4P9L
Crystal Structure of mouse Ryanodine Receptor 2 SPRY2 Domain (1080-1253) disease mutant A1107M
4P9L の概要
エントリーDOI | 10.2210/pdb4p9l/pdb |
関連するPDBエントリー | 4PNI |
分子名称 | Ryanodine receptor 2 (2 entities in total) |
機能のキーワード | ion channel, calcium, signalling, metal transport, transport protein |
由来する生物種 | Mus musculus (Mouse) |
タンパク質・核酸の鎖数 | 1 |
化学式量合計 | 19954.37 |
構造登録者 | |
主引用文献 | Lau, K.,Van Petegem, F. Crystal structures of wild type and disease mutant forms of the ryanodine receptor SPRY2 domain. Nat Commun, 5:5397-5397, 2014 Cited by PubMed Abstract: Ryanodine receptors (RyRs) form channels responsible for the release of Ca(2+) from the endoplasmic and sarcoplasmic reticulum. The SPRY2 domain in the skeletal muscle isoform (RyR1) has been proposed as a direct link with L-type calcium channels (CaV1.1), allowing for direct mechanical coupling between plasma membrane depolarization and Ca(2+) release. Here we present the crystal structures of the SPRY2 domain from RyR1 and RyR2 at 1.34-1.84 Å resolution. They form two antiparallel β sheets establishing a core, and four additional modules of which several are required for proper folding. A buried disease mutation, linked to hypertrophic cardiomyopathy and loss-of-function, induces local misfolding and strong destabilization. Isothermal titration calorimetry experiments negate the RyR1 SPRY2 domain as the major link with CaV1.1. Instead, docking into full-length RyR1 cryo-electron microscopy maps suggests that the SPRY2 domain forms a link between the N-terminal gating ring and the clamp region. PubMed: 25370123DOI: 10.1038/ncomms6397 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.4361 Å) |
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