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PoseEdit: enhanced ligand binding mode communication by interactive 2D diagrams

In this article, we present PoseEdit, a new, interactive frontend of the popular pose visualization tool PoseView. PoseEdit automatically produces high-quality 2D diagrams of intermolecular interactions in 3D binding sites calculated from ligands in complex with protein, DNA, and RNA. The PoseView d...

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Autores principales: Diedrich, Konrad, Krause, Bennet, Berg, Ole, Rarey, Matthias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10440272/
https://www.ncbi.nlm.nih.gov/pubmed/37515714
http://dx.doi.org/10.1007/s10822-023-00522-4
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author Diedrich, Konrad
Krause, Bennet
Berg, Ole
Rarey, Matthias
author_facet Diedrich, Konrad
Krause, Bennet
Berg, Ole
Rarey, Matthias
author_sort Diedrich, Konrad
collection PubMed
description In this article, we present PoseEdit, a new, interactive frontend of the popular pose visualization tool PoseView. PoseEdit automatically produces high-quality 2D diagrams of intermolecular interactions in 3D binding sites calculated from ligands in complex with protein, DNA, and RNA. The PoseView diagrams have been improved in several aspects, most notably in their interactivity. Thanks to the easy-to-use 2D editor of PoseEdit, the diagrams are extensively editable and extendible by the user, can be merged with other diagrams, and even be created from scratch. A large variety of graphical objects in the diagram can be moved, rotated, selected and highlighted, mirrored, removed, or even newly added. Furthermore, PoseEdit enables a synchronized 2D-3D view of macromolecule-ligand complexes simplifying the analysis of structural features and interactions. The representation of individual diagram objects regarding their visualized chemical properties, like stereochemistry, and general graphical styles, like the color of interactions, can additionally be edited. The primary objective of PoseEdit is to support scientists with an enhanced way to communicate ligand binding mode information through graphical 2D representations optimized with the scientist’s input in accordance with objective criteria and individual needs. PoseEdit is freely available on the ProteinsPlus web server (https://proteins.plus). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10822-023-00522-4.
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spelling pubmed-104402722023-08-22 PoseEdit: enhanced ligand binding mode communication by interactive 2D diagrams Diedrich, Konrad Krause, Bennet Berg, Ole Rarey, Matthias J Comput Aided Mol Des Article In this article, we present PoseEdit, a new, interactive frontend of the popular pose visualization tool PoseView. PoseEdit automatically produces high-quality 2D diagrams of intermolecular interactions in 3D binding sites calculated from ligands in complex with protein, DNA, and RNA. The PoseView diagrams have been improved in several aspects, most notably in their interactivity. Thanks to the easy-to-use 2D editor of PoseEdit, the diagrams are extensively editable and extendible by the user, can be merged with other diagrams, and even be created from scratch. A large variety of graphical objects in the diagram can be moved, rotated, selected and highlighted, mirrored, removed, or even newly added. Furthermore, PoseEdit enables a synchronized 2D-3D view of macromolecule-ligand complexes simplifying the analysis of structural features and interactions. The representation of individual diagram objects regarding their visualized chemical properties, like stereochemistry, and general graphical styles, like the color of interactions, can additionally be edited. The primary objective of PoseEdit is to support scientists with an enhanced way to communicate ligand binding mode information through graphical 2D representations optimized with the scientist’s input in accordance with objective criteria and individual needs. PoseEdit is freely available on the ProteinsPlus web server (https://proteins.plus). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10822-023-00522-4. Springer International Publishing 2023-07-29 2023 /pmc/articles/PMC10440272/ /pubmed/37515714 http://dx.doi.org/10.1007/s10822-023-00522-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Diedrich, Konrad
Krause, Bennet
Berg, Ole
Rarey, Matthias
PoseEdit: enhanced ligand binding mode communication by interactive 2D diagrams
title PoseEdit: enhanced ligand binding mode communication by interactive 2D diagrams
title_full PoseEdit: enhanced ligand binding mode communication by interactive 2D diagrams
title_fullStr PoseEdit: enhanced ligand binding mode communication by interactive 2D diagrams
title_full_unstemmed PoseEdit: enhanced ligand binding mode communication by interactive 2D diagrams
title_short PoseEdit: enhanced ligand binding mode communication by interactive 2D diagrams
title_sort poseedit: enhanced ligand binding mode communication by interactive 2d diagrams
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10440272/
https://www.ncbi.nlm.nih.gov/pubmed/37515714
http://dx.doi.org/10.1007/s10822-023-00522-4
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