7MDP
KRas G12C in complex with G-2897
7MDP の概要
| エントリーDOI | 10.2210/pdb7mdp/pdb |
| 分子名称 | Isoform 2B of GTPase KRas, 1,2-ETHANEDIOL, DIMETHYL SULFOXIDE, ... (12 entities in total) |
| 機能のキーワード | kras, gtpase, hydrolase, hydrolase-immune system complex, hydrolase/immune system |
| 由来する生物種 | Homo sapiens (Human) 詳細 |
| タンパク質・核酸の鎖数 | 3 |
| 化学式量合計 | 68897.33 |
| 構造登録者 | |
| 主引用文献 | Davies, C.W.,Oh, A.J.,Mroue, R.,Steffek, M.,Bruning, J.M.,Xiao, Y.,Feng, S.,Jayakar, S.,Chan, E.,Arumugam, V.,Uribe, S.C.,Drummond, J.,Frommlet, A.,Lu, C.,Franke, Y.,Merchant, M.,Koeppen, H.,Quinn, J.G.,Malhotra, S.,Do, S.,Gazzard, L.,Purkey, H.E.,Rudolph, J.,Mulvihill, M.M.,Koerber, J.T.,Wang, W.,Evangelista, M. Conformation-locking antibodies for the discovery and characterization of KRAS inhibitors. Nat.Biotechnol., 40:769-778, 2022 Cited by PubMed Abstract: Small molecules that stabilize inactive protein conformations are an underutilized strategy for drugging dynamic or otherwise intractable proteins. To facilitate the discovery and characterization of such inhibitors, we created a screening platform to identify conformation-locking antibodies for molecular probes (CLAMPs) that distinguish and induce rare protein conformational states. Applying the approach to KRAS, we discovered CLAMPs that recognize the open conformation of KRAS stabilized by covalent inhibitors. One CLAMP enables the visualization of KRAS covalent modification in vivo and can be used to investigate response heterogeneity to KRAS inhibitors in patient tumors. A second CLAMP enhances the affinity of weak ligands binding to the KRAS switch II region (SWII) by stabilizing a specific conformation of KRAS, thereby enabling the discovery of such ligands that could serve as leads for the development of drugs in a high-throughput screen. We show that combining the complementary properties of antibodies and small molecules facilitates the study and drugging of dynamic proteins. PubMed: 34992247DOI: 10.1038/s41587-021-01126-9 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.96 Å) |
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