Protein kinases as drug targets in parasitic protozoa

被引:76
作者
Doerig, C
Meijer, L
Mottram, JC
机构
[1] CHU Pitie Salpetriere, Inst Natl Sante & Rech Med, U511, F-75013 Paris, France
[2] CNRS, Biol Stn, F-29682 Roscoff, Bretagne, France
[3] Univ Glasgow, Wellcome Ctr Mol Parasitol, Glasgow G11 6NU, Lanark, Scotland
关键词
D O I
10.1016/S1471-4922(02)02321-8
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
The importance of protein kinases in cell signaling and cell cycle control has led to detailed structural and functional studies in various eukaryotes, and hence to the synthesis of specific chemical inhibitors for managing disease. Here, the current progress in applying developments from the wider protein kinase field to parasitic protozoa is reviewed. The availability of genome sequence data for several parasites has led to the identification of many protein kinases. Reverse genetics studies, including gene knockout and chemical genetics, can help to define the roles of the protein kinases and validate them as drug targets. In addition, screening chemical libraries with active recombinant protein kinases can identify lead compounds for drug design.
引用
收藏
页码:366 / 371
页数:6
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