Focal adhesion kinase
From Proteopedia
(Difference between revisions)
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**[[1k04]], [[1k05]], [[3s9o]], [[2l6h]], [[2l6g]], [[2l6f]] – hFAK1 – human<br /> | **[[1k04]], [[1k05]], [[3s9o]], [[2l6h]], [[2l6g]], [[2l6f]] – hFAK1 – human<br /> | ||
| - | **[[1k40]] – | + | **[[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 /> | ||
Revision as of 10:00, 18 May 2017
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3D Structures of focal adhesion kinase
Updated on 18-May-2017
References
- ↑ 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
- ↑ 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
- ↑ 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
