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MORPH-PRO: a novel algorithm and web server for protein morphing
BACKGROUND: Proteins are known to be dynamic in nature, changing from one conformation to another while performing vital cellular tasks. It is important to understand these movements in order to better understand protein function. At the same time, experimental techniques provide us with only single...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3738870/ https://www.ncbi.nlm.nih.gov/pubmed/23844614 http://dx.doi.org/10.1186/1748-7188-8-19 |
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author | Castellana, Natalie E Lushnikov, Andrey Rotkiewicz, Piotr Sefcovic, Natasha Pevzner, Pavel A Godzik, Adam Vyatkina, Kira |
author_facet | Castellana, Natalie E Lushnikov, Andrey Rotkiewicz, Piotr Sefcovic, Natasha Pevzner, Pavel A Godzik, Adam Vyatkina, Kira |
author_sort | Castellana, Natalie E |
collection | PubMed |
description | BACKGROUND: Proteins are known to be dynamic in nature, changing from one conformation to another while performing vital cellular tasks. It is important to understand these movements in order to better understand protein function. At the same time, experimental techniques provide us with only single snapshots of the whole ensemble of available conformations. Computational protein morphing provides a visualization of a protein structure transitioning from one conformation to another by producing a series of intermediate conformations. RESULTS: We present a novel, efficient morphing algorithm, Morph-Pro based on linear interpolation. We also show that apart from visualization, morphing can be used to provide plausible intermediate structures. We test this by using the intermediate structures of a c-Jun N-terminal kinase (JNK1) conformational change in a virtual docking experiment. The structures are shown to dock with higher score to known JNK1-binding ligands than structures solved using X-Ray crystallography. This experiment demonstrates the potential applications of the intermediate structures in modeling or virtual screening efforts. CONCLUSIONS: Visualization of protein conformational changes is important for characterization of protein function. Furthermore, the intermediate structures produced by our algorithm are good approximations to true structures. We believe there is great potential for these computationally predicted structures in protein-ligand docking experiments and virtual screening. The Morph-Pro web server can be accessed at http://morph-pro.bioinf.spbau.ru. |
format | Online Article Text |
id | pubmed-3738870 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-37388702013-08-09 MORPH-PRO: a novel algorithm and web server for protein morphing Castellana, Natalie E Lushnikov, Andrey Rotkiewicz, Piotr Sefcovic, Natasha Pevzner, Pavel A Godzik, Adam Vyatkina, Kira Algorithms Mol Biol Research BACKGROUND: Proteins are known to be dynamic in nature, changing from one conformation to another while performing vital cellular tasks. It is important to understand these movements in order to better understand protein function. At the same time, experimental techniques provide us with only single snapshots of the whole ensemble of available conformations. Computational protein morphing provides a visualization of a protein structure transitioning from one conformation to another by producing a series of intermediate conformations. RESULTS: We present a novel, efficient morphing algorithm, Morph-Pro based on linear interpolation. We also show that apart from visualization, morphing can be used to provide plausible intermediate structures. We test this by using the intermediate structures of a c-Jun N-terminal kinase (JNK1) conformational change in a virtual docking experiment. The structures are shown to dock with higher score to known JNK1-binding ligands than structures solved using X-Ray crystallography. This experiment demonstrates the potential applications of the intermediate structures in modeling or virtual screening efforts. CONCLUSIONS: Visualization of protein conformational changes is important for characterization of protein function. Furthermore, the intermediate structures produced by our algorithm are good approximations to true structures. We believe there is great potential for these computationally predicted structures in protein-ligand docking experiments and virtual screening. The Morph-Pro web server can be accessed at http://morph-pro.bioinf.spbau.ru. BioMed Central 2013-07-11 /pmc/articles/PMC3738870/ /pubmed/23844614 http://dx.doi.org/10.1186/1748-7188-8-19 Text en Copyright © 2013 Castellana et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Castellana, Natalie E Lushnikov, Andrey Rotkiewicz, Piotr Sefcovic, Natasha Pevzner, Pavel A Godzik, Adam Vyatkina, Kira MORPH-PRO: a novel algorithm and web server for protein morphing |
title | MORPH-PRO: a novel algorithm and web server for protein morphing |
title_full | MORPH-PRO: a novel algorithm and web server for protein morphing |
title_fullStr | MORPH-PRO: a novel algorithm and web server for protein morphing |
title_full_unstemmed | MORPH-PRO: a novel algorithm and web server for protein morphing |
title_short | MORPH-PRO: a novel algorithm and web server for protein morphing |
title_sort | morph-pro: a novel algorithm and web server for protein morphing |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3738870/ https://www.ncbi.nlm.nih.gov/pubmed/23844614 http://dx.doi.org/10.1186/1748-7188-8-19 |
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