Structure of PDB 3bur Chain B Binding Site BS01
Receptor Information
>3bur Chain B (length=325) Species:
9606
(Homo sapiens) [
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DLSAASHRIPLSDGNSIPIIGLGTYSEPKSTPKGACATSVKVAIDTGYRH
IDGAYIYQNEHEVGEAIREKIAEGKVRREDIFYCGKLWATNHVPEMVRPT
LERTLRVLQLDYVDLYIIEVPMAFKPGDEIYPRDENGKWLYHKSNLCATW
EAMEACKDAGLVKSLGVSNFNRRQLELILNKPGLKHKPVSNQVECHPYFT
QPKLLKFCQQHDIVITAYSPLGTSRNPIWVNVSSPPLLKDALLNSLGKRY
NKTAAQIVLRFNIQRGVVVIPKSFNLERIKENFQIFDFSLTEEEMKDIEA
LNKNVRFVELLMWRDHPEYPFHDEY
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
3bur Chain B Residue 327 [
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Receptor-Ligand Complex Structure
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PDB
3bur
Crystal Structure of Human Liver {Delta}4-3-Ketosteroid 5{beta}-Reductase (AKR1D1) and Implications for Substrate Binding and Catalysis.
Resolution
1.62 Å
Binding residue
(original residue number in PDB)
G24 T25 Y26 D53 Y58 N170 Q193 Y219 S220 P221 L222 T224 S225 L239 I271 P272 K273 S274 R279 E282 N283
Binding residue
(residue number reindexed from 1)
G23 T24 Y25 D52 Y57 N169 Q192 Y218 S219 P220 L221 T223 S224 L238 I270 P271 K272 S273 R278 E281 N282
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
D53 Y58 K87 E120
Catalytic site (residue number reindexed from 1)
D52 Y57 K86 E119
Enzyme Commision number
1.3.1.3
: Delta(4)-3-oxosteroid 5beta-reductase.
Gene Ontology
Molecular Function
GO:0004032
aldose reductase (NADPH) activity
GO:0004033
aldo-keto reductase (NADPH) activity
GO:0005496
steroid binding
GO:0005515
protein binding
GO:0016229
steroid dehydrogenase activity
GO:0016491
oxidoreductase activity
GO:0047086
ketosteroid monooxygenase activity
GO:0047787
Delta4-3-oxosteroid 5beta-reductase activity
Biological Process
GO:0006699
bile acid biosynthetic process
GO:0006707
cholesterol catabolic process
GO:0007586
digestion
GO:0008202
steroid metabolic process
GO:0008207
C21-steroid hormone metabolic process
GO:0008209
androgen metabolic process
GO:0016042
lipid catabolic process
GO:0030573
bile acid catabolic process
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
View graph for
Molecular Function
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Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:3bur
,
PDBe:3bur
,
PDBj:3bur
PDBsum
3bur
PubMed
18407998
UniProt
P51857
|AK1D1_HUMAN Aldo-keto reductase family 1 member D1 (Gene Name=AKR1D1)
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