Abstract:
:The complete nucleotide sequences of the vesicular stomatitis virus mRNA's encoding the glycoprotein (G) and the matrix protein (M) have been determined from cDNA clones that contain the complete coding sequences from each mRNA. The G protein mRNA is 1,665 nucleotides long, excluding polyadenylic acid, and encodes a protein of 511 amino acids including a signal peptide of 16 amino acids. G protein contains two large hydrophobic domains, one in the signal peptide and the other in the transmembrane segment near the COOH terminus. Two sites of glycosylation are predicted at amino acid residues 178 and 335. The close correspondence of the positions of these sites with the reported timing of the addition of the two oligosaccharides during synthesis of G suggests that glycosylation occurs as soon as the appropriate asparagine residues traverse the membrane of the rough endoplasmic reticulum. The mRNA encoding the vesicular stomatitis virus M protein is 831 nucleotides long, excluding polyadenylic acid, and encodes a protein of 229 amino acids. The predicted M protein sequence does not contain any long hydrophobic or nonpolar domains that might promote membrane association. The protein is rich in basic amino acids and contains a highly basic amino terminal domain. Details of construction of the nearly full-length cDNA clones are presented.
journal_name
J Viroljournal_title
Journal of virologyauthors
Rose JK,Gallione CJdoi
10.1128/JVI.39.2.519-528.1981subject
Has Abstractpub_date
1981-08-01 00:00:00pages
519-28issue
2eissn
0022-538Xissn
1098-5514journal_volume
39pub_type
杂志文章abstract::The Kaposi's sarcoma-associated herpesvirus (KSHV) open reading frame 57 (ORF57)-encoded protein (Mta) is a multifunctional regulator of viral gene expression. ORF57 is essential for viral replication, so elucidation of its molecular mechanisms is important for understanding KSHV infection. ORF57 has been implicated i...
journal_title:Journal of virology
pub_type: 杂志文章
doi:10.1128/JVI.03459-12
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pub_type: 杂志文章
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pub_type: 杂志文章
doi:10.1128/JVI.6.4.445-454.1970
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journal_title:Journal of virology
pub_type: 杂志文章
doi:10.1128/JVI.64.2.686-690.1990
更新日期:1990-02-01 00:00:00
abstract::The foot-and-mouth disease virus (FMDV) capsid protein precursor, P1-2A, is cleaved by 3C(pro) to generate VP0, VP3, VP1, and the peptide 2A. The capsid proteins self-assemble into empty capsid particles or viruses which do not contain 2A. In a cell culture-adapted strain of FMDV (O1 Manisa [Lindholm]), three differen...
journal_title:Journal of virology
pub_type: 杂志文章
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abstract::A chimeric poliovirus type 1 (PV1) genome was constructed in which the 3D RNA polymerase (3D(pol)) coding sequences were replaced with those from coxsackievirus B3 (CVB3). No infectious virus was produced from HeLa cells transfected with the chimeric RNA. Processing of the PV1 capsid protein precursor was incomplete, ...
journal_title:Journal of virology
pub_type: 杂志文章
doi:10.1128/JVI.73.11.9413-9421.1999
更新日期:1999-11-01 00:00:00
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journal_title:Journal of virology
pub_type: 杂志文章
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更新日期:2020-02-28 00:00:00
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journal_title:Journal of virology
pub_type: 杂志文章
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journal_title:Journal of virology
pub_type: 杂志文章
doi:10.1128/JVI.73.5.4136-4144.1999
更新日期:1999-05-01 00:00:00
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journal_title:Journal of virology
pub_type: 杂志文章
doi:10.1128/JVI.47.1.146-150.1983
更新日期:1983-07-01 00:00:00
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journal_title:Journal of virology
pub_type: 杂志文章
doi:10.1128/JVI.62.4.1194-1202.1988
更新日期:1988-04-01 00:00:00
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journal_title:Journal of virology
pub_type: 杂志文章
doi:10.1128/jvi.76.7.3257-3266.2002
更新日期:2002-04-01 00:00:00
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journal_title:Journal of virology
pub_type: 杂志文章
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更新日期:2012-04-01 00:00:00
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journal_title:Journal of virology
pub_type: 杂志文章
doi:10.1128/JVI.16.4.859-866.1975
更新日期:1975-10-01 00:00:00
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journal_title:Journal of virology
pub_type: 杂志文章
doi:10.1128/JVI.69.7.4440-4452.1995
更新日期:1995-07-01 00:00:00
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journal_title:Journal of virology
pub_type: 杂志文章
doi:10.1128/JVI.02483-16
更新日期:2017-04-13 00:00:00
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journal_title:Journal of virology
pub_type: 杂志文章
doi:10.1128/JVI.55.1.60-66.1985
更新日期:1985-07-01 00:00:00
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journal_title:Journal of virology
pub_type: 杂志文章
doi:10.1128/JVI.40.1.276-284.1981
更新日期:1981-10-01 00:00:00
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journal_title:Journal of virology
pub_type: 杂志文章
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更新日期:2016-08-26 00:00:00
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pub_type: 杂志文章
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更新日期:1997-05-01 00:00:00
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journal_title:Journal of virology
pub_type: 杂志文章
doi:10.1128/JVI.62.8.3040-3042.1988
更新日期:1988-08-01 00:00:00
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journal_title:Journal of virology
pub_type: 杂志文章
doi:10.1128/JVI.39.3.758-776.1981
更新日期:1981-09-01 00:00:00
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journal_title:Journal of virology
pub_type: 杂志文章
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更新日期:2013-03-01 00:00:00
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journal_title:Journal of virology
pub_type: 杂志文章
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更新日期:2006-06-01 00:00:00
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journal_title:Journal of virology
pub_type: 杂志文章
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更新日期:1997-10-01 00:00:00
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journal_title:Journal of virology
pub_type: 杂志文章
doi:10.1128/JVI.79.14.9254-9269.2005
更新日期:2005-07-01 00:00:00
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journal_title:Journal of virology
pub_type: 杂志文章
doi:10.1128/JVI.02295-07
更新日期:2008-02-01 00:00:00
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journal_title:Journal of virology
pub_type: 杂志文章
doi:10.1128/JVI.02343-08
更新日期:2009-05-01 00:00:00
abstract::HeLa cell nuclei, isolated 17 h after infection with human adenovirus type 2 (Ad2), were treated with 200 mM ammonium sulfate. The extract (S200 fraction) contained 50 to 70% of the nonintegrated Ad2 DNA, which was in the form of nucleoprotein complexes. These complexes contained native, intact Ad2 DNA (with the excep...
journal_title:Journal of virology
pub_type: 杂志文章
doi:10.1128/JVI.19.1.61-81.1976
更新日期:1976-07-01 00:00:00