Loading
PDBj
メニューPDBj@FacebookPDBj@TwitterPDBj@YouTubewwPDB FoundationwwPDB
RCSB PDBPDBeBMRBAdv. SearchSearch help

2V7U

X-ray crystal structure of 5'-fluorodeoxyadenosine synthase s158g mutant complexed with s-adenosylmethionine and chloride ion

2V7U の概要
エントリーDOI10.2210/pdb2v7u/pdb
関連するPDBエントリー1RQP 1RQR 2C2W 2C4T 2C4U 2C5B 2C5H 2CBX 2CC2 2V7T 2V7V 2V7W 2V7X
分子名称5'-FLUORO-5'-DEOXY ADENOSINE SYNTHETASE, S-ADENOSYLMETHIONINE, CHLORIDE ION, ... (4 entities in total)
機能のキーワードmechanism of fluorination, biosynthetic protein, transferase
由来する生物種STREPTOMYCES CATTLEYA
タンパク質・核酸の鎖数3
化学式量合計98416.07
構造登録者
Zhu, X.,O'Hagan, D.,Naismith, J.H. (登録日: 2007-08-02, 公開日: 2008-08-12, 最終更新日: 2023-12-13)
主引用文献Zhu, X.,Robinson, D.A.,McEwan, A.R.,O'Hagan, D.,Naismith, J.H.
Mechanism of enzymatic fluorination in Streptomyces cattleya.
J. Am. Chem. Soc., 129:14597-14604, 2007
Cited by
PubMed Abstract: Recently a fluorination enzyme was identified and isolated from Streptomyces cattleya, as the first committed step on the metabolic pathway to the fluorinated metabolites, fluoroacetate and 4-fluorothreonine. This enzyme, 5'-fluoro-5'-deoxy adenosine synthetase (FDAS), has been shown to catalyze C-F bond formation by nucleophilic attack of fluoride ion to S-adenosyl-l-methionine (SAM) with the concomitant displacement of l-methionine to generate 5'-fluoro-5'-deoxy adenosine (5'-FDA). Although the structures of FDAS bound to both SAM and products have been solved, the molecular mechanism remained to be elucidated. We now report site-directed mutagenesis studies, structural analyses, and isothermal calorimetry (ITC) experiments. The data establish the key residues required for catalysis and the order of substrate binding. Fluoride ion is not readily distinguished from water by protein X-ray crystallography; however, using chloride ion (also a substrate) with a mutant of low activity has enabled the halide ion to be located in nonproductive co-complexes with SAH and SAM. The kinetic data suggest the positively charged sulfur of SAM is a key requirement in stabilizing the transition state. We propose a molecular mechanism for FDAS in which fluoride weakly associates with the enzyme exchanging two water molecules for protein ligation. The binding of SAM expels remaining water associated with fluoride ion and traps the ion in a pocket positioned to react with SAM, generating l-methionine and 5'-FDA. l-methionine then dissociates from the enzyme followed by 5'-FDA.
PubMed: 17985882
DOI: 10.1021/ja0731569
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2 Å)
構造検証レポート
Validation report summary of 2v7u
検証レポート(詳細版)ダウンロードをダウンロード

226707

件を2024-10-30に公開中

PDB statisticsPDBj update infoContact PDBjnumon