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Atomistry » Fluorine » PDB 4csj-4dbq » 4d4v | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Atomistry » Fluorine » PDB 4csj-4dbq » 4d4v » |
Fluorine in PDB 4d4v: Focal Adhesion Kinase Catalytic DomainEnzymatic activity of Focal Adhesion Kinase Catalytic Domain
All present enzymatic activity of Focal Adhesion Kinase Catalytic Domain:
2.7.10.2; Protein crystallography data
The structure of Focal Adhesion Kinase Catalytic Domain, PDB code: 4d4v
was solved by
J.Le Coq,
A.Lin,
D.Lietha,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Fluorine Binding Sites:
The binding sites of Fluorine atom in the Focal Adhesion Kinase Catalytic Domain
(pdb code 4d4v). This binding sites where shown within
5.0 Angstroms radius around Fluorine atom.
In total 3 binding sites of Fluorine where determined in the Focal Adhesion Kinase Catalytic Domain, PDB code: 4d4v: Jump to Fluorine binding site number: 1; 2; 3; Fluorine binding site 1 out of 3 in 4d4vGo back to Fluorine Binding Sites List in 4d4v
Fluorine binding site 1 out
of 3 in the Focal Adhesion Kinase Catalytic Domain
Mono view Stereo pair view
Fluorine binding site 2 out of 3 in 4d4vGo back to Fluorine Binding Sites List in 4d4v
Fluorine binding site 2 out
of 3 in the Focal Adhesion Kinase Catalytic Domain
Mono view Stereo pair view
Fluorine binding site 3 out of 3 in 4d4vGo back to Fluorine Binding Sites List in 4d4v
Fluorine binding site 3 out
of 3 in the Focal Adhesion Kinase Catalytic Domain
Mono view Stereo pair view
Reference:
J.Zhou,
A.Bronowska,
J.Le Coq,
D.Lietha,
F.Grater.
Allosteric Regulation of Focal Adhesion Kinase By PIP2 and Atp. Biophys.J. V. 108 698 2015.
Page generated: Thu Aug 1 00:51:28 2024
ISSN: ISSN 0006-3495 PubMed: 25650936 DOI: 10.1016/J.BPJ.2014.11.3454 |
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