Structure of PDB 1mrq Chain A Binding Site BS01
Receptor Information
>1mrq Chain A (length=323) Species:
9606
(Homo sapiens) [
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QDSKYQCVKLNDGHFMPVLGFGTYAPAEVPKSKALEATKLAIEAGFRHID
SAHLYNNEEQVGLAIRSKIADGSVKREDIFYTSKLWCNSHRPELVRPALE
RSLKNLQLDYVDLYLIHFPVSVKPGEEVIPKDENGKILFDTVDLCATWEA
VEKCKDAGLAKSIGVSNFNRRQLEMILNKPGLKYKPVCNQVECHPYFNQR
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
1mrq Chain A Residue 500 [
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Receptor-Ligand Complex Structure
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PDB
1mrq
Human 20alpha-hydroxysteroid dehydrogenase: crystallographic and site-directed mutagenesis studies lead to the identification of an alternative binding site for C21-steroids.
Resolution
1.59 Å
Binding residue
(original residue number in PDB)
G22 T23 Y24 D50 Y55 H117 Q190 Y216 S217 L219 S221 H222 L236 A253 L268 K270 S271 R276 Q279 N280
Binding residue
(residue number reindexed from 1)
G22 T23 Y24 D50 Y55 H117 Q190 Y216 S217 L219 S221 H222 L236 A253 L268 K270 S271 R276 Q279 N280
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.-
1.1.1.112
: indanol dehydrogenase.
1.1.1.149
: 20alpha-hydroxysteroid dehydrogenase.
1.1.1.209
: 3(or 17)alpha-hydroxysteroid dehydrogenase.
1.1.1.210
: 3beta-(or 20alpha)-hydroxysteroid dehydrogenase.
1.1.1.357
: 3alpha-hydroxysteroid 3-dehydrogenase.
1.1.1.51
: 3(or 17)beta-hydroxysteroid 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:0004033
aldo-keto reductase (NADPH) activity
GO:0004303
estradiol 17-beta-dehydrogenase [NAD(P)+] activity
GO:0005515
protein binding
GO:0016491
oxidoreductase activity
GO:0016655
oxidoreductase activity, acting on NAD(P)H, quinone or similar compound as acceptor
GO:0030283
testosterone dehydrogenase [NAD(P)+] activity
GO:0031406
carboxylic acid binding
GO:0032052
bile acid binding
GO:0033703
3beta-hydroxy-5beta-steroid dehydrogenase activity
GO:0033764
steroid dehydrogenase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
GO:0047006
17-alpha,20-alpha-dihydroxypregn-4-en-3-one dehydrogenase activity
GO:0047023
androsterone dehydrogenase activity
GO:0047024
5alpha-androstane-3beta,17beta-diol dehydrogenase activity
GO:0047042
androsterone dehydrogenase (B-specific) activity
GO:0047044
androstan-3-alpha,17-beta-diol dehydrogenase activity
GO:0047045
testosterone 17-beta-dehydrogenase (NADP+) 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:0001523
retinoid metabolic process
GO:0006629
lipid metabolic process
GO:0006693
prostaglandin metabolic process
GO:0006805
xenobiotic metabolic process
GO:0007586
digestion
GO:0008206
bile acid metabolic process
GO:0015721
bile acid and bile salt transport
GO:0030299
intestinal cholesterol absorption
GO:0030855
epithelial cell differentiation
GO:0042448
progesterone metabolic process
GO:0042574
retinal metabolic process
GO:0042632
cholesterol homeostasis
GO:0044597
daunorubicin metabolic process
GO:0044598
doxorubicin metabolic process
GO:0046683
response to organophosphorus
GO:0071395
cellular response to jasmonic acid stimulus
GO:2000379
positive regulation of reactive oxygen species metabolic process
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
GO:0070062
extracellular exosome
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Cellular Component
External links
PDB
RCSB:1mrq
,
PDBe:1mrq
,
PDBj:1mrq
PDBsum
1mrq
PubMed
12899831
UniProt
Q04828
|AK1C1_HUMAN Aldo-keto reductase family 1 member C1 (Gene Name=AKR1C1)
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