Structure of PDB 2ii3 Chain F Binding Site BS02
Receptor Information
>2ii3 Chain F (length=234) Species:
9913
(Bos taurus) [
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GKDRTEPVKGFHKAMVKTMSAALKIPHFGYCDEVDLTELVKLREELKPIA
FARGIKLSFMPFFLKAASLGLLQFPILNASVDENCQNITYKASHNIGIAM
DTEQGLIVPNVKNVQIRSIFEIATELNRLQKLGSAGQLSTNDLIGGTFTL
SNIGSIGGTYAKPVILPPEVAIGALGTIKALPRFNEKGEVCKAQIMNVSW
SADHRIIDGATVSRFSNLWKSYLENPAFMLLDLK
Ligand information
Ligand ID
CAO
InChI
InChI=1S/C21H36N7O17P3S/c1-21(2,16(31)19(32)24-4-3-12(29)23-5-6-49-40)8-42-48(38,39)45-47(36,37)41-7-11-15(44-46(33,34)35)14(30)20(43-11)28-10-27-13-17(22)25-9-26-18(13)28/h9-11,14-16,20,30-31,40H,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
HWMGJMKHOJKGLQ-IBOSZNHHSA-N
SMILES
Software
SMILES
ACDLabs 10.04
O=C(NCCSO)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[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)NCCSO
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)NCCSO)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)NCCSO)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)NCCSO
Formula
C21 H36 N7 O17 P3 S
Name
OXIDIZED COENZYME A
ChEMBL
DrugBank
DB01846
ZINC
ZINC000098208732
PDB chain
2ii3 Chain F Residue 500 [
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Receptor-Ligand Complex Structure
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PDB
2ii3
A synchronized substrate-gating mechanism revealed by cubic-core structure of the bovine branched-chain alpha-ketoacid dehydrogenase complex.
Resolution
2.17 Å
Binding residue
(original residue number in PDB)
R230 S245 F246 M247 N339 G341 S342 T364 I365
Binding residue
(residue number reindexed from 1)
R43 S58 F59 M60 N152 G154 S155 T177 I178
Annotation score
3
Binding affinity
MOAD
: Kd=3uM
Enzymatic activity
Catalytic site (original residue number in PDB)
S338 H391
Catalytic site (residue number reindexed from 1)
S151 H204
Enzyme Commision number
2.3.1.168
: dihydrolipoyllysine-residue (2-methylpropanoyl)transferase.
Gene Ontology
Molecular Function
GO:0016746
acyltransferase activity
View graph for
Molecular Function
External links
PDB
RCSB:2ii3
,
PDBe:2ii3
,
PDBj:2ii3
PDBsum
2ii3
PubMed
17124494
UniProt
P11181
|ODB2_BOVIN Lipoamide acyltransferase component of branched-chain alpha-keto acid dehydrogenase complex, mitochondrial (Gene Name=DBT)
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