Structure of PDB 6esq Chain C Binding Site BS01
Receptor Information
>6esq Chain C (length=392) Species:
2186
(Methanothermococcus thermolithotrophicus) [
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MRDVAIIGYGQTKFGELWEDSFRDLIVEAGVKAIKDANVDGGDIDAMYIG
NMSGGLFVGQEHIASLIADHAGLNPVPCTRVEAACASGSLALRSAVLSVA
SGHHDVVLAGGVEKMTDVEDATAAIASASDQEWEAFFGATFPSLYAMMAR
RYMYQYGLTIEELSMWSVIAHENATKNKYAQFGFKTTLEQVMNASPVADP
LTLMHCSPVSDGASALIVCDADKAEEFAPKDEIIYIKASTQASDTIALHD
REDMTTLNAAKVASEKAYKLAKIAPEKIDVAEVHDCFAINGLILVEDLGF
CKKGDAGKVIDEGKIRIDYDDFVTVNPSGGLKAAGHALGATGIRQVGELY
WQLKQDKECKDRQATIKNGYGIAANVGGTGGTVCVHLLSDKR
Ligand information
Ligand ID
COA
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-IBOSZNHHSA-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
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
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
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
CHEMBL1213327
DrugBank
DB01992
ZINC
ZINC000008551087
PDB chain
6esq Chain C Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
6esq
Archaeal acetoacetyl-CoA thiolase/HMG-CoA synthase complex channels the intermediate via a fused CoA-binding site.
Resolution
2.95 Å
Binding residue
(original residue number in PDB)
F182 L203 M204 C206 S207 P208 V209 K332
Binding residue
(residue number reindexed from 1)
F182 L203 M204 C206 S207 P208 V209 K332
Annotation score
3
Enzymatic activity
Enzyme Commision number
2.3.1.9
: acetyl-CoA C-acetyltransferase.
Gene Ontology
Molecular Function
GO:0003985
acetyl-CoA C-acetyltransferase activity
GO:0016746
acyltransferase activity
GO:0016747
acyltransferase activity, transferring groups other than amino-acyl groups
View graph for
Molecular Function
External links
PDB
RCSB:6esq
,
PDBe:6esq
,
PDBj:6esq
PDBsum
6esq
PubMed
29531083
UniProt
A0A384E138
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