Cargando…
An evolutionary approach to systematic discovery of novel deubiquitinases, applied to Legionella
Deubiquitinating enzymes (DUBs) are important regulators of the posttranslational protein ubiquitination system. Mammalian genomes encode about 100 different DUBs, which can be grouped into seven different classes. Members of other DUB classes are found in pathogenic bacteria, which use them to targ...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Life Science Alliance LLC
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7391069/ https://www.ncbi.nlm.nih.gov/pubmed/32719160 http://dx.doi.org/10.26508/lsa.202000838 |
_version_ | 1783564571841134592 |
---|---|
author | Hermanns, Thomas Woiwode, Ilka Guerreiro, Ricardo FM Vogt, Robert Lammers, Michael Hofmann, Kay |
author_facet | Hermanns, Thomas Woiwode, Ilka Guerreiro, Ricardo FM Vogt, Robert Lammers, Michael Hofmann, Kay |
author_sort | Hermanns, Thomas |
collection | PubMed |
description | Deubiquitinating enzymes (DUBs) are important regulators of the posttranslational protein ubiquitination system. Mammalian genomes encode about 100 different DUBs, which can be grouped into seven different classes. Members of other DUB classes are found in pathogenic bacteria, which use them to target the host defense. By combining bioinformatical and experimental approaches, we address the question if the known DUB families have a common evolutionary ancestry and share conserved features that set them apart from other proteases. By systematically comparing family-specific hidden Markov models, we uncovered distant relationships between established DUBs and other cysteine protease families. Most DUB families share a conserved aromatic residue linked to the active site, which restricts the cleavage of substrates with side chains at the S2 position, corresponding to Gly-75 in ubiquitin. By applying these criteria to Legionella pneumophila ORFs, we identified lpg1621 and lpg1148 as deubiquitinases, characterized their cleavage specificities, and confirmed the importance of the aromatic gatekeeper motif for substrate selection. |
format | Online Article Text |
id | pubmed-7391069 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Life Science Alliance LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-73910692020-08-07 An evolutionary approach to systematic discovery of novel deubiquitinases, applied to Legionella Hermanns, Thomas Woiwode, Ilka Guerreiro, Ricardo FM Vogt, Robert Lammers, Michael Hofmann, Kay Life Sci Alliance Research Articles Deubiquitinating enzymes (DUBs) are important regulators of the posttranslational protein ubiquitination system. Mammalian genomes encode about 100 different DUBs, which can be grouped into seven different classes. Members of other DUB classes are found in pathogenic bacteria, which use them to target the host defense. By combining bioinformatical and experimental approaches, we address the question if the known DUB families have a common evolutionary ancestry and share conserved features that set them apart from other proteases. By systematically comparing family-specific hidden Markov models, we uncovered distant relationships between established DUBs and other cysteine protease families. Most DUB families share a conserved aromatic residue linked to the active site, which restricts the cleavage of substrates with side chains at the S2 position, corresponding to Gly-75 in ubiquitin. By applying these criteria to Legionella pneumophila ORFs, we identified lpg1621 and lpg1148 as deubiquitinases, characterized their cleavage specificities, and confirmed the importance of the aromatic gatekeeper motif for substrate selection. Life Science Alliance LLC 2020-07-27 /pmc/articles/PMC7391069/ /pubmed/32719160 http://dx.doi.org/10.26508/lsa.202000838 Text en © 2020 Hermanns et al. https://creativecommons.org/licenses/by/4.0/This article is available under a Creative Commons License (Attribution 4.0 International, as described at https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Research Articles Hermanns, Thomas Woiwode, Ilka Guerreiro, Ricardo FM Vogt, Robert Lammers, Michael Hofmann, Kay An evolutionary approach to systematic discovery of novel deubiquitinases, applied to Legionella |
title | An evolutionary approach to systematic discovery of novel deubiquitinases, applied to Legionella |
title_full | An evolutionary approach to systematic discovery of novel deubiquitinases, applied to Legionella |
title_fullStr | An evolutionary approach to systematic discovery of novel deubiquitinases, applied to Legionella |
title_full_unstemmed | An evolutionary approach to systematic discovery of novel deubiquitinases, applied to Legionella |
title_short | An evolutionary approach to systematic discovery of novel deubiquitinases, applied to Legionella |
title_sort | evolutionary approach to systematic discovery of novel deubiquitinases, applied to legionella |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7391069/ https://www.ncbi.nlm.nih.gov/pubmed/32719160 http://dx.doi.org/10.26508/lsa.202000838 |
work_keys_str_mv | AT hermannsthomas anevolutionaryapproachtosystematicdiscoveryofnoveldeubiquitinasesappliedtolegionella AT woiwodeilka anevolutionaryapproachtosystematicdiscoveryofnoveldeubiquitinasesappliedtolegionella AT guerreiroricardofm anevolutionaryapproachtosystematicdiscoveryofnoveldeubiquitinasesappliedtolegionella AT vogtrobert anevolutionaryapproachtosystematicdiscoveryofnoveldeubiquitinasesappliedtolegionella AT lammersmichael anevolutionaryapproachtosystematicdiscoveryofnoveldeubiquitinasesappliedtolegionella AT hofmannkay anevolutionaryapproachtosystematicdiscoveryofnoveldeubiquitinasesappliedtolegionella AT hermannsthomas evolutionaryapproachtosystematicdiscoveryofnoveldeubiquitinasesappliedtolegionella AT woiwodeilka evolutionaryapproachtosystematicdiscoveryofnoveldeubiquitinasesappliedtolegionella AT guerreiroricardofm evolutionaryapproachtosystematicdiscoveryofnoveldeubiquitinasesappliedtolegionella AT vogtrobert evolutionaryapproachtosystematicdiscoveryofnoveldeubiquitinasesappliedtolegionella AT lammersmichael evolutionaryapproachtosystematicdiscoveryofnoveldeubiquitinasesappliedtolegionella AT hofmannkay evolutionaryapproachtosystematicdiscoveryofnoveldeubiquitinasesappliedtolegionella |