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The human phosphatase interactome: An intricate family portrait

The concerted activities of kinases and phosphatases modulate the phosphorylation levels of proteins, lipids and carbohydrates in eukaryotic cells. Despite considerable effort, we are still missing a holistic picture representing, at a proteome level, the functional relationships between kinases, ph...

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Detalles Bibliográficos
Autores principales: Sacco, Francesca, Perfetto, Livia, Castagnoli, Luisa, Cesareni, Gianni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science B.V 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3437441/
https://www.ncbi.nlm.nih.gov/pubmed/22626554
http://dx.doi.org/10.1016/j.febslet.2012.05.008
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author Sacco, Francesca
Perfetto, Livia
Castagnoli, Luisa
Cesareni, Gianni
author_facet Sacco, Francesca
Perfetto, Livia
Castagnoli, Luisa
Cesareni, Gianni
author_sort Sacco, Francesca
collection PubMed
description The concerted activities of kinases and phosphatases modulate the phosphorylation levels of proteins, lipids and carbohydrates in eukaryotic cells. Despite considerable effort, we are still missing a holistic picture representing, at a proteome level, the functional relationships between kinases, phosphatases and their substrates. Here we focus on phosphatases and we review and integrate the available information that helps to place the members of the protein phosphatase superfamilies into the human protein interaction network. In addition we show how protein interaction domains and motifs, either covalently linked to the phosphatase domain or in regulatory/adaptor subunits, play a prominent role in substrate selection.
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spelling pubmed-34374412012-09-12 The human phosphatase interactome: An intricate family portrait Sacco, Francesca Perfetto, Livia Castagnoli, Luisa Cesareni, Gianni FEBS Lett Review The concerted activities of kinases and phosphatases modulate the phosphorylation levels of proteins, lipids and carbohydrates in eukaryotic cells. Despite considerable effort, we are still missing a holistic picture representing, at a proteome level, the functional relationships between kinases, phosphatases and their substrates. Here we focus on phosphatases and we review and integrate the available information that helps to place the members of the protein phosphatase superfamilies into the human protein interaction network. In addition we show how protein interaction domains and motifs, either covalently linked to the phosphatase domain or in regulatory/adaptor subunits, play a prominent role in substrate selection. Elsevier Science B.V 2012-08-14 /pmc/articles/PMC3437441/ /pubmed/22626554 http://dx.doi.org/10.1016/j.febslet.2012.05.008 Text en © 2012 Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/3.0/ Open Access under CC BY-NC-ND 3.0 (https://creativecommons.org/licenses/by-nc-nd/3.0/) license
spellingShingle Review
Sacco, Francesca
Perfetto, Livia
Castagnoli, Luisa
Cesareni, Gianni
The human phosphatase interactome: An intricate family portrait
title The human phosphatase interactome: An intricate family portrait
title_full The human phosphatase interactome: An intricate family portrait
title_fullStr The human phosphatase interactome: An intricate family portrait
title_full_unstemmed The human phosphatase interactome: An intricate family portrait
title_short The human phosphatase interactome: An intricate family portrait
title_sort human phosphatase interactome: an intricate family portrait
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3437441/
https://www.ncbi.nlm.nih.gov/pubmed/22626554
http://dx.doi.org/10.1016/j.febslet.2012.05.008
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