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5NQ6

Crystal structure of the inhibited form of the redox-sensitive SufE-like sulfur acceptor CsdE from Escherichia coli at 2.40 Angstrom Resolution

5NQ6 の概要
エントリーDOI10.2210/pdb5nq6/pdb
関連するPDBエントリー5FT4 5FT5 5FT6 5FT8
分子名称Sulfur acceptor protein CsdE, GLYCEROL, SULFATE ION, ... (4 entities in total)
機能のキーワードsulfur-binding protein, sulfur-acceptor protein, l-cysteine desulfurase, transpersulfuration, sulfur trafficking
由来する生物種Escherichia coli
タンパク質・核酸の鎖数2
化学式量合計34385.08
構造登録者
Penya-Soler, E.,Aranda, J.,Lopez-Estepa, M.,Gomez, S.,Garces, F.,Coll, M.,Fernandez, F.J.,Vega, M.C. (登録日: 2017-04-19, 公開日: 2018-03-28, 最終更新日: 2024-10-09)
主引用文献Pena-Soler, E.,Aranda, J.,Lopez-Estepa, M.,Gomez, S.,Garces, F.,Coll, M.,Fernandez, F.J.,Tunon, I.,Vega, M.C.
Insights into the inhibited form of the redox-sensitive SufE-like sulfur acceptor CsdE.
PLoS ONE, 12:e0186286-e0186286, 2017
Cited by
PubMed Abstract: Sulfur trafficking in living organisms relies on transpersulfuration reactions consisting in the enzyme-catalyzed transfer of S atoms via activated persulfidic S across protein-protein interfaces. The recent elucidation of the mechanistic basis for transpersulfuration in the CsdA-CsdE model system has paved the way for a better understanding of its role under oxidative stress. Herein we present the crystal structure of the oxidized, inactivated CsdE dimer at 2.4 Å resolution. The structure sheds light into the activation of the Cys61 nucleophile on its way from a solvent-secluded position in free CsdE to a fully extended conformation in the persulfurated CsdA-CsdE complex. Molecular dynamics simulations of available CsdE structures allow to delineate the sequence of conformational changes underwent by CsdE and to pinpoint the key role played by the deprotonation of the Cys61 thiol. The low-energy subunit orientation in the disulfide-bridged CsdE dimer demonstrates the likely physiologic relevance of this oxidative dead-end form of CsdE, suggesting that CsdE could act as a redox sensor in vivo.
PubMed: 29045454
DOI: 10.1371/journal.pone.0186286
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.4 Å)
構造検証レポート
Validation report summary of 5nq6
検証レポート(詳細版)ダウンロードをダウンロード

227561

件を2024-11-20に公開中

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