Structure of PDB 4dbw Chain A Binding Site BS02
Receptor Information
>4dbw Chain A (length=315) 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
FNSDSFASHPNYPYS
Ligand information
Ligand ID
511
InChI
InChI=1S/C18H14ClNO4/c1-24-14-6-7-16-15(9-14)12(8-17(21)22)10-20(16)18(23)11-2-4-13(19)5-3-11/h2-7,9-10H,8H2,1H3,(H,21,22)
InChIKey
DHEMTWWLRLOBKI-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.370
COc1ccc2n(cc(CC(O)=O)c2c1)C(=O)c3ccc(Cl)cc3
OpenEye OEToolkits 1.7.6
COc1ccc2c(c1)c(cn2C(=O)c3ccc(cc3)Cl)CC(=O)O
ACDLabs 12.01
Clc1ccc(cc1)C(=O)n3c2ccc(OC)cc2c(c3)CC(=O)O
Formula
C18 H14 Cl N O4
Name
[1-(4-chlorobenzoyl)-5-methoxy-1H-indol-3-yl]acetic acid;
2'-desmethyl-indomethacin
ChEMBL
CHEMBL503179
DrugBank
ZINC
ZINC000004298622
PDB chain
4dbw 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
4dbw
Development of potent and selective indomethacin analogues for the inhibition of AKR1C3 (Type 5 17 beta-hydroxysteroid dehydrogenase/prostaglandin F synthase) in castrate-resistant prostate cancer.
Resolution
1.802 Å
Binding residue
(original residue number in PDB)
Y24 L54 Y55 H117 S118 M120 N167 W227 F306 Y319
Binding residue
(residue number reindexed from 1)
Y19 L49 Y50 H112 S113 M115 N162 W222 F301 Y314
Annotation score
1
Binding affinity
MOAD
: ic50=0.1uM
BindingDB: IC50=0.96nM
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:4dbw
,
PDBe:4dbw
,
PDBj:4dbw
PDBsum
4dbw
PubMed
23432095
UniProt
P42330
|AK1C3_HUMAN Aldo-keto reductase family 1 member C3 (Gene Name=AKR1C3)
[
Back to BioLiP
]