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Seeking allosteric networks in PDZ domains

Ever since Ranganathan and coworkers subjected the covariation of amino acid residues in the postsynaptic density-95/Discs large/Zonula occludens 1 (PDZ) domain family to a statistical correlation analysis, PDZ domains have represented a paradigmatic family to explore single domain protein allostery...

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Autores principales: Gautier, Candice, Laursen, Louise, Jemth, Per, Gianni, Stefano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6508479/
https://www.ncbi.nlm.nih.gov/pubmed/30690500
http://dx.doi.org/10.1093/protein/gzy033
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author Gautier, Candice
Laursen, Louise
Jemth, Per
Gianni, Stefano
author_facet Gautier, Candice
Laursen, Louise
Jemth, Per
Gianni, Stefano
author_sort Gautier, Candice
collection PubMed
description Ever since Ranganathan and coworkers subjected the covariation of amino acid residues in the postsynaptic density-95/Discs large/Zonula occludens 1 (PDZ) domain family to a statistical correlation analysis, PDZ domains have represented a paradigmatic family to explore single domain protein allostery. Nevertheless, several theoretical and experimental studies in the past two decades have contributed contradicting results with regard to structural localization of the allosteric networks, or even questioned their actual existence in PDZ domains. In this review, we first describe theoretical and experimental approaches that were used to probe the energetic network(s) in PDZ domains. We then compare the proposed networks for two well-studied PDZ domains namely the third PDZ domain from PSD-95 and the second PDZ domain from PTP-BL. Our analysis highlights the contradiction between the different methods and calls for additional work to better understand these allosteric phenomena.
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spelling pubmed-65084792019-05-13 Seeking allosteric networks in PDZ domains Gautier, Candice Laursen, Louise Jemth, Per Gianni, Stefano Protein Eng Des Sel Review Ever since Ranganathan and coworkers subjected the covariation of amino acid residues in the postsynaptic density-95/Discs large/Zonula occludens 1 (PDZ) domain family to a statistical correlation analysis, PDZ domains have represented a paradigmatic family to explore single domain protein allostery. Nevertheless, several theoretical and experimental studies in the past two decades have contributed contradicting results with regard to structural localization of the allosteric networks, or even questioned their actual existence in PDZ domains. In this review, we first describe theoretical and experimental approaches that were used to probe the energetic network(s) in PDZ domains. We then compare the proposed networks for two well-studied PDZ domains namely the third PDZ domain from PSD-95 and the second PDZ domain from PTP-BL. Our analysis highlights the contradiction between the different methods and calls for additional work to better understand these allosteric phenomena. Oxford University Press 2018-10 2019-01-23 /pmc/articles/PMC6508479/ /pubmed/30690500 http://dx.doi.org/10.1093/protein/gzy033 Text en © The Author(s) 2019. Published by Oxford University Press. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Gautier, Candice
Laursen, Louise
Jemth, Per
Gianni, Stefano
Seeking allosteric networks in PDZ domains
title Seeking allosteric networks in PDZ domains
title_full Seeking allosteric networks in PDZ domains
title_fullStr Seeking allosteric networks in PDZ domains
title_full_unstemmed Seeking allosteric networks in PDZ domains
title_short Seeking allosteric networks in PDZ domains
title_sort seeking allosteric networks in pdz domains
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6508479/
https://www.ncbi.nlm.nih.gov/pubmed/30690500
http://dx.doi.org/10.1093/protein/gzy033
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