3A4X
Crystal structures of catalytic site mutants of active domain 2 of thermostable chitinase from Pyrococcus furiosus complexed with chito-oligosaccharides
3A4X の概要
| エントリーDOI | 10.2210/pdb3a4x/pdb |
| 関連するPDBエントリー | 3A4W 3AFB |
| 分子名称 | Chitinase, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-alpha-D-glucopyranose, MAGNESIUM ION, ... (6 entities in total) |
| 機能のキーワード | archaea, chitinase, glycosyl hydrolase, hydrolase |
| 由来する生物種 | Pyrococcus furiosus |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 71707.14 |
| 構造登録者 | Tsuji, H.,Nishimura, S.,Inui, T.,Ishikawa, K.,Nakamura, T.,Uegaki, K. (登録日: 2009-07-22, 公開日: 2010-06-09, 最終更新日: 2023-11-01) |
| 主引用文献 | Tsuji, H.,Nishimura, S.,Inui, T.,Kado, Y.,Ishikawa, K.,Nakamura, T.,Uegaki, K. Kinetic and crystallographic analyses of the catalytic domain of chitinase from Pyrococcus furiosus- the role of conserved residues in the active site Febs J., 277:2683-2695, 2010 Cited by PubMed Abstract: The hyperthermostable chitinase from the hyperthermophilic archaeon Pyrococcus furiosus has a unique multidomain structure containing two chitin-binding domains and two catalytic domains, and exhibits strong crystalline chitin hydrolyzing activity at high temperature. In order to investigate the structure-function relationship of this chitinase, we analyzed one of the catalytic domains (AD2) using mutational and kinetic approaches, and determined the crystal structure of AD2 complexed with chito-oligosaccharide substrate. Kinetic studies showed that, among the acidic residues in the signature sequence of family 18 chitinases (DXDXE motif), the second Asp (D(2)) and Glu (E) residues play critical roles in the catalysis of archaeal chitinase. Crystallographic analyses showed that the side-chain of the catalytic proton-donating E residue is restrained into the favorable conformer for proton donation by a hydrogen bond interaction with the adjacent D(2) residue. The comparison of active site conformations of family 18 chitinases provides a new criterion for the subclassification of family 18 chitinase based on the conformational change of the D(2) residue. PubMed: 20553502DOI: 10.1111/j.1742-464X.2010.07685.x 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.76 Å) |
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