Structure of PDB 2r9e Chain B Binding Site BS02
Receptor Information
>2r9e Chain B (length=379) Species:
2303
(Thermoplasma acidophilum) [
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EISKGLEDVNIKWTRLTTIDGNKGILRYGGYSVEDIIASGAQDEEIQYLF
LYGNLPTEQELRKYKETVQKGYKIPDFVINAIRQLPRESDAVAMQMAAVA
AMAASETKFKWNKDTDRDVAAEMIGRMSAITVNVYRHIMNMPAELPKPSD
SYAESFLNAAFGRKATKEEIDAMNTALILYTDHEVPASTTAGLVAVSTLS
DMYSGITAALAALKGPLHGGAAEAAIAQFDEIKDPAMVEKWFNDNIINGK
KRLMGFGHRVYKTYDPRAKIFKGIAEKLSSKKPEVHKVYEIATKLEDFGI
KAFGSKGIYPNTDYFSGIVYMSIGFPLRNNIYTALFALSRVTGWQAHFIE
YVEEQQRLIRPRAVYVGPAERKYVPIAER
Ligand information
Ligand ID
SDX
InChI
InChI=1S/C28H46N7O22P3/c1-27(2,21(41)24(42)31-7-5-16(37)30-6-3-4-14(36)8-28(45,26(43)44)9-17(38)39)11-54-60(51,52)57-59(49,50)53-10-15-20(56-58(46,47)48)19(40)25(55-15)35-13-34-18-22(29)32-12-33-23(18)35/h12-13,15,19-21,24-25,31,40-42,45H,3-11H2,1-2H3,(H,30,37)(H,38,39)(H,43,44)(H,49,50)(H,51,52)(H2,29,32,33)(H2,46,47,48)/t15-,19-,20-,21+,24+,25-,28-/m1/s1
InChIKey
JCKIRWYQPYQCEC-LWCHDFGBSA-N
SMILES
Software
SMILES
CACTVS 3.341
CC(C)(CO[P@](O)(=O)O[P@](O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O[P](O)(O)=O)n2cnc3c(N)ncnc23)[C@@H](O)[C@H](O)NCCC(=O)NCCCC(=O)C[C@@](O)(CC(O)=O)C(O)=O
ACDLabs 10.04
O=C(O)C(O)(CC(=O)O)CC(=O)CCCNC(=O)CCNC(O)C(O)C(C)(C)COP(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3OP(=O)(O)O
CACTVS 3.341
CC(C)(CO[P](O)(=O)O[P](O)(=O)OC[CH]1O[CH]([CH](O)[CH]1O[P](O)(O)=O)n2cnc3c(N)ncnc23)[CH](O)[CH](O)NCCC(=O)NCCCC(=O)C[C](O)(CC(O)=O)C(O)=O
OpenEye OEToolkits 1.5.0
CC(C)(COP(=O)(O)OP(=O)(O)OCC1C(C(C(O1)n2cnc3c2ncnc3N)O)OP(=O)(O)O)C(C(NCCC(=O)NCCCC(=O)CC(CC(=O)O)(C(=O)O)O)O)O
OpenEye OEToolkits 1.5.0
CC(C)(CO[P@@](=O)(O)O[P@@](=O)(O)OC[C@@H]1[C@H]([C@H]([C@@H](O1)n2cnc3c2ncnc3N)O)OP(=O)(O)O)[C@H]([C@@H](NCCC(=O)NCCCC(=O)C[C@@](CC(=O)O)(C(=O)O)O)O)O
Formula
C28 H46 N7 O22 P3
Name
s-citryldethia Coenzyme A
ChEMBL
DrugBank
ZINC
ZINC000263620588
PDB chain
2r9e Chain B Residue 701 [
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Receptor-Ligand Complex Structure
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PDB
2r9e
Snapshots of Intermediates in the Condensation Reaction Catalyzed by Citrate Synthase
Resolution
1.95 Å
Binding residue
(original residue number in PDB)
H187 P190 L221 H222 A225 R256 L257 M258 G259 F260 G261 H262 R263 R271 I312 N315 F340 R344
Binding residue
(residue number reindexed from 1)
H183 P186 L217 H218 A221 R252 L253 M254 G255 F256 G257 H258 R259 R267 I308 N311 F336 R340
Annotation score
2
Enzymatic activity
Catalytic site (original residue number in PDB)
S192 H222 H262 R271 D317
Catalytic site (residue number reindexed from 1)
S188 H218 H258 R267 D313
Enzyme Commision number
2.3.3.16
: citrate synthase (unknown stereospecificity).
Gene Ontology
Molecular Function
GO:0004108
citrate (Si)-synthase activity
GO:0016740
transferase activity
GO:0036440
citrate synthase activity
GO:0046912
acyltransferase activity, acyl groups converted into alkyl on transfer
Biological Process
GO:0005975
carbohydrate metabolic process
GO:0006099
tricarboxylic acid cycle
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2r9e
,
PDBe:2r9e
,
PDBj:2r9e
PDBsum
2r9e
PubMed
UniProt
P21553
|CISY_THEAC Citrate synthase (Gene Name=gltA)
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