High-molecular-mass APOBEC3G complexes restrict Alu retrotransposition. - Wikidata - wikimedia - TriplyDB

High-molecular-mass APOBEC3G complexes restrict Alu retrotransposition.

High-molecular-mass APOBEC3G complexes restrict Alu retrotransposition.

http://www.wikidata.org/entity/Q35070356

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Deaminase-independent inhibition of parvoviruses by the APOBEC3A cytidine deaminase APOBEC3 proteins mediate the clearance of foreign DNA from human cells HIV-1 replication and APOBEC3 antiviral activity are not regulated by P bodies LINE-1 ORF1 protein localizes in stress granules with other RNA-binding proteins, including components of RNA interference RNA-induced silencing complex Sole copy of Z2-type human cytidine deaminase APOBEC3H has inhibitory activity against retrotransposons and HIV-1 Crystal structure of the APOBEC3G catalytic domain reveals potential oligomerization interfaces Highly efficient purification of protein complexes from mammalian cells using a novel streptavidin-binding peptide and hexahistidine tandem tag system: application to Bruton's tyrosine kinase Structural model for deoxycytidine deamination mechanisms of the HIV-1 inactivation enzyme APOBEC3G Human LINE-1 restriction by APOBEC3C is deaminase independent and mediated by an ORF1p interaction that affects LINE reverse transcriptase activity Restriction of retroviral replication by APOBEC3G/F and TRIM5alpha HIV-1 Vif, APOBEC, and intrinsic immunity A single amino acid difference in human APOBEC3H variants determines HIV-1 Vif sensitivity Identification of amino acid residues in APOBEC3G required for regulation by human immunodeficiency virus type 1 Vif and Virion encapsidation 7SL RNA mediates virion packaging of the antiviral cytidine deaminase APOBEC3G Restricting retrotransposons: a review Guardian of the Human Genome: Host Defense Mechanisms against LINE-1 Retrotransposition Multiple APOBEC3 restriction factors for HIV-1 and one Vif to rule them all The APOBEC3 family of retroelement restriction factors Functional roles of non-coding Y RNAs Suppression of APOBEC3-mediated restriction of HIV-1 by Vif APOBEC3 Interference during Replication of Viral Genomes Newly synthesized APOBEC3G is incorporated into HIV virions, inhibited by HIV RNA, and subsequently activated by RNase H RNA-dependent oligomerization of APOBEC3G is required for restriction of HIV-1 Footprint of APOBEC3 on the genome of human retroelements Mapping the LINE1 ORF1 protein interactome reveals associated inhibitors of human retrotransposition The interaction between AID and CIB1 is nonessential for antibody gene diversification by gene conversion or class switch recombination APOBEC3G: an intracellular centurion Hypermutation of an ancient human retrovirus by APOBEC3G Bacterial Interactomes: Interacting Protein Partners Share Similar Function and Are Validated in Independent Assays More Frequently Than Previously Reported Multiple ways of targeting APOBEC3-virion infectivity factor interactions for anti-HIV-1 drug development.Two regions within the amino-terminal half of APOBEC3G cooperate to determine cytoplasmic localization.Reduced APOBEC3H variant anti-viral activities are associated with altered RNA binding activities.T cells contain an RNase-insensitive inhibitor of APOBEC3G deaminase activity.APOBEC3G and APOBEC3F require an endogenous cofactor to block HIV-1 replication.Distinct determinants in HIV-1 Vif and human APOBEC3 proteins are required for the suppression of diverse host anti-viral proteins Genetic editing of HBV DNA by monodomain human APOBEC3 cytidine deaminases and the recombinant nature of APOBEC3G.The SET complex acts as a barrier to autointegration of HIV-1 Massive APOBEC3 editing of hepatitis B viral DNA in cirrhosis.Functions and regulation of the APOBEC family of proteins A survey of genomic traces reveals a common sequencing error, RNA editing, and DNA editing.

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High-molecular-mass APOBEC3G complexes restrict Alu retrotransposition.

http://www.wikidata.org/entity/Q35070356

description

2006 nî lūn-bûn

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2006 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2006 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2006年の論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年论文

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name

High-molecular-mass APOBEC3G complexes restrict Alu retrotransposition.

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High-molecular-mass APOBEC3G complexes restrict Alu retrotransposition.

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type

label

High-molecular-mass APOBEC3G complexes restrict Alu retrotransposition.

@ast

High-molecular-mass APOBEC3G complexes restrict Alu retrotransposition.

@en

prefLabel

High-molecular-mass APOBEC3G complexes restrict Alu retrotransposition.

@ast

High-molecular-mass APOBEC3G complexes restrict Alu retrotransposition.

@en

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PNAS.0604524103

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Proceedings of the National Academy of Sciences of the United States of America

P1476

High-molecular-mass APOBEC3G complexes restrict Alu retrotransposition.

@en

P2093

Cécile Esnault

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H Ewa Witkowska

http://www.w3.org/2001/XMLSchema#string

Steven C Hall

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Thierry Heidmann

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Vanessa B Soros

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Warner C Greene

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Ya-Lin Chiu

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P2860

Human retroviral host restriction factors APOBEC3G and APOBEC3F localize to mRNA processing bodies

Ancient adaptive evolution of the primate antiviral DNA-editing enzyme APOBEC3G

An anthropoid-specific locus of orphan C to U RNA-editing enzymes on chromosome 22

Mammalian Staufen1 recruits Upf1 to specific mRNA 3'UTRs so as to elicit mRNA decay

Characterization of Staufen 1 ribonucleoprotein complexes

The cytidine deaminase CEM15 induces hypermutation in newly synthesized HIV-1 DNA

APOBEC3A is a potent inhibitor of adeno-associated virus and retrotransposons

The composition of Staufen-containing RNA granules from human cells indicates their role in the regulated transport and translation of messenger RNAs

APOBEC3A and APOBEC3B are potent inhibitors of LTR-retrotransposon function in human cells

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15588-15593

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10.1073/PNAS.0604524103

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42

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103

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Mario L. Santiago

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2006-10-09T00:00:00Z

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6764025

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17030807

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1592537

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