Structure of PDB 1j96 Chain A Binding Site BS01
Receptor Information
>1j96 Chain A (length=323) Species:
9606
(Homo sapiens) [
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DDSKYQCVKLNDGHFMPVLGFGTYAPAEVPKSKALEAVKLAIEAGFHHID
SAHVYNNEEQVGLAIRSKIADGSVKREDIFYTSKLWSNSHRPELVRPALE
RSLKNLQLDYVDLYLIHFPVSVKPGEEVIPKDENGKILFDTVDLCATWEA
MEKCKDAGLAKSIGVSNFNHRLLEMILNKPGLKYKPVCNQVECHPYFNQR
KLLDFCKSKDIVLVAYSALGSHREEPWVDPNSPVLLEDPVLCALAKKHKR
TPALIALRYQLQRGVVVLAKSYNEQRIRQNVQVFEFQLTSEEMKAIDGLN
RNVRYLTLDIFAGPPNYPFSDEY
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
1j96 Chain A Residue 901 [
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Receptor-Ligand Complex Structure
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PDB
1j96
Structure of the human 3alpha-hydroxysteroid dehydrogenase type 3 in complex with testosterone and NADP at 1.25-A resolution.
Resolution
1.25 Å
Binding residue
(original residue number in PDB)
G22 T23 Y24 D50 Y55 Q190 Y216 S217 L219 S221 H222 A253 K270 S271 R276 Q279 N280 L306
Binding residue
(residue number reindexed from 1)
G22 T23 Y24 D50 Y55 Q190 Y216 S217 L219 S221 H222 A253 K270 S271 R276 Q279 N280 L306
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
D50 Y55 K84 H117
Catalytic site (residue number reindexed from 1)
D50 Y55 K84 H117
Enzyme Commision number
1.-.-.-
1.1.1.112
: indanol dehydrogenase.
1.1.1.209
: 3(or 17)alpha-hydroxysteroid dehydrogenase.
1.1.1.357
: 3alpha-hydroxysteroid 3-dehydrogenase.
1.1.1.53
: 3alpha(or 20beta)-hydroxysteroid dehydrogenase.
1.1.1.62
: 17beta-estradiol 17-dehydrogenase.
1.3.1.20
: trans-1,2-dihydrobenzene-1,2-diol dehydrogenase.
Gene Ontology
Molecular Function
GO:0004032
aldose reductase (NADPH) activity
GO:0004303
estradiol 17-beta-dehydrogenase [NAD(P)+] activity
GO:0016491
oxidoreductase activity
GO:0016655
oxidoreductase activity, acting on NAD(P)H, quinone or similar compound as acceptor
GO:0031406
carboxylic acid binding
GO:0032052
bile acid binding
GO:0047023
androsterone dehydrogenase activity
GO:0047044
androstan-3-alpha,17-beta-diol dehydrogenase activity
GO:0047086
ketosteroid monooxygenase activity
GO:0047115
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase activity
GO:0047718
indanol dehydrogenase activity
Biological Process
GO:0006693
prostaglandin metabolic process
GO:0007186
G protein-coupled receptor signaling pathway
GO:0007586
digestion
GO:0008202
steroid metabolic process
GO:0008284
positive regulation of cell population proliferation
GO:0030855
epithelial cell differentiation
GO:0042448
progesterone metabolic process
GO:0044597
daunorubicin metabolic process
GO:0044598
doxorubicin metabolic process
GO:0051897
positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction
GO:0071395
cellular response to jasmonic acid stimulus
GO:0071799
cellular response to prostaglandin D stimulus
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
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Molecular Function
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Cellular Component
External links
PDB
RCSB:1j96
,
PDBe:1j96
,
PDBj:1j96
PDBsum
1j96
PubMed
11514561
UniProt
P52895
|AK1C2_HUMAN Aldo-keto reductase family 1 member C2 (Gene Name=AKR1C2)
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