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The Enzymatic Decarboxylation Mechanism of 5-Carboxy Uracil: A Comprehensive Quantum Chemical Study

机译:5-羧尿嘧啶的酶促脱羧机制:全普通化学研究

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摘要

Dynamic regulation of DNA methylation is an important process for the control of gene expression in mammals. It is believed that in the demethylation pathway of 5-methyl cytosine, the intermediate 5-carboxy cytosine (5caC ) can be actively decarboxylated alongside the substitution in the base excision repair. For the active decarboxylation of 5caC , a decarboxylase has not been identified so far. Due to the similar chemistry of the decarboxylation of 5-carboxy uracil (5caU ) to uracil (U ) in the pyrimidine salvage pathway catalyzed by the iso-orotate decarboxylase (IDCase), the study of this reaction might give valuable insights into the active 5caC decarboxylation process. In this work, we employ quantum chemical and molecular mechanic calculations and find that the catalytic mechanism of IDCase proceeds via a direct decarboxylation mechanism. Detailed investigations on the reaction coordinate reveal that it is a one-step mechanism with concerted proton transfer and C–C bond opening.
机译:DNA甲基化的动态调节是哺乳动物基因表达调控的重要过程。据信,在5-甲基胞嘧啶的去甲基化途径中,中间产物5-羧基胞嘧啶(5caC)可以在碱基切除修复过程中与取代物一起被积极脱羧。对于5caC的活性脱羧酶,目前尚未发现脱羧酶。由于在异羧酸脱羧酶(IDCase)催化的嘧啶补救途径中,5-羧基尿嘧啶(5caU)脱羧为尿嘧啶(U)的化学相似,因此对该反应的研究可能会对活性5caC脱羧过程提供有价值的见解。在这项工作中,我们采用量子化学和分子力学计算,发现IDCase的催化机制是通过直接脱羧机制进行的。对反应座标的详细研究表明,这是一个一步反应机制,具有协同质子转移和C–C键开放。

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