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Purine and pyrimidine transport in pathogenic protozoa: From biology to therapy

机译:嘌呤和嘧啶在致病性原生动物中的转运:从生物学到治疗

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摘要

Purine salvage is an essential function for all obligate parasitic protozoa studied to date and most are also capable of efficient uptake of preformed pyrimidines. Much progress has been made in the identification and characterisation of protozoan purine and pyrimidine transporters. While the genes encoding protozoan or metazoan pyrimidine transporters have yet to be identified, numerous purine transporters have now been cloned. All protozoan purine transporter-encoding genes characterised to date have been of the Equilibrative Nucleoside Transporter family conserved in a great variety of eukaryote organisms. However, these protozoan transporters have been shown to be sufficiently different from mammalian transporters to mediate selective uptake of therapeutic agents. Recent studies are increasingly addressing the structure and substrate recognition mechanisms of these vital transport proteins. (c) 2005 Federation of European Microbiological Societies. Published by Elsevier B.V. All rights reserved.
机译:嘌呤的挽救是迄今为止研究的所有专性寄生虫原生动物的一项基本功能,而且大多数还能够有效摄取预制的嘧啶。在原生动物嘌呤和嘧啶转运蛋白的鉴定和表征方面已经取得了很大进展。尽管尚未确定编码原生动物或后生嘧啶转运蛋白的基因,但现已克隆了许多嘌呤转运蛋白。迄今为止,所有表征为原生动物嘌呤转运蛋白的基因均属于在各种真核生物中均保守的平衡核苷转运蛋白家族。然而,这些原生动物转运蛋白已显示出与哺乳动物转运蛋白充分不同,以介导选择性吸收治疗剂。最近的研究越来越关注这些重要转运蛋白的结构和底物识别机制。 (c)2005年欧洲微生物学会联合会。由Elsevier B.V.发布。保留所有权利。

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