a bioinformatics approach to the structure, function, and evolution of the nucleoprotein of the order mononegavirales生物信息学方法的结构、功能和演化mononegavirales核蛋白质的顺序.pdfVIP

a bioinformatics approach to the structure, function, and evolution of the nucleoprotein of the order mononegavirales生物信息学方法的结构、功能和演化mononegavirales核蛋白质的顺序.pdf

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a bioinformatics approach to the structure, function, and evolution of the nucleoprotein of the order mononegavirales生物信息学方法的结构、功能和演化mononegavirales核蛋白质的顺序

A Bioinformatics Approach to the Structure, Function, and Evolution of the Nucleoprotein of the Order Mononegavirales 1 2 1 Sean B. Cleveland *, John Davies , Marcella A. McClure 1 Department of Microbiology and the Center for Computational Biology, Montana State University, Bozeman, Montana, United States of America, 2 Molecular and Cellular Toxicology Section, Laboratory of Molecular Immunology, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, Maryland, United States of America Abstract The goal of this Bioinformatic study is to investigate sequence conservation in relation to evolutionary function/structure of the nucleoprotein of the order Mononegavirales. In the combined analysis of 63 representative nucleoprotein (N) sequences from four viral families (Bornaviridae, Filoviridae, Rhabdoviridae, and Paramyxoviridae) we predict the regions of protein disorder, intra-residue contact and co-evolving residues. Correlations between location and conservation of predicted regions illustrate a strong division between families while high- lighting conservation within individual families. These results suggest the conserved regions among the nucleoproteins, specifically within Rhabdoviridae and Paramyxoviradae, but also generally among all members of the order, reflect an evolutionary advantage in maintaining these sites for the viral nucleoprotein as part of the transcription/replication machinery. Results indicate conservation for disorder in the C-terminus region of the representative proteins that is important for interacting with the phosphoprotein and the large subunit polymerase during transcription and replication. Additionally, the C-terminus region of the protein

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