7COV

Potato D-enzyme, native (substrate free)

7COV の概要

• エントリーDOI: 10.2210/pdb7cov/pdb
• 関連するPDBエントリー: 1X1N
• 分子名称: 4-alpha-glucanotransferase, chloroplastic/amyloplastic, CALCIUM ION, GLYCEROL, ... (4 entities in total)
• 機能のキーワード: d-enzyme, disproportionating enzyme, potato, cycloamylose, solanum tuberosum, plant protein, transferase
• 由来する生物種: Solanum tuberosum (Potato)
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 65798.23

構造登録者

Unno, H.,Imamura, K. (登録日: 2020-08-05, 公開日: 2020-08-26, 最終更新日: 2025-03-12)

主引用文献

Imamura, K.,Matsuura, T.,Nakagawa, A.,Kitamura, S.,Kusunoki, M.,Takaha, T.,Unno, H.
Structural analysis and reaction mechanism of the disproportionating enzyme (D-enzyme) from potato.
Protein Sci., 29:2085-2100, 2020

PubMed Abstract: Starch produced by plants is a stored form of energy and is an important dietary source of calories for humans and domestic animals. Disproportionating enzyme (D-enzyme) catalyzes intramolecular and intermolecular transglycosylation reactions of α-1, 4-glucan. D-enzyme is essential in starch metabolism in the potato. We present the crystal structures of potato D-enzyme, including two different types of complex structures: a primary Michaelis complex (substrate binding mode) for 26-meric cycloamylose (CA26) and a covalent intermediate for acarbose. Our study revealed that the acarbose and CA26 reactions catalyzed by potato D-enzyme involve the formation of a covalent intermediate with the donor substrate. HPAEC of reaction substrates and products revealed the activity of the potato D-enzyme on acarbose and CA26 as donor substrates. The structural and chromatography analyses provide insight into the mechanism of the coupling reaction of CA and glucose catalyzed by the potato D-enzyme. The enzymatic reaction mechanism does not involve residual hydrolysis. This could be particularly useful in preventing unnecessary starch degradation leading to reduced crop productivity. Optimization of this mechanism would be important for improvements of starch storage and productivity in crops.

PubMed: 32808707
DOI: 10.1002/pro.3932

実験手法

X-RAY DIFFRACTION (2 Å)