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Reaction Path Analysis for Demethylation Process of Histone Tail Lysine Residues

机译:组蛋白尾赖氨酸残基去甲基化过程的反应路径分析

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Histone proteins control many crucial cell regulatory processes post-translational modifications. Among these modifications, methylation is recently shown to be reversible with the discovery of Lysine-specific Demethylase (LSD1) enzyme. As many studies have showed the relation of some cancer-type and other diseases with the abnormalities in the balance of methylation/demethylation, drug molecule design based on the information gained from reaction path analysis becomes very useful. In this paper, a chemically-consistent reaction mechanism is proposed for the demethylation of histone tail lysine residues and the reaction path analysis of this mechanism is carried out. Potential and free energy profiles of the system, which does not include the residues of the enzyme, are calculated with semi-empirical and quantum mechanical (QM) methods. These results create a fundamental basis for further analysis of the demethylation process with enzyme and/or inhibitor molecules available in the literature.
机译:组蛋白蛋白控制许多关键的细胞调节过程翻译后修饰。在这些修饰中,最近显示甲基化与发现赖氨酸特异性去甲基酶(LSD1)酶的发现是可逆的。由于许多研究表明,一些癌症类型和其他疾病在甲基化/去甲基化平衡中的异常的关系,基于反应路径分析中获得的信息的药物分子设计变得非常有用。本文提出了一种化学 - 一致的反应机理,用于组蛋白尾赖氨酸残基的去甲基化,并进行该机制的反应路径分析。用半经验和量子机械(QM)方法计算该系统的潜在和自由能量谱,其不包括酶的残基。这些结果为进一步分析了文献中可用的酶和/或抑制剂分子进一步分析了对去甲基化方法的基础。

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