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Yosshi: a web-server for disulfide engineering by bioinformatic analysis of diverse protein families
Disulfide bonds play a significant role in protein stability, function or regulation but are poorly conserved among evolutionarily related proteins. The Yosshi can help to understand the role of S–S bonds by comparing sequences and structures of homologs with diverse properties and different disulfi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6602428/ https://www.ncbi.nlm.nih.gov/pubmed/31106356 http://dx.doi.org/10.1093/nar/gkz385 |
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author | Suplatov, Dmitry Timonina, Daria Sharapova, Yana Švedas, Vytas |
author_facet | Suplatov, Dmitry Timonina, Daria Sharapova, Yana Švedas, Vytas |
author_sort | Suplatov, Dmitry |
collection | PubMed |
description | Disulfide bonds play a significant role in protein stability, function or regulation but are poorly conserved among evolutionarily related proteins. The Yosshi can help to understand the role of S–S bonds by comparing sequences and structures of homologs with diverse properties and different disulfide connectivity patterns within a common structural fold of a superfamily, and assist to select the most promising hot-spots to improve stability of proteins/enzymes or modulate their functions by introducing naturally occurring crosslinks. The bioinformatic analysis is supported by the integrated Mustguseal web-server to construct large structure-guided sequence alignments of functionally diverse protein families that can include thousands of proteins based on all available information in public databases. The Yosshi+Mustguseal is a new integrated web-tool for a systematic homology-driven analysis and engineering of S–S bonds that facilitates a broader interpretation of disulfides not just as a factor of structural stability, but rather as a mechanism to implement functional diversity within a superfamily. The results can be downloaded as a content-rich PyMol session file or further studied online using the HTML5-based interactive analysis tools. Both web-servers are free and open to all users at https://biokinet.belozersky.msu.ru/yosshi and there is no login requirement. |
format | Online Article Text |
id | pubmed-6602428 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-66024282019-07-05 Yosshi: a web-server for disulfide engineering by bioinformatic analysis of diverse protein families Suplatov, Dmitry Timonina, Daria Sharapova, Yana Švedas, Vytas Nucleic Acids Res Web Server Issue Disulfide bonds play a significant role in protein stability, function or regulation but are poorly conserved among evolutionarily related proteins. The Yosshi can help to understand the role of S–S bonds by comparing sequences and structures of homologs with diverse properties and different disulfide connectivity patterns within a common structural fold of a superfamily, and assist to select the most promising hot-spots to improve stability of proteins/enzymes or modulate their functions by introducing naturally occurring crosslinks. The bioinformatic analysis is supported by the integrated Mustguseal web-server to construct large structure-guided sequence alignments of functionally diverse protein families that can include thousands of proteins based on all available information in public databases. The Yosshi+Mustguseal is a new integrated web-tool for a systematic homology-driven analysis and engineering of S–S bonds that facilitates a broader interpretation of disulfides not just as a factor of structural stability, but rather as a mechanism to implement functional diversity within a superfamily. The results can be downloaded as a content-rich PyMol session file or further studied online using the HTML5-based interactive analysis tools. Both web-servers are free and open to all users at https://biokinet.belozersky.msu.ru/yosshi and there is no login requirement. Oxford University Press 2019-07-02 2019-05-20 /pmc/articles/PMC6602428/ /pubmed/31106356 http://dx.doi.org/10.1093/nar/gkz385 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Web Server Issue Suplatov, Dmitry Timonina, Daria Sharapova, Yana Švedas, Vytas Yosshi: a web-server for disulfide engineering by bioinformatic analysis of diverse protein families |
title | Yosshi: a web-server for disulfide engineering by bioinformatic analysis of diverse protein families |
title_full | Yosshi: a web-server for disulfide engineering by bioinformatic analysis of diverse protein families |
title_fullStr | Yosshi: a web-server for disulfide engineering by bioinformatic analysis of diverse protein families |
title_full_unstemmed | Yosshi: a web-server for disulfide engineering by bioinformatic analysis of diverse protein families |
title_short | Yosshi: a web-server for disulfide engineering by bioinformatic analysis of diverse protein families |
title_sort | yosshi: a web-server for disulfide engineering by bioinformatic analysis of diverse protein families |
topic | Web Server Issue |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6602428/ https://www.ncbi.nlm.nih.gov/pubmed/31106356 http://dx.doi.org/10.1093/nar/gkz385 |
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