Structure of PDB 1w6u Chain B Binding Site BS02
Receptor Information
>1w6u Chain B (length=286) Species:
9606
(Homo sapiens) [
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MNTEALQSKFFSPLQKAMLPPNSFQGKVAFITGGGTGLGKGMTTLLSSLG
AQCVIASRKMDVLKATAEQISSQTGNKVHAIQCDVRDPDMVQNTVSELIK
VAGHPNIVINNAAGNFISPTERLSPNAWKTITDIVLNGTAFVTLEIGKQL
IKAQKGAAFLSITTIYAETGSGFVVPSASAKAGVEAMSKSLAAEWGKYGM
RFNVIQPGPIKTGTFEKEMIGRIPCGRLGTVEELANLAAFLCSDYASWIN
GAVIKFDGGEEVLISGEFNDLRKVTKEQWDTIEELI
Ligand information
Ligand ID
HXC
InChI
InChI=1S/C27H46N7O17P3S/c1-4-5-6-7-18(36)55-11-10-29-17(35)8-9-30-25(39)22(38)27(2,3)13-48-54(45,46)51-53(43,44)47-12-16-21(50-52(40,41)42)20(37)26(49-16)34-15-33-19-23(28)31-14-32-24(19)34/h14-16,20-22,26,37-38H,4-13H2,1-3H3,(H,29,35)(H,30,39)(H,43,44)(H,45,46)(H2,28,31,32)(H2,40,41,42)/t16-,20-,21-,22+,26-/m1/s1
InChIKey
OEXFMSFODMQEPE-HDRQGHTBSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
CCCCCC(=O)SCCNC(=O)CCNC(=O)[C@@H](C(C)(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)O
CACTVS 3.341
CCCCCC(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(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
ACDLabs 10.04
O=C(SCCNC(=O)CCNC(=O)C(O)C(C)(C)COP(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3OP(=O)(O)O)CCCCC
CACTVS 3.341
CCCCCC(=O)SCCNC(=O)CCNC(=O)[CH](O)C(C)(C)CO[P](O)(=O)O[P](O)(=O)OC[CH]1O[CH]([CH](O)[CH]1O[P](O)(O)=O)n2cnc3c(N)ncnc23
OpenEye OEToolkits 1.5.0
CCCCCC(=O)SCCNC(=O)CCNC(=O)C(C(C)(C)COP(=O)(O)OP(=O)(O)OCC1C(C(C(O1)n2cnc3c2ncnc3N)O)OP(=O)(O)O)O
Formula
C27 H46 N7 O17 P3 S
Name
HEXANOYL-COENZYME A
ChEMBL
DrugBank
DB02563
ZINC
ZINC000008551760
PDB chain
1w6u Chain B Residue 1331 [
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Receptor-Ligand Complex Structure
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PDB
1w6u
Structure and Reactivity of Human Mitochondrial 2,4-Dienoyl-Coa Reductase: Enzyme-Ligand Interactions in a Distinctive Short-Chain Reductase Active Site
Resolution
1.75 Å
Binding residue
(original residue number in PDB)
G147 N148 F149 I150 S157 N159 A160
Binding residue
(residue number reindexed from 1)
G114 N115 F116 I117 S124 N126 A127
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
G70 T196 A200 V207 P209 K214
Catalytic site (residue number reindexed from 1)
G37 T163 A167 V174 P176 K181
Enzyme Commision number
1.3.1.124
: 2,4-dienoyl-CoA reductase [(3E)-enoyl-CoA-producing].
Gene Ontology
Molecular Function
GO:0008670
2,4-dienoyl-CoA reductase (NADPH) activity
GO:0016491
oxidoreductase activity
GO:0042802
identical protein binding
GO:0070402
NADPH binding
Biological Process
GO:0006631
fatty acid metabolic process
GO:0006635
fatty acid beta-oxidation
GO:0120162
positive regulation of cold-induced thermogenesis
Cellular Component
GO:0005634
nucleus
GO:0005654
nucleoplasm
GO:0005739
mitochondrion
GO:0005759
mitochondrial matrix
GO:0005829
cytosol
GO:1902494
catalytic complex
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1w6u
,
PDBe:1w6u
,
PDBj:1w6u
PDBsum
1w6u
PubMed
15531764
UniProt
Q16698
|DECR_HUMAN 2,4-dienoyl-CoA reductase [(3E)-enoyl-CoA-producing], mitochondrial (Gene Name=DECR1)
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