The potential of the folic acid biosynthesis pathway as a target for the development of antibiotics has been acknowledged for many years and validated by the clinical use of several drugs. Recently, the crystal structures of all but one of the enzymes in the pathway from GTP to dihydrofolate have been determined. Given that structure-based drug design strategies are now widely employed, these recent developments have prompted a re-evaluation of the potential of each of the enzymes in the pathway as a target for development of specific inhibitors. Here, we review the current knowledge of the structure and mechanism of each enzyme in the bacterial folic acid biosynthesis pathway from GTP to dihydrofolate and draw conclusions regarding the potential of each enzyme as a target for therapeutic intervention. (C) 2002 Wiley Periodicals, Inc.
机构:NCI, Frederick Canc Res & Dev Ctr, Program Struct Biol, Frederick, MD 21702 USA
Blaszczyk, J
Shi, G
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机构:NCI, Frederick Canc Res & Dev Ctr, Program Struct Biol, Frederick, MD 21702 USA
Shi, G
Yan, H
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h-index: 0
机构:NCI, Frederick Canc Res & Dev Ctr, Program Struct Biol, Frederick, MD 21702 USA
Yan, H
Ji, X
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机构:
NCI, Frederick Canc Res & Dev Ctr, Program Struct Biol, Frederick, MD 21702 USANCI, Frederick Canc Res & Dev Ctr, Program Struct Biol, Frederick, MD 21702 USA
机构:NCI, Frederick Canc Res & Dev Ctr, Program Struct Biol, Frederick, MD 21702 USA
Blaszczyk, J
Shi, G
论文数: 0引用数: 0
h-index: 0
机构:NCI, Frederick Canc Res & Dev Ctr, Program Struct Biol, Frederick, MD 21702 USA
Shi, G
Yan, H
论文数: 0引用数: 0
h-index: 0
机构:NCI, Frederick Canc Res & Dev Ctr, Program Struct Biol, Frederick, MD 21702 USA
Yan, H
Ji, X
论文数: 0引用数: 0
h-index: 0
机构:
NCI, Frederick Canc Res & Dev Ctr, Program Struct Biol, Frederick, MD 21702 USANCI, Frederick Canc Res & Dev Ctr, Program Struct Biol, Frederick, MD 21702 USA