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3VDR

Crystal structure of D-3-hydroxybutyrate dehydrogenase, prepared in the presence of the substrate D-3-hydroxybutyrate and NAD(+)

3EEW」から置き換えられました
3VDR の概要
エントリーDOI10.2210/pdb3vdr/pdb
関連するPDBエントリー2YZ7 2ZEA 3VDQ
分子名称D-3-hydroxybutyrate dehydrogenase, CALCIUM ION, CHLORIDE ION, ... (8 entities in total)
機能のキーワードnad dependent enzymes, ketone bodies, oxidoreductase
由来する生物種Alcaligenes faecalis
タンパク質・核酸の鎖数4
化学式量合計114802.53
構造登録者
主引用文献Hoque, M.M.,Shimizu, S.,Juan, E.C.M.,Sato, Y.,Hossain, M.T.,Yamamoto, T.,Imamura, S.,Suzuki, K.,Amano, H.,Sekiguchi, T.,Tsunoda, M.,Takenaka, A.
Structure of D-3-hydroxybutyrate dehydrogenase prepared in the presence of the substrate D-3-hydroxybutyrate and NAD+.
Acta Crystallogr.,Sect.F, 65:331-335, 2009
Cited by
PubMed Abstract: D-3-hydroxybutyrate dehydrogenase from Alcaligenes faecalis catalyzes the reversible conversion between D-3-hydroxybutyrate and acetoacetate. The enzyme was crystallized in the presence of the substrate D-3-hydroxybutyrate and the cofactor NAD(+) at the optimum pH for the catalytic reaction. The structure, which was solved by X-ray crystallography, is isomorphous to that of the complex with the substrate analogue acetate. The product as well as the substrate molecule are accommodated well in the catalytic site. Their binding geometries suggest that the reversible reactions occur by shuttle movements of a hydrogen negative ion from the C3 atom of the substrate to the C4 atom of NAD(+) and from the C4 atom of NADH to the C3 atom of the product. The reaction might be further coupled to the withdrawal of a proton from the hydroxyl group of the substrate by the ionized Tyr155 residue. These structural features strongly support the previously proposed reaction mechanism of D-3-hydroxybutyrate dehydrogenase, which was based on the acetate-bound complex structure.
PubMed: 19342772
DOI: 10.1107/S1744309109008537
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (3 Å)
構造検証レポート
Validation report summary of 3vdr
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2026-02-11に公開中

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