Nihei_2002_Biochim.Biophys.Acta_1587_234

Reference

Title : Trypanosome alternative oxidase as a target of chemotherapy - Nihei_2002_Biochim.Biophys.Acta_1587_234
Author(s) : Nihei C , Fukai Y , Kita K
Ref : Biochimica & Biophysica Acta , 1587 :234 , 2002
Abstract :

Parasites have developed a variety of physiological functions necessary for their survival within the specialized environment of the host. Using metabolic systems that are very different from those of the host, they can adapt to low oxygen tension present within the host animals. Most parasites do not use the oxygen available within the host to generate ATP, but rather employ systems anaerobic metabolic pathways. The enzymes in these parasite-specific pathways are potential targets for chemotherapy.Cyanide-insensitive trypanosome alternative oxidase (TAO) is the terminal oxidase of the respiratory chain of long slender bloodstream forms of the African trypanosome, which causes sleeping sickness in human and nagana in cattle. TAO has been targeted for the development of anti-trypanosomal drugs because it does not exist in the host. Recently, we found the most potent inhibitor of TAO to date, ascofuranone, a compound isolated from the phytopathogenic fungus, Ascochyta visiae.

PubMedSearch : Nihei_2002_Biochim.Biophys.Acta_1587_234
PubMedID: 12084465
Gene_locus related to this paper: acreg-ascc

Related information

Gene_locus acreg-ascc

Citations formats

Nihei C, Fukai Y, Kita K (2002)
Trypanosome alternative oxidase as a target of chemotherapy
Biochimica & Biophysica Acta 1587 :234

Nihei C, Fukai Y, Kita K (2002)
Biochimica & Biophysica Acta 1587 :234