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Varicella-zoster virus ORF47 protein serine kinase: Characterization of a cloned, biologically active phosphotransferase and two viral substrates, ORF62 and ORF63
被引:62
作者:

Kenyon, TK
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机构: Univ Iowa, Dept Microbiol, Iowa City, IA 52242 USA

Lynch, J
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机构: Univ Iowa, Dept Microbiol, Iowa City, IA 52242 USA

Hay, J
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机构: Univ Iowa, Dept Microbiol, Iowa City, IA 52242 USA

Ruyechan, W
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机构: Univ Iowa, Dept Microbiol, Iowa City, IA 52242 USA

Grose, C
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机构: Univ Iowa, Dept Microbiol, Iowa City, IA 52242 USA
机构:
[1] Univ Iowa, Dept Microbiol, Iowa City, IA 52242 USA
[2] Univ Iowa, Dept Pediat, Iowa City, IA 52242 USA
[3] SUNY Buffalo, Dept Microbiol, Buffalo, NY 14260 USA
关键词:
D O I:
10.1128/JVI.75.18.8854-8858.2001
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Varicella-zoster virus (VZV) codes for a protein serine kinase called ORF47; the herpes simplex virus (HSV) homolog is UL13. No recombinant alphaherpesvirus serine kinase has been biologically active in vitro. We discovered that preservation of the intrinsic kinase activity of recombinant VZV ORF47 required unusually stringent in vitro conditions, including physiological concentrations of polyamines. In this assay, ORF47 phosphorylated two VZV regulatory proteins: the ORF62 protein (homolog of HSV ICP4) and the ORF63 protein (homolog of HSV ICP22). Of interest, ORF47 kinase also coprecipitated ORF63 protein from the kinase assay supernatant.
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页码:8854 / 8858
页数:5
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