Structure of PDB 2he5 Chain D Binding Site BS01
Receptor Information
>2he5 Chain D (length=314) Species:
10090
(Mus musculus) [
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HCVILNDGNFIPVLGFGTALPLECPKSKAKELTKIAIDAGFHHFDSASVY
NTEDHVGEAIRSKIADGTVRREDIFYTSKVWCTSLHPELVRASLERSLQK
LQFDYVDLYLIHYPMALKPGEENFPVDEHGKLIFDRVDLCATWEAMEKCK
DAGLTKSIGVSNFNYRQLEMILNKPGLKYKPVCNQVECHPYLNQMKLLDF
CKSKDIVLVAYGVLGTGWVDQNSPVLLDEPVLGSMAKKYNRTPALIALRY
QLQRGIVVLNTSLKEERIKENMQVFEFQLSSEDMKVLDGLNRNMRYIPAA
IFKGHPNWPFLDEY
Ligand information
Ligand ID
NDP
InChI
InChI=1S/C21H30N7O17P3/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/h1,3-4,7-8,10-11,13-16,20-21,29-31H,2,5-6H2,(H2,23,32)(H,36,37)(H,38,39)(H2,22,24,25)(H2,33,34,35)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
ACFIXJIJDZMPPO-NNYOXOHSSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=O)(O)O[P@@](=O)(O)OC[C@@H]4[C@H]([C@H]([C@@H](O4)N5C=CCC(=C5)C(=O)N)O)O)O)OP(=O)(O)O)N
CACTVS 3.341
NC(=O)C1=CN(C=CC1)[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)C1=CN(C=CC1)[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
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)OCC4C(C(C(O4)N5C=CCC(=C5)C(=O)N)O)O)O)OP(=O)(O)O)N
Formula
C21 H30 N7 O17 P3
Name
NADPH DIHYDRO-NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE
ChEMBL
CHEMBL407009
DrugBank
DB02338
ZINC
ZINC000008215411
PDB chain
2he5 Chain D Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
2he5
Crystal Structures of Mouse 17alpha-Hydroxysteroid Dehydrogenase (Apoenzyme and Enzyme-NADP(H) Binary Complex): Identification of Molecular Determinants Responsible for the Unique 17alpha-reductive Activity of this Enzyme.
Resolution
2.9 Å
Binding residue
(original residue number in PDB)
G22 A24 D50 Y55 Q190 Y216 G217 V218 L219 G220 T270 S271 R276
Binding residue
(residue number reindexed from 1)
G17 A19 D45 Y50 Q185 Y211 G212 V213 L214 G215 T261 S262 R267
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
D50 Y55 K84 H117
Catalytic site (residue number reindexed from 1)
D45 Y50 K79 H112
Enzyme Commision number
1.1.1.-
1.1.1.209
: 3(or 17)alpha-hydroxysteroid dehydrogenase.
Gene Ontology
Molecular Function
GO:0004033
aldo-keto reductase (NADPH) activity
GO:0005496
steroid binding
GO:0016491
oxidoreductase activity
GO:0033764
steroid dehydrogenase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
GO:0047023
androsterone dehydrogenase activity
GO:0047024
5alpha-androstane-3beta,17beta-diol dehydrogenase activity
GO:0070401
NADP+ binding
GO:0070402
NADPH binding
GO:0072555
17-beta-ketosteroid reductase (NADPH) activity
GO:0072582
17-beta-hydroxysteroid dehydrogenase (NADP+) activity
GO:1902121
lithocholic acid binding
Biological Process
GO:0006694
steroid biosynthetic process
GO:0008202
steroid metabolic process
Cellular Component
GO:0005737
cytoplasm
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2he5
,
PDBe:2he5
,
PDBj:2he5
PDBsum
2he5
PubMed
17034817
UniProt
Q91WR5
|AK1CL_MOUSE Aldo-keto reductase family 1 member C21 (Gene Name=Akr1c21)
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