5CSX
CRYSTAL STRUCTURE OF B-RAF IN COMPLEX WITH BI 882370
5CSX の概要
エントリーDOI | 10.2210/pdb5csx/pdb |
分子名称 | Serine/threonine-protein kinase B-raf, N-(3-{5-[(1-ethylpiperidin-4-yl)(methyl)amino]-3-(pyrimidin-5-yl)-1H-pyrrolo[3,2-b]pyridin-1-yl}-2,4-difluorophenyl)propane-1-sulfonamide, alpha-D-glucopyranose, ... (4 entities in total) |
機能のキーワード | kinase, transferase |
由来する生物種 | Homo sapiens (Human) |
タンパク質・核酸の鎖数 | 1 |
化学式量合計 | 32779.52 |
構造登録者 | |
主引用文献 | Waizenegger, I.C.,Baum, A.,Steurer, S.,Stadtmuller, H.,Bader, G.,Schaaf, O.,Garin-Chesa, P.,Schlattl, A.,Schweifer, N.,Haslinger, C.,Colbatzky, F.,Mousa, S.,Kalkuhl, A.,Kraut, N.,Adolf, G.R. A Novel RAF Kinase Inhibitor with DFG-Out-Binding Mode: High Efficacy in BRAF-Mutant Tumor Xenograft Models in the Absence of Normal Tissue Hyperproliferation. Mol.Cancer Ther., 15:354-365, 2016 Cited by PubMed: 26916115DOI: 10.1158/1535-7163.MCT-15-0617 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.51 Å) |
構造検証レポート
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