期刊
JOURNAL OF VIROLOGY
卷 76, 期 13, 页码 6857-6862出版社
AMER SOC MICROBIOLOGY
DOI: 10.1128/JVI.76.13.6857-6862.2002
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资金
- NIAID NIH HHS [AI 42510, AI 28691, P30 AI028691] Funding Source: Medline
Nef enhances the serine phosphorylation of the human immunodeficiency virus type 1 matrix (MA) protein, which suggests that MA may be a functional target of Nef. Using mutants that remain infectious despite the absence of most or all of MA, we show in the present study that the ability of Nef to enhance virus infectivity is not compromised even if MA is entirely replaced by a heterologous lipid anchor.
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