Revealing the mechanism for covalent inhibition of glycoside hydrolases by carbasugars at an atomic level

Mechanism-based inhibitors of glycoside hydrolases are useful probes for basic research and represent potential drug candidates. Here, the authors present a series of mechanism-based covalent α-galactosidase inhibitors and elucidate the kinetic and structural basis of their inhibitory activity.

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Autores principales: Weiwu Ren, Robert Pengelly, Marco Farren-Dai, Saeideh Shamsi Kazem Abadi, Verena Oehler, Oluwafemi Akintola, Jason Draper, Michael Meanwell, Saswati Chakladar, Katarzyna Świderek, Vicent Moliner, Robert Britton, Tracey M. Gloster, Andrew J. Bennet
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Lenguaje:EN
Publicado: Nature Portfolio 2018
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Acceso en línea:https://doaj.org/article/744697e101804594badef9eae41b0671
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spelling oai:doaj.org-article:744697e101804594badef9eae41b06712021-12-02T14:40:02ZRevealing the mechanism for covalent inhibition of glycoside hydrolases by carbasugars at an atomic level10.1038/s41467-018-05702-72041-1723https://doaj.org/article/744697e101804594badef9eae41b06712018-08-01T00:00:00Zhttps://doi.org/10.1038/s41467-018-05702-7https://doaj.org/toc/2041-1723Mechanism-based inhibitors of glycoside hydrolases are useful probes for basic research and represent potential drug candidates. Here, the authors present a series of mechanism-based covalent α-galactosidase inhibitors and elucidate the kinetic and structural basis of their inhibitory activity.Weiwu RenRobert PengellyMarco Farren-DaiSaeideh Shamsi Kazem AbadiVerena OehlerOluwafemi AkintolaJason DraperMichael MeanwellSaswati ChakladarKatarzyna ŚwiderekVicent MolinerRobert BrittonTracey M. GlosterAndrew J. BennetNature PortfolioarticleScienceQENNature Communications, Vol 9, Iss 1, Pp 1-12 (2018)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Weiwu Ren
Robert Pengelly
Marco Farren-Dai
Saeideh Shamsi Kazem Abadi
Verena Oehler
Oluwafemi Akintola
Jason Draper
Michael Meanwell
Saswati Chakladar
Katarzyna Świderek
Vicent Moliner
Robert Britton
Tracey M. Gloster
Andrew J. Bennet
Revealing the mechanism for covalent inhibition of glycoside hydrolases by carbasugars at an atomic level
description Mechanism-based inhibitors of glycoside hydrolases are useful probes for basic research and represent potential drug candidates. Here, the authors present a series of mechanism-based covalent α-galactosidase inhibitors and elucidate the kinetic and structural basis of their inhibitory activity.
format article
author Weiwu Ren
Robert Pengelly
Marco Farren-Dai
Saeideh Shamsi Kazem Abadi
Verena Oehler
Oluwafemi Akintola
Jason Draper
Michael Meanwell
Saswati Chakladar
Katarzyna Świderek
Vicent Moliner
Robert Britton
Tracey M. Gloster
Andrew J. Bennet
author_facet Weiwu Ren
Robert Pengelly
Marco Farren-Dai
Saeideh Shamsi Kazem Abadi
Verena Oehler
Oluwafemi Akintola
Jason Draper
Michael Meanwell
Saswati Chakladar
Katarzyna Świderek
Vicent Moliner
Robert Britton
Tracey M. Gloster
Andrew J. Bennet
author_sort Weiwu Ren
title Revealing the mechanism for covalent inhibition of glycoside hydrolases by carbasugars at an atomic level
title_short Revealing the mechanism for covalent inhibition of glycoside hydrolases by carbasugars at an atomic level
title_full Revealing the mechanism for covalent inhibition of glycoside hydrolases by carbasugars at an atomic level
title_fullStr Revealing the mechanism for covalent inhibition of glycoside hydrolases by carbasugars at an atomic level
title_full_unstemmed Revealing the mechanism for covalent inhibition of glycoside hydrolases by carbasugars at an atomic level
title_sort revealing the mechanism for covalent inhibition of glycoside hydrolases by carbasugars at an atomic level
publisher Nature Portfolio
publishDate 2018
url https://doaj.org/article/744697e101804594badef9eae41b0671
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