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Cytopathic Mechanisms of HIV-1

The human immunodeficiency virus type 1 (HIV-1) has been intensely investigated since its discovery in 1983 as the cause of acquired immune deficiency syndrome (AIDS). With relatively few proteins made by the virus, it is able to accomplish many tasks, with each protein serving multiple functions. T...

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Detalles Bibliográficos
Autor principal: Costin, Joshua M
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2174939/
https://www.ncbi.nlm.nih.gov/pubmed/17945027
http://dx.doi.org/10.1186/1743-422X-4-100
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author Costin, Joshua M
author_facet Costin, Joshua M
author_sort Costin, Joshua M
collection PubMed
description The human immunodeficiency virus type 1 (HIV-1) has been intensely investigated since its discovery in 1983 as the cause of acquired immune deficiency syndrome (AIDS). With relatively few proteins made by the virus, it is able to accomplish many tasks, with each protein serving multiple functions. The Envelope glycoprotein, composed of the two noncovalently linked subunits, SU (surface glycoprotein) and TM (transmembrane glycoprotein) is largely responsible for host cell recognition and entry respectively. While the roles of the N-terminal residues of TM is well established as a fusion pore and anchor for Env into cell membranes, the role of the C-terminus of the protein is not well understood and is fiercely debated. This review gathers information on TM in an attempt to shed some light on the functional regions of this protein.
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spelling pubmed-21749392008-01-05 Cytopathic Mechanisms of HIV-1 Costin, Joshua M Virol J Review The human immunodeficiency virus type 1 (HIV-1) has been intensely investigated since its discovery in 1983 as the cause of acquired immune deficiency syndrome (AIDS). With relatively few proteins made by the virus, it is able to accomplish many tasks, with each protein serving multiple functions. The Envelope glycoprotein, composed of the two noncovalently linked subunits, SU (surface glycoprotein) and TM (transmembrane glycoprotein) is largely responsible for host cell recognition and entry respectively. While the roles of the N-terminal residues of TM is well established as a fusion pore and anchor for Env into cell membranes, the role of the C-terminus of the protein is not well understood and is fiercely debated. This review gathers information on TM in an attempt to shed some light on the functional regions of this protein. BioMed Central 2007-10-18 /pmc/articles/PMC2174939/ /pubmed/17945027 http://dx.doi.org/10.1186/1743-422X-4-100 Text en Copyright © 2007 Costin; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Costin, Joshua M
Cytopathic Mechanisms of HIV-1
title Cytopathic Mechanisms of HIV-1
title_full Cytopathic Mechanisms of HIV-1
title_fullStr Cytopathic Mechanisms of HIV-1
title_full_unstemmed Cytopathic Mechanisms of HIV-1
title_short Cytopathic Mechanisms of HIV-1
title_sort cytopathic mechanisms of hiv-1
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2174939/
https://www.ncbi.nlm.nih.gov/pubmed/17945027
http://dx.doi.org/10.1186/1743-422X-4-100
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