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HEADER HYDROLASE 02-AUG-22 8AM2
TITLE HUMAN BUTYRYLCHOLINESTERASE IN COMPLEX WITH 2,2'-(((1E,1'E)-(2-
TITLE 2 PHENYLPYRIMIDINE-4,6-DIYL)BIS(METHANEYLYLIDENE))BIS(HYDRAZIN-1-YL-2-
TITLE 3 YLIDENE))BIS(N,N,N-TRIMETHYL-2-OXOETHAN-1-AMINIUM)
COMPND MOL_ID: 1;
COMPND 2 MOLECULE: CHOLINESTERASE;
COMPND 3 CHAIN: A;
COMPND 4 SYNONYM: ACYLCHOLINE ACYLHYDROLASE,BUTYRYLCHOLINE ESTERASE,CHOLINE
COMPND 5 ESTERASE II,PSEUDOCHOLINESTERASE;
COMPND 6 EC: 3.1.1.8;
COMPND 7 ENGINEERED: YES;
COMPND 8 MUTATION: YES;
COMPND 9 OTHER_DETAILS: ENGINEERED BUTYRYLCHOLINESTERASE FOR CRYSTALLISATION
SOURCE MOL_ID: 1;
SOURCE 2 ORGANISM_SCIENTIFIC: HOMO SAPIENS;
SOURCE 3 ORGANISM_COMMON: HUMAN;
SOURCE 4 ORGANISM_TAXID: 9606;
SOURCE 5 GENE: BCHE, CHE1;
SOURCE 6 EXPRESSION_SYSTEM: CRICETULUS GRISEUS;
SOURCE 7 EXPRESSION_SYSTEM_TAXID: 10029
KEYWDS INHIBITOR, COMPLEX, BUTYRYLCHOLINESTERASE, HYDROLASE
EXPDTA X-RAY DIFFRACTION
AUTHOR F.NACHON,X.BRAZZOLOTTO,J.DIAS
REVDAT 1 14-JUN-23 8AM2 0
JRNL AUTH F.NACHON,X.BRAZZOLOTTO,J.DIAS,C.COURAGEUX,W.DROZDZ,X.Y.CAO,
JRNL AUTH 2 A.R.STEFANKIEWICZ,J.M.LEHN
JRNL TITL GRID-TYPE QUATERNARY METALLOSUPRAMOLECULAR COMPOUNDS INHIBIT
JRNL TITL 2 HUMAN CHOLINESTERASES THROUGH DYNAMIC MULTIVALENT
JRNL TITL 3 INTERACTIONS.
JRNL REF CHEMBIOCHEM V. 23 00456 2022
JRNL REFN ESSN 1439-7633
JRNL PMID 36193860
JRNL DOI 10.1002/CBIC.202200456
REMARK 2
REMARK 2 RESOLUTION. 2.50 ANGSTROMS.
REMARK 3
REMARK 3 REFINEMENT.
REMARK 3 PROGRAM : PHENIX 1.19.2_4158
REMARK 3 AUTHORS : PAUL ADAMS,PAVEL AFONINE,VINCENT CHEN,IAN
REMARK 3 : DAVIS,KRESHNA GOPAL,RALF GROSSE-KUNSTLEVE,
REMARK 3 : LI-WEI HUNG,ROBERT IMMORMINO,TOM IOERGER,
REMARK 3 : AIRLIE MCCOY,ERIK MCKEE,NIGEL MORIARTY,
REMARK 3 : REETAL PAI,RANDY READ,JANE RICHARDSON,
REMARK 3 : DAVID RICHARDSON,TOD ROMO,JIM SACCHETTINI,
REMARK 3 : NICHOLAS SAUTER,JACOB SMITH,LAURENT
REMARK 3 : STORONI,TOM TERWILLIGER,PETER ZWART
REMARK 3
REMARK 3 REFINEMENT TARGET : GEOSTD + MONOMER LIBRARY + CDL V1.2
REMARK 3
REMARK 3 DATA USED IN REFINEMENT.
REMARK 3 RESOLUTION RANGE HIGH (ANGSTROMS) : 2.50
REMARK 3 RESOLUTION RANGE LOW (ANGSTROMS) : 55.25
REMARK 3 MIN(FOBS/SIGMA_FOBS) : 1.360
REMARK 3 COMPLETENESS FOR RANGE (%) : 97.5
REMARK 3 NUMBER OF REFLECTIONS : 26518
REMARK 3
REMARK 3 FIT TO DATA USED IN REFINEMENT.
REMARK 3 R VALUE (WORKING + TEST SET) : 0.172
REMARK 3 R VALUE (WORKING SET) : 0.170
REMARK 3 FREE R VALUE : 0.220
REMARK 3 FREE R VALUE TEST SET SIZE (%) : 4.000
REMARK 3 FREE R VALUE TEST SET COUNT : 1060
REMARK 3
REMARK 3 FIT TO DATA USED IN REFINEMENT (IN BINS).
REMARK 3 BIN RESOLUTION RANGE COMPL. NWORK NFREE RWORK RFREE
REMARK 3 1 55.2500 - 5.0000 0.95 3267 136 0.1755 0.2000
REMARK 3 2 5.0000 - 3.9700 0.97 3184 132 0.1298 0.1652
REMARK 3 3 3.9700 - 3.4700 0.97 3172 132 0.1534 0.1962
REMARK 3 4 3.4700 - 3.1500 0.98 3170 133 0.1733 0.2870
REMARK 3 5 3.1500 - 2.9200 0.98 3169 132 0.2074 0.2720
REMARK 3 6 2.9200 - 2.7500 0.98 3155 131 0.2012 0.2421
REMARK 3 7 2.7500 - 2.6100 0.99 3178 132 0.2111 0.2914
REMARK 3 8 2.6100 - 2.5000 0.99 3163 132 0.2336 0.3029
REMARK 3
REMARK 3 BULK SOLVENT MODELLING.
REMARK 3 METHOD USED : FLAT BULK SOLVENT MODEL
REMARK 3 SOLVENT RADIUS : 1.11
REMARK 3 SHRINKAGE RADIUS : 0.90
REMARK 3 K_SOL : NULL
REMARK 3 B_SOL : NULL
REMARK 3
REMARK 3 ERROR ESTIMATES.
REMARK 3 COORDINATE ERROR (MAXIMUM-LIKELIHOOD BASED) : 0.281
REMARK 3 PHASE ERROR (DEGREES, MAXIMUM-LIKELIHOOD BASED) : 22.556
REMARK 3
REMARK 3 B VALUES.
REMARK 3 FROM WILSON PLOT (A**2) : 46.82
REMARK 3 MEAN B VALUE (OVERALL, A**2) : 53.41
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 TWINNING INFORMATION.
REMARK 3 FRACTION: NULL
REMARK 3 OPERATOR: NULL
REMARK 3
REMARK 3 DEVIATIONS FROM IDEAL VALUES.
REMARK 3 RMSD COUNT
REMARK 3 BOND : 0.008 4545
REMARK 3 ANGLE : 0.957 6180
REMARK 3 CHIRALITY : 0.059 676
REMARK 3 PLANARITY : 0.007 783
REMARK 3 DIHEDRAL : 14.192 650
REMARK 3
REMARK 3 TLS DETAILS
REMARK 3 NUMBER OF TLS GROUPS : 6
REMARK 3 TLS GROUP : 1
REMARK 3 SELECTION: CHAIN A AND RESSEQ 1:65
REMARK 3 ORIGIN FOR THE GROUP (A): 132.0576 127.5494 17.5083
REMARK 3 T TENSOR
REMARK 3 T11: 0.6530 T22: 0.4961
REMARK 3 T33: 0.3796 T12: -0.0731
REMARK 3 T13: -0.1415 T23: -0.0084
REMARK 3 L TENSOR
REMARK 3 L11: 3.5230 L22: 1.4261
REMARK 3 L33: 1.8332 L12: -0.8717
REMARK 3 L13: 0.0644 L23: -0.0119
REMARK 3 S TENSOR
REMARK 3 S11: 0.0417 S12: 0.7824 S13: 0.0942
REMARK 3 S21: -0.5950 S22: -0.0525 S23: 0.1692
REMARK 3 S31: -0.2040 S32: -0.1671 S33: 0.0187
REMARK 3 TLS GROUP : 2
REMARK 3 SELECTION: CHAIN A AND RESSEQ 66:91
REMARK 3 ORIGIN FOR THE GROUP (A): 129.5952 110.9913 32.4581
REMARK 3 T TENSOR
REMARK 3 T11: 0.5253 T22: 0.4452
REMARK 3 T33: 0.4271 T12: -0.0889
REMARK 3 T13: -0.0532 T23: -0.0640
REMARK 3 L TENSOR
REMARK 3 L11: 1.8752 L22: 1.4488
REMARK 3 L33: 2.8295 L12: 1.1900
REMARK 3 L13: -1.5957 L23: -1.6799
REMARK 3 S TENSOR
REMARK 3 S11: -0.3006 S12: 0.1925 S13: -0.1761
REMARK 3 S21: -0.2917 S22: 0.3015 S23: -0.2508
REMARK 3 S31: 0.6402 S32: -0.1518 S33: -0.0548
REMARK 3 TLS GROUP : 3
REMARK 3 SELECTION: (CHAIN A AND RESSEQ 92:153) OR (CHAIN A AND RESSEQ
REMARK 3 164:231)
REMARK 3 ORIGIN FOR THE GROUP (A): 137.3797 130.0722 31.0346
REMARK 3 T TENSOR
REMARK 3 T11: 0.3789 T22: 0.3033
REMARK 3 T33: 0.2959 T12: -0.0457
REMARK 3 T13: -0.0347 T23: -0.0267
REMARK 3 L TENSOR
REMARK 3 L11: 1.6398 L22: 2.0229
REMARK 3 L33: 1.6976 L12: -0.2866
REMARK 3 L13: 0.3806 L23: 0.0489
REMARK 3 S TENSOR
REMARK 3 S11: -0.0007 S12: 0.1578 S13: -0.1104
REMARK 3 S21: -0.3495 S22: 0.0492 S23: 0.1428
REMARK 3 S31: -0.0322 S32: -0.0958 S33: -0.0446
REMARK 3 TLS GROUP : 4
REMARK 3 SELECTION: (CHAIN A AND RESSEQ 290:326) OR (CHAIN A AND RESSEQ
REMARK 3 397:515)
REMARK 3 ORIGIN FOR THE GROUP (A): 135.4610 130.6279 47.5844
REMARK 3 T TENSOR
REMARK 3 T11: 0.2639 T22: 0.2896
REMARK 3 T33: 0.2646 T12: -0.0123
REMARK 3 T13: -0.0423 T23: -0.0336
REMARK 3 L TENSOR
REMARK 3 L11: 1.2872 L22: 2.1571
REMARK 3 L33: 2.3846 L12: -0.0732
REMARK 3 L13: -0.1333 L23: 0.0327
REMARK 3 S TENSOR
REMARK 3 S11: 0.0195 S12: -0.2258 S13: 0.0405
REMARK 3 S21: 0.1306 S22: 0.0373 S23: 0.1654
REMARK 3 S31: -0.0561 S32: -0.1993 S33: -0.0548
REMARK 3 TLS GROUP : 5
REMARK 3 SELECTION: (CHAIN A AND RESSEQ 154:163) OR (CHAIN A AND RESSEQ
REMARK 3 232:289)
REMARK 3 ORIGIN FOR THE GROUP (A): 151.6143 107.1841 28.3340
REMARK 3 T TENSOR
REMARK 3 T11: 0.5472 T22: 0.4814
REMARK 3 T33: 0.6433 T12: 0.0432
REMARK 3 T13: 0.0402 T23: -0.1314
REMARK 3 L TENSOR
REMARK 3 L11: 3.1590 L22: 4.5446
REMARK 3 L33: 7.6346 L12: -1.3242
REMARK 3 L13: -2.1394 L23: 2.5680
REMARK 3 S TENSOR
REMARK 3 S11: -0.2729 S12: 0.1342 S13: -0.5640
REMARK 3 S21: 0.0196 S22: 0.3664 S23: -0.5385
REMARK 3 S31: 0.9778 S32: 0.8629 S33: -0.1118
REMARK 3 TLS GROUP : 6
REMARK 3 SELECTION: (CHAIN A AND RESSEQ 327:396) OR (CHAIN A AND RESSEQ
REMARK 3 516:529)
REMARK 3 ORIGIN FOR THE GROUP (A): 141.4229 110.1885 58.7281
REMARK 3 T TENSOR
REMARK 3 T11: 0.4155 T22: 0.3238
REMARK 3 T33: 0.3025 T12: 0.0014
REMARK 3 T13: -0.0592 T23: 0.0182
REMARK 3 L TENSOR
REMARK 3 L11: 7.6306 L22: 4.9925
REMARK 3 L33: 3.7385 L12: 1.9583
REMARK 3 L13: 1.9757 L23: -0.8078
REMARK 3 S TENSOR
REMARK 3 S11: 0.2319 S12: -0.7476 S13: -0.2121
REMARK 3 S21: 0.4040 S22: -0.0849 S23: -0.1029
REMARK 3 S31: 0.1824 S32: -0.1840 S33: -0.1728
REMARK 3
REMARK 3 NCS DETAILS
REMARK 3 NUMBER OF NCS GROUPS : NULL
REMARK 3
REMARK 3 OTHER REFINEMENT REMARKS: NULL
REMARK 4
REMARK 4 8AM2 COMPLIES WITH FORMAT V. 3.30, 13-JUL-11
REMARK 100
REMARK 100 THIS ENTRY HAS BEEN PROCESSED BY PDBE ON 09-AUG-22.
REMARK 100 THE DEPOSITION ID IS D_1292124726.
REMARK 200
REMARK 200 EXPERIMENTAL DETAILS
REMARK 200 EXPERIMENT TYPE : X-RAY DIFFRACTION
REMARK 200 DATE OF DATA COLLECTION : 24-NOV-16
REMARK 200 TEMPERATURE (KELVIN) : 100
REMARK 200 PH : 6.5
REMARK 200 NUMBER OF CRYSTALS USED : 1
REMARK 200
REMARK 200 SYNCHROTRON (Y/N) : Y
REMARK 200 RADIATION SOURCE : ESRF
REMARK 200 BEAMLINE : ID29
REMARK 200 X-RAY GENERATOR MODEL : NULL
REMARK 200 MONOCHROMATIC OR LAUE (M/L) : M
REMARK 200 WAVELENGTH OR RANGE (A) : 1.07252
REMARK 200 MONOCHROMATOR : NULL
REMARK 200 OPTICS : NULL
REMARK 200
REMARK 200 DETECTOR TYPE : PIXEL
REMARK 200 DETECTOR MANUFACTURER : DECTRIS PILATUS 6M
REMARK 200 INTENSITY-INTEGRATION SOFTWARE : XDS
REMARK 200 DATA SCALING SOFTWARE : XSCALE
REMARK 200
REMARK 200 NUMBER OF UNIQUE REFLECTIONS : 26526
REMARK 200 RESOLUTION RANGE HIGH (A) : 2.500
REMARK 200 RESOLUTION RANGE LOW (A) : 55.250
REMARK 200 REJECTION CRITERIA (SIGMA(I)) : NULL
REMARK 200
REMARK 200 OVERALL.
REMARK 200 COMPLETENESS FOR RANGE (%) : 97.5
REMARK 200 DATA REDUNDANCY : 6.400
REMARK 200 R MERGE (I) : 0.05889
REMARK 200 R SYM (I) : NULL
REMARK 200 FOR THE DATA SET : 25.0400
REMARK 200
REMARK 200 IN THE HIGHEST RESOLUTION SHELL.
REMARK 200 HIGHEST RESOLUTION SHELL, RANGE HIGH (A) : 2.50
REMARK 200 HIGHEST RESOLUTION SHELL, RANGE LOW (A) : 2.59
REMARK 200 COMPLETENESS FOR SHELL (%) : 98.8
REMARK 200 DATA REDUNDANCY IN SHELL : 6.60
REMARK 200 R MERGE FOR SHELL (I) : 0.47610
REMARK 200 R SYM FOR SHELL (I) : NULL
REMARK 200 FOR SHELL : 3.560
REMARK 200
REMARK 200 DIFFRACTION PROTOCOL: SINGLE WAVELENGTH
REMARK 200 METHOD USED TO DETERMINE THE STRUCTURE: MOLECULAR REPLACEMENT
REMARK 200 SOFTWARE USED: PHASER
REMARK 200 STARTING MODEL: 1P0I
REMARK 200
REMARK 200 REMARK: NULL
REMARK 280
REMARK 280 CRYSTAL
REMARK 280 SOLVENT CONTENT, VS (%): 61.75
REMARK 280 MATTHEWS COEFFICIENT, VM (ANGSTROMS**3/DA): 3.22
REMARK 280
REMARK 280 CRYSTALLIZATION CONDITIONS: AMMONIUM SULFATE 2.1 M, 2-(N
REMARK 280 -MORPHOLINO)-ETHANESULFONIC ACID 0.1 M, PH 6.5, VAPOR DIFFUSION,
REMARK 280 HANGING DROP, TEMPERATURE 298K
REMARK 290
REMARK 290 CRYSTALLOGRAPHIC SYMMETRY
REMARK 290 SYMMETRY OPERATORS FOR SPACE GROUP: I 4 2 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 -Y,X,Z
REMARK 290 4555 Y,-X,Z
REMARK 290 5555 -X,Y,-Z
REMARK 290 6555 X,-Y,-Z
REMARK 290 7555 Y,X,-Z
REMARK 290 8555 -Y,-X,-Z
REMARK 290 9555 X+1/2,Y+1/2,Z+1/2
REMARK 290 10555 -X+1/2,-Y+1/2,Z+1/2
REMARK 290 11555 -Y+1/2,X+1/2,Z+1/2
REMARK 290 12555 Y+1/2,-X+1/2,Z+1/2
REMARK 290 13555 -X+1/2,Y+1/2,-Z+1/2
REMARK 290 14555 X+1/2,-Y+1/2,-Z+1/2
REMARK 290 15555 Y+1/2,X+1/2,-Z+1/2
REMARK 290 16555 -Y+1/2,-X+1/2,-Z+1/2
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 0.000000 -1.000000 0.000000 0.00000
REMARK 290 SMTRY2 3 1.000000 0.000000 0.000000 0.00000
REMARK 290 SMTRY3 3 0.000000 0.000000 1.000000 0.00000
REMARK 290 SMTRY1 4 0.000000 1.000000 0.000000 0.00000
REMARK 290 SMTRY2 4 -1.000000 0.000000 0.000000 0.00000
REMARK 290 SMTRY3 4 0.000000 0.000000 1.000000 0.00000
REMARK 290 SMTRY1 5 -1.000000 0.000000 0.000000 0.00000
REMARK 290 SMTRY2 5 0.000000 1.000000 0.000000 0.00000
REMARK 290 SMTRY3 5 0.000000 0.000000 -1.000000 0.00000
REMARK 290 SMTRY1 6 1.000000 0.000000 0.000000 0.00000
REMARK 290 SMTRY2 6 0.000000 -1.000000 0.000000 0.00000
REMARK 290 SMTRY3 6 0.000000 0.000000 -1.000000 0.00000
REMARK 290 SMTRY1 7 0.000000 1.000000 0.000000 0.00000
REMARK 290 SMTRY2 7 1.000000 0.000000 0.000000 0.00000
REMARK 290 SMTRY3 7 0.000000 0.000000 -1.000000 0.00000
REMARK 290 SMTRY1 8 0.000000 -1.000000 0.000000 0.00000
REMARK 290 SMTRY2 8 -1.000000 0.000000 0.000000 0.00000
REMARK 290 SMTRY3 8 0.000000 0.000000 -1.000000 0.00000
REMARK 290 SMTRY1 9 1.000000 0.000000 0.000000 77.47000
REMARK 290 SMTRY2 9 0.000000 1.000000 0.000000 77.47000
REMARK 290 SMTRY3 9 0.000000 0.000000 1.000000 63.98500
REMARK 290 SMTRY1 10 -1.000000 0.000000 0.000000 77.47000
REMARK 290 SMTRY2 10 0.000000 -1.000000 0.000000 77.47000
REMARK 290 SMTRY3 10 0.000000 0.000000 1.000000 63.98500
REMARK 290 SMTRY1 11 0.000000 -1.000000 0.000000 77.47000
REMARK 290 SMTRY2 11 1.000000 0.000000 0.000000 77.47000
REMARK 290 SMTRY3 11 0.000000 0.000000 1.000000 63.98500
REMARK 290 SMTRY1 12 0.000000 1.000000 0.000000 77.47000
REMARK 290 SMTRY2 12 -1.000000 0.000000 0.000000 77.47000
REMARK 290 SMTRY3 12 0.000000 0.000000 1.000000 63.98500
REMARK 290 SMTRY1 13 -1.000000 0.000000 0.000000 77.47000
REMARK 290 SMTRY2 13 0.000000 1.000000 0.000000 77.47000
REMARK 290 SMTRY3 13 0.000000 0.000000 -1.000000 63.98500
REMARK 290 SMTRY1 14 1.000000 0.000000 0.000000 77.47000
REMARK 290 SMTRY2 14 0.000000 -1.000000 0.000000 77.47000
REMARK 290 SMTRY3 14 0.000000 0.000000 -1.000000 63.98500
REMARK 290 SMTRY1 15 0.000000 1.000000 0.000000 77.47000
REMARK 290 SMTRY2 15 1.000000 0.000000 0.000000 77.47000
REMARK 290 SMTRY3 15 0.000000 0.000000 -1.000000 63.98500
REMARK 290 SMTRY1 16 0.000000 -1.000000 0.000000 77.47000
REMARK 290 SMTRY2 16 -1.000000 0.000000 0.000000 77.47000
REMARK 290 SMTRY3 16 0.000000 0.000000 -1.000000 63.98500
REMARK 290
REMARK 290 REMARK: NULL
REMARK 300
REMARK 300 BIOMOLECULE: 1
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 APPLY THE FOLLOWING TO CHAINS: A, B, C
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 1
REMARK 465 ASP A 2
REMARK 500
REMARK 500 GEOMETRY AND STEREOCHEMISTRY
REMARK 500 SUBTOPIC: CLOSE CONTACTS IN SAME ASYMMETRIC UNIT
REMARK 500
REMARK 500 THE FOLLOWING ATOMS ARE IN CLOSE CONTACT.
REMARK 500
REMARK 500 ATM1 RES C SSEQI ATM2 RES C SSEQI DISTANCE
REMARK 500 O HOH A 702 O HOH A 861 1.95
REMARK 500 OD2 ASP A 378 O HOH A 701 2.00
REMARK 500 NZ LYS A 348 O HOH A 702 2.07
REMARK 500
REMARK 500 REMARK: NULL
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),1X,F6.3)
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 RES CSSEQI ATM2 DEVIATION
REMARK 500 GLU A 367 CG GLU A 367 CD 0.094
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 PHE A 43 -7.33 77.62
REMARK 500 ALA A 58 64.02 -102.75
REMARK 500 GLN A 67 148.81 -175.38
REMARK 500 CYS A 92 12.58 -141.57
REMARK 500 ASN A 106 52.13 -142.20
REMARK 500 ALA A 162 72.74 -158.15
REMARK 500 SER A 198 -124.60 59.54
REMARK 500 ASP A 297 -74.62 -135.25
REMARK 500 ASP A 379 -3.57 68.98
REMARK 500 PHE A 398 -56.66 -137.98
REMARK 500 PRO A 480 48.67 -86.46
REMARK 500 GLU A 506 -95.45 -69.85
REMARK 500
REMARK 500 REMARK: NULL
DBREF 8AM2 A 1 529 UNP P06276 CHLE_HUMAN 29 557
SEQADV 8AM2 GLN A 17 UNP P06276 ASN 45 ENGINEERED MUTATION
SEQADV 8AM2 GLN A 455 UNP P06276 ASN 483 ENGINEERED MUTATION
SEQADV 8AM2 GLN A 481 UNP P06276 ASN 509 ENGINEERED MUTATION
SEQADV 8AM2 GLN A 486 UNP P06276 ASN 514 ENGINEERED MUTATION
SEQRES 1 A 529 GLU ASP ASP ILE ILE ILE ALA THR LYS ASN GLY LYS VAL
SEQRES 2 A 529 ARG GLY MET GLN LEU THR VAL PHE GLY GLY THR VAL THR
SEQRES 3 A 529 ALA PHE LEU GLY ILE PRO TYR ALA GLN PRO PRO LEU GLY
SEQRES 4 A 529 ARG LEU ARG PHE LYS LYS PRO GLN SER LEU THR LYS TRP
SEQRES 5 A 529 SER ASP ILE TRP ASN ALA THR LYS TYR ALA ASN SER CYS
SEQRES 6 A 529 CYS GLN ASN ILE ASP GLN SER PHE PRO GLY PHE HIS GLY
SEQRES 7 A 529 SER GLU MET TRP ASN PRO ASN THR ASP LEU SER GLU ASP
SEQRES 8 A 529 CYS LEU TYR LEU ASN VAL TRP ILE PRO ALA PRO LYS PRO
SEQRES 9 A 529 LYS ASN ALA THR VAL LEU ILE TRP ILE TYR GLY GLY GLY
SEQRES 10 A 529 PHE GLN THR GLY THR SER SER LEU HIS VAL TYR ASP GLY
SEQRES 11 A 529 LYS PHE LEU ALA ARG VAL GLU ARG VAL ILE VAL VAL SER
SEQRES 12 A 529 MET ASN TYR ARG VAL GLY ALA LEU GLY PHE LEU ALA LEU
SEQRES 13 A 529 PRO GLY ASN PRO GLU ALA PRO GLY ASN MET GLY LEU PHE
SEQRES 14 A 529 ASP GLN GLN LEU ALA LEU GLN TRP VAL GLN LYS ASN ILE
SEQRES 15 A 529 ALA ALA PHE GLY GLY ASN PRO LYS SER VAL THR LEU PHE
SEQRES 16 A 529 GLY GLU SER ALA GLY ALA ALA SER VAL SER LEU HIS LEU
SEQRES 17 A 529 LEU SER PRO GLY SER HIS SER LEU PHE THR ARG ALA ILE
SEQRES 18 A 529 LEU GLN SER GLY SER PHE ASN ALA PRO TRP ALA VAL THR
SEQRES 19 A 529 SER LEU TYR GLU ALA ARG ASN ARG THR LEU ASN LEU ALA
SEQRES 20 A 529 LYS LEU THR GLY CYS SER ARG GLU ASN GLU THR GLU ILE
SEQRES 21 A 529 ILE LYS CYS LEU ARG ASN LYS ASP PRO GLN GLU ILE LEU
SEQRES 22 A 529 LEU ASN GLU ALA PHE VAL VAL PRO TYR GLY THR PRO LEU
SEQRES 23 A 529 SER VAL ASN PHE GLY PRO THR VAL ASP GLY ASP PHE LEU
SEQRES 24 A 529 THR ASP MET PRO ASP ILE LEU LEU GLU LEU GLY GLN PHE
SEQRES 25 A 529 LYS LYS THR GLN ILE LEU VAL GLY VAL ASN LYS ASP GLU
SEQRES 26 A 529 GLY THR ALA PHE LEU VAL TYR GLY ALA PRO GLY PHE SER
SEQRES 27 A 529 LYS ASP ASN ASN SER ILE ILE THR ARG LYS GLU PHE GLN
SEQRES 28 A 529 GLU GLY LEU LYS ILE PHE PHE PRO GLY VAL SER GLU PHE
SEQRES 29 A 529 GLY LYS GLU SER ILE LEU PHE HIS TYR THR ASP TRP VAL
SEQRES 30 A 529 ASP ASP GLN ARG PRO GLU ASN TYR ARG GLU ALA LEU GLY
SEQRES 31 A 529 ASP VAL VAL GLY ASP TYR ASN PHE ILE CYS PRO ALA LEU
SEQRES 32 A 529 GLU PHE THR LYS LYS PHE SER GLU TRP GLY ASN ASN ALA
SEQRES 33 A 529 PHE PHE TYR TYR PHE GLU HIS ARG SER SER LYS LEU PRO
SEQRES 34 A 529 TRP PRO GLU TRP MET GLY VAL MET HIS GLY TYR GLU ILE
SEQRES 35 A 529 GLU PHE VAL PHE GLY LEU PRO LEU GLU ARG ARG ASP GLN
SEQRES 36 A 529 TYR THR LYS ALA GLU GLU ILE LEU SER ARG SER ILE VAL
SEQRES 37 A 529 LYS ARG TRP ALA ASN PHE ALA LYS TYR GLY ASN PRO GLN
SEQRES 38 A 529 GLU THR GLN ASN GLN SER THR SER TRP PRO VAL PHE LYS
SEQRES 39 A 529 SER THR GLU GLN LYS TYR LEU THR LEU ASN THR GLU SER
SEQRES 40 A 529 THR ARG ILE MET THR LYS LEU ARG ALA GLN GLN CYS ARG
SEQRES 41 A 529 PHE TRP THR SER PHE PHE PRO LYS VAL
HET NAG B 1 14
HET NAG B 2 14
HET FUC B 3 10
HET NAG C 1 14
HET NAG C 2 14
HET FUC C 3 10
HET N0C A 601 32
HET NAG A 602 14
HET NAG A 603 14
HET NAG A 604 14
HET NAG A 605 14
HET GOL A 606 6
HET SO4 A 607 5
HET SO4 A 608 5
HET SO4 A 609 5
HET SO4 A 610 5
HET CL A 611 1
HET CL A 612 1
HET CL A 613 1
HETNAM NAG 2-ACETAMIDO-2-DEOXY-BETA-D-GLUCOPYRANOSE
HETNAM FUC ALPHA-L-FUCOPYRANOSE
HETNAM N0C ~{N}-[(~{E})-[2-PHENYL-6-[[2-[2-(TRIMETHYL-$L^{4}-
HETNAM 2 N0C AZANYL)ETHANOYL]HYDRAZINYL]METHYL]PYRIMIDIN-4-
HETNAM 3 N0C YL]METHYLIDENEAMINO]-2-(TRIMETHYL-$L^{4}-AZANYL)
HETNAM 4 N0C ETHANAMIDE
HETNAM GOL GLYCEROL
HETNAM SO4 SULFATE ION
HETNAM CL CHLORIDE ION
HETSYN NAG N-ACETYL-BETA-D-GLUCOSAMINE; 2-ACETAMIDO-2-DEOXY-BETA-
HETSYN 2 NAG D-GLUCOSE; 2-ACETAMIDO-2-DEOXY-D-GLUCOSE; 2-ACETAMIDO-
HETSYN 3 NAG 2-DEOXY-GLUCOSE; N-ACETYL-D-GLUCOSAMINE
HETSYN FUC ALPHA-L-FUCOSE; 6-DEOXY-ALPHA-L-GALACTOPYRANOSE; L-
HETSYN 2 FUC FUCOSE; FUCOSE
HETSYN GOL GLYCERIN; PROPANE-1,2,3-TRIOL
FORMUL 2 NAG 8(C8 H15 N O6)
FORMUL 2 FUC 2(C6 H12 O5)
FORMUL 4 N0C C22 H34 N8 O2 2+
FORMUL 9 GOL C3 H8 O3
FORMUL 10 SO4 4(O4 S 2-)
FORMUL 14 CL 3(CL 1-)
FORMUL 17 HOH *181(H2 O)
HELIX 1 AA1 LEU A 38 ARG A 42 5 5
HELIX 2 AA2 PHE A 76 MET A 81 1 6
HELIX 3 AA3 LEU A 125 ASP A 129 5 5
HELIX 4 AA4 GLY A 130 ARG A 138 1 9
HELIX 5 AA5 VAL A 148 LEU A 154 1 7
HELIX 6 AA6 ASN A 165 ILE A 182 1 18
HELIX 7 AA7 ALA A 183 PHE A 185 5 3
HELIX 8 AA8 SER A 198 SER A 210 1 13
HELIX 9 AA9 SER A 210 SER A 215 1 6
HELIX 10 AB1 SER A 235 THR A 250 1 16
HELIX 11 AB2 ASN A 256 LYS A 267 1 12
HELIX 12 AB3 ASP A 268 GLU A 276 1 9
HELIX 13 AB4 ALA A 277 VAL A 280 5 4
HELIX 14 AB5 MET A 302 LEU A 309 1 8
HELIX 15 AB6 GLY A 326 VAL A 331 1 6
HELIX 16 AB7 THR A 346 PHE A 358 1 13
HELIX 17 AB8 SER A 362 THR A 374 1 13
HELIX 18 AB9 GLU A 383 PHE A 398 1 16
HELIX 19 AC1 PHE A 398 GLU A 411 1 14
HELIX 20 AC2 PRO A 431 GLY A 435 5 5
HELIX 21 AC3 GLU A 441 PHE A 446 1 6
HELIX 22 AC4 GLY A 447 GLN A 455 5 9
HELIX 23 AC5 THR A 457 GLY A 478 1 22
HELIX 24 AC6 ARG A 515 PHE A 525 1 11
HELIX 25 AC7 PHE A 526 VAL A 529 5 4
SHEET 1 AA1 3 ILE A 5 THR A 8 0
SHEET 2 AA1 3 GLY A 11 ARG A 14 -1 O VAL A 13 N ILE A 6
SHEET 3 AA1 3 ILE A 55 ASN A 57 1 O TRP A 56 N ARG A 14
SHEET 1 AA211 MET A 16 VAL A 20 0
SHEET 2 AA211 GLY A 23 PRO A 32 -1 O ALA A 27 N MET A 16
SHEET 3 AA211 TYR A 94 PRO A 100 -1 O LEU A 95 N ILE A 31
SHEET 4 AA211 ILE A 140 MET A 144 -1 O SER A 143 N ASN A 96
SHEET 5 AA211 ALA A 107 ILE A 113 1 N LEU A 110 O ILE A 140
SHEET 6 AA211 GLY A 187 GLU A 197 1 O ASN A 188 N ALA A 107
SHEET 7 AA211 ARG A 219 GLN A 223 1 O GLN A 223 N GLY A 196
SHEET 8 AA211 ILE A 317 ASN A 322 1 O LEU A 318 N LEU A 222
SHEET 9 AA211 ALA A 416 PHE A 421 1 O PHE A 417 N VAL A 319
SHEET 10 AA211 LYS A 499 LEU A 503 1 O LEU A 501 N PHE A 418
SHEET 11 AA211 ILE A 510 THR A 512 -1 O MET A 511 N TYR A 500
SHEET 1 AA3 2 SER A 64 CYS A 65 0
SHEET 2 AA3 2 LEU A 88 SER A 89 1 O SER A 89 N SER A 64
SSBOND 1 CYS A 65 CYS A 92 1555 1555 2.04
SSBOND 2 CYS A 252 CYS A 263 1555 1555 2.04
SSBOND 3 CYS A 400 CYS A 519 1555 1555 2.04
LINK ND2 ASN A 57 C1 NAG A 602 1555 1555 1.45
LINK ND2 ASN A 106 C1 NAG A 603 1555 1555 1.46
LINK ND2 ASN A 241 C1 NAG C 1 1555 1555 1.46
LINK ND2 ASN A 256 C1 NAG A 604 1555 1555 1.44
LINK ND2 ASN A 341 C1 NAG B 1 1555 1555 1.43
LINK ND2 ASN A 485 C1 NAG A 605 1555 1555 1.44
LINK O4 NAG B 1 C1 NAG B 2 1555 1555 1.44
LINK O6 NAG B 1 C1 FUC B 3 1555 1555 1.45
LINK O4 NAG C 1 C1 NAG C 2 1555 1555 1.47
LINK O6 NAG C 1 C1 FUC C 3 1555 1555 1.44
CISPEP 1 ALA A 101 PRO A 102 0 -2.80
CRYST1 154.940 154.940 127.970 90.00 90.00 90.00 I 4 2 2 16
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 0.006454 0.000000 0.000000 0.00000
SCALE2 0.000000 0.006454 0.000000 0.00000
SCALE3 0.000000 0.000000 0.007814 0.00000
TER 4235 VAL A 529
MASTER 406 0 19 25 16 0 0 6 4577 1 202 41
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