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Selective Inhibitors of Protein Methyltransferases

[Image: see text] Mounting evidence suggests that protein methyltransferases (PMTs), which catalyze methylation of histone and nonhistone proteins, play a crucial role in diverse biological processes and human diseases. In particular, PMTs have been recognized as major players in regulating gene exp...

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Autores principales: Kaniskan, H. Ümit, Konze, Kyle D., Jin, Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4345896/
https://www.ncbi.nlm.nih.gov/pubmed/25406853
http://dx.doi.org/10.1021/jm501234a
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author Kaniskan, H. Ümit
Konze, Kyle D.
Jin, Jian
author_facet Kaniskan, H. Ümit
Konze, Kyle D.
Jin, Jian
author_sort Kaniskan, H. Ümit
collection PubMed
description [Image: see text] Mounting evidence suggests that protein methyltransferases (PMTs), which catalyze methylation of histone and nonhistone proteins, play a crucial role in diverse biological processes and human diseases. In particular, PMTs have been recognized as major players in regulating gene expression and chromatin state. PMTs are divided into two categories: protein lysine methyltransferases (PKMTs) and protein arginine methyltransferases (PRMTs). There has been a steadily growing interest in these enzymes as potential therapeutic targets and therefore discovery of PMT inhibitors has also been pursued increasingly over the past decade. Here, we present a perspective on selective, small-molecule inhibitors of PMTs with an emphasis on their discovery, characterization, and applicability as chemical tools for deciphering the target PMTs’ physiological functions and involvement in human diseases. We highlight the current state of PMT inhibitors and discuss future directions and opportunities for PMT inhibitor discovery.
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spelling pubmed-43458962015-11-19 Selective Inhibitors of Protein Methyltransferases Kaniskan, H. Ümit Konze, Kyle D. Jin, Jian J Med Chem [Image: see text] Mounting evidence suggests that protein methyltransferases (PMTs), which catalyze methylation of histone and nonhistone proteins, play a crucial role in diverse biological processes and human diseases. In particular, PMTs have been recognized as major players in regulating gene expression and chromatin state. PMTs are divided into two categories: protein lysine methyltransferases (PKMTs) and protein arginine methyltransferases (PRMTs). There has been a steadily growing interest in these enzymes as potential therapeutic targets and therefore discovery of PMT inhibitors has also been pursued increasingly over the past decade. Here, we present a perspective on selective, small-molecule inhibitors of PMTs with an emphasis on their discovery, characterization, and applicability as chemical tools for deciphering the target PMTs’ physiological functions and involvement in human diseases. We highlight the current state of PMT inhibitors and discuss future directions and opportunities for PMT inhibitor discovery. American Chemical Society 2014-11-19 2015-02-26 /pmc/articles/PMC4345896/ /pubmed/25406853 http://dx.doi.org/10.1021/jm501234a Text en Copyright © 2014 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Kaniskan, H. Ümit
Konze, Kyle D.
Jin, Jian
Selective Inhibitors of Protein Methyltransferases
title Selective Inhibitors of Protein Methyltransferases
title_full Selective Inhibitors of Protein Methyltransferases
title_fullStr Selective Inhibitors of Protein Methyltransferases
title_full_unstemmed Selective Inhibitors of Protein Methyltransferases
title_short Selective Inhibitors of Protein Methyltransferases
title_sort selective inhibitors of protein methyltransferases
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4345896/
https://www.ncbi.nlm.nih.gov/pubmed/25406853
http://dx.doi.org/10.1021/jm501234a
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