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Dimerization inhibitors of HIV-1 reverse transcriptase, protease and integrase: A single mode of inhibition for the three HIV enzymes?

机译:HIV-1逆转录酶,蛋白酶和整合酶的二聚化抑制剂:三种HIV酶的单一抑制方式?

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摘要

The genome of human immunodeficiency virus type 1 (HIV-1) encodes 15 distinct proteins, three of which provide essential enzymatic functions: a reverse transcriptase (RT), an integrase (IN), and a protease (PR). Since these enzymes are all homodimers, pseudohomodimers or multimers, disruption of protein-protein interactions in these retroviral enzymes may constitute an alternative way to achieve HIV-1 inhibition. A growing number. of dimerization inhibitors for these enzymes is being reported. This mini review summarizes some approaches that have been followed for the development of compounds that inhibit those three enzymes by interfering with the dimerization interfaces between the enzyme subunits. (c) 2006 Elsevier B.V. All rights reserved.
机译:人类1型免疫缺陷病毒(HIV-1)的基因组编码15种不同的蛋白质,其中三种提供基本的酶促功能:逆转录酶(RT),整合酶(IN)和蛋白酶(PR)。由于这些酶都是同型二聚体,假同型二聚体或多聚体,因此破坏这些逆转录病毒酶中的蛋白质间相互作用可能构成实现HIV-1抑制的另一种方法。越来越多。已经报道了针对这些酶的二聚化抑制剂。这篇简短的综述总结了开发通过干扰酶亚基之间的二聚化界面来抑制这三种酶的化合物所遵循的一些方法。 (c)2006 Elsevier B.V.保留所有权利。

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