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Large-scale analysis of influenza A virus nucleoprotein sequence conservation reveals potential drug-target sites

机译:流感的大规模分析病毒核蛋白序列保护揭示了潜在的药物靶位位点

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The nucleoprotein (NP) of the influenza A virus encapsidates the viral RNA and participates in the infectious life cycle of the virus. The aims of this study were to find the degree of conservation of NP among all virus subtypes and hosts and to identify conserved binding sites, which may be utilised as potential drug target sites. The analysis of conservation based on 4430 amino acid sequences identified high conservation in known functional regions as well as novel highly conserved sites. Highly variable clusters identified on the surface of NP may be associated with adaptation to different hosts and avoidance of the host immune defence. Ligand binding potential overlapping with high conservation was found in the tail-loop binding site and near the putative RNA binding region. The results provide the basis for developing antivirals that may be universally effective and have a reduced potential to induce resistance through mutations.
机译:流感病毒的核蛋白(NP)封装病毒RNA并参与病毒的传染性生命周期。 本研究的目的是在所有病毒亚型和宿主中寻找NP的守恒程度,并鉴定保守的结合位点,其可用于潜在的药物靶位位点。 基于4430氨基酸序列的守恒分析确定了已知的功能区的高保守以及新的高度保守场所。 在NP的表面上鉴定的高度可变簇可以与适应不同宿主的适应性和避免宿主免疫防御。 在尾环结合位点和推定的RNA结合区域附近发现具有高保守的配体结合潜在重叠。 结果为开发可能是普遍有效的抗病毒的基础,并且通过突变具有降低的耐受抗性的可能性。

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