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Structure of the Human Autophagy Initiating Kinase ULK1 in Complex with Potent Inhibitors

[Image: see text] Autophagy is a conserved cellular process that involves the degradation of cellular components for energy maintenance and cytoplasmic quality control that has recently gained interest as a novel target for a variety of human diseases, including cancer. A prime candidate to determin...

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Autores principales: Lazarus, Michael B., Novotny, Chris J., Shokat, Kevan M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4301081/
https://www.ncbi.nlm.nih.gov/pubmed/25551253
http://dx.doi.org/10.1021/cb500835z
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author Lazarus, Michael B.
Novotny, Chris J.
Shokat, Kevan M.
author_facet Lazarus, Michael B.
Novotny, Chris J.
Shokat, Kevan M.
author_sort Lazarus, Michael B.
collection PubMed
description [Image: see text] Autophagy is a conserved cellular process that involves the degradation of cellular components for energy maintenance and cytoplasmic quality control that has recently gained interest as a novel target for a variety of human diseases, including cancer. A prime candidate to determine the potential therapeutic benefit of targeting autophagy is the kinase ULK1, whose activation initiates autophagy. Here, we report the first structures of ULK1, in complex with multiple potent inhibitors. These structures show features unique to the enzyme and will provide a path for the rational design of selective compounds as cellular probes and potential therapeutics.
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spelling pubmed-43010812015-12-31 Structure of the Human Autophagy Initiating Kinase ULK1 in Complex with Potent Inhibitors Lazarus, Michael B. Novotny, Chris J. Shokat, Kevan M. ACS Chem Biol [Image: see text] Autophagy is a conserved cellular process that involves the degradation of cellular components for energy maintenance and cytoplasmic quality control that has recently gained interest as a novel target for a variety of human diseases, including cancer. A prime candidate to determine the potential therapeutic benefit of targeting autophagy is the kinase ULK1, whose activation initiates autophagy. Here, we report the first structures of ULK1, in complex with multiple potent inhibitors. These structures show features unique to the enzyme and will provide a path for the rational design of selective compounds as cellular probes and potential therapeutics. American Chemical Society 2014-12-31 2015-01-16 /pmc/articles/PMC4301081/ /pubmed/25551253 http://dx.doi.org/10.1021/cb500835z 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 Lazarus, Michael B.
Novotny, Chris J.
Shokat, Kevan M.
Structure of the Human Autophagy Initiating Kinase ULK1 in Complex with Potent Inhibitors
title Structure of the Human Autophagy Initiating Kinase ULK1 in Complex with Potent Inhibitors
title_full Structure of the Human Autophagy Initiating Kinase ULK1 in Complex with Potent Inhibitors
title_fullStr Structure of the Human Autophagy Initiating Kinase ULK1 in Complex with Potent Inhibitors
title_full_unstemmed Structure of the Human Autophagy Initiating Kinase ULK1 in Complex with Potent Inhibitors
title_short Structure of the Human Autophagy Initiating Kinase ULK1 in Complex with Potent Inhibitors
title_sort structure of the human autophagy initiating kinase ulk1 in complex with potent inhibitors
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4301081/
https://www.ncbi.nlm.nih.gov/pubmed/25551253
http://dx.doi.org/10.1021/cb500835z
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