1KXH
Crystal structure of the complex between an inactive mutant of psychrophilic alpha-amylase (D174N) and acarbose
1KXH の概要
エントリーDOI | 10.2210/pdb1kxh/pdb |
関連するPDBエントリー | 1AQH 1AQM 1BOI 1G94 1G9H |
関連するBIRD辞書のPRD_ID | PRD_900007 |
分子名称 | alpha-amylase, 4,6-dideoxy-4-{[(1S,4R,5S,6S)-4,5,6-trihydroxy-3-(hydroxymethyl)cyclohex-2-en-1-yl]amino}-alpha-D-glucopyranose-(1-4)-alpha-D-glucopyranose-(1-4)-alpha-D-glucopyranose, CALCIUM ION, ... (5 entities in total) |
機能のキーワード | (beta/alpha)8 barrel, hydrolase |
由来する生物種 | Pseudoalteromonas haloplanktis |
タンパク質・核酸の鎖数 | 1 |
化学式量合計 | 49667.58 |
構造登録者 | |
主引用文献 | Aghajari, N.,Roth, M.,Haser, R. Crystallographic evidence of a transglycosylation reaction: ternary complexes of a psychrophilic alpha-amylase. Biochemistry, 41:4273-4280, Cited by PubMed Abstract: The psychrophilic Pseudoalteromonas haloplanctis alpha-amylase is shown to form ternary complexes with two alpha-amylase inhibitors present in the active site region, namely, a molecule of Tris and a trisaccharide inhibitor or heptasaccharide inhibitor, respectively. The crystal structures of these complexes have been determined by X-ray crystallography to 1.80 and 1.74 A resolution, respectively. In both cases, the prebound inhibitor Tris is expelled from the active site by the incoming oligosaccharide inhibitor substrate analogue, but stays linked to it, forming well-defined ternary complexes with the enzyme. These results illustrate competition in the crystalline state between two inhibitors, an oligosaccharide substrate analogue and a Tris molecule, bound at the same time in the active site region. Taken together, these structures show that the enzyme performs transglycosylation in the complex with the pseudotetrasaccharide acarbose (confirmed by a mutant structure), leading to a well-defined heptasaccharide, considered as a more potent inhibitor. Furthermore, the substrate-induced ordering of water molecules within a channel highlights a possible pathway used for hydrolysis of starch and related poly- and oligosaccharides. PubMed: 11914073DOI: 10.1021/bi0160516 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.3 Å) |
構造検証レポート
検証レポート(詳細版)をダウンロード