贾第鞭毛虫糖代谢途径的重建。

International journal of proteomics Pub Date : 2012-01-01 Epub Date: 2012-10-18 DOI:10.1155/2012/980829
Jian Han, Lesley J Collins
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引用次数: 17

摘要

贾第鞭毛虫是人类的一种“重要”病原体,但作为一种外交发掘,它在进化上与其他真核生物距离较远,对其核心代谢途径的了解相对较少。KEGG是一个被广泛引用的提供代谢信息的网站,它还没有包括许多来自贾第鞭毛虫物种的酶。在这里,我们使用标准的生物信息学方法确定贾第鞭毛虫的核心糖代谢。通过将贾第鞭毛虫蛋白质组与其他已知物种的酶进行比较,我们确定了糖酵解途径中的酶,以及一些参与TCA循环和氧化磷酸化的酶。然而,后两种途径中的大多数酶都无法识别,这表明可能缺乏这些功能。我们还发现贾第鞭毛虫糖酵解途径中的酶与细菌中的酶更相似。由于这些酶不同于在哺乳动物(贾第鞭毛虫的宿主生物)中发现的酶,我们提出了这些细菌样酶可能成为治疗贾第鞭毛虫感染的新药物靶点的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Reconstruction of Sugar Metabolic Pathways of Giardia lamblia.

Giardia lamblia is an "important" pathogen of humans, but as a diplomonad excavate it is evolutionarily distant from other eukaryotes and relatively little is known about its core metabolic pathways. KEGG, the widely referenced site for providing information of metabolism, does not yet include many enzymes from Giardia species. Here we identify Giardia's core sugar metabolism using standard bioinformatic approaches. By comparing Giardia proteomes with known enzymes from other species, we have identified enzymes in the glycolysis pathway, as well as some enzymes involved in the TCA cycle and oxidative phosphorylation. However, the majority of enzymes from the latter two pathways were not identifiable, indicating the likely absence of these functionalities. We have also found enzymes from the Giardia glycolysis pathway that appear more similar to those from bacteria. Because these enzymes are different from those found in mammals, the host organisms for Giardia, we raise the possibility that these bacteria-like enzymes could be novel drug targets for treating Giardia infections.

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