Structure of PDB 6fa3 Chain F Binding Site BS02
Receptor Information
>6fa3 Chain F (length=165) Species:
9606
(Homo sapiens) [
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FQGMTEYKLVVVGAGGVGKSALTIQLIQNHFVDEYDPTIEDSYRKQVVID
GETCLLDILDTAGHMRDQYMRTGEGFLCVFAINNTKSFEDIHHYREQIKR
VKDSEDVPMVLVGNKCDLPSRTVDTKQAQDLARSYGIPFIETSAKTRQGV
DDAFYTLVREIRKHK
Ligand information
Ligand ID
MG
InChI
InChI=1S/Mg/q+2
InChIKey
JLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341
[Mg++]
Formula
Mg
Name
MAGNESIUM ION
ChEMBL
DrugBank
DB01378
ZINC
PDB chain
6fa3 Chain F Residue 202 [
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Receptor-Ligand Complex Structure
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PDB
6fa3
Small molecule inhibitors of RAS-effector protein interactions derived using an intracellular antibody fragment.
Resolution
1.82 Å
Binding residue
(original residue number in PDB)
S17 T35
Binding residue
(residue number reindexed from 1)
S20 T38
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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Molecular Function
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Cellular Component
External links
PDB
RCSB:6fa3
,
PDBe:6fa3
,
PDBj:6fa3
PDBsum
6fa3
PubMed
30093669
UniProt
P01116
|RASK_HUMAN GTPase KRas (Gene Name=KRAS)
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