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Determinants for Substrate Specificity of Protein Phosphatase 2A
Protein phosphatase 2A- (PP2A-) catalyzed dephosphorylation of target substrate proteins is widespread and critical for cellular function. PP2A is predominantly found as a heterotrimeric complex of a catalytic subunit (C), a scaffolding subunit (A), and one member of 4 families of regulatory subunit...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE-Hindawi Access to Research
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3132988/ https://www.ncbi.nlm.nih.gov/pubmed/21755039 http://dx.doi.org/10.4061/2011/398751 |
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author | Slupe, Andrew M. Merrill, Ronald A. Strack, Stefan |
author_facet | Slupe, Andrew M. Merrill, Ronald A. Strack, Stefan |
author_sort | Slupe, Andrew M. |
collection | PubMed |
description | Protein phosphatase 2A- (PP2A-) catalyzed dephosphorylation of target substrate proteins is widespread and critical for cellular function. PP2A is predominantly found as a heterotrimeric complex of a catalytic subunit (C), a scaffolding subunit (A), and one member of 4 families of regulatory subunits (B). Substrate specificity of the holoenzyme complex is determined by the subcellular locale the complex is confined to, selective incorporation of the B subunit, interactions with endogenous inhibitory proteins, and specific intermolecular interactions between PP2A and target substrates. Here, we discuss recent studies that have advanced our understanding of the molecular determinants for PP2A substrate specificity. |
format | Online Article Text |
id | pubmed-3132988 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | SAGE-Hindawi Access to Research |
record_format | MEDLINE/PubMed |
spelling | pubmed-31329882011-07-13 Determinants for Substrate Specificity of Protein Phosphatase 2A Slupe, Andrew M. Merrill, Ronald A. Strack, Stefan Enzyme Res Review Article Protein phosphatase 2A- (PP2A-) catalyzed dephosphorylation of target substrate proteins is widespread and critical for cellular function. PP2A is predominantly found as a heterotrimeric complex of a catalytic subunit (C), a scaffolding subunit (A), and one member of 4 families of regulatory subunits (B). Substrate specificity of the holoenzyme complex is determined by the subcellular locale the complex is confined to, selective incorporation of the B subunit, interactions with endogenous inhibitory proteins, and specific intermolecular interactions between PP2A and target substrates. Here, we discuss recent studies that have advanced our understanding of the molecular determinants for PP2A substrate specificity. SAGE-Hindawi Access to Research 2011-07-02 /pmc/articles/PMC3132988/ /pubmed/21755039 http://dx.doi.org/10.4061/2011/398751 Text en Copyright © 2011 Andrew M. Slupe et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Slupe, Andrew M. Merrill, Ronald A. Strack, Stefan Determinants for Substrate Specificity of Protein Phosphatase 2A |
title | Determinants for Substrate Specificity of Protein Phosphatase 2A |
title_full | Determinants for Substrate Specificity of Protein Phosphatase 2A |
title_fullStr | Determinants for Substrate Specificity of Protein Phosphatase 2A |
title_full_unstemmed | Determinants for Substrate Specificity of Protein Phosphatase 2A |
title_short | Determinants for Substrate Specificity of Protein Phosphatase 2A |
title_sort | determinants for substrate specificity of protein phosphatase 2a |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3132988/ https://www.ncbi.nlm.nih.gov/pubmed/21755039 http://dx.doi.org/10.4061/2011/398751 |
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