Structure and reactivity in the non-mevalonate pathway of isoprenoid biosynthesis

被引:11
|
作者
Hunter, WN [1 ]
Bond, CS [1 ]
Gabrielsen, M [1 ]
Kemp, LE [1 ]
机构
[1] Univ Dundee, Sch Life Sci, Div Biol Chem & Mol Microbiol, Dundee DD1 5EH, Scotland
关键词
cytidylytransferase; enzyme; manganese; synthase; X-ray crystallography; zinc;
D O I
10.1042/bst0310537
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
The function, structure and mechanism of two Escherichia coli enzymes involved in the non-mevalonate route of isoprenoid biosynthesis, 2C-methyl-D-erythritol 4-phosphate cytidylyltransferase and 2C-methyl-D-erythritol 2,4-cyclodiphosphate synthase, are reviewed. Comparisons of each with enzymes from microbial pathogens highlight important conservation of sequence suggestive of similarities in secondary structure, subunit folds, quaternary structure and active sites. Since both enzymes are validated drug targets, the models provide templates for structure-based design of anti-microbial agents targeting a number of serious human diseases.
引用
收藏
页码:537 / 542
页数:6
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