7RMR

Crystal structure of [I11L]cycloviolacin O2

7RMR の概要

• エントリーDOI: 10.2210/pdb7rmr/pdb
• 関連するPDBエントリー: 7RMQ
• 分子名称: [I11L]cycloviolacin O2, D-[I11L]cycloviolacin O2, THIOCYANATE ION, ... (4 entities in total)
• 機能のキーワード: cyclic peptides, cyclotides, quasi-racemic, plant protein
• 由来する生物種: Viola odorata (Sweet violet); 詳細
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 6449.69

構造登録者

Huang, Y.H.,Du, Q.,Craik, D.J. (登録日: 2021-07-28, 公開日: 2021-09-22, 最終更新日: 2024-11-20)

主引用文献

Huang, Y.H.,Du, Q.,Jiang, Z.,King, G.J.,Collins, B.M.,Wang, C.K.,Craik, D.J.
Enabling Efficient Folding and High-Resolution Crystallographic Analysis of Bracelet Cyclotides.
Molecules, 26:-, 2021

PubMed Abstract: Cyclotides have attracted great interest as drug design scaffolds because of their unique cyclic cystine knotted topology. They are classified into three subfamilies, among which the bracelet subfamily represents the majority and comprises the most bioactive cyclotides, but are the most poorly utilized in drug design applications. A long-standing challenge has been the very low in vitro folding yields of bracelets, hampering efforts to characterize their structures and activities. Herein, we report substantial increases in bracelet folding yields enabled by a single point mutation of residue Ile-11 to Leu or Gly. We applied this discovery to synthesize mirror image enantiomers and used quasi-racemic crystallography to elucidate the first crystal structures of bracelet cyclotides. This study provides a facile strategy to produce bracelet cyclotides, leading to a general method to easily access their atomic resolution structures and providing a basis for development of biotechnological applications.

PubMed: 34577034
DOI: 10.3390/molecules26185554

実験手法

X-RAY DIFFRACTION (1.04 Å)