5JSI
Structure of membrane protein
5JSI の概要
エントリーDOI | 10.2210/pdb5jsi/pdb |
分子名称 | Bacteriorhodopsin, EICOSANE, IODIDE ION, ... (6 entities in total) |
機能のキーワード | membrane protein, iodide, unknown function, transferase |
由来する生物種 | Candidatus Actinomarina minuta 詳細 |
タンパク質・核酸の鎖数 | 2 |
化学式量合計 | 58487.49 |
構造登録者 | Melnikov, I.,Polovinkin, V.,Kovalev, K.,Shevchenko, V.,Gushchin, I.,Popov, A.,Gordeliy, V. (登録日: 2016-05-08, 公開日: 2017-05-31, 最終更新日: 2025-04-09) |
主引用文献 | Melnikov, I.,Polovinkin, V.,Kovalev, K.,Gushchin, I.,Shevtsov, M.,Shevchenko, V.,Mishin, A.,Alekseev, A.,Rodriguez-Valera, F.,Borshchevskiy, V.,Cherezov, V.,Leonard, G.A.,Gordeliy, V.,Popov, A. Fast iodide-SAD phasing for high-throughput membrane protein structure determination. Sci Adv, 3:e1602952-e1602952, 2017 Cited by PubMed Abstract: We describe a fast, easy, and potentially universal method for the de novo solution of the crystal structures of membrane proteins via iodide-single-wavelength anomalous diffraction (I-SAD). The potential universality of the method is based on a common feature of membrane proteins-the availability at the hydrophobic-hydrophilic interface of positively charged amino acid residues with which iodide strongly interacts. We demonstrate the solution using I-SAD of four crystal structures representing different classes of membrane proteins, including a human G protein-coupled receptor (GPCR), and we show that I-SAD can be applied using data collection strategies based on either standard or serial x-ray crystallography techniques. PubMed: 28508075DOI: 10.1126/sciadv.1602952 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2 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
