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In Silico Insights of L-Glutamate: Structural Features in Vacuum and in Complex with Its Receptor

Structural properties of the glutamate in vacuum and in complex with its receptor were analyzed. The analysis was focused on global properties, attempting to characterize features such as overall flexibility and common trends in the conformation set. The glutamate, as other ligands in complex with t...

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Detalles Bibliográficos
Autores principales: Gonzalez, Janneth, Barreto, George E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3836412/
https://www.ncbi.nlm.nih.gov/pubmed/24307941
http://dx.doi.org/10.1155/2013/872058
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author Gonzalez, Janneth
Barreto, George E.
author_facet Gonzalez, Janneth
Barreto, George E.
author_sort Gonzalez, Janneth
collection PubMed
description Structural properties of the glutamate in vacuum and in complex with its receptor were analyzed. The analysis was focused on global properties, attempting to characterize features such as overall flexibility and common trends in the conformation set. The glutamate, as other ligands in complex with the receptor, adopts a spatial conformation that corresponds to one of the possible molecular equilibrium states in physiological conditions. The glutamate forms an extended structure for all cases, but the energy of the glutamate round out form is lower than the extended glutamate form. The results showed the glutamate as a flexible molecule, which can easily adapt to different interacting environments, and it can be considered as an approximation to address why glutamate interacts with a great number of molecules.
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spelling pubmed-38364122013-12-04 In Silico Insights of L-Glutamate: Structural Features in Vacuum and in Complex with Its Receptor Gonzalez, Janneth Barreto, George E. J Amino Acids Research Article Structural properties of the glutamate in vacuum and in complex with its receptor were analyzed. The analysis was focused on global properties, attempting to characterize features such as overall flexibility and common trends in the conformation set. The glutamate, as other ligands in complex with the receptor, adopts a spatial conformation that corresponds to one of the possible molecular equilibrium states in physiological conditions. The glutamate forms an extended structure for all cases, but the energy of the glutamate round out form is lower than the extended glutamate form. The results showed the glutamate as a flexible molecule, which can easily adapt to different interacting environments, and it can be considered as an approximation to address why glutamate interacts with a great number of molecules. Hindawi Publishing Corporation 2013 2013-11-06 /pmc/articles/PMC3836412/ /pubmed/24307941 http://dx.doi.org/10.1155/2013/872058 Text en Copyright © 2013 J. Gonzalez and G. E. Barreto. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Gonzalez, Janneth
Barreto, George E.
In Silico Insights of L-Glutamate: Structural Features in Vacuum and in Complex with Its Receptor
title In Silico Insights of L-Glutamate: Structural Features in Vacuum and in Complex with Its Receptor
title_full In Silico Insights of L-Glutamate: Structural Features in Vacuum and in Complex with Its Receptor
title_fullStr In Silico Insights of L-Glutamate: Structural Features in Vacuum and in Complex with Its Receptor
title_full_unstemmed In Silico Insights of L-Glutamate: Structural Features in Vacuum and in Complex with Its Receptor
title_short In Silico Insights of L-Glutamate: Structural Features in Vacuum and in Complex with Its Receptor
title_sort in silico insights of l-glutamate: structural features in vacuum and in complex with its receptor
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3836412/
https://www.ncbi.nlm.nih.gov/pubmed/24307941
http://dx.doi.org/10.1155/2013/872058
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