Casein kinase-2–mediated phosphorylation increases the SUMO-dependent activity of the cytomegalovirus transactivator IE2
Author:
Funder
Department of Biotechnology, Ministry of Science and Technology
Tata Institute of Fundamental Research
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference39 articles.
1. Structural analysis of the major immediate early gene of human cytomegalovirus;Stenberg;Microbiology,1984
2. Human cytomegalovirus with IE-2 (UL122) deleted fails to express early lytic genes;Marchini;J. Virol,2001
3. Inhibition of cellular DNA synthesis by the human cytomegalovirus IE86 protein is necessary for efficient virus replication;Petrik;J. Virol,2006
4. Human cytomegalovirus UL84 oligomerization and heterodimerization domains act as transdominant inhibitors of oriLyt-dependent DNA replication: evidence that IE2–L84 and UL84–UL84 interactions are required for lytic DNA replication;Colletti;J. Virol,2004
5. The human cytomegalovirus 80-kilodalton but not the 72-kilodalton immediate-early protein transactivates heterologous promoters in a TATA box-dependent mechanism and interacts directly with TFIID;Hagemeier;J. Virol,1992
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