Structure of PDB 7mu7 Chain B Binding Site BS01
Receptor Information
>7mu7 Chain B (length=260) Species:
9606
(Homo sapiens) [
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DLLEYDYEYDENGDRVVLGKGTYGIVYAGRDLSNQVRIAIKEIPERSQPL
HEEIALHKHLKHKNIVQYLGSFSENGFIKIFMEQVPGGSLSALLRSKWGP
LKDNEQTIGFYTKQILEGLKYLHDNQIVHRDIKGDNVLINTYSGVLKISD
FGTSKRLAGTGTLQYMAPEIIDKGPRGYGKAADIWSLGCTIIEMATGKPP
FYELGEPQAAMFKVGMFKVHPEIPESMSAEAKAFILKCFEPDPDKRACAN
DLLVDEFLKV
Ligand information
Ligand ID
RFG
InChI
InChI=1S/C19H19N9O2/c1-12(2)27-11-22-25-17(27)14-5-4-6-15(23-14)24-18(29)13-10-28(26-19(13)30-3)16-9-20-7-8-21-16/h4-12H,1-3H3,(H,23,24,29)
InChIKey
FTPVMITWJIXRGQ-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 2.0.7
CC(C)n1cnnc1c2cccc(n2)NC(=O)c3cn(nc3OC)c4cnccn4
ACDLabs 12.01
C(Nc2nc(c1nncn1C(C)C)ccc2)(c3cn(nc3OC)c4cnccn4)=O
CACTVS 3.385
COc1nn(cc1C(=O)Nc2cccc(n2)c3nncn3C(C)C)c4cnccn4
Formula
C19 H19 N9 O2
Name
3-methoxy-N-{6-[4-(propan-2-yl)-4H-1,2,4-triazol-3-yl]pyridin-2-yl}-1-(pyrazin-2-yl)-1H-pyrazole-4-carboxamide
ChEMBL
CHEMBL4632672
DrugBank
ZINC
PDB chain
7mu7 Chain B Residue 1003 [
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Receptor-Ligand Complex Structure
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PDB
7mu7
Discovery of Potent, Selective and CNS-Penetrant Apoptosis Signal-regulating Kinase 1 (ASK1) Inhibitors that Modulate Brain Inflammation in Vivo
Resolution
2.298 Å
Binding residue
(original residue number in PDB)
A707 K709 M754 E755 Q756 V757 G759 G760 L810 D822
Binding residue
(residue number reindexed from 1)
A39 K41 M82 E83 Q84 V85 G87 G88 L138 D150
Annotation score
1
Enzymatic activity
Enzyme Commision number
2.7.11.25
: mitogen-activated protein kinase kinase kinase.
Gene Ontology
Molecular Function
GO:0004672
protein kinase activity
GO:0005524
ATP binding
Biological Process
GO:0006468
protein phosphorylation
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:7mu7
,
PDBe:7mu7
,
PDBj:7mu7
PDBsum
7mu7
PubMed
UniProt
Q99683
|M3K5_HUMAN Mitogen-activated protein kinase kinase kinase 5 (Gene Name=MAP3K5)
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