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- Table of Contents
Facts about DNA dC->dU-editing enzyme APOBEC-3G.
The consequent detrimental levels of mutations in the proviral genome, together with a deamination- independent mechanism which operates before the proviral integration, together exert effective antiretroviral effects in infected cells. Selectively targets single-stranded DNA and does not deaminate double-stranded DNA or single-or double- stranded RNA.
| Human | |
|---|---|
| Gene Name: | APOBEC3G |
| Uniprot: | Q9HC16 |
| Entrez: | 60489 |

| Belongs to: |
|---|
| cytidine and deoxycytidylate deaminase family |

APOBEC-related cytidine deaminase; APOBEC-related protein 9; APOBEC-related protein; apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like 3G; ARCD; ARP-9; bK150C2.7; CEM-15; CEM15ARP9; dJ494G10.1; DNA dC->dU-editing enzyme APOBEC-3G; EC 3.5.4; EC 3.5.4.-; EC 3.5.4.5; FLJ12740DNA dC->dU editing enzyme; MDS019; phorbolin-like protein MDS019
Mass (kDA):
46.408 kDA

| Human | |
|---|---|
| Location: | 22q13.1 |
| Sequence: | 22; NC_000022.11 (39077005..39087743) |
Expressed in spleen, testes, ovary and peripheral blood leukocytes and CD4+ lymphocytes. Also expressed in non-permissive peripheral blood mononuclear cells, and several tumor cell lines; no expression detected in permissive lymphoid and non-lymphoid cell lines. Exists only in the LMM form in peripheral blood-derived resting CD4 T-cells and monocytes, both of which are refractory to HIV-1 infection. LMM is converted to a HMM complex when resting CD4 T-cells are activated or when monocytes are induced to differentiate into macrophages. This change correlates with increased susceptibility of these cells to HIV-1 infection.
Cytoplasm. Nucleus. Cytoplasm, P-body. Mainly cytoplasmic. Small amount are found in the nucleus. During HIV-1 infection, virion-encapsidated in absence of HIV-1 VIF.





PMID: 14557625 by Kao S., et al. The human immunodeficiency virus type 1 Vif protein reduces intracellular expression and inhibits packaging of APOBEC3G (CEM15), a cellular inhibitor of virus infectivity.
PMID: 11863358 by Jarmuz A., et al. An anthropoid-specific locus of orphan C to U RNA-editing enzymes on chromosome 22.