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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DOI10.2210/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
Miotto, M.C.,Marks, A.R. (登録日: 2022-03-11, 公開日: 2022-08-03, 最終更新日: 2024-11-06)
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: 35857850
DOI: 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
Validation report summary of 7ua3
検証レポート(詳細版)ダウンロードをダウンロード

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件を2024-11-06に公開中

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