7RXQ

Crystal structure of junctophilin-2 in complex with a CaV1.1 peptide

7RXQ の概要

• エントリーDOI: 10.2210/pdb7rxq/pdb
• 関連するPDBエントリー: 7RW4 7RXE
• 分子名称: Junctophilin-2 N-terminal fragment, Voltage-dependent L-type calcium channel subunit alpha-1S, ETHANOL, ... (5 entities in total)
• 機能のキーワード: complex, membrane, ion channel, structural protein
• 由来する生物種: Homo sapiens (Human); 詳細
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 38340.06

構造登録者

Yang, Z.,Panwar, P.,Van Petegem, F. (登録日: 2021-08-23, 公開日: 2022-02-23, 最終更新日: 2023-10-18)

主引用文献

Yang, Z.F.,Panwar, P.,McFarlane, C.R.,Tuinte, W.E.,Campiglio, M.,Van Petegem, F.
Structures of the junctophilin/voltage-gated calcium channel interface reveal hot spot for cardiomyopathy mutations.
Proc.Natl.Acad.Sci.USA, 119:e2120416119-e2120416119, 2022

PubMed Abstract: SignificanceIon channels have evolved the ability to communicate with one another, either through protein-protein interactions, or indirectly via intermediate diffusible messenger molecules. In special cases, the channels are part of different membranes. In muscle tissue, the T-tubule membrane is in proximity to the sarcoplasmic reticulum, allowing communication between L-type calcium channels and ryanodine receptors. This process is critical for excitation-contraction coupling and requires auxiliary proteins like junctophilin (JPH). JPHs are targets for disease-associated mutations, most notably hypertrophic cardiomyopathy mutations in the JPH2 isoform. Here we provide high-resolution snapshots of JPH, both alone and in complex with a calcium channel peptide, and show how this interaction is targeted by cardiomyopathy mutations.

PubMed: 35238659
DOI: 10.1073/pnas.2120416119

実験手法

X-RAY DIFFRACTION (2.03 Å)