Loading
PDBj
メニューPDBj@FacebookPDBj@TwitterPDBj@YouTubewwPDB FoundationwwPDB
RCSB PDBPDBeBMRBAdv. SearchSearch help

1DQ0

Locked, metal-free concanavalin A, a minor species in solution

1DQ0 の概要
エントリーDOI10.2210/pdb1dq0/pdb
関連するPDBエントリー1DQ1 1DQ2 1DQ4 1DQ5 1DQ6 1ENR
分子名称Concanavalin-Br (2 entities in total)
機能のキーワードminor structural species, solution, locked state, demetallized concanavalin a, beta-sheet, sugar binding protein
由来する生物種Canavalia ensiformis (jack bean)
タンパク質・核酸の鎖数1
化学式量合計25622.38
構造登録者
Bouckaert, J.,Dewallef, Y.,Poortmans, F.,Wyns, L.,Loris, R. (登録日: 1999-12-29, 公開日: 2000-01-19, 最終更新日: 2023-08-09)
主引用文献Bouckaert, J.,Dewallef, Y.,Poortmans, F.,Wyns, L.,Loris, R.
The structural features of concanavalin A governing non-proline peptide isomerization
J.Biol.Chem., 275:19778-19787, 2000
Cited by
PubMed Abstract: The reversible binding of manganese and calcium to concanavalin A determines the carbohydrate binding of the lectin by inducing large conformational changes. These changes are governed by the isomerization of a non-proline peptide bond, Ala-207-Asp-208, positioned in a beta-strand in between the calcium binding site S2 and the carbohydrate specificity-determining loop. The replacement of calcium by manganese allowed us to investigate the structures of the carbohydrate binding, locked state and the inactive, unlocked state of concanavalin A, both with and without metal ions bound. Crystals of unlocked metal-free concanavalin A convert to the locked form with the binding of two Mn(2+) ions. Removal of these ions from the crystals traps metal-free concanavalin A in its locked state, a minority species in solution. The ligation of a metal ion in S2 to unlocked concanavalin A causes bending of the beta-strand foregoing the S2 ligand residues Asp-10 and Tyr-12. This bending disrupts conventional beta-sheet hydrogen bonding and forces the Thr-11 side chain against the Ala-207-Asp-208 peptide bond. The steric strain exerted by Thr-11 is presumed to drive the trans-to-cis isomerization. Upon isomerization, Asp-208 flips into its carbohydrate binding position, and the conformation of the carbohydrate specificity determining loop changes dramatically.
PubMed: 10748006
DOI: 10.1074/jbc.M001251200
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.7 Å)
構造検証レポート
Validation report summary of 1dq0
検証レポート(詳細版)ダウンロードをダウンロード

226707

件を2024-10-30に公開中

PDB statisticsPDBj update infoContact PDBjnumon