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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...

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Detalles Bibliográficos
Autores principales: Bajusz, Dávid, Pándy-Szekeres, Gáspár, Takács, Ágnes, de Araujo, Elvin D, Keserű, György M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
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.
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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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