3PRI
Crystal Structure of Human B-Raf Kinase in Complex with a Non-Oxime Furopyridine Inhibitor
Summary for 3PRI
Entry DOI | 10.2210/pdb3pri/pdb |
Related | 3PPJ 3PPK 3PRF |
Descriptor | Serine/threonine-protein kinase B-raf, 3-(4-{[2-(pyrimidin-2-yl)furo[2,3-c]pyridin-3-yl]amino}-1H-indazol-3-yl)propan-1-ol (2 entities in total) |
Functional Keywords | protein kinase, atp-competitive inhibitor, transferase-transferase inhibitor complex, transferase/transferase inhibitor |
Biological source | Homo sapiens (human) |
Cellular location | Nucleus (By similarity): P15056 |
Total number of polymer chains | 2 |
Total formula weight | 71208.08 |
Authors | Voegtli, W.C.,Vigers, G.P.A.,Morales, T.,Brandhuber, B.J. (deposition date: 2010-11-29, release date: 2011-02-02, Last modification date: 2024-02-21) |
Primary citation | Ren, L.,Wenglowsky, S.,Miknis, G.,Rast, B.,Buckmelter, A.J.,Ely, R.J.,Schlachter, S.,Laird, E.R.,Randolph, N.,Callejo, M.,Martinson, M.,Galbraith, S.,Brandhuber, B.J.,Vigers, G.,Morales, T.,Voegtli, W.C.,Lyssikatos, J. Non-oxime inhibitors of B-Raf(V600E) kinase. Bioorg.Med.Chem.Lett., 21:1243-1247, 2011 Cited by PubMed: 21251822DOI: 10.1016/j.bmcl.2010.12.061 PDB entries with the same primary citation |
Experimental method |
Structure validation
Download full validation report