4YJQ
SYK kinase domain in complex with inhibitor GTC000224
4YJQ の概要
エントリーDOI | 10.2210/pdb4yjq/pdb |
分子名称 | Tyrosine-protein kinase SYK, 3-[1H-indazol-4-yl(2-{[3-(4-methyl-1,3-oxazol-5-yl)phenyl]amino}pyrimidin-4-yl)amino]propan-1-ol (3 entities in total) |
機能のキーワード | syk, non-receptor tyrosine kinase, spleen tyrosine kinase, transferase, phosphorylation, transferase-transferase inhibitor complex |
由来する生物種 | Homo sapiens (Human) |
細胞内の位置 | Cell membrane : P43405 |
タンパク質・核酸の鎖数 | 1 |
化学式量合計 | 33252.09 |
構造登録者 | |
主引用文献 | Liddle, J.,Atkinson, F.L.,Barker, M.D.,Carter, P.S.,Curtis, N.R.,Davis, R.P.,Douault, C.,Dickson, M.C.,Elwes, D.,Garton, N.S.,Gray, M.,Hayhow, T.G.,Hobbs, C.I.,Jones, E.,Leach, S.,Leavens, K.,Lewis, H.D.,McCleary, S.,Neu, M.,Patel, V.K.,Preston, A.G.,Ramirez-Molina, C.,Shipley, T.J.,Skone, P.A.,Smithers, N.,Somers, D.O.,Walker, A.L.,Watson, R.J.,Weingarten, G.G. Discovery of GSK143, a highly potent, selective and orally efficacious spleen tyrosine kinase inhibitor. Bioorg. Med. Chem. Lett., 21:6188-6194, 2011 Cited by PubMed Abstract: The lead optimisation of the diaminopyrimidine carboxamide series of spleen tyrosine kinase inhibitors is described. The medicinal chemistry strategy was focused on optimising the human whole blood activity whilst achieving a sufficient margin over liability kinases and hERG activity. GSK143 is a potent and highly selective SYK inhibitor showing good efficacy in the rat Arthus model. PubMed: 21903390DOI: 10.1016/j.bmcl.2011.07.082 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.34 Å) |
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