Structure of PDB 7w9u Chain A Binding Site BS01
Receptor Information
>7w9u Chain A (length=132) Species:
9606
(Homo sapiens) [
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NDKVYENVTGLVKAVIEMSSKIQPAPPEEYVPMVKEVGLALRTLLATVDE
TIPLLPASTHREIEMAQKLLNSDLGELINKMKLAQQYVMTSLQQEYKKQM
LTAAHALAVDAKNLLDVIDQARLKMLGQTRPH
Ligand information
Ligand ID
ZN
InChI
InChI=1S/Zn/q+2
InChIKey
PTFCDOFLOPIGGS-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Zn++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Zn+2]
Formula
Zn
Name
ZINC ION
ChEMBL
CHEMBL1236970
DrugBank
DB14532
ZINC
PDB chain
7w9u Chain A Residue 1102 [
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Receptor-Ligand Complex Structure
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PDB
7w9u
Crystal Structure of Zn bound human Focal Adhesion Targeting (FAT) domain of the Focal Adhesion Kinase
Resolution
2.163 Å
Binding residue
(original residue number in PDB)
E940 E959
Binding residue
(residue number reindexed from 1)
E17 E36
Annotation score
1
Enzymatic activity
Enzyme Commision number
2.7.10.2
: non-specific protein-tyrosine kinase.
Gene Ontology
Molecular Function
GO:0004713
protein tyrosine kinase activity
Biological Process
GO:0006468
protein phosphorylation
GO:0007172
signal complex assembly
Cellular Component
GO:0005925
focal adhesion
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Molecular Function
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Cellular Component
External links
PDB
RCSB:7w9u
,
PDBe:7w9u
,
PDBj:7w9u
PDBsum
7w9u
PubMed
UniProt
Q05397
|FAK1_HUMAN Focal adhesion kinase 1 (Gene Name=PTK2)
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