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Applications of molecular replacement to G protein-coupled receptors
G protein-coupled receptors (GPCRs) are a large class of integral membrane proteins involved in regulating virtually every aspect of human physiology. Despite their profound importance in human health and disease, structural information regarding GPCRs has been extremely limited until recently. With...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3817703/ https://www.ncbi.nlm.nih.gov/pubmed/24189241 http://dx.doi.org/10.1107/S090744491301322X |
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author | Kruse, Andrew C. Manglik, Aashish Kobilka, Brian K. Weis, William I. |
author_facet | Kruse, Andrew C. Manglik, Aashish Kobilka, Brian K. Weis, William I. |
author_sort | Kruse, Andrew C. |
collection | PubMed |
description | G protein-coupled receptors (GPCRs) are a large class of integral membrane proteins involved in regulating virtually every aspect of human physiology. Despite their profound importance in human health and disease, structural information regarding GPCRs has been extremely limited until recently. With the advent of a variety of new biochemical and crystallographic techniques, the structural biology of GPCRs has advanced rapidly, offering key molecular insights into GPCR activation and signal transduction. To date, almost all GPCR structures have been solved using molecular-replacement techniques. Here, the unique aspects of molecular replacement as applied to individual GPCRs and to signaling complexes of these important proteins are discussed. |
format | Online Article Text |
id | pubmed-3817703 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-38177032013-11-06 Applications of molecular replacement to G protein-coupled receptors Kruse, Andrew C. Manglik, Aashish Kobilka, Brian K. Weis, William I. Acta Crystallogr D Biol Crystallogr Research Papers G protein-coupled receptors (GPCRs) are a large class of integral membrane proteins involved in regulating virtually every aspect of human physiology. Despite their profound importance in human health and disease, structural information regarding GPCRs has been extremely limited until recently. With the advent of a variety of new biochemical and crystallographic techniques, the structural biology of GPCRs has advanced rapidly, offering key molecular insights into GPCR activation and signal transduction. To date, almost all GPCR structures have been solved using molecular-replacement techniques. Here, the unique aspects of molecular replacement as applied to individual GPCRs and to signaling complexes of these important proteins are discussed. International Union of Crystallography 2013-11-01 2013-10-18 /pmc/articles/PMC3817703/ /pubmed/24189241 http://dx.doi.org/10.1107/S090744491301322X Text en © Kruse et al. 2013 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited. |
spellingShingle | Research Papers Kruse, Andrew C. Manglik, Aashish Kobilka, Brian K. Weis, William I. Applications of molecular replacement to G protein-coupled receptors |
title | Applications of molecular replacement to G protein-coupled receptors |
title_full | Applications of molecular replacement to G protein-coupled receptors |
title_fullStr | Applications of molecular replacement to G protein-coupled receptors |
title_full_unstemmed | Applications of molecular replacement to G protein-coupled receptors |
title_short | Applications of molecular replacement to G protein-coupled receptors |
title_sort | applications of molecular replacement to g protein-coupled receptors |
topic | Research Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3817703/ https://www.ncbi.nlm.nih.gov/pubmed/24189241 http://dx.doi.org/10.1107/S090744491301322X |
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