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The folic acid biosynthesis pathway in bacteria: evaluation of potential for antibacterial drug discovery.

机译:细菌中的叶酸生物合成途径:评估抗菌药物发现的潜力。

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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.
机译:叶酸生物合成途径作为开发抗生素的目标的潜力已经被认识了很多年,并已通过几种药物的临床使用得到了证实。最近,已经确定了从GTP到二氢叶酸途径中除一种酶外的所有酶的晶体结构。考虑到基于结构的药物设计策略已被广泛采用,这些最新进展促使人们重新评估了该途径中每种酶作为开发特定抑制剂的目标的潜力。在这里,我们回顾了细菌叶酸从GTP到二氢叶酸的生物合成途径中每种酶的结构和机理的当前知识,并就每种酶作为治疗干预目标的潜力得出了结论。 BioEssays 24:637-648,2002。

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