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针对抗寄生虫药物靶点——锥虫硫醇还原酶的分子研究。

Molecular studies on trypanothione reductase, a target for antiparasitic drugs.

作者信息

Walsh C, Bradley M, Nadeau K

机构信息

Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115.

出版信息

Trends Biochem Sci. 1991 Aug;16(8):305-9. doi: 10.1016/0968-0004(91)90124-e.

Abstract

Trypanosoma and Leishmania are parasitic protozoa that cause a variety of diseases, which include African sleeping sickness and oriental sore. Attempts to determine pharmaceutically exploitable differences between host and parasite biochemistry have identified the unique trypanothione pathway as a possible target. This pathway includes the enzyme trypanothione reductase, the parasite analogue of glutathione reductase.

摘要

锥虫和利什曼原虫是引起多种疾病的寄生原生动物,这些疾病包括非洲昏睡病和东方疖。试图确定宿主与寄生虫生物化学之间可用于药物开发的差异,已确定独特的三硫醇途径是一个可能的靶点。该途径包括三硫醇还原酶,它是谷胱甘肽还原酶的寄生虫类似物。

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