8TLR
Crystal Structure of human HRAS G12C covalently bound to AMG 510
8TLR の概要
| エントリーDOI | 10.2210/pdb8tlr/pdb |
| 分子名称 | GTPase HRas, GUANOSINE-5'-DIPHOSPHATE, AMG 510 (bound form), ... (5 entities in total) |
| 機能のキーワード | hras, h-ras, sotorasib, ras, oncoprotein |
| 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 | 19951.40 |
| 構造登録者 | |
| 主引用文献 | Morstein, J.,Bowcut, V.,Fernando, M.,Yang, Y.,Zhu, L.,Jenkins, M.L.,Evans, J.T.,Guiley, K.Z.,Peacock, D.M.,Krahnke, S.,Lin, Z.,Taran, K.A.,Huang, B.J.,Stephen, A.G.,Burke, J.E.,Lightstone, F.C.,Shokat, K.M. Targeting Ras-, Rho-, and Rab-family GTPases via a conserved cryptic pocket. Cell, 187:6379-, 2024 Cited by PubMed Abstract: The family of Ras-like GTPases consists of over 150 different members, regulated by an even larger number of guanine exchange factors (GEFs) and GTPase-activating proteins (GAPs) that comprise cellular switch networks that govern cell motility, growth, polarity, protein trafficking, and gene expression. Efforts to develop selective small molecule probes and drugs for these proteins have been hampered by the high affinity of guanosine triphosphate (GTP) and lack of allosteric regulatory sites. This paradigm was recently challenged by the discovery of a cryptic allosteric pocket in the switch II region of K-Ras. Here, we ask whether similar pockets are present in GTPases beyond K-Ras. We systematically surveyed members of the Ras, Rho, and Rab family of GTPases and found that many GTPases exhibit targetable switch II pockets. Notable differences in the composition and conservation of key residues offer potential for the development of optimized inhibitors for many members of this previously undruggable family. PubMed: 39255801DOI: 10.1016/j.cell.2024.08.017 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.70003947485 Å) |
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