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Fuzzle 2.0: Ligand Binding in Natural Protein Building Blocks
Modern proteins have been shown to share evolutionary relationships via subdomain-sized fragments. The assembly of such fragments through duplication and recombination events led to the complex structures and functions we observe today. We previously implemented a pipeline that identified more than...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8416435/ https://www.ncbi.nlm.nih.gov/pubmed/34485385 http://dx.doi.org/10.3389/fmolb.2021.715972 |
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author | Ferruz, Noelia Michel, Florian Lobos, Francisco Schmidt, Steffen Höcker, Birte |
author_facet | Ferruz, Noelia Michel, Florian Lobos, Francisco Schmidt, Steffen Höcker, Birte |
author_sort | Ferruz, Noelia |
collection | PubMed |
description | Modern proteins have been shown to share evolutionary relationships via subdomain-sized fragments. The assembly of such fragments through duplication and recombination events led to the complex structures and functions we observe today. We previously implemented a pipeline that identified more than 1,000 of these fragments that are shared by different protein folds and developed a web interface to analyze and search for them. This resource named Fuzzle helps structural and evolutionary biologists to identify and analyze conserved parts of a protein but it also provides protein engineers with building blocks for example to design proteins by fragment combination. Here, we describe a new version of this web resource that was extended to include ligand information. This addition is a significant asset to the database since now protein fragments that bind specific ligands can be identified and analyzed. Often the mode of ligand binding is conserved in proteins thereby supporting a common evolutionary origin. The same can now be explored for subdomain-sized fragments within this database. This ligand binding information can also be used in protein engineering to graft binding pockets into other protein scaffolds or to transfer functional sites via recombination of a specific fragment. Fuzzle 2.0 is freely available at https://fuzzle.uni-bayreuth.de/2.0. |
format | Online Article Text |
id | pubmed-8416435 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84164352021-09-04 Fuzzle 2.0: Ligand Binding in Natural Protein Building Blocks Ferruz, Noelia Michel, Florian Lobos, Francisco Schmidt, Steffen Höcker, Birte Front Mol Biosci Molecular Biosciences Modern proteins have been shown to share evolutionary relationships via subdomain-sized fragments. The assembly of such fragments through duplication and recombination events led to the complex structures and functions we observe today. We previously implemented a pipeline that identified more than 1,000 of these fragments that are shared by different protein folds and developed a web interface to analyze and search for them. This resource named Fuzzle helps structural and evolutionary biologists to identify and analyze conserved parts of a protein but it also provides protein engineers with building blocks for example to design proteins by fragment combination. Here, we describe a new version of this web resource that was extended to include ligand information. This addition is a significant asset to the database since now protein fragments that bind specific ligands can be identified and analyzed. Often the mode of ligand binding is conserved in proteins thereby supporting a common evolutionary origin. The same can now be explored for subdomain-sized fragments within this database. This ligand binding information can also be used in protein engineering to graft binding pockets into other protein scaffolds or to transfer functional sites via recombination of a specific fragment. Fuzzle 2.0 is freely available at https://fuzzle.uni-bayreuth.de/2.0. Frontiers Media S.A. 2021-08-18 /pmc/articles/PMC8416435/ /pubmed/34485385 http://dx.doi.org/10.3389/fmolb.2021.715972 Text en Copyright © 2021 Ferruz, Michel, Lobos, Schmidt and Höcker. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Molecular Biosciences Ferruz, Noelia Michel, Florian Lobos, Francisco Schmidt, Steffen Höcker, Birte Fuzzle 2.0: Ligand Binding in Natural Protein Building Blocks |
title | Fuzzle 2.0: Ligand Binding in Natural Protein Building Blocks |
title_full | Fuzzle 2.0: Ligand Binding in Natural Protein Building Blocks |
title_fullStr | Fuzzle 2.0: Ligand Binding in Natural Protein Building Blocks |
title_full_unstemmed | Fuzzle 2.0: Ligand Binding in Natural Protein Building Blocks |
title_short | Fuzzle 2.0: Ligand Binding in Natural Protein Building Blocks |
title_sort | fuzzle 2.0: ligand binding in natural protein building blocks |
topic | Molecular Biosciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8416435/ https://www.ncbi.nlm.nih.gov/pubmed/34485385 http://dx.doi.org/10.3389/fmolb.2021.715972 |
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