Pyridoxine 5′-phosphate synthase:: de novo synthesis of vitamin B6 and beyond

被引:19
作者
Garrido-Franco, M [1 ]
机构
[1] Univ Dundee, Div Biol Chem & Mol Microbiol, Sch Life Sci, Dundee DD1 5EH, Scotland
[2] Max Planck Inst Biochem, Abt Strukturforsch, D-82152 Planegg Martinsried, Germany
来源
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS | 2003年 / 1647卷 / 1-2期
关键词
drug design; enzyme-ligand complex; open-closed transition; PdxJ; reaction mechanism; vitamin B-6;
D O I
10.1016/S1570-9639(03)00065-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Vitamin B-6 is an essential component in human diet. However, some organisms have the required machinery for its synthesis. There are two independent and autoexclusive groups of genes, pdx and SOR1 Pyridoxine 5'-phosphate (PNP) synthase is the key enzyme in the pdx group. It catalyses a multistep ring closure reaction yielding PNP and inorganic phosphate (Pi). This is the last step in the de novo synthetic pathway; afterwards, PNP enters the salvage pathway to be transformed to the pyridoxal 5'-phosphate cofactor. Because PNP synthase is not present in humans but is found in many human pathogens, the enzyme can be regarded as a potential target for the development of novel drugs. We have recently solved the structure of PNP synthase in complex with several ligands. The structural information allowed us to characterise the active site of the enzyme and identify the catalytically important residues. Furthermore, a detailed reaction mechanism could be proposed. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:92 / 97
页数:6
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