Structure of PDB 1w8d Chain A Binding Site BS01
Receptor Information
>1w8d Chain A (length=288) Species:
9606
(Homo sapiens) [
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NTEALQSKFFSPLQKAMLPPNSFQGKVAFITGGGTGLGKGMTTLLSSLGA
QCVIASRKMDVLKATAEQISSQTGNKVHAIQCDVRDPDMVQNTVSELIKV
AGHPNIVINNAAGNFISPTERLSPNAWKTITDIVLNGTAFVTLEIGKQLI
KAQKGAAFLSITTIYAETGSGFVVPSASAKAGVEAMSKSLAAEWGKYGMR
FNVIQPGPIKTLDPTGTFEKEMIGRIPCGRLGTVEELANLAAFLCSDYAS
WINGAVIKFDGGEEVLISGEFNDLRKVTKEQWDTIEEL
Ligand information
Ligand ID
NAP
InChI
InChI=1S/C21H28N7O17P3/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(44-46(33,34)35)14(30)11(43-21)6-41-48(38,39)45-47(36,37)40-5-10-13(29)15(31)20(42-10)27-3-1-2-9(4-27)18(23)32/h1-4,7-8,10-11,13-16,20-21,29-31H,5-6H2,(H7-,22,23,24,25,32,33,34,35,36,37,38,39)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
XJLXINKUBYWONI-NNYOXOHSSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1cc(c[n+](c1)C2C(C(C(O2)COP(=O)([O-])OP(=O)(O)OCC3C(C(C(O3)n4cnc5c4ncnc5N)OP(=O)(O)O)O)O)O)C(=O)N
CACTVS 3.341
NC(=O)c1ccc[n+](c1)[CH]2O[CH](CO[P]([O-])(=O)O[P](O)(=O)OC[CH]3O[CH]([CH](O[P](O)(O)=O)[CH]3O)n4cnc5c(N)ncnc45)[CH](O)[CH]2O
CACTVS 3.341
NC(=O)c1ccc[n+](c1)[C@@H]2O[C@H](CO[P]([O-])(=O)O[P@@](O)(=O)OC[C@H]3O[C@H]([C@H](O[P](O)(O)=O)[C@@H]3O)n4cnc5c(N)ncnc45)[C@@H](O)[C@H]2O
OpenEye OEToolkits 1.5.0
c1cc(c[n+](c1)[C@H]2[C@@H]([C@@H]([C@H](O2)CO[P@@](=O)([O-])O[P@](=O)(O)OC[C@@H]3[C@H]([C@H]([C@@H](O3)n4cnc5c4ncnc5N)OP(=O)(O)O)O)O)O)C(=O)N
Formula
C21 H28 N7 O17 P3
Name
NADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE;
2'-MONOPHOSPHOADENOSINE 5'-DIPHOSPHORIBOSE
ChEMBL
CHEMBL295069
DrugBank
DB03461
ZINC
PDB chain
1w8d Chain A Residue 1330 [
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Receptor-Ligand Complex Structure
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PDB
1w8d
Structure and Reactivity of Human Mitochondrial 2,4-Dienoyl-Coa Reductase: Enzyme-Ligand Interactions in a Distinctive Short-Chain Reductase Active Site
Resolution
2.2 Å
Binding residue
(original residue number in PDB)
G66 T69 G70 L71 S90 R91 K92 D117 V118 N144 A145 A146 I195 T196 K214 P242 I243
Binding residue
(residue number reindexed from 1)
G32 T35 G36 L37 S56 R57 K58 D83 V84 N110 A111 A112 I161 T162 K180 P208 I209
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
G70 T196 A200 V207 P209 K214
Catalytic site (residue number reindexed from 1)
G36 T162 A166 V173 P175 K180
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:1w8d
,
PDBe:1w8d
,
PDBj:1w8d
PDBsum
1w8d
PubMed
15531764
UniProt
Q16698
|DECR_HUMAN 2,4-dienoyl-CoA reductase [(3E)-enoyl-CoA-producing], mitochondrial (Gene Name=DECR1)
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