Paradigms of convergent evolution in enzymes.

Ioannis G Riziotis, Jenny C Kafas, Gabriel Ong, Neera Borkakoti, António J M Ribeiro, Janet M Thornton
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Abstract

There are many occurrences of enzymes catalysing the same reaction but having significantly different structures. Leveraging the comprehensive information on enzymes stored in the Mechanism and Catalytic Site Atlas (M-CSA), we present a collection of 34 cases for which there is sufficient evidence of functional convergence without an evolutionary link. For each case, we compare enzymes which have identical Enzyme Commission numbers (i.e. catalyse the same reaction), but different identifiers in the CATH data resource (i.e. different folds). We focus on similarities between their sequences, structures, active site geometries, cofactors and catalytic mechanisms. These features are then assessed to evaluate whether all the evidence for these structurally diverse proteins supports their independent evolution to catalyse the same chemical reaction. Our approach combines published literature information with knowledge-based computational resources from, amongst others, M-CSA, PDBe and PDBsum, supported by tailor-made software to explore active site structures and assess similarities in mechanism. We find that there are multiple types of convergent functional evolution observed to date, and it is necessary to investigate sequence, structure, active site geometry and enzyme mechanisms to describe such convergence accurately.

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酶的趋同进化范例。
有许多酶催化相同的反应,但结构却大相径庭。利用机制和催化位点图集(M-CSA)中储存的酶的全面信息,我们收集了34种有充分证据表明功能趋同而无进化联系的情况。在每个案例中,我们比较了具有相同酶委员会编号(即催化相同反应)但在 CATH 数据资源中具有不同标识符(即不同折叠)的酶。我们将重点放在它们的序列、结构、活性位点几何图形、辅助因子和催化机制之间的相似性上。然后对这些特征进行评估,以确定这些结构不同的蛋白质的所有证据是否都支持它们催化相同化学反应的独立进化。我们的方法将已发表的文献信息与来自 M-CSA、PDBe 和 PDBsum 等基于知识的计算资源相结合,并辅以量身定制的软件来探索活性位点结构和评估机制的相似性。我们发现,迄今为止观察到的趋同功能进化有多种类型,有必要对序列、结构、活性位点几何和酶机制进行研究,以准确描述这种趋同。
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