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2D24

Crystal structure of ES complex of catalytic-site mutant xylanase from Streptomyces olivaceoviridis E-86

2D24 の概要
エントリーDOI10.2210/pdb2d24/pdb
関連するPDBエントリー1ISW 1ISX 1XYF 2D1Z 2D20 2D22 2D23
分子名称ENDO-1,4-BETA-D-XYLANASE, alpha-D-xylopyranose-(1-4)-alpha-D-xylopyranose-(1-4)-alpha-D-xylopyranose-(1-4)-alpha-D-xylopyranose-(1-4)-alpha-D-xylopyranose, alpha-D-xylopyranose-(1-4)-alpha-D-xylopyranose-(1-4)-alpha-D-xylopyranose-(1-4)-alpha-D-xylopyranose, ... (7 entities in total)
機能のキーワードtim-barrel, retaining enzyme, catalytic-site mutant, chemical rescue, michaelis complex, hydrolase
由来する生物種Streptomyces olivaceoviridis
タンパク質・核酸の鎖数2
化学式量合計96483.01
構造登録者
Suzuki, R.,Kuno, A.,Fujimoto, Z.,Ito, S.,Kawahara, S.I.,Kaneko, S.,Hasegawa, T.,Taira, K. (登録日: 2005-09-02, 公開日: 2006-10-10, 最終更新日: 2024-10-16)
主引用文献Suzuki, R.,Fujimoto, Z.,Ito, S.,Kawahara, S.,Kaneko, S.,Taira, K.,Hasegawa, T.,Kuno, A.
Crystallographic snapshots of an entire reaction cycle for a retaining xylanase from Streptomyces olivaceoviridis E-86
J.Biochem., 146:61-70, 2009
Cited by
PubMed Abstract: Retaining glycosyl hydrolases, which catalyse both glycosylation and deglycosylation in a concerted manner, are the most abundant hydrolases. To date, their visualization has tended to be focused on glycosylation because glycosylation reactions can be visualized by inactivating deglycosylation step and/or using substrate analogues to isolate covalent intermediates. Furthermore, during structural analyses of glycosyl hydrolases with hydrolytic reaction products by the conventional soaking method, mutarotation of an anomeric carbon in the reaction products promptly and certainly occurs. This undesirable structural alteration hinders visualization of the second step in the reaction. Here, we investigated X-ray crystallographic visualization as a possible method for visualizing the conformational itinerary of a retaining xylanase from Streptomyces olivaceoviridis E-86. To clearly define the stereochemistry at the anomeric carbon during the deglycosylation step, extraneous nucleophiles, such as azide, were adopted to substitute for the missing base catalyst in an appropriate mutant. The X-ray crystallographic visualization provided snapshots of the components of the entire reaction, including the E*S complex, the covalent intermediate, breakdown of the intermediate and the enzyme-product (E*P)complex.
PubMed: 19279191
DOI: 10.1093/jb/mvp047
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.85 Å)
構造検証レポート
Validation report summary of 2d24
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2024-10-30に公開中

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