Structure of PDB 4yvv Chain B Binding Site BS02
Receptor Information
>4yvv Chain B (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
GBM
InChI
InChI=1S/C23H28ClN3O5S/c1-32-21-12-9-17(24)15-20(21)22(28)25-14-13-16-7-10-19(11-8-16)33(30,31)27-23(29)26-18-5-3-2-4-6-18/h7-12,15,18H,2-6,13-14H2,1H3,(H,25,28)(H2,26,27,29)
InChIKey
ZNNLBTZKUZBEKO-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 12.01
O=C(NC1CCCCC1)NS(=O)(=O)c3ccc(CCNC(=O)c2c(OC)ccc(Cl)c2)cc3
CACTVS 3.385
COc1ccc(Cl)cc1C(=O)NCCc2ccc(cc2)[S](=O)(=O)NC(=O)NC3CCCCC3
OpenEye OEToolkits 1.9.2
COc1ccc(cc1C(=O)NCCc2ccc(cc2)S(=O)(=O)NC(=O)NC3CCCCC3)Cl
Formula
C23 H28 Cl N3 O5 S
Name
5-chloro-N-(2-{4-[(cyclohexylcarbamoyl)sulfamoyl]phenyl}ethyl)-2-methoxybenzamide;
Glibenclamide;
Glyburide
ChEMBL
CHEMBL472
DrugBank
DB01016
ZINC
ZINC000000537805
PDB chain
4yvv Chain B 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
4yvv
In vitro inhibition of AKR1Cs by sulphonylureas and the structural basis
Resolution
2.3 Å
Binding residue
(original residue number in PDB)
Y24 L54 Y55 W86 H117 W227 F306
Binding residue
(residue number reindexed from 1)
Y19 L49 Y50 W81 H112 W222 F301
Annotation score
1
Binding affinity
MOAD
: ic50=3.72uM
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:4yvv
,
PDBe:4yvv
,
PDBj:4yvv
PDBsum
4yvv
PubMed
26362498
UniProt
P42330
|AK1C3_HUMAN Aldo-keto reductase family 1 member C3 (Gene Name=AKR1C3)
[
Back to BioLiP
]