COVID-2019 Genome Sequence Analysis: Phylogenetic Molecular Evolution and Docking of Structural Modelling of Receptor Binding Domain of S Protein in Active Site of ACE2

Abaysew Ayele, Baba Abdissa, Dereje Taye, Bereket Yemane, R. Majumdar
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引用次数: 1

Abstract

Meanwhile the outbreak of the Covid-19 since December, 2019 in China, it has killed more than a hundred thousand of people of all ages and sex across the globe in a short span of time. On the bases of this study the nearest family member of the virus and its receptor binding domain of S protein including its model structure and function of its active sites were naked through Multiple Sequence Alignment, modelling and molecular docking software accordingly its repository genome databases. The virus was genetically associated and molecular evolutionary related with (RaTG13) and it scores 96.12% homology with 99% query coverage followed by bat-SL-CoVZC45 and bat-SL-CoVZXC21 notch 89.12% and 88.65% respectively. However, SARS and MERS corona type virus those outbreak earlier respectively less likely family members of 2019-nCoV. Though the virus has a close genetic association with those previous SARS coronaviruses, and certainly the spike protein used as a binding receptor to fight against human receptor protein of ACE 2, but on the basis of FRODOC and HDOCK server analysis multi favorable active sites of S protein was discovered such GLN493 shown as a finest key in both model and possessed a unique traits on it resulting unexpected rate of transmission and number of people died while compared to the previous one. TYR500, ASN501, GLN498 and others residues preferably contemplate site also. In particular, the diversity of the virus in the world may be due to the genome structure of the virus and S gene changed over the time, across the world against to host of human genetic diversity, which may be more robust, and may be a new and unique feature. This is because it is characterized close to contact with distance divergence between wild type novel coronavirus which was risen from China against to the genomes from Lebanon, India, Italy, and USA and so on. Thus, the World Health Organization and its researchers should focus on immunologic research and effective drug and vaccine development that will help to address the epidemiology of the virus, which can provide a long-term solution.
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2019冠状病毒病基因组序列分析:系统发育分子进化与ACE2活性位点S蛋白受体结合结构域结构建模对接
与此同时,自2019年12月在中国爆发的新冠肺炎疫情,在短时间内已导致全球10万多名不同年龄和性别的人死亡。在此基础上,通过多序列比对、建模和分子对接软件,对该病毒最近的家族成员及其S蛋白受体结合域及其模型结构和活性位点的功能进行了裸露,从而获得了该病毒库基因组数据库。该病毒与(RaTG13)具有遗传相关性和分子进化相关性,同源性为96.12%,查询覆盖率为99%,其次是bat-SL-CoVZC45和bat-SL-CoVZXC21,同源性分别为89.12%和88.65%。然而,SARS和MERS冠状病毒这些爆发较早的病毒分别不太可能是2019-nCoV的家族成员。虽然病毒密切遗传协会与先前的SARS冠状病毒,当然突起蛋白作为绑定受体对抗的人类高手2受体蛋白质,但FRODOC和HDOCK服务器的基础上分析多优惠活动网站S蛋白被发现等GLN493显示最好的关键模型和具有独特的传播特征,产生意想不到的速度和时死亡的人数与前一个相比。TYR500、ASN501、GLN498等残基也优先考虑选址。特别是病毒在世界范围内的多样性,可能是由于病毒的基因组结构和S基因随着时间的推移发生了变化,世界各地对宿主人类的遗传多样性,这可能是更加健壮的,并可能是一个新的和独特的特征。这是因为从中国产生的新型冠状病毒野生型与黎巴嫩、印度、意大利、美国等国家的基因组存在距离差异,具有接近接触的特点。因此,世界卫生组织及其研究人员应该把重点放在免疫学研究和有效的药物和疫苗开发上,这将有助于解决病毒的流行病学问题,这可以提供一个长期的解决办法。
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