Decaprenyl-phosphoryl-ribose 2'-epimerase (DprE1): challenging target for antitubercular drug discovery.

Q1 Chemistry Chemistry Central Journal Pub Date : 2018-06-23 DOI:10.1186/s13065-018-0441-2
Jineetkumar Gawad, Chandrakant Bonde
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引用次数: 20

Abstract

Tuberculosis has proved harmful to the entire history of mankind from past several decades. Decaprenyl-phosphoryl-ribose 2'-epimerase (DprE1) is a recent target which was identified in 2009 but unfortunately it is neither explored nor crossed phase II. In past several decades few targets were identified for effective antitubercular drug discovery. Resistance is the major problem for effective antitubercular drug discovery. Arabinose is constituent of mycobacterium cell wall. Biosynthesis of arabinose is FAD dependant two step epimerisation reaction which is catalysed by DprE1 and DprE2 flavoprotein enzymes. The current review is mainly emphases on DprE1 as a perspective challenge for further research.

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十戊烯基磷酸基核糖2'-外甲酰基酶(DprE1):抗结核药物发现的挑战性靶点。
过去几十年来,结核病已被证明对整个人类历史都是有害的。decaprenyl - phospylyl -ribose 2’- epimase (DprE1)是2009年发现的一个新靶点,但遗憾的是,它既没有被探索,也没有经过II期交叉。在过去的几十年里,人们发现的有效的抗结核药物靶点很少。耐药性是发现有效抗结核药物的主要问题。阿拉伯糖是分枝杆菌细胞壁的组成成分。阿拉伯糖的生物合成是由DprE1和DprE2黄蛋白酶催化的FAD依赖的两步外聚反应。目前的综述主要侧重于DprE1作为进一步研究的前景挑战。
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来源期刊
Chemistry Central Journal
Chemistry Central Journal 化学-化学综合
CiteScore
4.40
自引率
0.00%
发文量
0
审稿时长
3.5 months
期刊介绍: BMC Chemistry is an open access, peer reviewed journal that considers all articles in the broad field of chemistry, including research on fundamental concepts, new developments and the application of chemical sciences to broad range of research fields, industry, and other disciplines. It provides an inclusive platform for the dissemination and discussion of chemistry to aid the advancement of all areas of research. Sections: -Analytical Chemistry -Organic Chemistry -Environmental and Energy Chemistry -Agricultural and Food Chemistry -Inorganic Chemistry -Medicinal Chemistry -Physical Chemistry -Materials and Macromolecular Chemistry -Green and Sustainable Chemistry
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