Loading
PDBj
メニューPDBj@FacebookPDBj@X(formerly Twitter)PDBj@BlueSkyPDBj@YouTubewwPDB FoundationwwPDBDonate
RCSB PDBPDBeBMRBAdv. SearchSearch help

3Q0E

Crystals Structure of Aspartate beta-Semialdehyde Dehydrogenase from Vibrio Cholerae with product of S-allyl-L-cysteine sulfoxide

3Q0E の概要
エントリーDOI10.2210/pdb3q0e/pdb
関連するPDBエントリー3PWK 3PWS 3PYL 3PYX 3PZB 3PZR 3Q11 3Q1L
分子名称Aspartate-semialdehyde dehydrogenase, CYSTEINE, SULFATE ION, ... (6 entities in total)
機能のキーワードoxydoreductase, nadp, oxidoreductase
由来する生物種Vibrio cholerae
タンパク質・核酸の鎖数2
化学式量合計81700.95
構造登録者
Pavlovsky, A.G.,Liu, X.,Viola, R.E. (登録日: 2010-12-15, 公開日: 2012-02-22, 最終更新日: 2024-10-16)
主引用文献Pavlovsky, A.G.,Liu, X.,Faehnle, C.R.,Potente, N.,Viola, R.E.
Structural characterization of inhibitors with selectivity against members of a homologous enzyme family.
Chem.Biol.Drug Des., 79:128-136, 2012
Cited by
PubMed Abstract: The aspartate biosynthetic pathway provides essential metabolites for many important biological functions, including the production of four essential amino acids. As this critical pathway is only present in plants and microbes, any disruptions will be fatal to these organisms. An early pathway enzyme, l-aspartate-β-semialdehyde dehydrogenase, produces a key intermediate at the first branch point of this pathway. Developing potent and selective inhibitors against several orthologs in the l-aspartate-β-semialdehyde dehydrogenase family can serve as lead compounds for antibiotic development. Kinetic studies of two small molecule fragment libraries have identified inhibitors that show good selectivity against l-aspartate-β-semialdehyde dehydrogenases from two different bacterial species, Streptococcus pneumoniae and Vibrio cholerae, despite the presence of an identical constellation of active site amino acids in this homologous enzyme family. Structural characterization of enzyme-inhibitor complexes have elucidated different modes of binding between these structurally related enzymes. This information provides the basis for a structure-guided approach to the development of more potent and more selective inhibitors.
PubMed: 22039970
DOI: 10.1111/j.1747-0285.2011.01267.x
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.8 Å)
構造検証レポート
Validation report summary of 3q0e
検証レポート(詳細版)ダウンロードをダウンロード

252091

件を2026-04-15に公開中

PDB statisticsPDBj update infoContact PDBjnumon