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Comparison of Orexin 1 and Orexin 2 Ligand Binding Modes Using X-ray Crystallography and Computational Analysis
[Image: see text] The orexin system, which consists of the two G protein-coupled receptors OX(1) and OX(2), activated by the neuropeptides OX-A and OX-B, is firmly established as a key regulator of behavioral arousal, sleep, and wakefulness and has been an area of intense research effort over the pa...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7050010/ https://www.ncbi.nlm.nih.gov/pubmed/31860301 http://dx.doi.org/10.1021/acs.jmedchem.9b01787 |
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author | Rappas, Mathieu Ali, Ammar A. E. Bennett, Kirstie A. Brown, Jason D. Bucknell, Sarah J. Congreve, Miles Cooke, Robert M. Cseke, Gabriella de Graaf, Chris Doré, Andrew S. Errey, James C. Jazayeri, Ali Marshall, Fiona H. Mason, Jonathan S. Mould, Richard Patel, Jayesh C. Tehan, Benjamin G. Weir, Malcolm Christopher, John A. |
author_facet | Rappas, Mathieu Ali, Ammar A. E. Bennett, Kirstie A. Brown, Jason D. Bucknell, Sarah J. Congreve, Miles Cooke, Robert M. Cseke, Gabriella de Graaf, Chris Doré, Andrew S. Errey, James C. Jazayeri, Ali Marshall, Fiona H. Mason, Jonathan S. Mould, Richard Patel, Jayesh C. Tehan, Benjamin G. Weir, Malcolm Christopher, John A. |
author_sort | Rappas, Mathieu |
collection | PubMed |
description | [Image: see text] The orexin system, which consists of the two G protein-coupled receptors OX(1) and OX(2), activated by the neuropeptides OX-A and OX-B, is firmly established as a key regulator of behavioral arousal, sleep, and wakefulness and has been an area of intense research effort over the past two decades. X-ray structures of the receptors in complex with 10 new antagonist ligands from diverse chemotypes are presented, which complement the existing structural information for the system and highlight the critical importance of lipophilic hotspots and water molecules for these peptidergic GPCR targets. Learnings from the structural information regarding the utility of pharmacophore models and how selectivity between OX(1) and OX(2) can be achieved are discussed. |
format | Online Article Text |
id | pubmed-7050010 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-70500102020-03-03 Comparison of Orexin 1 and Orexin 2 Ligand Binding Modes Using X-ray Crystallography and Computational Analysis Rappas, Mathieu Ali, Ammar A. E. Bennett, Kirstie A. Brown, Jason D. Bucknell, Sarah J. Congreve, Miles Cooke, Robert M. Cseke, Gabriella de Graaf, Chris Doré, Andrew S. Errey, James C. Jazayeri, Ali Marshall, Fiona H. Mason, Jonathan S. Mould, Richard Patel, Jayesh C. Tehan, Benjamin G. Weir, Malcolm Christopher, John A. J Med Chem [Image: see text] The orexin system, which consists of the two G protein-coupled receptors OX(1) and OX(2), activated by the neuropeptides OX-A and OX-B, is firmly established as a key regulator of behavioral arousal, sleep, and wakefulness and has been an area of intense research effort over the past two decades. X-ray structures of the receptors in complex with 10 new antagonist ligands from diverse chemotypes are presented, which complement the existing structural information for the system and highlight the critical importance of lipophilic hotspots and water molecules for these peptidergic GPCR targets. Learnings from the structural information regarding the utility of pharmacophore models and how selectivity between OX(1) and OX(2) can be achieved are discussed. American Chemical Society 2019-12-20 2020-02-27 /pmc/articles/PMC7050010/ /pubmed/31860301 http://dx.doi.org/10.1021/acs.jmedchem.9b01787 Text en Copyright © 2019 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 | Rappas, Mathieu Ali, Ammar A. E. Bennett, Kirstie A. Brown, Jason D. Bucknell, Sarah J. Congreve, Miles Cooke, Robert M. Cseke, Gabriella de Graaf, Chris Doré, Andrew S. Errey, James C. Jazayeri, Ali Marshall, Fiona H. Mason, Jonathan S. Mould, Richard Patel, Jayesh C. Tehan, Benjamin G. Weir, Malcolm Christopher, John A. Comparison of Orexin 1 and Orexin 2 Ligand Binding Modes Using X-ray Crystallography and Computational Analysis |
title | Comparison of Orexin
1 and Orexin 2 Ligand Binding Modes Using X-ray Crystallography
and Computational Analysis |
title_full | Comparison of Orexin
1 and Orexin 2 Ligand Binding Modes Using X-ray Crystallography
and Computational Analysis |
title_fullStr | Comparison of Orexin
1 and Orexin 2 Ligand Binding Modes Using X-ray Crystallography
and Computational Analysis |
title_full_unstemmed | Comparison of Orexin
1 and Orexin 2 Ligand Binding Modes Using X-ray Crystallography
and Computational Analysis |
title_short | Comparison of Orexin
1 and Orexin 2 Ligand Binding Modes Using X-ray Crystallography
and Computational Analysis |
title_sort | comparison of orexin
1 and orexin 2 ligand binding modes using x-ray crystallography
and computational analysis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7050010/ https://www.ncbi.nlm.nih.gov/pubmed/31860301 http://dx.doi.org/10.1021/acs.jmedchem.9b01787 |
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