7UA3
Structure of PKA phosphorylated human RyR2-R2474S in the closed state in the presence of Calmodulin
これはPDB形式変換不可エントリーです。
7UA3 の概要
エントリーDOI | 10.2210/pdb7ua3/pdb |
EMDBエントリー | 26413 |
分子名称 | Ryanodine receptor 2, Peptidyl-prolyl cis-trans isomerase FKBP1B, Calmodulin-1, ... (5 entities in total) |
機能のキーワード | calcium channel, membrane protein |
由来する生物種 | Homo sapiens (human) 詳細 |
タンパク質・核酸の鎖数 | 12 |
化学式量合計 | 2379787.27 |
構造登録者 | |
主引用文献 | Miotto, M.C.,Weninger, G.,Dridi, H.,Yuan, Q.,Liu, Y.,Wronska, A.,Melville, Z.,Sittenfeld, L.,Reiken, S.,Marks, A.R. Structural analyses of human ryanodine receptor type 2 channels reveal the mechanisms for sudden cardiac death and treatment. Sci Adv, 8:eabo1272-eabo1272, 2022 Cited by PubMed Abstract: Ryanodine receptor type 2 (RyR2) mutations have been linked to an inherited form of exercise-induced sudden cardiac death called catecholaminergic polymorphic ventricular tachycardia (CPVT). CPVT results from stress-induced sarcoplasmic reticular Ca leak via the mutant RyR2 channels during diastole. We present atomic models of human wild-type (WT) RyR2 and the CPVT mutant RyR2-R2474S determined by cryo-electron microscopy with overall resolutions in the range of 2.6 to 3.6 Å, and reaching local resolutions of 2.25 Å, unprecedented for RyR2 channels. Under nonactivating conditions, the RyR2-R2474S channel is in a "primed" state between the closed and open states of WT RyR2, rendering it more sensitive to activation that results in stress-induced Ca leak. The Rycal drug ARM210 binds to RyR2-R2474S, reverting the primed state toward the closed state. Together, these studies provide a mechanism for CPVT and for the therapeutic actions of ARM210. PubMed: 35857850DOI: 10.1126/sciadv.abo1272 主引用文献が同じPDBエントリー |
実験手法 | ELECTRON MICROSCOPY (2.97 Å) |
構造検証レポート
検証レポート(詳細版)をダウンロード