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4P2L

Quiescin Sulfhydryl Oxidase from Rattus norvegicus

4P2L の概要
エントリーDOI10.2210/pdb4p2l/pdb
関連するPDBエントリー3LLK 3Q6O 3QCP 3T58
分子名称Sulfhydryl oxidase 1, FLAVIN-ADENINE DINUCLEOTIDE (3 entities in total)
機能のキーワードdisulfide formation, enzyme intermediate, thioredoxin fold, erv fold, oxidoreductase
由来する生物種Rattus norvegicus (Rat)
タンパク質・核酸の鎖数2
化学式量合計115176.42
構造登録者
Gat, Y.,Fass, D. (登録日: 2014-03-04, 公開日: 2014-06-25, 最終更新日: 2024-11-13)
主引用文献Gat, Y.,Vardi-Kilshtain, A.,Grossman, I.,Major, D.T.,Fass, D.
Enzyme structure captures four cysteines aligned for disulfide relay.
Protein Sci., 23:1102-1112, 2014
Cited by
PubMed Abstract: Thioredoxin superfamily proteins introduce disulfide bonds into substrates, catalyze the removal of disulfides, and operate in electron relays. These functions rely on one or more dithiol/disulfide exchange reactions. The flavoenzyme quiescin sulfhydryl oxidase (QSOX), a catalyst of disulfide bond formation with an interdomain electron transfer step in its catalytic cycle, provides a unique opportunity for exploring the structural environment of enzymatic dithiol/disulfide exchange. Wild-type Rattus norvegicus QSOX1 (RnQSOX1) was crystallized in a conformation that juxtaposes the two redox-active di-cysteine motifs in the enzyme, presenting the entire electron-transfer pathway and proton-transfer participants in their native configurations. As such a state cannot generally be enriched and stabilized for analysis, RnQSOX1 gives unprecedented insight into the functional group environments of the four cysteines involved in dithiol/disulfide exchange and provides the framework for analysis of the energetics of electron transfer in the presence of the bound flavin adenine dinucleotide cofactor. Hybrid quantum mechanics/molecular mechanics (QM/MM) free energy simulations based on the X-ray crystal structure suggest that formation of the interdomain disulfide intermediate is highly favorable and secures the flexible enzyme in a state from which further electron transfer via the flavin can occur.
PubMed: 24888638
DOI: 10.1002/pro.2496
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.9 Å)
構造検証レポート
Validation report summary of 4p2l
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2026-04-15に公開中

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