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Molecular docking analysis of penta galloyl glucose with the bcl-2 family of anti-apoptotic targets
Apoptosis requires cellular proteins from the B-cell lymphoma 2 (BCL-2) family linked to breast cancer. Therefore, it is of interest to document the Molecular docking analysis data of penta galloyl glucose with the bcl-2 family of anti-apoptotic targets (Bcl-2, BCL-XL, Caspase 3, and Caspase 9). Dat...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Biomedical Informatics
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9070626/ https://www.ncbi.nlm.nih.gov/pubmed/35574508 http://dx.doi.org/10.6026/97320630017861 |
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author | Dharmalingam, Karthick Dharmalingam, Velvizhi Durairaj, Satheesh Sharma, Praveen Jayaraman, Selvaraj Choudhary, Sarita |
author_facet | Dharmalingam, Karthick Dharmalingam, Velvizhi Durairaj, Satheesh Sharma, Praveen Jayaraman, Selvaraj Choudhary, Sarita |
author_sort | Dharmalingam, Karthick |
collection | PubMed |
description | Apoptosis requires cellular proteins from the B-cell lymphoma 2 (BCL-2) family linked to breast cancer. Therefore, it is of interest to document the Molecular docking analysis data of penta galloyl glucose with the bcl-2 family of anti-apoptotic targets (Bcl-2, BCL-XL, Caspase 3, and Caspase 9). Data shows that Pentagalloyl glucose have optimal binding features with Bcl-2, BCL-XL, Caspase 3, and Caspase 9 proteins with binding energy of -8.6,-7,-7.5 and 4.4 kcal/mol respectively for further consideration in this context. |
format | Online Article Text |
id | pubmed-9070626 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Biomedical Informatics |
record_format | MEDLINE/PubMed |
spelling | pubmed-90706262022-05-12 Molecular docking analysis of penta galloyl glucose with the bcl-2 family of anti-apoptotic targets Dharmalingam, Karthick Dharmalingam, Velvizhi Durairaj, Satheesh Sharma, Praveen Jayaraman, Selvaraj Choudhary, Sarita Bioinformation Research Article Apoptosis requires cellular proteins from the B-cell lymphoma 2 (BCL-2) family linked to breast cancer. Therefore, it is of interest to document the Molecular docking analysis data of penta galloyl glucose with the bcl-2 family of anti-apoptotic targets (Bcl-2, BCL-XL, Caspase 3, and Caspase 9). Data shows that Pentagalloyl glucose have optimal binding features with Bcl-2, BCL-XL, Caspase 3, and Caspase 9 proteins with binding energy of -8.6,-7,-7.5 and 4.4 kcal/mol respectively for further consideration in this context. Biomedical Informatics 2021-10-31 /pmc/articles/PMC9070626/ /pubmed/35574508 http://dx.doi.org/10.6026/97320630017861 Text en © 2021 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 Dharmalingam, Karthick Dharmalingam, Velvizhi Durairaj, Satheesh Sharma, Praveen Jayaraman, Selvaraj Choudhary, Sarita Molecular docking analysis of penta galloyl glucose with the bcl-2 family of anti-apoptotic targets |
title | Molecular docking analysis of penta galloyl glucose with the bcl-2 family of anti-apoptotic targets |
title_full | Molecular docking analysis of penta galloyl glucose with the bcl-2 family of anti-apoptotic targets |
title_fullStr | Molecular docking analysis of penta galloyl glucose with the bcl-2 family of anti-apoptotic targets |
title_full_unstemmed | Molecular docking analysis of penta galloyl glucose with the bcl-2 family of anti-apoptotic targets |
title_short | Molecular docking analysis of penta galloyl glucose with the bcl-2 family of anti-apoptotic targets |
title_sort | molecular docking analysis of penta galloyl glucose with the bcl-2 family of anti-apoptotic targets |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9070626/ https://www.ncbi.nlm.nih.gov/pubmed/35574508 http://dx.doi.org/10.6026/97320630017861 |
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