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SH2db, an information system for the SH2 domain
SH2 domains are key mediators of phosphotyrosine-based signalling, and therapeutic targets for diverse, mostly oncological, disease indications. They have a highly conserved structure with a central beta sheet that divides the binding surface of the protein into two main pockets, responsible for pho...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10320075/ https://www.ncbi.nlm.nih.gov/pubmed/37207333 http://dx.doi.org/10.1093/nar/gkad420 |
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author | Bajusz, Dávid Pándy-Szekeres, Gáspár Takács, Ágnes de Araujo, Elvin D Keserű, György M |
author_facet | Bajusz, Dávid Pándy-Szekeres, Gáspár Takács, Ágnes de Araujo, Elvin D Keserű, György M |
author_sort | Bajusz, Dávid |
collection | PubMed |
description | SH2 domains are key mediators of phosphotyrosine-based signalling, and therapeutic targets for diverse, mostly oncological, disease indications. They have a highly conserved structure with a central beta sheet that divides the binding surface of the protein into two main pockets, responsible for phosphotyrosine binding (pY pocket) and substrate specificity (pY + 3 pocket). In recent years, structural databases have proven to be invaluable resources for the drug discovery community, as they contain highly relevant and up-to-date information on important protein classes. Here, we present SH2db, a comprehensive structural database and webserver for SH2 domain structures. To organize these protein structures efficiently, we introduce (i) a generic residue numbering scheme to enhance the comparability of different SH2 domains, (ii) a structure-based multiple sequence alignment of all 120 human wild-type SH2 domain sequences and their PDB and AlphaFold structures. The aligned sequences and structures can be searched, browsed and downloaded from the online interface of SH2db (http://sh2db.ttk.hu), with functions to conveniently prepare multiple structures into a Pymol session, and to export simple charts on the contents of the database. Our hope is that SH2db can assist researchers in their day-to-day work by becoming a one-stop shop for SH2 domain related research. |
format | Online Article Text |
id | pubmed-10320075 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-103200752023-07-06 SH2db, an information system for the SH2 domain Bajusz, Dávid Pándy-Szekeres, Gáspár Takács, Ágnes de Araujo, Elvin D Keserű, György M Nucleic Acids Res Web Server Issue SH2 domains are key mediators of phosphotyrosine-based signalling, and therapeutic targets for diverse, mostly oncological, disease indications. They have a highly conserved structure with a central beta sheet that divides the binding surface of the protein into two main pockets, responsible for phosphotyrosine binding (pY pocket) and substrate specificity (pY + 3 pocket). In recent years, structural databases have proven to be invaluable resources for the drug discovery community, as they contain highly relevant and up-to-date information on important protein classes. Here, we present SH2db, a comprehensive structural database and webserver for SH2 domain structures. To organize these protein structures efficiently, we introduce (i) a generic residue numbering scheme to enhance the comparability of different SH2 domains, (ii) a structure-based multiple sequence alignment of all 120 human wild-type SH2 domain sequences and their PDB and AlphaFold structures. The aligned sequences and structures can be searched, browsed and downloaded from the online interface of SH2db (http://sh2db.ttk.hu), with functions to conveniently prepare multiple structures into a Pymol session, and to export simple charts on the contents of the database. Our hope is that SH2db can assist researchers in their day-to-day work by becoming a one-stop shop for SH2 domain related research. Oxford University Press 2023-05-19 /pmc/articles/PMC10320075/ /pubmed/37207333 http://dx.doi.org/10.1093/nar/gkad420 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Web Server Issue Bajusz, Dávid Pándy-Szekeres, Gáspár Takács, Ágnes de Araujo, Elvin D Keserű, György M SH2db, an information system for the SH2 domain |
title | SH2db, an information system for the SH2 domain |
title_full | SH2db, an information system for the SH2 domain |
title_fullStr | SH2db, an information system for the SH2 domain |
title_full_unstemmed | SH2db, an information system for the SH2 domain |
title_short | SH2db, an information system for the SH2 domain |
title_sort | sh2db, an information system for the sh2 domain |
topic | Web Server Issue |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10320075/ https://www.ncbi.nlm.nih.gov/pubmed/37207333 http://dx.doi.org/10.1093/nar/gkad420 |
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