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基于蛋白质结构的系统发育分析推断现代代谢网络的起源。

The origin of modern metabolic networks inferred from phylogenomic analysis of protein architecture.

作者信息

Caetano-Anollés Gustavo, Kim Hee Shin, Mittenthal Jay E

机构信息

Departments of Crop Sciences and Cell and Developmental Biology, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA.

出版信息

Proc Natl Acad Sci U S A. 2007 May 29;104(22):9358-63. doi: 10.1073/pnas.0701214104. Epub 2007 May 21.

Abstract

Metabolism represents a complex collection of enzymatic reactions and transport processes that convert metabolites into molecules capable of supporting cellular life. Here we explore the origins and evolution of modern metabolism. Using phylogenomic information linked to the structure of metabolic enzymes, we sort out recruitment processes and discover that most enzymatic activities were associated with the nine most ancient and widely distributed protein fold architectures. An analysis of newly discovered functions showed enzymatic diversification occurred early, during the onset of the modern protein world. Most importantly, phylogenetic reconstruction exercises and other evidence suggest strongly that metabolism originated in enzymes with the P-loop hydrolase fold in nucleotide metabolism, probably in pathways linked to the purine metabolic subnetwork. Consequently, the first enzymatic takeover of an ancient biochemistry or prebiotic chemistry was related to the synthesis of nucleotides for the RNA world.

摘要

新陈代谢是一个复杂的酶促反应和转运过程的集合,它将代谢物转化为能够支持细胞生命的分子。在这里,我们探索现代新陈代谢的起源和进化。利用与代谢酶结构相关的系统基因组信息,我们梳理出招募过程,并发现大多数酶活性与九种最古老且分布广泛的蛋白质折叠结构相关。对新发现功能的分析表明,酶的多样化在现代蛋白质世界开始时就已早期发生。最重要的是,系统发育重建研究和其他证据强烈表明,新陈代谢起源于核苷酸代谢中具有P环水解酶折叠的酶,可能是在与嘌呤代谢子网相关的途径中。因此,对古代生物化学或前体生物化学的首次酶促接管与RNA世界中核苷酸的合成有关。

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