• 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

腮腺炎病毒(宫原株)基质蛋白编码基因的核苷酸序列。

Nucleotide sequence of the gene encoding the matrix protein of mumps virus (Miyahara strain).

作者信息

Tanabayashi K, Takeuchi K, Hishiyama M, Yamada A, Sugiura A

机构信息

Department of Measles Virus, National Institute of Health, Tokyo, Japan.

出版信息

Virus Genes. 1990 Apr;3(4):361-5. doi: 10.1007/BF00569042.

DOI:10.1007/BF00569042
PMID:2349787
Abstract

The nucleotide sequence of the gene encoding the matrix (M) protein of mumps virus (MuV), Miyahara strain, has been determined from several overlapping cDNA clones. The M protein mRNA is 1248 nucleotides in length, exclusive of the poly(A) tail, and codes for a protein of 375 amino acids (Mr41,556). Comparison of the deduced amino acid sequence of the M protein of the Miyahara strain with that of the SBL-1 strain revealed that the M proteins of both strains are highly conserved. A significantly lower rate of nucleotide differences conducive to amino acid differences in the M gene compared with other genes appeared to indicate the importance of the conserved primary structure of the M protein for its function.

摘要

通过几个重叠的cDNA克隆,已确定了腮腺炎病毒(MuV)宫原株编码基质(M)蛋白的基因的核苷酸序列。M蛋白mRNA长度为1248个核苷酸,不包括聚腺苷酸尾,编码一个由375个氨基酸组成的蛋白质(Mr41,556)。将宫原株M蛋白的推导氨基酸序列与SBL-1株的进行比较,发现两株的M蛋白高度保守。与其他基因相比,M基因中导致氨基酸差异的核苷酸差异率显著较低,这似乎表明M蛋白保守的一级结构对其功能很重要。

相似文献

1
Nucleotide sequence of the gene encoding the matrix protein of mumps virus (Miyahara strain).腮腺炎病毒(宫原株)基质蛋白编码基因的核苷酸序列。
Virus Genes. 1990 Apr;3(4):361-5. doi: 10.1007/BF00569042.
2
Nucleotide sequence of the matrix, fusion and putative SH protein genes of mumps virus and their deduced amino acid sequences.腮腺炎病毒基质蛋白、融合蛋白及假定的SH蛋白基因的核苷酸序列及其推导的氨基酸序列。
Virus Res. 1989 Jan;12(1):61-75. doi: 10.1016/0168-1702(89)90054-3.
3
Complete nucleotide sequence of the matrix protein mRNA of mumps virus.腮腺炎病毒基质蛋白mRNA的完整核苷酸序列
Virology. 1989 Feb;168(2):426-8. doi: 10.1016/0042-6822(89)90288-2.
4
Molecular cloning and sequence analysis of the mumps virus gene encoding the L protein and the trailer sequence.编码L蛋白的腮腺炎病毒基因及拖尾序列的分子克隆与序列分析。
Virology. 1992 Jun;188(2):926-30. doi: 10.1016/0042-6822(92)90555-4.
5
Nucleotide sequence of the leader and nucleocapsid protein gene of mumps virus and epitope mapping with the in vitro expressed nucleocapsid protein.腮腺炎病毒前导区和核衣壳蛋白基因的核苷酸序列以及用体外表达的核衣壳蛋白进行表位作图
Virology. 1990 Jul;177(1):124-30. doi: 10.1016/0042-6822(90)90466-5.
6
The mumps virus nucleocapsid mRNA sequence and homology among the Paramyxoviridae proteins.腮腺炎病毒核衣壳mRNA序列及副黏病毒科蛋白质间的同源性。
Virus Res. 1989 Jan;12(1):77-86. doi: 10.1016/0168-1702(89)90055-5.
7
The mumps virus fusion protein mRNA sequence and homology among the paramyxoviridae proteins.腮腺炎病毒融合蛋白mRNA序列及副黏病毒科蛋白质间的同源性。
J Gen Virol. 1989 Apr;70 ( Pt 4):801-7. doi: 10.1099/0022-1317-70-4-801.
8
Molecular cloning and sequence analysis of the mumps virus gene encoding the P protein: mumps virus P gene is monocistronic.编码腮腺炎病毒P蛋白的基因的分子克隆及序列分析:腮腺炎病毒P基因是单顺反子的。
J Gen Virol. 1988 Aug;69 ( Pt 8):2043-9. doi: 10.1099/0022-1317-69-8-2043.
9
Molecular cloning and characterization of six genes, determination of gene order and intergenic sequences and leader sequence of mumps virus.腮腺炎病毒六个基因的分子克隆与特性分析、基因顺序及基因间序列和前导序列的确定
J Gen Virol. 1988 Nov;69 ( Pt 11):2893-900. doi: 10.1099/0022-1317-69-11-2893.
10
Complete nucleotide sequence of the hemagglutinin-neuraminidase (HN) mRNA of mumps virus and comparison of paramyxovirus HN proteins.腮腺炎病毒血凝素神经氨酸酶(HN)mRNA的完整核苷酸序列及副粘病毒HN蛋白的比较
Virus Res. 1989 Jan;12(1):87-96. doi: 10.1016/0168-1702(89)90056-7.

引用本文的文献

1
Function of small hydrophobic proteins of paramyxovirus.副粘病毒小疏水蛋白的功能。
J Virol. 2006 Feb;80(4):1700-9. doi: 10.1128/JVI.80.4.1700-1709.2006.
2
In vitro transcription and replication of the mumps virus genome.腮腺炎病毒基因组的体外转录与复制
Arch Virol. 1993;128(1-2):177-83. doi: 10.1007/BF01309799.

本文引用的文献

1
Compilation and analysis of sequences upstream from the translational start site in eukaryotic mRNAs.真核生物mRNA翻译起始位点上游序列的汇编与分析。
Nucleic Acids Res. 1984 Jan 25;12(2):857-72. doi: 10.1093/nar/12.2.857.
2
The reactions of monoclonal antibodies with structural proteins of mumps virus.单克隆抗体与腮腺炎病毒结构蛋白的反应。
J Immunol. 1984 May;132(5):2622-9.
3
Cloning and sequencing of the mumps virus fusion protein gene.腮腺炎病毒融合蛋白基因的克隆与测序
Virology. 1987 Aug;159(2):381-8. doi: 10.1016/0042-6822(87)90477-6.
4
Molecular cloning and sequence analysis of the mumps virus gene encoding the P protein: mumps virus P gene is monocistronic.编码腮腺炎病毒P蛋白的基因的分子克隆及序列分析:腮腺炎病毒P基因是单顺反子的。
J Gen Virol. 1988 Aug;69 ( Pt 8):2043-9. doi: 10.1099/0022-1317-69-8-2043.
5
Sequence determination of the mumps virus HN gene.腮腺炎病毒HN基因的序列测定
Virology. 1988 Jun;164(2):318-25. doi: 10.1016/0042-6822(88)90544-2.
6
Molecular cloning and characterization of six genes, determination of gene order and intergenic sequences and leader sequence of mumps virus.腮腺炎病毒六个基因的分子克隆与特性分析、基因顺序及基因间序列和前导序列的确定
J Gen Virol. 1988 Nov;69 ( Pt 11):2893-900. doi: 10.1099/0022-1317-69-11-2893.
7
The nucleotide sequence of the gene encoding the Newcastle disease virus membrane protein and comparisons of membrane protein sequences.编码新城疫病毒膜蛋白的基因的核苷酸序列及膜蛋白序列比较。
Virology. 1987 Feb;156(2):221-8. doi: 10.1016/0042-6822(87)90401-6.
8
mRNA sequence and deduced amino acid sequence of the mumps virus small hydrophobic protein gene.腮腺炎病毒小疏水蛋白基因的mRNA序列及推导的氨基酸序列。
J Virol. 1989 Mar;63(3):1413-5. doi: 10.1128/JVI.63.3.1413-1415.1989.
9
Complete nucleotide sequence of the matrix protein mRNA of mumps virus.腮腺炎病毒基质蛋白mRNA的完整核苷酸序列
Virology. 1989 Feb;168(2):426-8. doi: 10.1016/0042-6822(89)90288-2.
10
Sequence variation of the P gene among mumps virus strains.腮腺炎病毒株中P基因的序列变异
Virology. 1989 Sep;172(1):374-6. doi: 10.1016/0042-6822(89)90144-x.