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2
Conformational changes accompany activation of reovirus RNA-dependent RNA transcription.呼肠孤病毒RNA依赖性RNA转录激活伴随着构象变化。
J Struct Biol. 2008 May;162(2):277-89. doi: 10.1016/j.jsb.2008.01.006. Epub 2008 Jan 26.
3
MEGA4: Molecular Evolutionary Genetics Analysis (MEGA) software version 4.0.MEGA4:分子进化遗传学分析(MEGA)软件版本4.0。
Mol Biol Evol. 2007 Aug;24(8):1596-9. doi: 10.1093/molbev/msm092. Epub 2007 May 7.
4
Genetic variation of the lambdaA and lambdaC protein encoding genes of avian reoviruses.禽呼肠孤病毒λA和λC蛋白编码基因的遗传变异
Res Vet Sci. 2007 Dec;83(3):394-402. doi: 10.1016/j.rvsc.2007.01.002. Epub 2007 Mar 2.
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Sequences of avian reovirus M1, M2 and M3 genes and predicted structure/function of the encoded mu proteins.禽呼肠孤病毒M1、M2和M3基因序列以及编码的μ蛋白的预测结构/功能
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Structure of avian orthoreovirus virion by electron cryomicroscopy and image reconstruction.通过电子冷冻显微镜和图像重建解析禽正呼肠孤病毒病毒粒子的结构
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Mutations in the putative zinc-binding motif of UL52 demonstrate a complex interdependence between the UL5 and UL52 subunits of the human herpes simplex virus type 1 helicase/primase complex.单纯疱疹病毒1型解旋酶/引发酶复合体的UL5和UL52亚基之间,UL52假定锌结合基序中的突变表现出复杂的相互依赖性。
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Phylogenetic analysis of the sigma 2 protein gene of turkey reoviruses.火鸡呼肠孤病毒σ2蛋白基因的系统发育分析
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正呼肠孤病毒主要核心蛋白的保守结构/功能

Conserved structure/function of the orthoreovirus major core proteins.

作者信息

Xu Wanhong, Coombs Kevin M

机构信息

Department of Medical Microbiology and Infectious Diseases, University of Manitoba, Winnipeg, Manitoba, Canada.

出版信息

Virus Res. 2009 Sep;144(1-2):44-57. doi: 10.1016/j.virusres.2009.03.020. Epub 2009 Apr 7.

DOI:10.1016/j.virusres.2009.03.020
PMID:19720241
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5123878/
Abstract

Orthoreoviruses are infectious agents with genomes of 10 segments of double-stranded RNA. Detailed molecular information is available for all 10 segments of several mammalian orthoreoviruses, and for most segments of several avian orthoreoviruses (ARV). We, and others, have reported sequences of the L2, all S-class, and all M-class genome segments of two different avian reoviruses, strains ARV138 and ARV176. We here determined L1 and L3 genome segment nucleotide sequences for both strains to complete full genome characterization of this orthoreovirus subgroup. ARV L1 segments were 3958 nucleotides long and encode lambda A major core shell proteins of 1293 residues. L3 segments were 3907 nucleotides long and encode lambda C core turret proteins of 1285 residues. These newly determined ARV segments were aligned with all currently available homologous mammalian reovirus (MRV) and aquareovirus (AqRV) genome segments. Identical and conserved amino acid residues amongst these diverse groups were mapped into known mammalian reovirus lambda 1 core shell and lambda 2 core turret proteins to predict conserved structure/function domains. Most identical and conserved residues were located near predicted catalytic domains in the lambda-class guanylyltransferase, and forming patches that traverse the lambda-class core shell, which may contribute to the unusual RNA transcription processes in this group of viruses.

摘要

正呼肠孤病毒是一种感染性因子,其基因组由10个双链RNA片段组成。关于几种哺乳动物正呼肠孤病毒的所有10个片段以及几种禽正呼肠孤病毒(ARV)的大多数片段,都有详细的分子信息。我们和其他人已经报道了两种不同禽呼肠孤病毒ARV138和ARV176的L2、所有S类和所有M类基因组片段的序列。我们在此确定了这两种病毒株的L1和L3基因组片段核苷酸序列,以完成该正呼肠孤病毒亚组的全基因组特征分析。ARV的L1片段长3958个核苷酸,编码含1293个残基的λA主要核心壳蛋白。L3片段长3907个核苷酸,编码含1285个残基的λC核心炮塔蛋白。这些新确定的ARV片段与所有目前可用的同源哺乳动物呼肠孤病毒(MRV)和水生呼肠孤病毒(AqRV)基因组片段进行了比对。将这些不同病毒组中相同和保守的氨基酸残基定位到已知的哺乳动物呼肠孤病毒λ1核心壳蛋白和λ2核心炮塔蛋白中,以预测保守的结构/功能域。大多数相同和保守的残基位于λ类鸟苷酸转移酶预测的催化结构域附近,并形成贯穿λ类核心壳的斑块,这可能有助于该组病毒中不同寻常的RNA转录过程。