Introduction of H2C2-type zinc-binding residues into HIV-2 Vpr increases its expression level
Author:
Affiliation:
1. Department of Bioorganic Medicinal Chemistry; Faculty of Life Sciences; Kumamoto University; Japan
2. Research Institute for Drug Discovery; School of Pharmacy; Kumamoto University; Japan
Funder
Japan Society for the Promotion of Science
Publisher
Wiley
Subject
General Biochemistry, Genetics and Molecular Biology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/2211-5463.12358/fullpdf
Reference38 articles.
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2. MDM2 is a novel E3 ligase for HIV-1 Vif;Izumi;Retrovirology,2009
3. Amino acid residues 88 and 89 in the central hydrophilic region of human immunodeficiency virus type 1 Vif are critical for viral infectivity by enhancing the steady-state expression of Vif;Fujita;J Virol,2003
4. Core binding factor beta protects HIV, type 1 accessory protein viral infectivity factor from MDM2-mediated degradation;Matsui;J Biol Chem,2016
5. High level expression of human immunodeficiency virus type-1 Vif inhibits viral infectivity by modulating proteolytic processing of the Gag precursor at the p2/nucleocapsid processing site;Akari;J Biol Chem,2004
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