6YQ1
FOCAL ADHESION KINASE CATALYTIC DOMAIN IN COMPLEX WITH N-Methyl-N-(3-{[2-(2-oxo-1,2,3,4-tetrahydro-quinolin-6-ylamino)-5-trifluoromethyl-pyrimidin-4-ylamino]-methyl}-pyridin-2-yl)-methanesulfonamide
Summary for 6YQ1
Entry DOI | 10.2210/pdb6yq1/pdb |
Descriptor | Focal adhesion kinase 1, ~{N}-methyl-~{N}-[3-[[[2-[(2-oxidanylidene-3,4-dihydro-1~{H}-quinolin-6-yl)amino]-5-(trifluoromethyl)pyrimidin-4-yl]amino]methyl]pyridin-2-yl]methanesulfonamide, SODIUM ION, ... (5 entities in total) |
Functional Keywords | protein tyrosine kinase, atp binding, transferase, transferase-inhibitor complex |
Biological source | Homo sapiens (Human) |
Total number of polymer chains | 4 |
Total formula weight | 131422.00 |
Authors | Musil, D.,Heinrich, T.,Amaral, M. (deposition date: 2020-04-16, release date: 2021-02-10, Last modification date: 2024-01-24) |
Primary citation | Berger, B.T.,Amaral, M.,Kokh, D.B.,Nunes-Alves, A.,Musil, D.,Heinrich, T.,Schroder, M.,Neil, R.,Wang, J.,Navratilova, I.,Bomke, J.,Elkins, J.M.,Muller, S.,Frech, M.,Wade, R.C.,Knapp, S. Structure-kinetic relationship reveals the mechanism of selectivity of FAK inhibitors over PYK2. Cell Chem Biol, 28:686-, 2021 Cited by PubMed: 33497606DOI: 10.1016/j.chembiol.2021.01.003 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.784 Å) |
Structure validation
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