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SCOTCH: subtype A coreceptor tropism classification in HIV-1

机译:苏格兰威士忌:亚型艾滋病毒1中的核心深度染色分类

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Motivation: The V3 loop of the gp120 glycoprotein of the Human Immunodeficiency Virus 1 (HIV-1) is considered to be responsible for viral coreceptor tropism. gp120 interacts with the CD4 receptor of the host cell and subsequently V3 binds either CCR5 or CXCR4. Due to the fact that the CCR5 coreceptor is targeted by entry inhibitors, a reliable prediction of the coreceptor usage of HIV-1 is of great interest for antiretroviral therapy. Although several methods for the prediction of coreceptor tropism are available, almost all of them have been developed based on only subtype B sequences, and it has been shown in several studies that the prediction of non-B sequences, in particular subtype A sequences, are less reliable. Thus, the aim of the current study was to develop a reliable prediction model for subtype A viruses.
机译:刺激:人免疫缺陷病毒1(HIV-1)的GP120糖蛋白的V3环被认为是病毒核心冠状枢转的原因。 GP120与宿主细胞的CD4受体相互作用,随后V3结合CCR5或CXCR4。 由于CCR5团簇由进入抑制剂靶向,可靠地预测HIV-1的抗逆转录病毒治疗的兴趣。 虽然可获得有几种用于预测的核心体的方法,但几乎所有这些都是基于亚型B序列开发的,并且已经在几项研究中示出了,即非B序列的预测,特别是亚型序列。 不那么可靠。 因此,目前研究的目的是为亚型病毒开发可靠的预测模型。

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