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2F2J

Solution structure of [W19K, P20N, V21K]-kalata B1

2F2J の概要
エントリーDOI10.2210/pdb2f2j/pdb
関連するPDBエントリー2F2I
分子名称Kalata-B1 (1 entity in total)
機能のキーワードcystine knot, circular backbone, beta-hairpin, antimicrobial protein
タンパク質・核酸の鎖数1
化学式量合計2907.35
構造登録者
Clark, R.J.,Daly, N.L.,Craik, D.J. (登録日: 2005-11-17, 公開日: 2006-01-31, 最終更新日: 2024-10-23)
主引用文献Clark, R.J.,Daly, N.L.,Craik, D.J.
Structural plasticity of the cyclic cystine knot framework: implications for biological activity and drug design
Biochem.J., 394:85-93, 2006
Cited by
PubMed Abstract: The cyclotide family of plant proteins is of interest because of their unique topology, which combines a head-to-tail cyclic backbone with an embedded cystine knot, and because their remarkable chemical and biological properties make them ideal candidates as grafting templates for biologically active peptide epitopes. The present study describes the first steps towards exploiting the cyclotide framework by synthesizing and structurally characterizing two grafted analogues of the cyclotide kalata B1. The modified peptides have polar or charged residues substituted for residues that form part of a surface-exposed hydrophobic patch that plays a significant role in the folding and biological activity of kalata B1. Both analogues retain the native cyclotide fold, but lack the undesired haemolytic activity of their parent molecule, kalata B1. This finding confirms the tolerance of the cyclotide framework to residue substitutions and opens up possibilities for the substitution of biologically active peptide epitopes into the framework.
PubMed: 16300479
DOI: 10.1042/BJ20051691
主引用文献が同じPDBエントリー
実験手法
SOLUTION NMR
構造検証レポート
Validation report summary of 2f2j
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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