Structure of PDB 2c6x Chain B Binding Site BS01
Receptor Information
>2c6x Chain B (length=363) Species:
1423
(Bacillus subtilis) [
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VHYGLKGITCVETSISHIDGEKGRLIYRGHHAKDIALNHSFEEAAYLILF
GKLPSTEELQVFKDKLAAERNLPEHIERLIQSLPNNMDDMSVLRTVVSAL
GENTYTFHPKTEEAIRLIAITPSIIAYRKRWTRGEQAIAPSSQYGHVENY
YYMLTGEQPSEAKKKALETYMILATEHGMNASTFSARVTLSTESDLVSAV
TAALGTMKGPLHGGAPSAVTKMLEDIGEKEHAEAYLKEKLEKGERLMGFG
HRVYKTKDPRAEALRQKAEEVAGNDRDLDLALHVEAEAIRLLEIYKPGRK
LYTNVEFYAAAVMRAIDFDDELFTPTFSASRMVGWCAHVLEQAENNMIFR
PSAQYTGAIPEEV
Ligand information
Ligand ID
COZ
InChI
InChI=1S/C21H36N7O16P3S/c1-21(2,16(31)19(32)24-4-3-12(29)23-5-6-48)8-41-47(38,39)44-46(36,37)40-7-11-15(43-45(33,34)35)14(30)20(42-11)28-10-27-13-17(22)25-9-26-18(13)28/h9-11,14-16,20,30-31,48H,3-8H2,1-2H3,(H,23,29)(H,24,32)(H,36,37)(H,38,39)(H2,22,25,26)(H2,33,34,35)/t11-,14-,15-,16-,20-/m1/s1
InChIKey
RGJOEKWQDUBAIZ-HDCXRZRFSA-N
SMILES
Software
SMILES
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(=O)NCCC(=O)NCCS)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(=O)NCCC(=O)NCCS)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)C(=O)NCCC(=O)NCCS
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(=O)NCCC(=O)NCCS
ACDLabs 10.04
O=C(NCCS)CCNC(=O)C(O)C(C)(C)COP(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3OP(=O)(O)O
Formula
C21 H36 N7 O16 P3 S
Name
COENZYME A
ChEMBL
DrugBank
ZINC
ZINC000008215426
PDB chain
2c6x Chain B Residue 1365 [
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Receptor-Ligand Complex Structure
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PDB
2c6x
Domain Closure in Citrate Synthases Adapted to the Range of Biological Temperatures
Resolution
3.4 Å
Binding residue
(original residue number in PDB)
R246 L247 M248 F250 G251 K297 R300 L302 E307
Binding residue
(residue number reindexed from 1)
R245 L246 M247 F249 G250 K296 R299 L301 E306
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
S183 H213 H252 R261 E307
Catalytic site (residue number reindexed from 1)
S182 H212 H251 R260 E306
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
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:2c6x
,
PDBe:2c6x
,
PDBj:2c6x
PDBsum
2c6x
PubMed
UniProt
P39119
|CISY_BACSU Citrate synthase 1 (Gene Name=citA)
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