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首页> 外文期刊>Evolutionary Bioinformatics >In Silico Analysis of Hepatitis B Virus Genotype D Subgenotype D1 Circulating in Pakistan, China, and India
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In Silico Analysis of Hepatitis B Virus Genotype D Subgenotype D1 Circulating in Pakistan, China, and India

机译:在巴基斯坦,中国和印度循环乙型肝炎病毒基因型D株D1的硅藻分析

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The focus of this study was the computational analysis of hepatitis B virus (HBV) genotype D subgenotype D1 in Pakistan, China, and India. In total, 54 complete genome sequences of HBV genotype D subgenotype D1 were downloaded from National Center for Biotechnology Information (NCBI). Of these, 6 complete genome sequences were from Pakistan, 14 were from China, and 34 were from India. Sequence alignment showed less than 4% divergence in these sequences. C and X genes showed divergence of less than 3%. Comparison over the S gene showed more than 97% similarity among the nucleotide sequences of genotype D subgenotype D1. The identity and similarity matrix of 54 nucleotide sequences of HBV genotype D subgenotype D1 from Pakistan, China, and India revealed more than 93% identity and 93% similarity. Phylogenetic analysis highlighted that complete genome isolates of HBV circulating in Pakistan had the closest evolutionary relationship with its neighboring countries China and India. China’s (HQ833466) and Pakistan’s (AB583680.1) isolates shared the same ancestor. Gene structure analysis showed that “P” gene exons were the longest, about three-fourth of the genome size, whereas gene “S” had the second longest coding regions with 2 exons and 1 intron. However, “C” and “X” genes had 1 smallest exon. X proteins had proven role in spreading of the HBV infection diseases. For HBx analysis, 1 X protein sequence of HBV genotype D subgenotype D1 belonging to each country was obtained. Homology models of the 3 X proteins generated using SWISS-MODEL revealed GMQE (Global Model Quality Estimation)?=?0.1. Global and local quality estimate scores including Z -scores for Qualitative Model Energy Analysis (QMEAN) C-beta, all-atom, solvation, and torsion energy scores were similar indicating good quality, accuracy, and reliability of the predicted models. Three-dimensional (3D) visualization showed similar structures and Ramachandran plots showed a high percentage of protein residues into the favorable region for X protein models.
机译:本研究的重点是乙型肝炎病毒(HBV)基因型D株D1在巴基斯坦,中国和印度的计算分析。总共,从国家生物技术信息(NCBI)下载了54个完整的HBV基因型D株D1。其中,来自巴基斯坦的6个完整的基因组序列,14名来自中国,34名来自印度。序列对准显示在这些序列中差异小于4%。 C和X基因显示出差异小于3%。对S基因的比较在基因型D株D1的核苷酸序列中显示出超过97%的相似性。巴基斯坦,中国和印度HBV基因型D株D1的54个核苷酸序列的同一性和相似性矩阵显示出超过93%的身份和93%相似性。系统发育分析强调,巴基斯坦循环的HBV完全基因组分离株与其邻国中国和印度具有最近的进化关系。中国(HQ833466)和巴基斯坦(AB583680.1)分享了同样的祖先。基因结构分析表明,“P”基因外显子是基因组大小的最长,约四分之三,而基因“S”具有第二最长的编码区,具有2个外显子和1个内含子。但是,“C”和“X”基因有1个最小的外显子。 X蛋白在蔓延的HBV感染疾病中证明了作用。对于HBX分析,获得了属于每个国家的HBV基因型D株D1的1 x蛋白质序列。使用瑞士模型产生的3 X蛋白的同源型模型显示GmQe(全球型号质量估计)?=?0.1。全局和地方优质估算分数包括用于定性模型能量分析(Qmean)C-Beta,全原子,求解和扭转能量分数的Z-κchores类似的表明预测模型的质量好,准确性和可靠性相似。三维(3D)可视化显示出类似的结构,并且Ramachandran图显示出高百分比的蛋白质残基进入X蛋白模型的有利区域。

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