLUTION BIN.
REMARK   3   TOTAL NUMBER OF BINS USED           : 20
REMARK   3   BIN RESOLUTION RANGE HIGH       (A) : 1.66
REMARK   3   BIN RESOLUTION RANGE LOW        (A) : 1.70
REMARK   3   REFLECTION IN BIN     (WORKING SET) : 5575
REMARK   3   BIN COMPLETENESS (WORKING+TEST) (%) : 98.60
REMARK   3   BIN R VALUE           (WORKING SET) : 0.2110
REMARK   3   BIN FREE R VALUE SET COUNT          : 282
REMARK   3   BIN FREE R VALUE                    : 0.2570
REMARK   3
REMARK   3  NUMBER OF NON-HYDROGEN ATOMS USED IN REFINEMENT.
REMARK   3   PROTEIN ATOMS            : 3945
REMARK   3   NUCLEIC ACID ATOMS       : 0
REMARK   3   HETEROGEN ATOMS          : 0
REMARK   3   SOLVENT ATOMS            : 208
REMARK   3
REMARK   3  B VALUES.
REMARK   3   FROM WILSON PLOT           (A**2) : NULL
REMARK   3   MEAN B VALUE      (OVERALL, A**2) : 19.59
REMARK   3   OVERALL ANISOTROPIC B VALUE.
REMARK   3    B11 (A**2) : 0.24000
REMARK   3    B22 (A**2) : 0.21000
REMARK   3    B33 (A**2) : -0.45000
REMARK   3    B12 (A**2) : 0.00000
REMARK   3    B13 (A**2) : 0.00000
REMARK   3    B23 (A**2) : 0.00000
REMARK   3
REMARK   3  ESTIMATED OVERALL COORDINATE ERROR.
REMARK   3   ESU BASED ON R VALUE                            (A): 0.082
REMARK   3   ESU BASED ON FREE R VALUE                       (A): 0.082
REMARK   3   ESU BASED ON MAXIMUM LIKELIHOOD                 (A): 0.052
REMARK   3   ESU FOR B VALUES BASED ON MAXIMUM LIKELIHOOD (A**2): 1.522
REMARK   3
REMARK   3 CORRELATION COEFFICIENTS.
REMARK   3   CORRELATION COEFFICIENT FO-FC      : 0.958
REMARK   3   CORRELATION COEFFICIENT FO-FC FREE : 0.950
REMARK   3
REMARK   3  RMS DEVIATIONS FROM IDEAL VALUES        COUNT    RMS    WEIGHT
REMARK   3   BOND LENGTHS REFINED ATOMS        (A):  4064 ; 0.012 ; 0.012
REMARK   3   BOND LENGTHS OTHERS               (A):  3684 ; 0.001 ; 0.016
REMARK   3   BOND ANGLES REFINED ATOMS   (DEGREES):  5560 ; 1.984 ; 1.785
REMARK   3   BOND ANGLES OTHERS          (DEGREES):  8472 ; 0.691 ; 1.734
REMARK   3   TORSION ANGLES, PERIOD 1    (DEGREES):   517 ; 6.733 ; 5.000
REMARK   3   TORSION ANGLES, PERIOD 2    (DEGREES):    30 ; 9.455 ; 5.000
REMARK   3   TORSION ANGLES, PERIOD 3    (DEGREES):   565 ;11.209 ;10.000
REMARK   3   TORSION ANGLES, PERIOD 4    (DEGREES):  NULL ;  NULL ;  NULL
REMARK   3   CHIRAL-CENTER RESTRAINTS       (A**3):   598 ; 0.104 ; 0.200
REMARK   3   GENERAL PLANES REFINED ATOMS      (A):  4964 ; 0.011 ; 0.020
REMARK   3   GENERAL PLANES OTHERS             (A):   996 ; 0.001 ; 0.020
REMARK   3   NON-BONDED CONTACTS REFINED ATOMS (A):  NULL ;  NULL ;  NULL
REMARK   3   NON-BONDED CONTACTS OTHERS        (A):  NULL ;  NULL ;  NULL
REMARK   3   NON-BONDED TORSION REFINED ATOMS  (A):  NULL ;  NULL ;  NULL
REMARK   3   NON-BONDED TORSION OTHERS         (A):  NULL ;  NULL ;  NULL
REMARK   3   H-BOND (X...Y) REFINED ATOMS      (A):  NULL ;  NULL ;  NULL
REMARK   3   H-BOND (X...Y) OTHERS             (A):  NULL ;  NULL ;  NULL
REMARK   3   POTENTIAL METAL-ION REFINED ATOMS (A):  NULL ;  NULL ;  NULL
REMARK   3   POTENTIAL METAL-ION OTHERS        (A):  NULL ;  NULL ;  NULL
REMARK   3   SYMMETRY VDW REFINED ATOMS        (A):  NULL ;  NULL ;  NULL
REMARK   3   SYMMETRY VDW OTHERS               (A):  NULL ;  NULL ;  NULL
REMARK   3   SYMMETRY H-BOND REFINED ATOMS     (A):  NULL ;  NULL ;  NULL
REMARK   3   SYMMETRY H-BOND OTHERS            (A):  NULL ;  NULL ;  NULL
REMARK   3   SYMMETRY METAL-ION REFINED ATOMS  (A):  NULL ;  NULL ;  NULL
REMARK   3   SYMMETRY METAL-ION OTHERS         (A):  NULL ;  NULL ;  NULL
REMARK   3
REMARK   3  ISOTROPIC THERMAL FACTOR RESTRAINTS.     COUNT   RMS    WEIGHT
REMARK   3   MAIN-CHAIN BOND REFINED ATOMS  (A**2):  2074 ; 2.079 ; 1.900
REMARK   3   MAIN-CHAIN BOND OTHER ATOMS    (A**2):  2074 ; 2.078 ; 1.900
REMARK   3   MAIN-CHAIN ANGLE REFINED ATOMS (A**2):  2589 ; 2.836 ; 3.414
REMARK   3   MAIN-CHAIN ANGLE OTHER ATOMS   (A**2):  2590 ; 2.836 ; 3.415
REMARK   3   SIDE-CHAIN BOND REFINED ATOMS  (A**2):  1990 ; 2.828 ; 2.156
REMARK   3   SIDE-CHAIN BOND OTHER ATOMS    (A**2):  1991 ; 2.828 ; 2.157
REMARK   3   SIDE-CHAIN ANGLE REFINED ATOMS (A**2):  NULL ;  NULL ;  NULL
REMARK   3   SIDE-CHAIN ANGLE OTHER ATOMS   (A**2):  2972 ; 4.176 ; 3.836
REMARK   3   LONG RANGE B REFINED ATOMS     (A**2):  4530 ; 4.917 ;20.030
REMARK   3   LONG RANGE B OTHER ATOMS       (A**2):  4506 ; 4.912 ;19.820
REMARK   3
REMARK   3 ANISOTROPIC THERMAL FACTOR RESTRAINTS.    COUNT   RMS   WEIGHT
REMARK   3   RIGID-BOND RESTRAINTS          (A**2):  NULL ;  NULL ;  NULL
REMARK   3   SPHERICITY; FREE ATOMS         (A**2):  NULL ;  NULL ;  NULL
REMARK   3   SPHERICITY; BONDED ATOMS       (A**2):  NULL ;  NULL ;  NULL
REMARK   3
REMARK   3  NCS RESTRAINTS STATISTICS
REMARK   3   NUMBER OF DIFFERENT NCS GROUPS : NULL
REMARK   3
REMARK   3  TLS DETAILS
REMARK   3   NUMBER OF TLS GROUPS  : NULL
REMARK   3
REMARK   3  BULK SOLVENT MODELLING.
REMARK   3   METHOD USED : MASK
REMARK   3   PARAMETERS FOR MASK CALCULATION
REMARK   3   VDW PROBE RADIUS   : 1.20
REMARK   3   ION PROBE RADIUS   : 0.80
REMARK   3   SHRINKAGE RADIUS   : 0.80
REMARK   3
REMARK   3  OTHER REFINEMENT REMARKS: HYDROGENS HAVE BEEN ADDED IN THE RIDING
REMARK   3  POSITIONS
REMARK   4
REMARK   4 9UM6 COMPLIES WITH FORMAT V. 3.30, 13-JUL-11
REMARK 100
REMARK 100 THIS ENTRY HAS BEEN PROCESSED BY PDBJ ON 23-APR-25.
REMARK 100 THE DEPOSITION ID IS D_1300058596.
REMARK 200
REMARK 200 EXPERIMENTAL DETAILS
REMARK 200  EXPERIMENT TYPE                : X-RAY DIFFRACTION
REMARK 200  DATE OF DATA COLLECTION        : 18-OCT-24
REMARK 200  TEMPERATURE           (KELVIN) : 100
REMARK 200  PH                             : NULL
REMARK 200  NUMBER OF CRYSTALS USED        : 1
REMARK 200
REMARK 200  SYNCHROTRON              (Y/N) : Y
REMARK 200  RADIATION SOURCE               : PAL/PLS
REMARK 200  BEAMLINE                       : 7A (6B, 6C1)
REMARK 200  X-RAY GENERATOR MODEL          : NULL
REMARK 200  MONOCHROMATIC OR LAUE    (M/L) : M
REMARK 200  WAVELENGTH OR RANGE        (A) : 0.97934
REMARK 200  MONOCHROMATOR                  : NULL
REMARK 200  OPTICS                         : NULL
REMARK 200
REMARK 200  DETECTOR TYPE                  : PIXEL
REMARK 200  DETECTOR MANUFACTURER          : DECTRIS EIGER2 S 9M
REMARK 200  INTENSITY-INTEGRATION SOFTWARE : HKL-2000
REMARK 200  DATA SCALING SOFTWARE          : HKL-2000
REMARK 200
REMARK 200  NUMBER OF UNIQUE REFLECTIONS   : 81578
REMARK 200  RESOLUTION RANGE HIGH      (A) : 1.660
REMARK 200  RESOLUTION RANGE LOW       (A) : 50.000
REMARK 200  REJECTION CRITERIA  (SIGMA(I)) : NULL
REMARK 200
REMARK 200 OVERALL.
REMARK 200  COMPLETENESS FOR RANGE     (%) : 99.9
REMARK 200  DATA REDUNDANCY                : 12.50
REMARK 200  R MERGE                    (I) : 0.14900
REMARK 200  R SYM                      (I) : NULL
REMARK 200   FOR THE DATA SET  : 10.8000
REMARK 200
REMARK 200 IN THE HIGHEST RESOLUTION SHELL.
REMARK 200  HIGHEST RESOLUTION SHELL, RANGE HIGH (A) : 1.66
REMARK 200  HIGHEST RESOLUTION SHELL, RANGE LOW  (A) : 1.69
REMARK 200  COMPLETENESS FOR SHELL     (%) : 99.5
REMARK 200  DATA REDUNDANCY IN SHELL       : 9.40
REMARK 200  R MERGE FOR SHELL          (I) : 0.49100
REMARK 200  R SYM FOR SHELL            (I) : NULL
REMARK 200   FOR SHELL         : NULL
REMARK 200
REMARK 200 DIFFRACTION PROTOCOL: SINGLE WAVELENGTH
REMARK 200 METHOD USED TO DETERMINE THE STRUCTURE: MOLECULAR REPLACEMENT
REMARK 200 SOFTWARE USED: MOLREP
REMARK 200 STARTING MODEL: 7YME
REMARK 200
REMARK 200 REMARK: NULL
REMARK 280
REMARK 280 CRYSTAL
REMARK 280 SOLVENT CONTENT, VS   (%): 58.24
REMARK 280 MATTHEWS COEFFICIENT, VM (ANGSTROMS**3/DA): 2.95
REMARK 280
REMARK 280 CRYSTALLIZATION CONDITIONS: 12% (W/V) PEG 3350, 4% (V/V) TACSIMATE
REMARK 280  PH 4.0, VAPOR DIFFUSION, SITTING DROP, TEMPERATURE 293K
REMARK 290
REMARK 290 CRYSTALLOGRAPHIC SYMMETRY
REMARK 290 SYMMETRY OPERATORS FOR SPACE GROUP: P 21 21 21
REMARK 290
REMARK 290      SYMOP   SYMMETRY
REMARK 290     NNNMMM   OPERATOR
REMARK 290       1555   X,Y,Z
REMARK 290       2555   -X+1/2,-Y,Z+1/2
REMARK 290       3555   -X,Y+1/2,-Z+1/2
REMARK 290       4555   X+1/2,-Y+1/2,-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       20.56700
REMARK 290   SMTRY2   2  0.000000 -1.000000  0.000000        0.00000
REMARK 290   SMTRY3   2  0.000000  0.000000  1.000000       71.13800
REMARK 290   SMTRY1   3 -1.000000  0.000000  0.000000        0.00000
REMARK 290   SMTRY2   3  0.000000  1.000000  0.000000       58.17950
REMARK 290   SMTRY3   3  0.000000  0.000000 -1.000000       71.13800
REMARK 290   SMTRY1   4  1.000000  0.000000  0.000000       20.56700
REMARK 290   SMTRY2   4  0.000000 -1.000000  0.000000       58.17950
REMARK 290   SMTRY3   4  0.000000  0.000000 -1.000000        0.00000
REMARK 290
REMARK 290 REMARK: NULL
REMARK 300
REMARK 300 BIOMOLECULE: 1, 2
REMARK 300 SEE REMARK 350 FOR THE AUTHOR PROVIDED AND/OR PROGRAM
REMARK 300 GENERATED ASSEMBLY INFORMATION FOR THE STRUCTURE IN
REMARK 300 THIS ENTRY. THE REMARK MAY ALSO PROVIDE INFORMATION ON
REMARK 300 BURIED SURFACE AREA.
REMARK 350
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 AUTHOR DETERMINED BIOLOGICAL UNIT: MONOMERIC
REMARK 350 SOFTWARE DETERMINED QUATERNARY STRUCTURE: MONOMERIC
REMARK 350 SOFTWARE USED: PISA
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 350
REMARK 350 BIOMOLECULE: 2
REMARK 350 AUTHOR DETERMINED BIOLOGICAL UNIT: MONOMERIC
REMARK 350 APPLY THE FOLLOWING TO CHAINS: B
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     GLU A    39
REMARK 465     PRO A    40
REMARK 465     ALA A    41
REMARK 465     ALA A    42
REMARK 465     HIS A   303
REMARK 465     HIS A   304
REMARK 465     HIS A   305
REMARK 465     GLU B    39
REMARK 465     PRO B    40
REMARK 465     LEU B   300
REMARK 465     GLU B   301
REMARK 465     HIS B   302
REMARK 465     HIS B   303
REMARK 465     HIS B   304
REMARK 465     HIS B   305
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 PROTEIN: ENGH AND HUBER, 1999
REMARK 500 EXPECTED VALUES NUCLEIC ACID: CLOWNEY ET AL 1996
REMARK 500
REMARK 500  M RES CSSEQI ATM1   ATM2   ATM3
REMARK 500    CYS A 180   CB  -  CA  -  C   ANGL. DEV. =   8.0 DEGREES
REMARK 500    ARG A 266   NE  -  CZ  -  NH1 ANGL. DEV. =   3.4 DEGREES
REMARK 500    ILE B 102   CA  -  C   -  N   ANGL. DEV. = -15.4 DEGREES
REMARK 500    ILE B 102   O   -  C   -  N   ANGL. DEV. =  16.3 DEGREES
REMARK 500
REMARK 500 REMARK: NULL
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 EXPECTED VALUES: GJ KLEYWEGT AND TA JONES (1996). PHI/PSI-
REMARK 500 CHOLOGY: RAMACHANDRAN REVISITED. STRUCTURE 4, 1395 - 1400
REMARK 500
REMARK 500  M RES CSSEQI        PSI       PHI
REMARK 500    SER A 169     -124.37     60.21
REMARK 500    HIS A 223      -86.21   -123.32
REMARK 500    PHE A 299       46.81     75.03
REMARK 500    ILE B 102       58.30     37.82
REMARK 500    SER B 169     -128.69     61.91
REMARK 500    HIS B 223      -89.69   -126.04
REMARK 500
REMARK 500 REMARK: NULL
REMARK 500
REMARK 500 GEOMETRY AND STEREOCHEMISTRY
REMARK 500 SUBTOPIC: PLANAR GROUPS
REMARK 500
REMARK 500 PLANAR GROUPS IN THE FOLLOWING RESIDUES HAVE A TOTAL
REMARK 500 RMS DISTANCE OF ALL ATOMS FROM THE BEST-FIT PLANE
REMARK 500 BY MORE THAN AN EXPECTED VALUE OF 6*RMSD, WITH AN
REMARK 500 RMSD 0.02 ANGSTROMS, OR AT LEAST ONE ATOM HAS
REMARK 500 AN RMSD GREATER THAN THIS VALUE
REMARK 500 (M=MODEL NUMBER; RES=RESIDUE NAME; C=CHAIN IDENTIFIER;
REMARK 500 SSEQ=SEQUENCE NUMBER; I=INSERTION CODE).
REMARK 500
REMARK 500  M RES CSSEQI        RMS     TYPE
REMARK 500    ARG A 137         0.14    SIDE CHAIN
REMARK 500    ARG A 176         0.09    SIDE CHAIN
REMARK 500    ARG B 137         0.07    SIDE CHAIN
REMARK 500    ARG B 182         0.10    SIDE CHAIN
REMARK 500
REMARK 500 REMARK: NULL
DBREF1 9UM6 A   39   299  UNP                  A0A1M7II12_9ACTN
DBREF2 9UM6 A     A0A1M7II12                         39         299
DBREF1 9UM6 B   39   299  UNP                  A0A1M7II12_9ACTN
DBREF2 9UM6 B     A0A1M7II12                         39         299
SEQADV 9UM6 GLU A   39  UNP  A0A1M7II1 ALA    39 ENGINEERED MUTATION
SEQADV 9UM6 PRO A   40  UNP  A0A1M7II1 GLN    40 ENGINEERED MUTATION
SEQADV 9UM6 ALA A  109  UNP  A0A1M7II1 ASN   109 ENGINEERED MUTATION
SEQADV 9UM6 THR A  129  UNP  A0A1M7II1 VAL   129 ENGINEERED MUTATION
SEQADV 9UM6 ARG A  155  UNP  A0A1M7II1 ALA   155 ENGINEERED MUTATION
SEQADV 9UM6 CYS A  180  UNP  A0A1M7II1 LEU   180 ENGINEERED MUTATION
SEQADV 9UM6 THR A  196  UNP  A0A1M7II1 GLY   196 ENGINEERED MUTATION
SEQADV 9UM6 LYS A  198  UNP  A0A1M7II1 ARG   198 ENGINEERED MUTATION
SEQADV 9UM6 CYS A  202  UNP  A0A1M7II1 ALA   202 ENGINEERED MUTATION
SEQADV 9UM6 CYS A  242  UNP  A0A1M7II1 ARG   242 ENGINEERED MUTATION
SEQADV 9UM6 ARG A  283  UNP  A0A1M7II1 SER   283 ENGINEERED MUTATION
SEQADV 9UM6 ASP A  284  UNP  A0A1M7II1 THR   284 ENGINEERED MUTATION
SEQADV 9UM6 GLY A  288  UNP  A0A1M7II1 ALA   288 ENGINEERED MUTATION
SEQADV 9UM6 CYS A  291  UNP  A0A1M7II1 SER   291 ENGINEERED MUTATION
SEQADV 9UM6 LEU A  300  UNP  A0A1M7II1           EXPRESSION TAG
SEQADV 9UM6 GLU A  301  UNP  A0A1M7II1           EXPRESSION TAG
SEQADV 9UM6 HIS A  302  UNP  A0A1M7II1           EXPRESSION TAG
SEQADV 9UM6 HIS A  303  UNP  A0A1M7II1           EXPRESSION TAG
SEQADV 9UM6 HIS A  304  UNP  A0A1M7II1           EXPRESSION TAG
SEQADV 9UM6 HIS A  305  UNP  A0A1M7II1           EXPRESSION TAG
SEQADV 9UM6 GLU B   39  UNP  A0A1M7II1 ALA    39 ENGINEERED MUTATION
SEQADV 9UM6 PRO B   40  UNP  A0A1M7II1 GLN    40 ENGINEERED MUTATION
SEQADV 9UM6 ALA B  109  UNP  A0A1M7II1 ASN   109 ENGINEERED MUTATION
SEQADV 9UM6 THR B  129  UNP  A0A1M7II1 VAL   129 ENGINEERED MUTATION
SEQADV 9UM6 ARG B  155  UNP  A0A1M7II1 ALA   155 ENGINEERED MUTATION
SEQADV 9UM6 CYS B  180  UNP  A0A1M7II1 LEU   180 ENGINEERED MUTATION
SEQADV 9UM6 THR B  196  UNP  A0A1M7II1 GLY   196 ENGINEERED MUTATION
SEQADV 9UM6 LYS B  198  UNP  A0A1M7II1 ARG   198 ENGINEERED MUTATION
SEQADV 9UM6 CYS B  202  UNP  A0A1M7II1 ALA   202 ENGINEERED MUTATION
SEQADV 9UM6 CYS B  242  UNP  A0A1M7II1 ARG   242 ENGINEERED MUTATION
SEQADV 9UM6 ARG B  283  UNP  A0A1M7II1 SER   283 ENGINEERED MUTATION
SEQADV 9UM6 ASP B  284  UNP  A0A1M7II1 THR   284 ENGINEERED MUTATION
SEQADV 9UM6 GLY B  288  UNP  A0A1M7II1 ALA   288 ENGINEERED MUTATION
SEQADV 9UM6 CYS B  291  UNP  A0A1M7II1 SER   291 ENGINEERED MUTATION
SEQADV 9UM6 LEU B  300  UNP  A0A1M7II1           EXPRESSION TAG
SEQADV 9UM6 GLU B  301  UNP  A0A1M7II1           EXPRESSION TAG
SEQADV 9UM6 HIS B  302  UNP  A0A1M7II1           EXPRESSION TAG
SEQADV 9UM6 HIS B  303  UNP  A0A1M7II1           EXPRESSION TAG
SEQADV 9UM6 HIS B  304  UNP  A0A1M7II1           EXPRESSION TAG
SEQADV 9UM6 HIS B  305  UNP  A0A1M7II1           EXPRESSION TAG
SEQRES   1 A  267  GLU PRO ALA ALA ASP ASN PRO TYR GLN ARG GLY PRO ASP
SEQRES   2 A  267  PRO THR ASN ALA SER ILE GLU ALA ALA THR GLY PRO PHE
SEQRES   3 A  267  ALA VAL GLY THR GLN PRO ILE VAL GLY ALA SER GLY PHE
SEQRES   4 A  267  GLY GLY GLY GLN ILE TYR TYR PRO THR ASP THR SER GLN
SEQRES   5 A  267  THR TYR GLY ALA VAL VAL ILE VAL PRO GLY PHE ILE SER
SEQRES   6 A  267  VAL TRP ALA GLN LEU ALA TRP LEU GLY PRO ARG LEU ALA
SEQRES   7 A  267  SER GLN GLY PHE VAL VAL ILE GLY ILE GLU THR SER THR
SEQRES   8 A  267  ILE THR ASP LEU PRO ASP PRO ARG GLY ASP GLN ALA LEU
SEQRES   9 A  267  ALA ALA LEU ASP TRP ALA THR THR ARG SER PRO VAL ARG
SEQRES  10 A  267  SER ARG ILE ASP ARG THR ARG LEU ALA ALA ALA GLY TRP
SEQRES  11 A  267  SER MET GLY GLY GLY GLY LEU ARG ARG ALA ALA CYS GLN
SEQRES  12 A  267  ARG PRO SER LEU LYS ALA ILE VAL GLY MET ALA PRO TRP
SEQRES  13 A  267  ASN THR GLU LYS ASN TRP SER CYS VAL THR VAL PRO THR
SEQRES  14 A  267  LEU PHE PHE GLY GLY SER SER ASP ALA VAL ALA SER PRO
SEQRES  15 A  267  ASN ASP HIS ALA LYS PRO PHE TYR ASN SER ILE THR ARG
SEQRES  16 A  267  ALA GLU LYS ASP TYR ILE GLU LEU CYS ASN ALA ASP HIS
SEQRES  17 A  267  PHE PHE PRO THR SER ALA ASN THR THR MET ALA LYS TYR
SEQRES  18 A  267  PHE ILE SER TRP LEU LYS ARG TRP VAL ASP ASN ASP THR
SEQRES  19 A  267  ARG TYR THR GLN PHE LEU CYS PRO GLY PRO ARG ASP GLY
SEQRES  20 A  267  LEU PHE GLY PRO VAL CYS ALA SER MET ASN THR CYS PRO
SEQRES  21 A  267  PHE LEU GLU HIS HIS HIS HIS
SEQRES   1 B  267  GLU PRO ALA ALA ASP ASN PRO TYR GLN ARG GLY PRO ASP
SEQRES   2 B  267  PRO THR ASN ALA SER ILE GLU ALA ALA THR GLY PRO PHE
SEQRES   3 B  267  ALA VAL GLY THR GLN PRO ILE VAL GLY ALA SER GLY PHE
SEQRES   4 B  267  GLY GLY GLY GLN ILE TYR TYR PRO THR ASP THR SER GLN
SEQRES   5 B  267  THR TYR GLY ALA VAL VAL ILE VAL PRO GLY PHE ILE SER
SEQRES   6 B  267  VAL TRP ALA GLN LEU ALA TRP LEU GLY PRO ARG LEU ALA
SEQRES   7 B  267  SER GLN GLY PHE VAL VAL ILE GLY ILE GLU THR SER THR
SEQRES   8 B  267  ILE THR ASP LEU PRO ASP PRO ARG GLY ASP GLN ALA LEU
SEQRES   9 B  267  ALA ALA LEU ASP TRP ALA THR THR ARG SER PRO VAL ARG
SEQRES  10 B  267  SER ARG ILE ASP ARG THR ARG LEU ALA ALA ALA GLY TRP
SEQRES  11 B  267  SER MET GLY GLY GLY GLY LEU ARG ARG ALA ALA CYS GLN
SEQRES  12 B  267  ARG PRO SER LEU LYS ALA ILE VAL GLY MET ALA PRO TRP
SEQRES  13 B  267  ASN THR GLU LYS ASN TRP SER CYS VAL THR VAL PRO THR
SEQRES  14 B  267  LEU PHE PHE GLY GLY SER SER ASP ALA VAL ALA SER PRO
SEQRES  15 B  267  ASN ASP HIS ALA LYS PRO PHE TYR ASN SER ILE THR ARG
SEQRES  16 B  267  ALA GLU LYS ASP TYR ILE GLU LEU CYS ASN ALA ASP HIS
SEQRES  17 B  267  PHE PHE PRO THR SER ALA ASN THR THR MET ALA LYS TYR
SEQRES  18 B  267  PHE ILE SER TRP LEU LYS ARG TRP VAL ASP ASN ASP THR
SEQRES  19 B  267  ARG TYR THR GLN PHE LEU CYS PRO GLY PRO ARG ASP GLY
SEQRES  20 B  267  LEU PHE GLY PRO VAL CYS ALA SER MET ASN THR CYS PRO
SEQRES  21 B  267  PHE LEU GLU HIS HIS HIS HIS
FORMUL   3  HOH   *208(H2 O)
HELIX    1 AA1 THR A   53  ALA A   59  1                                   7
HELIX    2 AA2 VAL A  104  ALA A  109  5                                   6
HELIX    3 AA3 TRP A  110  SER A  117  1                                   8
HELIX    4 AA4 LEU A  133  ARG A  151  1                                  19
HELIX    5 AA5 VAL A  154  SER A  156  5                                   3
HELIX    6 AA6 SER A  169  GLY A  174  1                                   6
HELIX    7 AA7 GLY A  174  ARG A  182  1                                   9
HELIX    8 AA8 HIS A  223  ILE A  231  1                                   9
HELIX    9 AA9 PHE A  247  SER A  251  5                                   5
HELIX   10 AB1 ASN A  253  ASP A  269  1                                  17
HELIX   11 AB2 ASP A  271  ARG A  273  5                                   3
HELIX   12 AB3 TYR A  274  CYS A  279  1                                   6
HELIX   13 AB4 THR B   53  ALA B   59  1                                   7
HELIX   14 AB5 VAL B  104  ALA B  109  5                                   6
HELIX   15 AB6 TRP B  110  SER B  117  1                                   8
HELIX   16 AB7 LEU B  133  ARG B  151  1                                  19
HELIX   17 AB8 VAL B  154  SER B  156  5                                   3
HELIX   18 AB9 SER B  169  GLY B  174  1                                   6
HELIX   19 AC1 GLY B  174  ARG B  182  1                                   9
HELIX   20 AC2 HIS B  223  ILE B  231  1                                   9
HELIX   21 AC3 PHE B  247  SER B  251  5                                   5
HELIX   22 AC4 ASN B  253  ASP B  269  1                                  17
HELIX   23 AC5 ASP B  271  ARG B  273  5                                   3
HELIX   24 AC6 TYR B  274  CYS B  279  1                                   6
SHEET    1 AA1 9 VAL A  66  PRO A  70  0
SHEET    2 AA1 9 GLY A  79  PRO A  85 -1  O  ILE A  82   N  GLN A  69
SHEET    3 AA1 9 VAL A 121  GLU A 126 -1  O  VAL A 122   N  TYR A  83
SHEET    4 AA1 9 TYR A  92  VAL A  98  1  N  VAL A  95   O  ILE A 123
SHEET    5 AA1 9 ILE A 158  TRP A 168  1  O  ASP A 159   N  TYR A  92
SHEET    6 AA1 9 ALA A 187  MET A 191  1  O  MET A 191   N  GLY A 167
SHEET    7 AA1 9 THR A 207  GLY A 212  1  O  LEU A 208   N  ILE A 188
SHEET    8 AA1 9 LYS A 236  LEU A 241  1  O  LEU A 241   N  GLY A 211
SHEET    9 AA1 9 VAL A 290  ASN A 295 -1  O  MET A 294   N  TYR A 238
SHEET    1 AA2 9 VAL B  66  PRO B  70  0
SHEET    2 AA2 9 GLY B  79  PRO B  85 -1  O  TYR B  84   N  GLY B  67
SHEET    3 AA2 9 VAL B 121  GLU B 126 -1  O  VAL B 122   N  TYR B  83
SHEET    4 AA2 9 TYR B  92  VAL B  98  1  N  VAL B  95   O  ILE B 123
SHEET    5 AA2 9 ILE B 158  TRP B 168  1  O  ALA B 166   N  VAL B  96
SHEET    6 AA2 9 ALA B 187  MET B 191  1  O  MET B 191   N  GLY B 167
SHEET    7 AA2 9 THR B 207  GLY B 212  1  O  PHE B 210   N  GLY B 190
SHEET    8 AA2 9 LYS B 236  LEU B 241  1  O  LEU B 241   N  GLY B 211
SHEET    9 AA2 9 VAL B 290  ASN B 295 -1  O  MET B 294   N  TYR B 238
SSBOND   1 CYS A  180    CYS A  202                          1555   1555  2.10
SSBOND   2 CYS A  242    CYS A  291                          1555   1555  2.14
SSBOND   3 CYS A  279    CYS A  297                          1555   1555  2.03
SSBOND   4 CYS B  180    CYS B  202                          1555   1555  2.09
SSBOND   5 CYS B  242    CYS B  291                          1555   1555  2.17
SSBOND   6 CYS B  279    CYS B  297                          1555   1555  2.12
CISPEP   1 CYS A  279    PRO A  280          0        13.36
CISPEP   2 CYS A  297    PRO A  298          0         5.71
CISPEP   3 PRO B   99    GLY B  100          0        13.75
CISPEP   4 CYS B  279    PRO B  280          0         5.74
CISPEP   5 GLY B  288    PRO B  289          0        -0.45
CISPEP   6 CYS B  297    PRO B  298          0         4.64
CRYST1   41.134  116.359  142.276  90.00  90.00  90.00 P 21 21 21    8
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      0.024311  0.000000  0.000000        0.00000
SCALE2      0.000000  0.008594  0.000000        0.00000
SCALE3      0.000000  0.000000  0.007029        0.00000
TER    1982      HIS A 302
TER    3947      PHE B 299
MASTER      329    0    0   24   18    0    0    6 4153    2   12   42
END