Literature DB >> 1662698

The most abundant protein in bovine herpes 1 virions is a homologue of herpes simplex virus type 1 UL47.

D E Carpenter1, V Misra.   

Abstract

The bovine herpesvirus type 1 (BHV-1) protein VP8 is present, in large amounts, in the tegument of virions. As a preliminary step towards determining the function of VP8 and the biological relevance for its abundant presence, we describe the mapping of the location of its gene and determination of its nucleotide sequence. The gene for VP8 was located between 0.088 and 0.108 map units on the BHV-1 genome and contained a 2226 bp reading frame encoding a 742 amino acid protein. The protein, produced in vitro by transcribing and translating the reading frame, was precipitated by monoclonal antibodies and polyclonal serum directed against VP8. The primary structure of VP8 showed considerable homology with the product of the UL47 reading frame of herpes simplex virus type 1.

Entities:  

Mesh:

Substances:

Year:  1991        PMID: 1662698     DOI: 10.1099/0022-1317-72-12-3077

Source DB:  PubMed          Journal:  J Gen Virol        ISSN: 0022-1317            Impact factor:   3.891


  19 in total

1.  Identification and functional characterization of the Varicella zoster virus ORF11 gene product.

Authors:  Xibing Che; Stefan L Oliver; Marvin H Sommer; Jaya Rajamani; Mike Reichelt; Ann M Arvin
Journal:  Virology       Date:  2011-01-26       Impact factor: 3.616

2.  Nucleocytoplasmic shuttling of bovine herpesvirus 1 UL47 protein in infected cells.

Authors:  Janneke Verhagen; Ian Hutchinson; Gillian Elliott
Journal:  J Virol       Date:  2006-01       Impact factor: 5.103

3.  Characterization of a CRM1-dependent nuclear export signal in the C terminus of herpes simplex virus type 1 tegument protein UL47.

Authors:  Paul Williams; Janneke Verhagen; Gillian Elliott
Journal:  J Virol       Date:  2008-08-20       Impact factor: 5.103

4.  US3 Kinase-Mediated Phosphorylation of Tegument Protein VP8 Plays a Critical Role in the Cellular Localization of VP8 and Its Effect on the Lipid Metabolism of Bovine Herpesvirus 1-Infected Cells.

Authors:  Kuan Zhang; Tara Donovan; Soumya Sucharita; Robert Brownlie; Marlene Snider; Suresh K Tikoo; Sylvia van Drunen Littel-van den Hurk
Journal:  J Virol       Date:  2019-03-05       Impact factor: 5.103

5.  Characterization of the nuclear localization and nuclear export signals of bovine herpesvirus 1 VP22.

Authors:  Chunfu Zheng; Robert Brownlie; Lorne A Babiuk; Sylvia van Drunen Littel-van den Hurk
Journal:  J Virol       Date:  2005-09       Impact factor: 5.103

6.  Identification and characterization of the pseudorabies virus tegument proteins UL46 and UL47: role for UL47 in virion morphogenesis in the cytoplasm.

Authors:  Martina Kopp; Barbara G Klupp; Harald Granzow; Walter Fuchs; Thomas C Mettenleiter
Journal:  J Virol       Date:  2002-09       Impact factor: 5.103

7.  Protein and DNA elements involved in transactivation of the promoter of the bovine herpesvirus (BHV) 1 IE-1 transcription unit by the BHV alpha gene trans-inducing factor.

Authors:  V Misra; A C Bratanich; D Carpenter; P O'Hare
Journal:  J Virol       Date:  1994-08       Impact factor: 5.103

8.  A UL47 gene deletion mutant of bovine herpesvirus type 1 exhibits impaired growth in cell culture and lack of virulence in cattle.

Authors:  Vladislav A Lobanov; Sheryl L Maher-Sturgess; Marlene G Snider; Zoe Lawman; Lorne A Babiuk; Sylvia van Drunen Littel-van den Hurk
Journal:  J Virol       Date:  2010-01       Impact factor: 5.103

9.  Herpes simplex virus type 1 UL46 and UL47 deletion mutants lack VP11 and VP12 or VP13 and VP14, respectively, and exhibit altered viral thymidine kinase expression.

Authors:  Y Zhang; J L McKnight
Journal:  J Virol       Date:  1993-03       Impact factor: 5.103

10.  The dominant phosphoprotein pp65 (UL83) of human cytomegalovirus is dispensable for growth in cell culture.

Authors:  S Schmolke; H F Kern; P Drescher; G Jahn; B Plachter
Journal:  J Virol       Date:  1995-10       Impact factor: 5.103

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.