5C9C
CRYSTAL STRUCTURE OF BRAF(V600E) IN COMPLEX WITH LY3009120 COMPND
5C9C の概要
エントリーDOI | 10.2210/pdb5c9c/pdb |
分子名称 | Serine/threonine-protein kinase B-raf, 1-(3,3-dimethylbutyl)-3-{2-fluoro-4-methyl-5-[7-methyl-2-(methylamino)pyrido[2,3-d]pyrimidin-6-yl]phenyl}urea, CHLORIDE ION, ... (4 entities in total) |
機能のキーワード | transferase-transferase inhibitor complex, transferase/transferase inhibitor |
由来する生物種 | Homo sapiens (Human) |
細胞内の位置 | Nucleus : P15056 |
タンパク質・核酸の鎖数 | 2 |
化学式量合計 | 71379.71 |
構造登録者 | |
主引用文献 | Peng, S.B.,Henry, J.R.,Kaufman, M.D.,Lu, W.P.,Smith, B.D.,Vogeti, S.,Rutkoski, T.J.,Wise, S.,Chun, L.,Zhang, Y.,Van Horn, R.D.,Yin, T.,Zhang, X.,Yadav, V.,Chen, S.H.,Gong, X.,Ma, X.,Webster, Y.,Buchanan, S.,Mochalkin, I.,Huber, L.,Kays, L.,Donoho, G.P.,Walgren, J.,McCann, D.,Patel, P.,Conti, I.,Plowman, G.D.,Starling, J.J.,Flynn, D.L. Inhibition of RAF Isoforms and Active Dimers by LY3009120 Leads to Anti-tumor Activities in RAS or BRAF Mutant Cancers. Cancer Cell, 28:384-398, 2015 Cited by PubMed Abstract: LY3009120 is a pan-RAF and RAF dimer inhibitor that inhibits all RAF isoforms and occupies both protomers in RAF dimers. Biochemical and cellular analyses revealed that LY3009120 inhibits ARAF, BRAF, and CRAF isoforms with similar affinity, while vemurafenib or dabrafenib have little or modest CRAF activity compared to their BRAF activities. LY3009120 induces BRAF-CRAF dimerization but inhibits the phosphorylation of downstream MEK and ERK, suggesting that it effectively inhibits the kinase activity of BRAF-CRAF heterodimers. Further analyses demonstrated that LY3009120 also inhibits various forms of RAF dimers including BRAF or CRAF homodimers. Due to these unique properties, LY3009120 demonstrates minimal paradoxical activation, inhibits MEK1/2 phosphorylation, and exhibits anti-tumor activities across multiple models carrying KRAS, NRAS, or BRAF mutation. PubMed: 26343583DOI: 10.1016/j.ccell.2015.08.002 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.7 Å) |
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