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- Table of Contents
Facts about DNA dC->dU-editing enzyme APOBEC-3F.
Following the penetration of retroviral nucleocapsids into target cells of infection and the initiation of reverse transcription, it can cause the conversion of cytosine to uracil in the minus-sense single-strand viral DNA, resulting in G-to-A hypermutations in the following plus-strand viral DNA. The consequent detrimental levels of mutations in the proviral genome, along with a deamination- independent mechanism that works before the proviral integration, together exert efficient antiretroviral effects in infected cells.
Human | |
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Gene Name: | APOBEC3F |
Uniprot: | Q8IUX4 |
Entrez: | 200316 |
Belongs to: |
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cytidine and deoxycytidylate deaminase family |
apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like 3F; Apolipoprotein B mRNA-editing enzyme catalytic polypeptide-like 3F; ARP8; BK150C2.4.MRNA; DNA dC->dU-editing enzyme APOBEC-3F; EC 3.5.4; EC 3.5.4.-; induced upon T-cell activation; KA6; MGC74891
Mass (kDA):
45.02 kDA
Human | |
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Location: | 22q13.1 |
Sequence: | 22; NC_000022.11 (39019081..39055972) |
Widely expressed. Highly expressed in ovary.
Cytoplasm. Cytoplasm, P-body.
PMID: 11863358 by Jarmuz A., et al. An anthropoid-specific locus of orphan C to U RNA-editing enzymes on chromosome 22.
PMID: 12683974 by Wedekind J.E., et al. Messenger RNA editing in mammals: new members of the APOBEC family seeking roles in the family business.