Structure of PDB 1qyv Chain A Binding Site BS01
Receptor Information
>1qyv Chain A (length=276) Species:
9606
(Homo sapiens) [
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ARTVVLITGCSSGIGLHLAVRLASDPSQSFKVYATLRDLKTQGRLWEAAR
ALACPPGSLETLQLDVRDSKSVAAARERVTEGRVDVLVCNAGLGLLGPLE
ALGEDAVASVLDVNVVGTVRMLQAFLPDMKRRGSGRVLVTGSVGGLMGLP
FNDVYCASKFALEGLCESLAVLLLPFGVHLSLIECGPVHTSPEEVLDRTD
IHTFHRFYQYLAHSKQVFREAAQNPEEVAEVFLTALRAPKPTLRYFTTER
FLPLLRMRLDDPSGSNYVTAMHREVF
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
1qyv Chain A Residue 361 [
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Receptor-Ligand Complex Structure
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PDB
1qyv
Cofactor hydrogen bonding onto the protein main chain is conserved in the short chain dehydrogenase/reductase family and contributes to nicotinamide orientation.
Resolution
1.81 Å
Binding residue
(original residue number in PDB)
G9 S11 S12 G13 I14 R37 D65 V66 N90 A91 G92 T140 G141 S142 K159 C185 G186 V188 T190
Binding residue
(residue number reindexed from 1)
G9 S11 S12 G13 I14 R37 D65 V66 N90 A91 G92 T140 G141 S142 K159 C185 G186 V188 T190
Annotation score
4
Enzymatic activity
Enzyme Commision number
1.1.1.51
: 3(or 17)beta-hydroxysteroid dehydrogenase.
1.1.1.62
: 17beta-estradiol 17-dehydrogenase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0004303
estradiol 17-beta-dehydrogenase [NAD(P)+] activity
GO:0005496
steroid binding
GO:0005515
protein binding
GO:0016491
oxidoreductase activity
GO:0030283
testosterone dehydrogenase [NAD(P)+] activity
GO:0036094
small molecule binding
GO:0042803
protein homodimerization activity
GO:0047035
testosterone dehydrogenase (NAD+) activity
GO:0047045
testosterone 17-beta-dehydrogenase (NADP+) activity
GO:0050661
NADP binding
GO:0070401
NADP+ binding
GO:0072582
17-beta-hydroxysteroid dehydrogenase (NADP+) activity
GO:1903924
estradiol binding
Biological Process
GO:0006629
lipid metabolic process
GO:0006694
steroid biosynthetic process
GO:0006703
estrogen biosynthetic process
GO:0007040
lysosome organization
GO:0007519
skeletal muscle tissue development
GO:0008210
estrogen metabolic process
GO:0010467
gene expression
GO:0060348
bone development
GO:0060612
adipose tissue development
GO:0061370
testosterone biosynthetic process
GO:0071248
cellular response to metal ion
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1qyv
,
PDBe:1qyv
,
PDBj:1qyv
PDBsum
1qyv
PubMed
14966133
UniProt
P14061
|DHB1_HUMAN 17-beta-hydroxysteroid dehydrogenase type 1 (Gene Name=HSD17B1)
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