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Paradigm development: Comparative and predictive 3D modeling of HIV-1 Virion Infectivity Factor (vif)

机译:范式发展:HIV-1病毒粒子感染因子(vif)的比较和预测性3D建模

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摘要

Obtaining structural information about Vif is of interest for several reasons that include the study of the interaction of Vif with APOBEC3G, a resistance factor. Vif is a potential drug target and its function is essential for the HIV-1 infectivity process. To study Vif mechanism of action, we need to decipher its structure. Pivotal in this approach is the painstaking prediction of its protein structure. The three-dimensional (3D) crystal structure for Vif has not been established. In order to understand its mechanism of action, information on the structure of Vif is very much needed. Therefore we undertook this study based on the hypothesis that information from structurally homologous proteins can be used to predict the 3D structure of Vif by computer modeling and threading. As a result the structure of HIV-1 Vif has been modeled and deposited in the theoretical models section and accepted with the PDB code 1VZF. Here, we present the results of the comparative modeling strategy we used to predict the 3D structure of Vif.
机译:获得有关Vif的结构信息之所以引起人们的兴趣,有几个原因,其中包括研究Vif与抗药性因子APOBEC3G的相互作用。 Vif是潜在的药物靶标,其功能对于HIV-1感染过程至关重要。要研究Vif的作用机理,我们需要破译其结构。这种方法的关键是对其蛋白质结构的艰苦预测。 Vif的三维(3D)晶体结构尚未建立。为了了解其作用机理,非常需要有关Vif结构的信息。因此,我们基于以下假设进行了这项研究:来自结构同源蛋白的信息可用于通过计算机建模和线程预测Vif的3D结构。结果,对HIV-1 Vif的结构进行了建模,并将其存放在理论模型部分中,并被PDB代码1VZF接受。在这里,我们介绍了用于预测Vif的3D结构的比较建模策略的结果。

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