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Molecular docking analysis of a virulence factor protein dentilisin from Treponema denticola with oxazole piperazine derivatives

Dentilisin is a surface protease synthesized by the cell wall of Treponema denticola. This protein aids in the invasion of the periodontal tissue by causing infection. To identify drug molecules that have better results, homology modeling of the dentilisin protein was constructed, and molecular dock...

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Autores principales: Parthiban, Kandeeban, Veeraraghavan, Vishnu Priya, Sekaran, Surya, Rengasamy, Gayathri, Eswaramoorthy, Rajalakshmanan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Biomedical Informatics 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10504502/
https://www.ncbi.nlm.nih.gov/pubmed/37720272
http://dx.doi.org/10.6026/97320630019057
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author Parthiban, Kandeeban
Veeraraghavan, Vishnu Priya
Sekaran, Surya
Rengasamy, Gayathri
Eswaramoorthy, Rajalakshmanan
author_facet Parthiban, Kandeeban
Veeraraghavan, Vishnu Priya
Sekaran, Surya
Rengasamy, Gayathri
Eswaramoorthy, Rajalakshmanan
author_sort Parthiban, Kandeeban
collection PubMed
description Dentilisin is a surface protease synthesized by the cell wall of Treponema denticola. This protein aids in the invasion of the periodontal tissue by causing infection. To identify drug molecules that have better results, homology modeling of the dentilisin protein was constructed, and molecular docking was performed with the oxazole compounds (1-6) taken from previous studies that are not yet clinically used. Data shows that compounds 1, 2, 3 show better inhibiting properties.
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spelling pubmed-105045022023-09-17 Molecular docking analysis of a virulence factor protein dentilisin from Treponema denticola with oxazole piperazine derivatives Parthiban, Kandeeban Veeraraghavan, Vishnu Priya Sekaran, Surya Rengasamy, Gayathri Eswaramoorthy, Rajalakshmanan Bioinformation Research Article Dentilisin is a surface protease synthesized by the cell wall of Treponema denticola. This protein aids in the invasion of the periodontal tissue by causing infection. To identify drug molecules that have better results, homology modeling of the dentilisin protein was constructed, and molecular docking was performed with the oxazole compounds (1-6) taken from previous studies that are not yet clinically used. Data shows that compounds 1, 2, 3 show better inhibiting properties. Biomedical Informatics 2023-01-31 /pmc/articles/PMC10504502/ /pubmed/37720272 http://dx.doi.org/10.6026/97320630019057 Text en © 2023 Biomedical Informatics https://creativecommons.org/licenses/by/3.0/This is an Open Access article which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. This is distributed under the terms of the Creative Commons Attribution License.
spellingShingle Research Article
Parthiban, Kandeeban
Veeraraghavan, Vishnu Priya
Sekaran, Surya
Rengasamy, Gayathri
Eswaramoorthy, Rajalakshmanan
Molecular docking analysis of a virulence factor protein dentilisin from Treponema denticola with oxazole piperazine derivatives
title Molecular docking analysis of a virulence factor protein dentilisin from Treponema denticola with oxazole piperazine derivatives
title_full Molecular docking analysis of a virulence factor protein dentilisin from Treponema denticola with oxazole piperazine derivatives
title_fullStr Molecular docking analysis of a virulence factor protein dentilisin from Treponema denticola with oxazole piperazine derivatives
title_full_unstemmed Molecular docking analysis of a virulence factor protein dentilisin from Treponema denticola with oxazole piperazine derivatives
title_short Molecular docking analysis of a virulence factor protein dentilisin from Treponema denticola with oxazole piperazine derivatives
title_sort molecular docking analysis of a virulence factor protein dentilisin from treponema denticola with oxazole piperazine derivatives
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10504502/
https://www.ncbi.nlm.nih.gov/pubmed/37720272
http://dx.doi.org/10.6026/97320630019057
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