Focal adhesion kinase

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FAK ATP-binding site is the <scene name='48/480805/Cv/5'>location of inhibitor binding</scene><ref>PMID:19030106</ref>.
FAK ATP-binding site is the <scene name='48/480805/Cv/5'>location of inhibitor binding</scene><ref>PMID:19030106</ref>.
 +
== 3D Structures of focal adhesion kinase ==
 +
[[Focal adhesion kinase 3D structures]]
</StructureSection>
</StructureSection>
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**[[1k04]], [[1k05]], [[3s9o]], [[2l6h]], [[2l6g]], [[2l6f]] – hFAK1 – human<br />
**[[1k04]], [[1k05]], [[3s9o]], [[2l6h]], [[2l6g]], [[2l6f]] – hFAK1 – human<br />
-
**[[1k40]] – mFAK1 – mouse<br />
 
-
**[[5f28]] – mFAK1 + MEF2C<br />
 
**[[1ow6]], [[1ow7]] - hFAK1 + paxillin LD4 motif<br />
**[[1ow6]], [[1ow7]] - hFAK1 + paxillin LD4 motif<br />
**[[1ow8]] - hFAK1 + paxillin LD2 motif<br />
**[[1ow8]] - hFAK1 + paxillin LD2 motif<br />
**[[3b71]] - hFAK1 + ADP + ATP<BR />
**[[3b71]] - hFAK1 + ADP + ATP<BR />
 +
**[[1k40]] – mFAK1 – mouse<br />
 +
**[[5f28]] – mFAK1 + MEF2C<br />
**[[1ktm]], [[1qvx]], [[1pv3]] - cFAK1 – chicken – NMR
**[[1ktm]], [[1qvx]], [[1pv3]] - cFAK1 – chicken – NMR
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**[[1mp8]] - hFAK1 <br />
**[[1mp8]] - hFAK1 <br />
-
**[[2etm]], [[3bz3]], [[4gu9]], [[4kab]], [[4k9y]], [[4i4e]], [[4i4f]], [[4k8a]], [[4gu6]], [[4brx]], [[4ebv]], [[4ebw]], [[3pxk]], [[4q9s]] - hFAK1 + inhibitor<br />
+
**[[2etm]], [[3bz3]], [[4gu9]], [[4kab]], [[4k9y]], [[4i4e]], [[4i4f]], [[4k8a]], [[4gu6]], [[4brx]], [[4ebv]], [[4ebw]], [[3pxk]], [[4q9s]], [[6i8z]] - hFAK1 + inhibitor<br />
**[[4kao]] - hFAK1 (mutant) + pyrazole derivative<br />
**[[4kao]] - hFAK1 (mutant) + pyrazole derivative<br />
**[[2ijm]] - hFAK1 + ADP + ATP<BR />
**[[2ijm]] - hFAK1 + ADP + ATP<BR />
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**[[2j0l]] - cFAK1 phosphorylated<br />
**[[2j0l]] - cFAK1 phosphorylated<br />
**[[2jkk]], [[2jkm]], [[2jko]], [[2jkq]], [[4d58]] - cFAK1 + pyrimidine derivative<br />
**[[2jkk]], [[2jkm]], [[2jko]], [[2jkq]], [[4d58]] - cFAK1 + pyrimidine derivative<br />
-
**[[4c7t]] - cFAK1 + inhibitor<br />
+
**[[4c7t]], [[6gcr]], [[6gcw]], [[6gcx]] - cFAK1 + inhibitor<br />
*''FAK1 FERM domain''
*''FAK1 FERM domain''
-
**[[2j0j]], [[2j0k]], [[2j0m]] - cFAK1 kinase + FERM domains<br />
 
-
**[[2aeh]], [[2al6]] - cFAK1<br />
 
-
**[[3zdt]] - cFAK1 (mutant)<br />
 
**[[4cye]] - hFAK1<br />
**[[4cye]] - hFAK1<br />
**[[4ny0]] - hFAK1 (mutant)<br />
**[[4ny0]] - hFAK1 (mutant)<br />
 +
**[[2j0j]], [[2j0k]], [[2j0m]] - cFAK1 kinase + FERM domains<br />
 +
**[[2aeh]], [[2al6]], [[6cb0]] - cFAK1<br />
 +
**[[3zdt]] - cFAK1 (mutant)<br />
*''FAK1 FAT domain''
*''FAK1 FAT domain''

Revision as of 08:41, 3 July 2019

Focal adhesion kinase 1 kinase domain complex with pyrimidine derivative inhibitor and sulfate (PDB code 2jkk)

Drag the structure with the mouse to rotate

3D Structures of focal adhesion kinase

Updated on 03-July-2019

References

  1. Mitra SK, Hanson DA, Schlaepfer DD. Focal adhesion kinase: in command and control of cell motility. Nat Rev Mol Cell Biol. 2005 Jan;6(1):56-68. PMID:15688067 doi:http://dx.doi.org/10.1038/nrm1549
  2. Cabrita MA, Jones LM, Quizi JL, Sabourin LA, McKay BC, Addison CL. Focal adhesion kinase inhibitors are potent anti-angiogenic agents. Mol Oncol. 2011 Dec;5(6):517-26. doi: 10.1016/j.molonc.2011.10.004. Epub 2011 Oct, 20. PMID:22075057 doi:http://dx.doi.org/10.1016/j.molonc.2011.10.004
  3. Lietha D, Eck MJ. Crystal structures of the FAK kinase in complex with TAE226 and related bis-anilino pyrimidine inhibitors reveal a helical DFG conformation. PLoS ONE. 2008;3(11):e3800. Epub 2008 Nov 24. PMID:19030106 doi:10.1371/journal.pone.0003800

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Michal Harel, Alexander Berchansky

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