4DBH
Crystal structure of Cg1458 with inhibitor
4DBH の概要
| エントリーDOI | 10.2210/pdb4dbh/pdb |
| 関連するPDBエントリー | 4DBF |
| 分子名称 | 2-HYDROXYHEPTA-2,4-DIENE-1,7-DIOATE ISOMERASE, MAGNESIUM ION, OXALATE ION, ... (4 entities in total) |
| 機能のキーワード | oxaloacetate decarboxylase, oxalate, mg++, isomerase |
| 由来する生物種 | Corynebacterium glutamicum |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 62649.93 |
| 構造登録者 | |
| 主引用文献 | Ran, T.,Gao, Y.,Marsh, M.,Zhu, W.,Wang, M.,Mao, X.,Xu, L.,Xu, D.,Wang, W. Crystal structures of Cg1458 reveal a catalytic lid domain and a common catalytic mechanism for FAH family. Biochem.J., 449:51-60, 2013 Cited by PubMed Abstract: Cg1458 was recently characterized as a novel soluble oxaloacetate decarboxylase. However, sequence alignment identified that Cg1458 has no similarity with other oxaloacetate decarboxylases and instead belongs to the FAH (fumarylacetoacetate hydrolase) family. Differences in the function of Cg1458 and other FAH proteins may suggest a different catalytic mechanism. To help elucidate the catalytic mechanism of Cg1458, crystal structures of Cg1458 in both the open and closed conformations have been determined for the first time up to a resolution of 1.9 Å (1 Å=0.1 nm) and 2.0 Å respectively. Comparison of both structures and detailed biochemical studies confirmed the presence of a catalytic lid domain which is missing in the native enzyme structure. In this lid domain, a glutamic acid-histidine dyad was found to be critical in mediating enzymatic catalysis. On the basis of structural modelling and comparison, as well as large-scale sequence alignment studies, we further determined that the catalytic mechanism of Cg1458 is actually through a glutamic acid-histidine-water triad, and this catalytic triad is common among FAH family proteins that catalyse the cleavage of the C-C bond of the substrate. Two sequence motifs, HxxE and Hxx…xxE have been identified as the basis for this mechanism. PubMed: 23046410DOI: 10.1042/BJ20120913 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.94 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






