三氯生
酰基载体蛋白
酶
还原酶
生物化学
异烟肼
生物
化学
肺结核
生物合成
医学
病理
作者
R. Prisca Massengo-Tiassé,John E. Cronan
标识
DOI:10.1007/s00018-009-8704-7
摘要
The enoyl-acyl carrier protein reductase (ENR) is the last enzyme in the fatty acid elongation cycle. Unlike most enzymes in this essential pathway, ENR displays an unusual diversity among organisms. The growing interest in ENRs is mainly due to the fact that a variety of both synthetic and natural antibacterial compounds are shown to specifically target their activity. The primary anti-tuberculosis drug, isoniazid, and the broadly used antibacterial compound, triclosan, both target this enzyme. In this review, we discuss the diversity of ENRs, and their inhibitors in the light of current research progress.
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