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首页> 外文期刊>FEBS Letters >Prediction of proteinase cleavage sites in polyproteins of coronaviruses and its applications in analyzing SARS‐CoV genomes
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Prediction of proteinase cleavage sites in polyproteins of coronaviruses and its applications in analyzing SARS‐CoV genomes

机译:冠状病毒多蛋白蛋白酶切割位点的预测及其在SARS-CoV基因组分析中的应用

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摘要

>Recently, we have developed a coronavirus-specific gene-finding system, ZCURVE_CoV 1.0. In this paper, the system is further improved by taking the prediction of cleavage sites of viral proteinases in polyproteins into account. The cleavage sites of the 3C-like proteinase and papain-like proteinase are highly conserved. Based on the method of traditional positional weight matrix trained by the peptides around cleavage sites, the present method also sufficiently considers the length conservation of non-structural proteins cleaved by the 3C-like proteinase and papain-like proteinase to reduce the false positive prediction rate. The improved system, ZCURVE_CoV 2.0, has been run for each of the 24 completely sequenced coronavirus genomes in GenBank. Consequently, all the non-structural proteins in the 24 genomes are accurately predicted. Compared with known annotations, the performance of the present method is satisfactory. The software ZCURVE_CoV 2.0 is freely available at href="http://tubic.tju.edu.cn/sars/" title="Link to external resource: http://tubic.tju.edu.cn/sars/" target="_blank">http://tubic.tju.edu.cn/sars/.
机译:>最近,我们开发了一种冠状病毒特异性基因发现系统ZCURVE_CoV 1.0。在本文中,该系统通过考虑对多蛋白中病毒蛋白酶切割位点的预测而得到进一步改进。 3C样蛋白酶和木瓜蛋白酶样蛋白酶的切割位点是高度保守的。基于传统的位置权重矩阵由裂解位点周围肽段训练的方法,本方法还充分考虑了3C样蛋白酶和木瓜蛋白酶样裂解的非结构蛋白的长度保守性,以降低假阳性预测率。针对GenBank中24个完全测序的冠状病毒基因组中的每一个,都运行了改进的系统ZCURVE_CoV 2.0。因此,可以准确预测24个基因组中的所有非结构蛋白。与已知注释相比,本方法的性能令人满意。 ZCURVE_CoV 2.0软件可在href =“ http://tubic.tju.edu.cn/sars/” title =“链接到外部资源:http://tubic.tju.edu.cn/sars/上免费获得。 “ target =” _blank“> http://tubic.tju.edu.cn/sars/ 。

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