Multifaceted HIV‐1 Vif interactions with human E3 ubiquitin ligase and APOBEC3s
Author:
Affiliation:
1. Department of Molecular Biophysics and Biochemistry Yale University New Haven CT USA
Funder
NIH Clinical Center
Publisher
Wiley
Subject
Cell Biology,Molecular Biology,Biochemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/febs.15550
Reference102 articles.
1. Broad antiretroviral defence by human APOBEC3G through lethal editing of nascent reverse transcripts
2. The cytidine deaminase CEM15 induces hypermutation in newly synthesized HIV-1 DNA
3. Hypermutation of HIV-1 DNA in the Absence of the Vif Protein
4. APOBEC3F Can Inhibit the Accumulation of HIV-1 Reverse Transcription Products in the Absence of Hypermutation
5. APOBEC3G Inhibits DNA Strand Transfer during HIV-1 Reverse Transcription
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1. Structural insights into PPP2R5A degradation by HIV-1 Vif;Nature Structural & Molecular Biology;2024-05-24
2. Variability in HIV-1 Transmitted/Founder Virus Susceptibility to Combined APOBEC3F and APOBEC3G Host Restriction;2024-01-26
3. Stability of APOBEC3F in the Presence of the APOBEC3 Antagonist HIV-1 Vif Increases at the Expense of Co-Expressed APOBEC3H Haplotype I;Viruses;2023-02-07
4. Structural basis for recruitment of host CypA and E3 ubiquitin ligase by maedi-visna virus Vif;Science Advances;2023-01-13
5. Evidence linking APOBEC3B genesis and evolution of innate immune antagonism by gamma-herpesvirus ribonucleotide reductases;eLife;2022-12-02
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