4ITJ
Crystal structure of RIP1 kinase in complex with necrostatin-4
4ITJ の概要
エントリーDOI | 10.2210/pdb4itj/pdb |
関連するPDBエントリー | 4ITH 4ITI |
分子名称 | Receptor-interacting serine/threonine-protein kinase 1, N-[(1S)-1-(2-chloro-6-fluorophenyl)ethyl]-5-cyano-1-methyl-1H-pyrrole-2-carboxamide, IODIDE ION, ... (4 entities in total) |
機能のキーワード | alpha/beta, rip1 kinase, necroptosis, necrostatins, kinase, transferase-transferase inhibitor complex, transferase/transferase inhibitor |
由来する生物種 | Homo sapiens (human) |
細胞内の位置 | Cytoplasm: Q13546 |
タンパク質・核酸の鎖数 | 2 |
化学式量合計 | 68691.07 |
構造登録者 | |
主引用文献 | Xie, T.,Peng, W.,Liu, Y.,Yan, C.,Maki, J.,Degterev, A.,Yuan, J.,Shi, Y. Structural Basis of RIP1 Inhibition by Necrostatins. Structure, 21:493-499, 2013 Cited by PubMed Abstract: Necroptosis is a cellular mechanism that mediates necrotic cell death. The receptor-interacting serine/threonine protein kinase 1 (RIP1) is an essential upstream signaling molecule in tumor-necrosis-factor-α-induced necroptosis. Necrostatins, a series of small-molecule inhibitors, suppress necroptosis by specifically inhibiting RIP1 kinase activity. Both RIP1 structure and the mechanisms by which necrostatins inhibit RIP1 remain unknown. Here, we report the crystal structures of the RIP1 kinase domain individually bound to necrostatin-1 analog, necrostatin-3 analog, and necrostatin-4. Necrostatin, caged in a hydrophobic pocket between the N- and C-lobes of the kinase domain, stabilizes RIP1 in an inactive conformation through interactions with highly conserved amino acids in the activation loop and the surrounding structural elements. Structural comparison of RIP1 with the inhibitor-bound oncogenic kinase B-RAF reveals partially overlapping binding sites for necrostatin and for the anticancer compound PLX4032. Our study provides a structural basis for RIP1 inhibition by necrostatins and offers insights into potential structure-based drug design. PubMed: 23473668DOI: 10.1016/j.str.2013.01.016 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.8 Å) |
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