Structure of PDB 7u8h Chain A Binding Site BS01
Receptor Information
>7u8h Chain A (length=169) Species:
9606
(Homo sapiens) [
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GMTEYKLVVVGAVGVGKSALTIQLIQNHFVDEYDPTIEDCYRKQVVIDGE
TCLLDILDTAGQEEYSAMRDQYMRTGEGFLCVFAINNTKSFEDIHHYREQ
IKRVKDSEDVPMVLVGNKSDLPSRTVDTKQAQDLARSYGIPFIETSAKTR
QGVDDAFYTLVREIRKHKE
Ligand information
Ligand ID
2XO
InChI
InChI=1S/C8H8N2S/c11-5-8-9-6-3-1-2-4-7(6)10-8/h1-4,11H,5H2,(H,9,10)
InChIKey
XGIDEUICZZXBFQ-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.6
c1ccc2c(c1)[nH]c(n2)CS
CACTVS 3.385
SCc1[nH]c2ccccc2n1
ACDLabs 12.01
n2c1ccccc1nc2CS
Formula
C8 H8 N2 S
Name
1H-benzimidazol-2-ylmethanethiol
ChEMBL
CHEMBL2358377
DrugBank
ZINC
ZINC000000127800
PDB chain
7u8h Chain A Residue 201 [
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Receptor-Ligand Complex Structure
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PDB
7u8h
Fragment Optimization of Reversible Binding to the Switch II Pocket on KRAS Leads to a Potent, In Vivo Active KRAS G12C Inhibitor.
Resolution
1.702 Å
Binding residue
(original residue number in PDB)
V7 C39 D54 L56 Y71 T74
Binding residue
(residue number reindexed from 1)
V8 C40 D55 L57 Y72 T75
Annotation score
1
Enzymatic activity
Enzyme Commision number
3.6.5.2
: small monomeric GTPase.
Gene Ontology
Molecular Function
GO:0003924
GTPase activity
GO:0005525
GTP binding
Biological Process
GO:0007165
signal transduction
Cellular Component
GO:0016020
membrane
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Cellular Component
External links
PDB
RCSB:7u8h
,
PDBe:7u8h
,
PDBj:7u8h
PDBsum
7u8h
PubMed
36300829
UniProt
P01116
|RASK_HUMAN GTPase KRas (Gene Name=KRAS)
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