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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...

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Detalles Bibliográficos
Autores principales: Slupe, Andrew M., Merrill, Ronald A., Strack, Stefan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE-Hindawi Access to Research 2011
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.
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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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