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O-GlcNAcase: Promiscuous Hexosaminidase or Key Regulator of O-GlcNAc Signaling?

O-GlcNAc signaling is regulated by an opposing pair of enzymes: O-GlcNAc transferase installs and O-GlcNAcase (OGA) removes the modification from proteins. The dynamics and regulation of this process are only beginning to be understood as the physiological functions of both enzymes are being probed...

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Autores principales: Alonso, Jana, Schimpl, Marianne, van Aalten, Daan M. F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4263850/
https://www.ncbi.nlm.nih.gov/pubmed/25336650
http://dx.doi.org/10.1074/jbc.R114.609198
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author Alonso, Jana
Schimpl, Marianne
van Aalten, Daan M. F.
author_facet Alonso, Jana
Schimpl, Marianne
van Aalten, Daan M. F.
author_sort Alonso, Jana
collection PubMed
description O-GlcNAc signaling is regulated by an opposing pair of enzymes: O-GlcNAc transferase installs and O-GlcNAcase (OGA) removes the modification from proteins. The dynamics and regulation of this process are only beginning to be understood as the physiological functions of both enzymes are being probed using genetic and pharmacological approaches. This minireview charts the discovery and functional and structural analysis of OGA and summarizes the insights gained from recent studies using OGA inhibition, gene knock-out, and overexpression. We identify several areas of “known unknowns” that would benefit from future research, such as the enigmatic C-terminal domain of OGA.
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spelling pubmed-42638502014-12-16 O-GlcNAcase: Promiscuous Hexosaminidase or Key Regulator of O-GlcNAc Signaling? Alonso, Jana Schimpl, Marianne van Aalten, Daan M. F. J Biol Chem Minireviews O-GlcNAc signaling is regulated by an opposing pair of enzymes: O-GlcNAc transferase installs and O-GlcNAcase (OGA) removes the modification from proteins. The dynamics and regulation of this process are only beginning to be understood as the physiological functions of both enzymes are being probed using genetic and pharmacological approaches. This minireview charts the discovery and functional and structural analysis of OGA and summarizes the insights gained from recent studies using OGA inhibition, gene knock-out, and overexpression. We identify several areas of “known unknowns” that would benefit from future research, such as the enigmatic C-terminal domain of OGA. American Society for Biochemistry and Molecular Biology 2014-12-12 2014-10-21 /pmc/articles/PMC4263850/ /pubmed/25336650 http://dx.doi.org/10.1074/jbc.R114.609198 Text en © 2014 by The American Society for Biochemistry and Molecular Biology, Inc. Author's Choice—Final version full access. Creative Commons Attribution Unported License (http://creativecommons.org/licenses/by/3.0/) applies to Author Choice Articles
spellingShingle Minireviews
Alonso, Jana
Schimpl, Marianne
van Aalten, Daan M. F.
O-GlcNAcase: Promiscuous Hexosaminidase or Key Regulator of O-GlcNAc Signaling?
title O-GlcNAcase: Promiscuous Hexosaminidase or Key Regulator of O-GlcNAc Signaling?
title_full O-GlcNAcase: Promiscuous Hexosaminidase or Key Regulator of O-GlcNAc Signaling?
title_fullStr O-GlcNAcase: Promiscuous Hexosaminidase or Key Regulator of O-GlcNAc Signaling?
title_full_unstemmed O-GlcNAcase: Promiscuous Hexosaminidase or Key Regulator of O-GlcNAc Signaling?
title_short O-GlcNAcase: Promiscuous Hexosaminidase or Key Regulator of O-GlcNAc Signaling?
title_sort o-glcnacase: promiscuous hexosaminidase or key regulator of o-glcnac signaling?
topic Minireviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4263850/
https://www.ncbi.nlm.nih.gov/pubmed/25336650
http://dx.doi.org/10.1074/jbc.R114.609198
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