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7JJO

Structural Basis of the Activation of Heterotrimeric Gs-protein by Isoproterenol-bound Beta1-Adrenergic Receptor

7JJO の概要
エントリーDOI10.2210/pdb7jjo/pdb
EMDBエントリー22357
分子名称Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1, Nanobody 35, Guanine nucleotide-binding protein G(s) subunit alpha isoforms short, ... (6 entities in total)
機能のキーワードgs protein, gpcr-gs complex, agonist, signaling protein
由来する生物種Bos taurus (Bovine)
詳細
タンパク質・核酸の鎖数5
化学式量合計163136.03
構造登録者
主引用文献Su, M.,Zhu, L.,Zhang, Y.,Paknejad, N.,Dey, R.,Huang, J.,Lee, M.Y.,Williams, D.,Jordan, K.D.,Eng, E.T.,Ernst, O.P.,Meyerson, J.R.,Hite, R.K.,Walz, T.,Liu, W.,Huang, X.Y.
Structural Basis of the Activation of Heterotrimeric Gs-Protein by Isoproterenol-Bound beta 1 -Adrenergic Receptor.
Mol.Cell, 80:59-, 2020
Cited by
PubMed Abstract: Cardiac disease remains the leading cause of morbidity and mortality worldwide. The β-adrenergic receptor (β-AR) is a major regulator of cardiac functions and is downregulated in the majority of heart failure cases. A key physiological process is the activation of heterotrimeric G-protein Gs by β-ARs, leading to increased heart rate and contractility. Here, we use cryo-electron microscopy and functional studies to investigate the molecular mechanism by which β-AR activates Gs. We find that the tilting of α5-helix breaks a hydrogen bond between the sidechain of His373 in the C-terminal α5-helix and the backbone carbonyl of Arg38 in the N-terminal αN-helix of Gα. Together with the disruption of another interacting network involving Gln59 in the α1-helix, Ala352 in the β6-α5 loop, and Thr355 in the α5-helix, these conformational changes might lead to the deformation of the GDP-binding pocket. Our data provide molecular insights into the activation of G-proteins by G-protein-coupled receptors.
PubMed: 32818430
DOI: 10.1016/j.molcel.2020.08.001
主引用文献が同じPDBエントリー
実験手法
ELECTRON MICROSCOPY (2.6 Å)
構造検証レポート
Validation report summary of 7jjo
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2026-02-04に公開中

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