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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Science B.V
2012
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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. |
format | Online Article Text |
id | pubmed-3437441 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Elsevier Science B.V |
record_format | MEDLINE/PubMed |
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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