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The Search for Covalently Ligandable Proteins in Biological Systems
This commentary highlights the recent article published in Nature, June 2016, titled: “Proteome-wide covalent ligand discovery in native biological systems”. They screened the whole proteome of different human cell lines and cell lysates. Around 700 druggable cysteines in the whole proteome were fou...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274003/ https://www.ncbi.nlm.nih.gov/pubmed/27598117 http://dx.doi.org/10.3390/molecules21091170 |
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author | Badshah, Syed Lal Mabkhot, Yahia Nasser |
author_facet | Badshah, Syed Lal Mabkhot, Yahia Nasser |
author_sort | Badshah, Syed Lal |
collection | PubMed |
description | This commentary highlights the recent article published in Nature, June 2016, titled: “Proteome-wide covalent ligand discovery in native biological systems”. They screened the whole proteome of different human cell lines and cell lysates. Around 700 druggable cysteines in the whole proteome were found to bind the electrophilic fragments in both active and inactive states of the proteins. Their experiment and computational docking results agreed with one another. The usefulness of this study in terms of bringing a change in medicinal chemistry is highlighted here. |
format | Online Article Text |
id | pubmed-6274003 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62740032018-12-28 The Search for Covalently Ligandable Proteins in Biological Systems Badshah, Syed Lal Mabkhot, Yahia Nasser Molecules Commentary This commentary highlights the recent article published in Nature, June 2016, titled: “Proteome-wide covalent ligand discovery in native biological systems”. They screened the whole proteome of different human cell lines and cell lysates. Around 700 druggable cysteines in the whole proteome were found to bind the electrophilic fragments in both active and inactive states of the proteins. Their experiment and computational docking results agreed with one another. The usefulness of this study in terms of bringing a change in medicinal chemistry is highlighted here. MDPI 2016-09-02 /pmc/articles/PMC6274003/ /pubmed/27598117 http://dx.doi.org/10.3390/molecules21091170 Text en © 2016 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Commentary Badshah, Syed Lal Mabkhot, Yahia Nasser The Search for Covalently Ligandable Proteins in Biological Systems |
title | The Search for Covalently Ligandable Proteins in Biological Systems |
title_full | The Search for Covalently Ligandable Proteins in Biological Systems |
title_fullStr | The Search for Covalently Ligandable Proteins in Biological Systems |
title_full_unstemmed | The Search for Covalently Ligandable Proteins in Biological Systems |
title_short | The Search for Covalently Ligandable Proteins in Biological Systems |
title_sort | search for covalently ligandable proteins in biological systems |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274003/ https://www.ncbi.nlm.nih.gov/pubmed/27598117 http://dx.doi.org/10.3390/molecules21091170 |
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