5YND
Crystal structure of Pullulanase from Klebsiella pneumoniae complex at 1 mM gamma-cyclodextrin
5YND の概要
エントリーDOI | 10.2210/pdb5ynd/pdb |
関連するBIRD辞書のPRD_ID | PRD_900010 |
分子名称 | DUF3372 domain-containing protein, alpha-D-glucopyranose-(1-4)-alpha-D-glucopyranose-(1-4)-alpha-D-glucopyranose-(1-4)-alpha-D-glucopyranose, CALCIUM ION, ... (6 entities in total) |
機能のキーワード | hydrolase, alpha-amylase, pullulanase, klebsiella pneumoniae, crystal, gamma-cyclodextrin, co-crystallization |
由来する生物種 | Klebsiella pneumoniae |
タンパク質・核酸の鎖数 | 1 |
化学式量合計 | 120858.60 |
構造登録者 | Saka, N.,Iwamoto, H.,Takahashi, N.,Mizutani, K.,Mikami, B. (登録日: 2017-10-24, 公開日: 2018-10-24, 最終更新日: 2024-10-30) |
主引用文献 | Saka, N.,Iwamoto, H.,Malle, D.,Takahashi, N.,Mizutani, K.,Mikami, B. Elucidation of the mechanism of interaction between Klebsiella pneumoniae pullulanase and cyclodextrin Acta Crystallogr D Struct Biol, 74:1115-1123, 2018 Cited by PubMed Abstract: Crystal structures of Klebsiella pneumoniae pullulanase (KPP) in complex with α-cyclodextrin (α-CD), β-cyclodextrin (β-CD) and γ-cyclodextrin (γ-CD) were refined at around 1.98-2.59 Å resolution from data collected at SPring-8. In the structures of the complexes obtained with 1 mM α-CD or γ-CD, one molecule of CD was found at carbohydrate-binding module 41 only (CBM41). In the structures of the complexes obtained with 1 mM β-CD or with 10 mM α-CD or γ-CD, two molecules of CD were found at CBM41 and in the active-site cleft, where the hydrophobic residue of Phe746 occupies the inside cavity of the CD rings. In contrast to α-CD and γ-CD, one β-CD molecule was found at the active site only in the presence of 0.1 mM β-CD. These results were coincident with the solution experiments, which showed that β-CD inhibits this enzyme more than a thousand times more potently than α-CD and γ-CD. The strong inhibition of β-CD is caused by the optimized interaction between β-CD and the side chain of Phe746. The increased K values of the F746A mutant for β-CD supported the importance of Phe746 in the strong interaction of pullulanase with β-CD. PubMed: 30387770DOI: 10.1107/S2059798318014523 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.227 Å) |
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