Structure of PDB 2r26 Chain C Binding Site BS02
Receptor Information
>2r26 Chain C (length=379) Species:
2303
(Thermoplasma acidophilum) [
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EISKGLEDVNIKWTRLTTIDGNKGILRYGGYSVEDIIASGAQDEEIQYLF
LYGNLPTEQELRKYKETVQKGYKIPDFVINAIRQLPRESDAVAMQMAAVA
AMAASETKFKWNKDTDRDVAAEMIGRMSAITVNVYRHIMNMPAELPKPSD
SYAESFLNAAFGRKATKEEIDAMNTALILYTDHEVPASTTAGLVAVSTLS
DMYSGITAALAALKGPLHGGAAEAAIAQFDEIKDPAMVEKWFNDNIINGK
KRLMGFGHRVYKTYDPRAKIFKGIAEKLSSKKPEVHKVYEIATKLEDFGI
KAFGSKGIYPNTDYFSGIVYMSIGFPLRNNIYTALFALSRVTGWQAHFIE
YVEEQQRLIRPRAVYVGPAERKYVPIAER
Ligand information
Ligand ID
CMC
InChI
InChI=1S/C23H38N7O18P3S/c1-23(2,18(35)21(36)26-4-3-13(31)25-5-6-52-8-14(32)33)9-45-51(42,43)48-50(40,41)44-7-12-17(47-49(37,38)39)16(34)22(46-12)30-11-29-15-19(24)27-10-28-20(15)30/h10-12,16-18,22,34-35H,3-9H2,1-2H3,(H,25,31)(H,26,36)(H,32,33)(H,40,41)(H,42,43)(H2,24,27,28)(H2,37,38,39)/t12-,16-,17-,18+,22-/m1/s1
InChIKey
OBUOSIHPWVNVJN-GRFIIANRSA-N
SMILES
Software
SMILES
ACDLabs 12.01
O=C(O)CSCCNC(=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 3.370
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)C(=O)NCCC(=O)NCCSCC(O)=O
OpenEye OEToolkits 1.7.2
CC(C)(COP(=O)(O)OP(=O)(O)OCC1C(C(C(O1)n2cnc3c2ncnc3N)O)OP(=O)(O)O)C(C(=O)NCCC(=O)NCCSCC(=O)O)O
OpenEye OEToolkits 1.7.2
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(=O)NCCC(=O)NCCSCC(=O)O)O
CACTVS 3.370
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(=O)NCCC(=O)NCCSCC(O)=O
Formula
C23 H38 N7 O18 P3 S
Name
CARBOXYMETHYL COENZYME *A
ChEMBL
DrugBank
ZINC
ZINC000085534448
PDB chain
2r26 Chain C Residue 702 [
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Receptor-Ligand Complex Structure
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PDB
2r26
The Structure of the Ternary Complex of Carboxymethyl Coenzyme A and Oxalateacetate with Citrate Synthase from the Thermophilic Archaeonthermoplasma Acidophilum
Resolution
2.5 Å
Binding residue
(original residue number in PDB)
L221 H222 A225 R256 L257 M258 G259 F260 G261 R263 I312 N315 D317
Binding residue
(residue number reindexed from 1)
L217 H218 A221 R252 L253 M254 G255 F256 G257 R259 I308 N311 D313
Annotation score
3
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
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2r26
,
PDBe:2r26
,
PDBj:2r26
PDBsum
2r26
PubMed
UniProt
P21553
|CISY_THEAC Citrate synthase (Gene Name=gltA)
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