RNF7
Gene Ontology Biological Process
Gene Ontology Molecular Function
Gene Ontology Cellular Component
APOBEC3F
Gene Ontology Biological Process
- DNA cytosine deamination [IDA]
- DNA demethylation [IDA]
- base conversion or substitution editing [IDA]
- cytidine deamination [IDA]
- defense response to virus [IDA]
- innate immune response [IDA]
- negative regulation of single stranded viral RNA replication via double stranded DNA intermediate [IDA]
- negative regulation of transposition [IDA]
- negative regulation of viral genome replication [IDA]
- negative regulation of viral process [IDA]
- positive regulation of defense response to virus by host [IDA]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
Biochemical Activity (Ubiquitination)
An interaction is inferred from the biochemical effect of one protein upon another, for example, GTP-GDP exchange activity or phosphorylation of a substrate by a kinase. The bait protein executes the activity on the substrate hit protein. A Modification value is recorded for interactions of this type with the possible values Phosphorylation, Ubiquitination, Sumoylation, Dephosphorylation, Methylation, Prenylation, Acetylation, Deubiquitination, Proteolytic Processing, Glucosylation, Nedd(Rub1)ylation, Deacetylation, No Modification, Demethylation.
Publication
ARIH2 Is a Vif-Dependent Regulator of CUL5-Mediated APOBEC3G Degradation in HIV Infection.
The Cullin-RING E3 ligase (CRL) family is commonly hijacked by pathogens to redirect the host ubiquitin proteasome machinery to specific targets. During HIV infection, CRL5 is hijacked by HIV Vif to target viral restriction factors of the APOBEC3 family for ubiquitination and degradation. Here, using a quantitative proteomics approach, we identify the E3 ligase ARIH2 as a regulator of CRL5-mediated ... [more]
Throughput
- Low Throughput
Additional Notes
- E2: UBE2R1.
- Note: Substrate adapter for CRL5 implicated to be the Vif(HIV)-CBFB-ELOBC complex formed by Vif to hijack CRL5
Curated By
- BioGRID