Apolipoprotein B MRNA Editing Enzyme, Catalytic Polypeptide-Like 3G Proteins (APOBEC3G)

APOBEC3G is a member of the cytidine deaminase gene family. Additionally we are shipping APOBEC3G Antibodies (182) and and many more products for this protein.

list all proteins Gene Name GeneID UniProt
APOBEC3G 60489 Q9HC16
APOBEC3G 449577  
APOBEC3G    
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Top APOBEC3G Proteins at antibodies-online.com

Showing 8 out of 9 products:

Catalog No. Origin Source Conjugate Images Quantity Delivery Price Details
Insect Cells Human His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg 50 Days
$6,749.58
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Wheat germ Human GST tag 10 μg 11 to 12 Days
$414.29
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HEK-293 Cells Human Myc-DYKDDDDK Tag Validation with Western Blot 20 μg 11 Days
$888.80
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Yeast Rhesus Monkey His tag   1 mg 60 to 71 Days
$3,014.00
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Yeast REACT_Green monkey His tag   1 mg 60 to 71 Days
$3,036.00
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Yeast REACT_Woolly monkey His tag   1 mg 60 to 71 Days
$3,048.83
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Yeast Chimpanzee His tag   1 mg 60 to 71 Days
$3,058.00
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Yeast Cynomolgus His tag   1 mg 60 to 71 Days
$3,058.00
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APOBEC3G Proteins by Origin and Source

Origin Expressed in Conjugate
Human , ,
, ,
Chimpanzee

Cynomolgus

More Proteins for Apolipoprotein B MRNA Editing Enzyme, Catalytic Polypeptide-Like 3G (APOBEC3G) Interaction Partners

Human Apolipoprotein B MRNA Editing Enzyme, Catalytic Polypeptide-Like 3G (APOBEC3G) interaction partners

  1. This study presents structural investigations on the interactions between cytidine deaminase APOBEC3G and DNA. The deamination of two cytidines by A3G is only exerted in single-stranded DNA with the target motif 5'-CCC-3'. The substrate DNA binds to A3G catalytic domain (A3G-CD2) in CCC and TCC modes.

  2. Thus it was concluded that APOBEC3G rs8177832 AA genotype contributes in genetic predisposition to HIV-1 infection in Pakistani population.

  3. APOBEC3G inhibited the 5'UTR activity of Enterovirus 71 by competitively binding to the 5'UTR through its nucleic acid binding activity.

  4. It is the major target for C-to-T substitutions in the HPV genomes.

  5. induces site-specific C-to-U RNA editing in natural killer cells, lymphoma cell lines, and, to a lesser extent, CD8-positive T cells upon cellular crowding and hypoxia

  6. This is first report from India which represented the occurrence of APOBEC3G polymorphisms in HIV patients and its association with HIV acquisition and disease progression.

  7. It has been shown that HCMV has evolved mutational robustness against IFN-beta by limiting the presence of APOBEC3G hot spots in essential open reading frames of its genome.

  8. We found that A3G regulates the expression of several cellular proteins, which influences the capacity of the host cell to replicate measles virus.

  9. Low APOBEC3G expression is associated with HIV-1 replication.

  10. study concludes that hA3G may restrict porcine endogenous retrovirus (PERV) by both deamination-dependent mechanisms and inhibition of DNA strand transfer during PERV reverse transcription.

  11. two stem-loop structures within the 5'-untranslated region of A3G mRNA are crucial for translation inhibition by Vif in HIV-infected cells, and most Vif alleles neutralize A3G translation efficiently

  12. DNA substrate selection by APOBEC3G

  13. these findings indicate that A3G is associated with cervical intraepithelial neoplasia , suggesting its important roles in human papillomavirus-induced pathophysiological processes such as cervical intraepithelial neoplasia progression and viral elimination

  14. These findings report genetic variants possibly associated with susceptibility to HIV-1 infection (CUL5 rs11212495, rs7103534, rs7117111) and partial viral load control (APOBEC3G rs2294367).

  15. analysis indicated that IL-6 also increased the expression of A3B through JAK1/STAT3 signaling pathway, which formed a positive feedback to maintain the continuous expression of A3B and IL-6, and thereby promoted the prolonged non-resolving inflammation

  16. The goal of this methods review is through example of our research on APOBEC3G, describe the application of cross-linking methods to characterize and quantify macromolecular interactions and their functional implications

  17. Our results identify APOBEC3G as a new candidate biomarker for tumor-infiltrating T lymphocytes and favorable prognoses for HGSOC.

  18. propose that APOBEC3G has the ability to induce T cell plasticity and modulate immune response.

  19. The results show for the first time the nuclear translocation of A3G in activated-proliferating CD4(+) T cells.

  20. Mouse mammary tumour virus only moderately susceptible to inhibition by the human APOBEC3G.

Rhesus Monkey Apolipoprotein B MRNA Editing Enzyme, Catalytic Polypeptide-Like 3G (APOBEC3G) interaction partners

  1. The authors found one novel transcript and 10 genetic variants of APOBEC3G, among them, L71R showed resistance to HIV-2-Vif-mediated APOBEC3G degradation, strongly suggesting that L71R could play an important role in the host's antiviral defense.

  2. APOBEC3G polymorphism as a selective barrier to cross-species transmission and emergence of pathogenic SIV and AIDS in a primate host.

  3. The arginine at position 14 of the SIV Vif is a critical residue for virus restriction by rhA3D, rhA3G and rhA3H.

  4. APOBEC3F/G-specific responses in HIV-1-infected rhesus macaques are CD8+ T cell mediated.

  5. Vif proteins of human and simian immunodeficiency viruses require cellular CBFbeta to degrade APOBEC3G.

  6. simian immunodeficiency virus (SIV) Vif binds to and requires CBF-beta to degrade rhesus macaque APOBEC3G

  7. Increased APOBEC3G and APOBEC3F expression is associated with low viral load and prolonged survival in simian immunodeficiency virus infected rhesus monkeys.

  8. APOBEC3 proteins restrict xenotropic murine leukemia virus-related virus infections in a Macaca mulatta model.

  9. Alteration of the conserved sequence at positions 14 to 17 from DRMR to SERQ, which is the sequence in AGM Vif, caused HIV-1 Vif to functionally interact with rhAPOBEC3G and agmAPOBEC3G

  10. Upregulation of APOBEC3G may restrict spread of SIV in the brain and thus limit brain damage during lentiviral infection

APOBEC3G Protein Profile

Protein Summary

This gene is a member of the cytidine deaminase gene family. It is one of seven related genes or pseudogenes found in a cluster, thought to result from gene duplication, on chromosome 22. Members of the cluster encode proteins that are structurally and functionally related to the C to U RNA-editing cytidine deaminase APOBEC1. It is thought that the proteins may be RNA editing enzymes and have roles in growth or cell cycle control. The protein encoded by this gene has been found to be a specific inhibitor of human immunodeficiency virus-1 (HIV-1) infectivity.

Gene names and symbols associated with APOBEC3G

  • apolipoprotein B mRNA editing enzyme catalytic subunit 3G (APOBEC3G)
  • A3G protein
  • ARCD protein
  • ARP-9 protein
  • ARP9 protein
  • bK150C2.7 protein
  • CEM-15 protein
  • CEM15 protein
  • dJ494G10.1 protein

Protein level used designations for APOBEC3G

APOBEC-related cytidine deaminase , APOBEC-related protein 9 , DNA dC->dU editing enzyme , DNA dC->dU-editing enzyme APOBEC-3G , apolipoprotein B editing enzyme catalytic polypeptide-like 3G , apolipoprotein B mRNA editing enzyme cytidine deaminase , deoxycytidine deaminase , phorbolin-like protein MDS019 , apolipoprotein B mRNA editing enzyme catalytic polypeptide-like 3G , apolipoprotein B mRNA editing enzyme, catalytic peptide-like 3G

GENE ID SPECIES
60489 Homo sapiens
449577 Pan troglodytes
574398 Macaca mulatta
100303423 Papio anubis
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