Structure of PDB 7khj Chain A Binding Site BS01
Receptor Information
>7khj Chain A (length=288) Species:
9606
(Homo sapiens) [
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NNYSYIDPTQLPYDHKWEFPRNRLSFGKTLGAGGKVVEATAQGLIKSDAA
MTVAVKMLKPSTEREALMSELKVLSYLGNHENIVNLLGACTHGGPTLVIT
EYCCYGDLLNFLRRKRDSFHNALDLEDLLSFSYQVAKGMAFLASKNCIHR
DLAARNILLTHGRITKICDFGLARVIKNDSNYVDKARLPVKWMAPESIFN
SVYTFESDVWSYGIFLWELFSLGSSPYPGMPVDSKFYKMIKEGFRMSSPE
HAPAEMYDIMKTCWDADPDKRPTFKQIVQDIEKQISES
Ligand information
Ligand ID
WEG
InChI
InChI=1S/C16H12N4/c1-2-4-11(5-3-1)15-7-12-6-13(8-17-16(12)20-15)14-9-18-19-10-14/h1-10H,(H,17,20)(H,18,19)
InChIKey
NSAWQZXLJIAJFT-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.385
[nH]1cc(cn1)c2cnc3[nH]c(cc3c2)c4ccccc4
OpenEye OEToolkits 2.0.7
c1ccc(cc1)c2cc3cc(cnc3[nH]2)c4c[nH]nc4
ACDLabs 12.01
c1ccc(cc1)c2nc4c(c2)cc(c3cnnc3)cn4
Formula
C16 H12 N4
Name
2-phenyl-5-(1H-pyrazol-4-yl)-1H-pyrrolo[2,3-b]pyridine
ChEMBL
DrugBank
ZINC
PDB chain
7khj Chain A Residue 1001 [
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Receptor-Ligand Complex Structure
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PDB
7khj
Association of Combination of Conformation-Specific KIT Inhibitors With Clinical Benefit in Patients With Refractory Gastrointestinal Stromal Tumors: A Phase 1b/2a Nonrandomized Clinical Trial.
Resolution
2.8 Å
Binding residue
(original residue number in PDB)
Y672 C673 C674 Y675 G676 L799
Binding residue
(residue number reindexed from 1)
Y102 C103 C104 Y105 G106 L158
Annotation score
1
Enzymatic activity
Enzyme Commision number
2.7.10.1
: receptor protein-tyrosine kinase.
Gene Ontology
Molecular Function
GO:0004672
protein kinase activity
GO:0004713
protein tyrosine kinase activity
GO:0004714
transmembrane receptor protein tyrosine kinase activity
GO:0005524
ATP binding
Biological Process
GO:0006468
protein phosphorylation
GO:0007169
cell surface receptor protein tyrosine kinase signaling pathway
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Molecular Function
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Biological Process
External links
PDB
RCSB:7khj
,
PDBe:7khj
,
PDBj:7khj
PDBsum
7khj
PubMed
34236401
UniProt
P10721
|KIT_HUMAN Mast/stem cell growth factor receptor Kit (Gene Name=KIT)
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