Structure of PDB 4wrh Chain A Binding Site BS02
Receptor Information
>4wrh Chain A (length=316) Species:
9606
(Homo sapiens) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
QCVKLNDGHFMPVLGFGTYAPPEVPRSKALEVTKLAIEAGFRHIDSAHLY
NNEEQVGLAIRSKIADGSVKREDIFYTSKLWSTFHRPELVRPALENSLKK
AQLDYVDLYLIHSPMSLKPGEELSPTDENGKVIFDIVDLCTTWEAMEKCK
DAGLAKSIGVSNFNRRQLEMILNKPGLKYKPVCNQVECHPYFNRSKLLDF
CKSKDIVLVAYSALGSQRDKRWVDPNSPVLLEDPVLCALAKKHKRTPALI
ALRYQLQRGVVVLAKSYNEQRIRQNVQVFEFQLTAEDMKAIDGLDRNLHY
FNSDSFASHPNYPYSD
Ligand information
Ligand ID
YY2
InChI
InChI=1S/C14H21ClN2O3/c1-14(2,3)17-12(18)8-20-13-10(15)5-9(7-16)6-11(13)19-4/h5-6H,7-8,16H2,1-4H3,(H,17,18)
InChIKey
HEOFBSUCMHLHRB-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.385
COc1cc(CN)cc(Cl)c1OCC(=O)NC(C)(C)C
OpenEye OEToolkits 1.9.2
CC(C)(C)NC(=O)COc1c(cc(cc1Cl)CN)OC
ACDLabs 12.01
Clc1cc(cc(OC)c1OCC(=O)NC(C)(C)C)CN
Formula
C14 H21 Cl N2 O3
Name
2-[4-(aminomethyl)-2-chloro-6-methoxyphenoxy]-N-tert-butylacetamide
ChEMBL
DrugBank
ZINC
PDB chain
4wrh Chain A Residue 402 [
Download ligand structure
] [
Download structure with residue number starting from 1
] [
View ligand structure
]
Receptor-Ligand Complex Structure
Global view
Local view
Structure summary
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
PDB
4wrh
Breakdown product of N-(tert-butyl)-2-(2-chloro-4-(((3-mercapto-5-methyl-4H-1,2,4-triazol-4-yl)amino)methyl)-6-methoxyphenoxy)acetamide trapped in active site of AKR1C3
Resolution
1.6 Å
Binding residue
(original residue number in PDB)
W86 S118 M120 N167 F306 F311 P318
Binding residue
(residue number reindexed from 1)
W81 S113 M115 N162 F301 F306 P313
Annotation score
1
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.-
1.1.1.188
: prostaglandin-F synthase.
1.1.1.210
: 3beta-(or 20alpha)-hydroxysteroid dehydrogenase.
1.1.1.239
: 3alpha-(17beta)-hydroxysteroid dehydrogenase (NAD(+)).
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.
1.1.1.64
: testosterone 17beta-dehydrogenase (NADP(+)).
Gene Ontology
Molecular Function
GO:0001758
retinal dehydrogenase activity
GO:0004032
aldose reductase (NADPH) activity
GO:0004033
aldo-keto reductase (NADPH) activity
GO:0004303
estradiol 17-beta-dehydrogenase [NAD(P)+] activity
GO:0004745
all-trans-retinol dehydrogenase (NAD+) 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:0032052
bile acid binding
GO:0036130
prostaglandin H2 endoperoxidase reductase activity
GO:0036131
prostaglandin D2 11-ketoreductase activity
GO:0045550
geranylgeranyl reductase activity
GO:0045703
ketoreductase activity
GO:0047017
prostaglandin F synthase activity
GO:0047020
15-hydroxyprostaglandin-D dehydrogenase (NADP+) activity
GO:0047023
androsterone dehydrogenase activity
GO:0047024
5alpha-androstane-3beta,17beta-diol dehydrogenase activity
GO:0047035
testosterone dehydrogenase (NAD+) 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:0047787
Delta4-3-oxosteroid 5beta-reductase activity
GO:0052650
all-trans-retinol dehydrogenase (NADP+) activity
Biological Process
GO:0001523
retinoid metabolic process
GO:0006629
lipid metabolic process
GO:0006693
prostaglandin metabolic process
GO:0007186
G protein-coupled receptor signaling pathway
GO:0007584
response to nutrient
GO:0008202
steroid metabolic process
GO:0008284
positive regulation of cell population proliferation
GO:0008584
male gonad development
GO:0009267
cellular response to starvation
GO:0016488
farnesol catabolic process
GO:0019371
cyclooxygenase pathway
GO:0030216
keratinocyte differentiation
GO:0042448
progesterone metabolic process
GO:0042572
retinol metabolic process
GO:0042574
retinal metabolic process
GO:0043170
macromolecule metabolic process
GO:0044597
daunorubicin metabolic process
GO:0044598
doxorubicin metabolic process
GO:0048385
regulation of retinoic acid receptor signaling pathway
GO:0051897
positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction
GO:0061370
testosterone biosynthetic process
GO:0070293
renal absorption
GO:0071277
cellular response to calcium ion
GO:0071379
cellular response to prostaglandin stimulus
GO:0071384
cellular response to corticosteroid stimulus
GO:0071395
cellular response to jasmonic acid stimulus
GO:0071799
cellular response to prostaglandin D stimulus
GO:1900053
negative regulation of retinoic acid biosynthetic process
GO:2000224
regulation of testosterone biosynthetic process
GO:2000353
positive regulation of endothelial cell apoptotic process
GO:2000379
positive regulation of reactive oxygen species metabolic process
Cellular Component
GO:0005634
nucleus
GO:0005737
cytoplasm
GO:0005829
cytosol
GO:0070062
extracellular exosome
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:4wrh
,
PDBe:4wrh
,
PDBj:4wrh
PDBsum
4wrh
PubMed
UniProt
P42330
|AK1C3_HUMAN Aldo-keto reductase family 1 member C3 (Gene Name=AKR1C3)
[
Back to BioLiP
]