酶
生物合成
抗生素
药品
药物发现
叶酸
生物化学
代谢途径
生物
GTP'
细菌
叶酸拮抗剂
计算生物学
化学
药理学
医学
遗传学
内科学
作者
Alun Bermingham,Jeremy P. Derrick
出处
期刊:BioEssays
[Wiley]
日期:2002-06-21
卷期号:24 (7): 637-648
被引量:282
摘要
Abstract 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. BioEssays 24:637–648, 2002. © 2002 Wiley Periodicals, Inc.
科研通智能强力驱动
Strongly Powered by AbleSci AI