Divergent retroviral late-budding domains recruit vacuolar protein sorting factors by using alternative adaptor proteins (Q24296475)

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Language	Label	Description	Also known as
English	Divergent retroviral late-budding domains recruit vacuolar protein sorting factors by using alternative adaptor proteins	scientific article

Statements

instance of

scholarly article

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title

Divergent retroviral late-budding domains recruit vacuolar protein sorting factors by using alternative adaptor proteins (English)

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author name string

Juan Martin-Serrano

series ordinal

1

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Anton Yarovoy

series ordinal

2

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David Perez-Caballero

series ordinal

3

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Paul D Bieniasz

series ordinal

4

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Anton Yaravoy

series ordinal

5

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original language of film or TV show

English

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publication date

14 October 2003

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published in

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

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volume

100

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issue

21

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page(s)

12414-9

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cites work

Equine infectious anemia virus utilizes host vesicular protein sorting machinery during particle release

1 reference

stated in

PubMed Central

TSG101 interaction with HRS mediates endosomal trafficking and receptor down-regulation

1 reference

stated in

PubMed Central

Role of ESCRT-I in retroviral budding

1 reference

stated in

PubMed Central

YPXL/I is a protein interaction motif recognized by aspergillus PalA and its human homologue, AIP1/Alix

1 reference

stated in

PubMed Central

Overexpression of the N-terminal domain of TSG101 inhibits HIV-1 budding by blocking late domain function

1 reference

stated in

PubMed Central

Tsg101 and the vacuolar protein sorting pathway are essential for HIV-1 budding

1 reference

stated in

PubMed Central

CHMP1 functions as a member of a newly defined family of vesicle trafficking proteins

1 reference

stated in

PubMed Central

Tsg101, a homologue of ubiquitin-conjugating (E2) enzymes, binds the L domain in HIV type 1 Pr55(Gag)

1 reference

stated in

PubMed Central

TSG101/mammalian VPS23 and mammalian VPS28 interact directly and are recruited to VPS4-induced endosomes

1 reference

stated in

PubMed Central

A role for ubiquitin ligase recruitment in retrovirus release

1 reference

stated in

PubMed Central

Proteasome inhibition interferes with gag polyprotein processing, release, and maturation of HIV-1 and HIV-2

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stated in

PubMed Central

ATPase-defective mammalian VPS4 localizes to aberrant endosomes and impairs cholesterol trafficking

1 reference

stated in

PubMed Central

The Vps4p AAA ATPase regulates membrane association of a Vps protein complex required for normal endosome function

1 reference

stated in

PubMed Central

Hrs is associated with STAM, a signal-transducing adaptor molecule. Its suppressive effect on cytokine-induced cell growth

1 reference

stated in

PubMed Central

An assembly domain of the Rous sarcoma virus Gag protein required late in budding

1 reference

stated in

PubMed Central

Effect of mutations affecting the p6 gag protein on human immunodeficiency virus particle release

1 reference

stated in

PubMed Central

Bro1 is an endosome-associated protein that functions in the MVB pathway in Saccharomyces cerevisiae.

1 reference

stated in

PubMed Central

Endosome-associated complex, ESCRT-II, recruits transport machinery for protein sorting at the multivesicular body

1 reference

stated in

PubMed Central

Escrt-III: an endosome-associated heterooligomeric protein complex required for mvb sorting

1 reference

stated in

PubMed Central

Ubiquitin-dependent sorting into the multivesicular body pathway requires the function of a conserved endosomal protein sorting complex, ESCRT-I.

1 reference

stated in

PubMed Central

A PPxY motif within the VP40 protein of Ebola virus interacts physically and functionally with a ubiquitin ligase: implications for filovirus budding

1 reference

stated in

PubMed Central

Receptor downregulation and multivesicular-body sorting

1 reference

stated in

PubMed Central

HIV-1 and Ebola virus encode small peptide motifs that recruit Tsg101 to sites of particle assembly to facilitate egress

1 reference

stated in

PubMed Central

Hrs, a Tyrosine Kinase Substrate with a Conserved Double Zinc Finger Domain, Is Localized to the Cytoplasmic Surface of Early Endosomes

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Identifiers

DOI

10.1073/PNAS.2133846100

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OpenCitations bibliographic resource ID

914511

1 reference

stated in

OpenCitations Corpus

PMC publication ID

218772

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PubMed publication ID

14519844

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