3Q6W
Structure of dually-phosphorylated MET receptor kinase in complex with an MK-2461 analog with specificity for the activated receptor
Summary for 3Q6W
Entry DOI | 10.2210/pdb3q6w/pdb |
Related | 3Q6U |
Descriptor | Hepatocyte growth factor receptor, 3-{5-oxo-3-[1-(piperidin-4-yl)-1H-pyrazol-4-yl]-5H-benzo[4,5]cyclohepta[1,2-b]pyridin-7-yl}-N-(pyridin-2-ylmethyl)propanamide (3 entities in total) |
Functional Keywords | tyrosine kinase, two phosphotyrosine resiudes, transferase-transferase inhibitor complex, transferase/transferase inhibitor |
Biological source | Homo sapiens (human) |
Cellular location | Membrane; Single-pass type I membrane protein. Isoform 3: Secreted: P08581 |
Total number of polymer chains | 1 |
Total formula weight | 35631.98 |
Authors | Soisson, S.M.,Rickert, K.W.,Patel, S.B.,Lumb, K.J. (deposition date: 2011-01-03, release date: 2011-01-19, Last modification date: 2017-11-08) |
Primary citation | Rickert, K.W.,Patel, S.B.,Allison, T.J.,Byrne, N.J.,Darke, P.L.,Ford, R.E.,Guerin, D.J.,Hall, D.L.,Kornienko, M.,Lu, J.,Munshi, S.K.,Reid, J.C.,Shipman, J.M.,Stanton, E.F.,Wilson, K.J.,Young, J.R.,Soisson, S.M.,Lumb, K.J. Structural basis for selective small molecule kinase inhibition of activated c-Met. J.Biol.Chem., 286:11218-11225, 2011 Cited by PubMed: 21247903DOI: 10.1074/jbc.M110.204404 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.75 Å) |
Structure validation
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