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PMID: 15567490 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S. Review

Retrovirus budding.

Virus research ·Vol. 106 ·No. 2 ·2004-12-00 ·Pages 87-102

Demirov DG, Freed EO

Abstract

The release of retrovirus particles from the infected cell is greatly stimulated by short motifs, known as "late" or "L" domains, present within the Gag precursor protein. Three distinct classes of L domains have been identified; these bear the core sequence: Pro-Thr/Ser-Ala-Pro [P(T/S)AP], Pro-Pro-x-Tyr (PPxY), or Tyr-Pro-x-Leu (YPxL). A number of recent studies have demonstrated that L domains function by interacting with components of the machinery responsible for sorting cellular proteins into the multivesicular body (MVB) pathway. This review traces the history of L domain discovery and characterization, and highlights the relationship between L domain activity, retrovirus release, and the host endosomal sorting machinery.

MeSH Terms
Gene Expression Regulation, Viral Gene Products, gag/chemistry,genetics,metabolism,physiology Retroviridae/chemistry,genetics,growth & development,physiology Ubiquitin/metabolism Virus Assembly/physiology
Chemicals
Gene Products, gag Ubiquitin
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Demirov Dimiter G
Virus-Cell Interaction Section, HIV Drug Resistance Program, National Cancer Institute at Frederick, Bldg. 535/Rm. 124, Frederick, MD 21702-1201, USA.
Freed Eric O
Article Info
Journal
Virus research
Abbr.
Virus Res
ISSN
0168-1702
Published
2004-12-00
Pages
87-102
Language
English
Region
Netherlands
NLM ID
8410979
Subset
IM
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