• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

小鼠巨细胞病毒蛋白酶和衣壳装配蛋白基因的克隆与序列分析

Cloning and sequence analysis of murine cytomegalovirus protease and capsid assembly protein genes.

作者信息

Loutsch J M, Galvin N J, Bryant M L, Holwerda B C

机构信息

Department of Pathology, St. Louis University Health Sciences Center, MO 63104.

出版信息

Biochem Biophys Res Commun. 1994 Aug 30;203(1):472-8. doi: 10.1006/bbrc.1994.2206.

DOI:10.1006/bbrc.1994.2206
PMID:8074692
Abstract

The murine cytomegalovirus UL80 open reading frame was cloned and the predicted amino acid sequence compared with those from other herpesviruses. The open reading frame encodes a fused protease-capsid assembly protein precursor and maintains conserved features including the active site serine, conserved regions CD1 through CD5, the release and maturation sites, and a potential internal cleavage site within the protease. However, the murine cytomegalovirus protease differs in comparison with the other proteases because it contains a unique 15-16 amino acid insertion between CD3 and CD1. The assembly protein sequences are relatively divergent, but they can be arranged into groups defined by herpesvirus subfamily, with each group possessing a conserved motif at its carboxyl terminus.

摘要

克隆了鼠巨细胞病毒UL80开放阅读框,并将预测的氨基酸序列与其他疱疹病毒的序列进行了比较。该开放阅读框编码一种融合的蛋白酶-衣壳装配蛋白前体,并保留了保守特征,包括活性位点丝氨酸、CD1至CD5保守区域、释放和成熟位点以及蛋白酶内潜在的内部切割位点。然而,与其他蛋白酶相比,鼠巨细胞病毒蛋白酶有所不同,因为它在CD3和CD1之间包含一个独特的15-16个氨基酸的插入序列。装配蛋白序列相对分散,但可以根据疱疹病毒亚科分为不同的组,每组在其羧基末端具有一个保守基序。

相似文献

1
Cloning and sequence analysis of murine cytomegalovirus protease and capsid assembly protein genes.小鼠巨细胞病毒蛋白酶和衣壳装配蛋白基因的克隆与序列分析
Biochem Biophys Res Commun. 1994 Aug 30;203(1):472-8. doi: 10.1006/bbrc.1994.2206.
2
An insect picorna-like virus, Plautia stali intestine virus, has genes of capsid proteins in the 3' part of the genome.一种昆虫类微小核糖核酸病毒,斯氏负蝽肠道病毒,在基因组的3'部分具有衣壳蛋白基因。
Virology. 1998 Apr 25;244(1):50-8. doi: 10.1006/viro.1998.9094.
3
Complete nucleotide sequence of the chiba virus genome and functional expression of the 3C-like protease in Escherichia coli.千叶病毒基因组的完整核苷酸序列及3C样蛋白酶在大肠杆菌中的功能表达
Virology. 2000 Dec 20;278(2):490-500. doi: 10.1006/viro.2000.0672.
4
Sequence analysis and expression of the murine cytomegalovirus phosphoprotein pp50, a homolog of the human cytomegalovirus UL44 gene product.小鼠巨细胞病毒磷蛋白pp50(人巨细胞病毒UL44基因产物的同源物)的序列分析与表达
Virology. 1994 May 1;200(2):413-27. doi: 10.1006/viro.1994.1205.
5
Molecular characterization of the outer capsid spike protein (VP4) gene from human group C rotavirus.人C组轮状病毒外衣壳刺突蛋白(VP4)基因的分子特征分析
Virology. 1994 Oct;204(1):442-6. doi: 10.1006/viro.1994.1551.
6
Beet yellows closterovirus: complete genome structure and identification of a leader papain-like thiol protease.甜菜黄化线形病毒:完整基因组结构及一种先导类木瓜蛋白酶样巯基蛋白酶的鉴定
Virology. 1994 Jan;198(1):311-24. doi: 10.1006/viro.1994.1034.
7
Conservation of the segment 4 gene sequence and of a leucine zipper motif in VP4 among five US bluetongue viruses.美国五种蓝舌病毒中第4节段基因序列及VP4中亮氨酸拉链基序的保守性
Virology. 1993 Aug;195(2):772-9. doi: 10.1006/viro.1993.1429.
8
Sequence variability of the human cytomegalovirus UL141 Open Reading Frame in clinical strains.临床毒株中人巨细胞病毒UL141开放阅读框的序列变异性
Arch Virol. 2006 Apr;151(4):827-35. doi: 10.1007/s00705-005-0638-2. Epub 2005 Sep 30.
9
Proteolytic activity of human cytomegalovirus UL80 protease cleavage site mutants.人巨细胞病毒UL80蛋白酶切割位点突变体的蛋白水解活性
J Virol. 1994 Jun;68(6):3742-52. doi: 10.1128/JVI.68.6.3742-3752.1994.
10
Soybean dwarf luteovirus contains the third variant genome type in the luteovirus group.大豆矮缩黄症病毒含有黄症病毒属中的第三种变异基因组类型。
Virology. 1994 Feb;198(2):671-9. doi: 10.1006/viro.1994.1079.

引用本文的文献

1
Engineered RNase P Ribozymes Effectively Inhibit the Infection of Murine Cytomegalovirus in Animals.工程化 RNase P 核酶有效地抑制了动物体内鼠巨细胞病毒的感染。
Theranostics. 2018 Nov 9;8(20):5634-5644. doi: 10.7150/thno.27776. eCollection 2018.
2
Inhibition of Murine Cytomegalovirus Infection in Animals by RNase P-Associated External Guide Sequences.核糖核酸酶P相关的外部引导序列对动物体内小鼠巨细胞病毒感染的抑制作用
Mol Ther Nucleic Acids. 2017 Dec 15;9:322-332. doi: 10.1016/j.omtn.2017.10.007. Epub 2017 Oct 16.
3
Murine cytomegalovirus protein pM79 is a key regulator for viral late transcription.
鼠巨细胞病毒蛋白 pM79 是病毒晚期转录的关键调节因子。
J Virol. 2013 Aug;87(16):9135-47. doi: 10.1128/JVI.00688-13. Epub 2013 Jun 12.
4
Inactivation of enveloped virus by laser-driven protein aggregation.激光驱动蛋白聚集使包膜病毒失活。
J Biomed Opt. 2012 Dec;17(12):128002. doi: 10.1117/1.JBO.17.12.128002.
5
Temporal profiling of the coding and noncoding murine cytomegalovirus transcriptomes.鼠巨细胞病毒编码和非编码转录本的时间特征分析。
J Virol. 2011 Jun;85(12):6065-76. doi: 10.1128/JVI.02341-10. Epub 2011 Apr 6.
6
Effective inhibition in animals of viral pathogenesis by a ribozyme derived from RNase P catalytic RNA.一种源自核糖核酸酶P催化RNA的核酶对动物病毒致病机制的有效抑制作用。
Proc Natl Acad Sci U S A. 2008 Aug 5;105(31):10919-24. doi: 10.1073/pnas.0804922105. Epub 2008 Jul 28.
7
Identification of proteins associated with murine cytomegalovirus virions.与鼠巨细胞病毒病毒粒子相关的蛋白质的鉴定
J Virol. 2004 Oct;78(20):11187-97. doi: 10.1128/JVI.78.20.11187-11197.2004.
8
Generation of mutant murine cytomegalovirus strains from overlapping cosmid and plasmid clones.从重叠黏粒和质粒克隆中产生突变型鼠巨细胞病毒株。
J Virol. 2000 Oct;74(19):8972-9. doi: 10.1128/jvi.74.19.8972-8979.2000.
9
Cytomegalovirus assembly protein precursor and proteinase precursor contain two nuclear localization signals that mediate their own nuclear translocation and that of the major capsid protein.巨细胞病毒装配蛋白前体和蛋白酶前体含有两个核定位信号,这两个信号介导它们自身以及主要衣壳蛋白的核转运。
J Virol. 1998 Oct;72(10):7722-32. doi: 10.1128/JVI.72.10.7722-7732.1998.
10
Molecular and biotechnological aspects of microbial proteases.微生物蛋白酶的分子与生物技术方面
Microbiol Mol Biol Rev. 1998 Sep;62(3):597-635. doi: 10.1128/MMBR.62.3.597-635.1998.