<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Boulay A</submitter><funding>CREATE Responsible Health and Healthcare Data Science</funding><funding>Natural Sciences and Engineering Research Council of Canada</funding><funding>Fonds de recherche du Québec secteur Santé (FRQS)</funding><funding>Natural Sciences and Engineering Research Council of Canada (NSERC)</funding><funding>Bijzonder Onderzoeksfonds</funding><funding>Research Foundation-Flanders (FWO)</funding><funding>Fonds de recherche du Québec secteur Nature et technologies (FRQNT)</funding><funding>Research Scholars—Junior 1</funding><funding>Fonds de recherche du Québec secteur Nature et technologies</funding><funding>2024 from the European Society of Clinical Microbiology and Infectious Diseases</funding><funding>Research Scholars-Junior 1</funding><funding>CREATE Responsible Health and Healthcare Data Science (RHHDS)</funding><funding>Research Foundation—Flanders</funding><funding>Mitacs Globalink Research program</funding><funding>Compute Ontario</funding><funding>Fonds de recherche du Québec secteur Santé</funding><pagination>btaf531</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12518921</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>41(10)</volume><pubmed_abstract>&lt;h4>Summary&lt;/h4>SPAED is an accessible tool for the accurate segmentation of protein domains that leverages information contained in the predicted aligned error (PAE) matrix obtained from AlphaFold to better identify domain-linker boundaries and detect terminal disordered regions. On a dataset of 376 bacteriophage endolysins (proteins that degrade the bacterial cell wall), SPAED achieves a mean intersect-over-union score of 96% and a domain-boundary-distance score of 89% compared to 94% and 70%, respectively, for the state-of-the-art tool Chainsaw.&lt;h4>Availability and implementation&lt;/h4>Implemented in Python, SPAED is accessible on the web (https://spaed.ca) and available for download from https://github.com/Rousseau-Team/spaed or https://pypi.org/project/spaed. The data used to test SPAED</pubmed_abstract><journal>Bioinformatics (Oxford, England)</journal><pubmed_title>SPAED: harnessing AlphaFold output for accurate segmentation of phage endolysin domains.</pubmed_title><pmcid>PMC12518921</pmcid><funding_grant_id>1S15424N</funding_grant_id><funding_grant_id>01P10022</funding_grant_id><funding_grant_id>307935</funding_grant_id><funding_grant_id>325947</funding_grant_id><funding_grant_id>IT41138</funding_grant_id><pubmed_authors>Vazquez R</pubmed_authors><pubmed_authors>Cremelie E</pubmed_authors><pubmed_authors>Briers Y</pubmed_authors><pubmed_authors>Rousseau E</pubmed_authors><pubmed_authors>Boulay A</pubmed_authors><pubmed_authors>Galiez C</pubmed_authors></additional><is_claimable>false</is_claimable><name>SPAED: harnessing AlphaFold output for accurate segmentation of phage endolysin domains.</name><description>&lt;h4>Summary&lt;/h4>SPAED is an accessible tool for the accurate segmentation of protein domains that leverages information contained in the predicted aligned error (PAE) matrix obtained from AlphaFold to better identify domain-linker boundaries and detect terminal disordered regions. On a dataset of 376 bacteriophage endolysins (proteins that degrade the bacterial cell wall), SPAED achieves a mean intersect-over-union score of 96% and a domain-boundary-distance score of 89% compared to 94% and 70%, respectively, for the state-of-the-art tool Chainsaw.&lt;h4>Availability and implementation&lt;/h4>Implemented in Python, SPAED is accessible on the web (https://spaed.ca) and available for download from https://github.com/Rousseau-Team/spaed or https://pypi.org/project/spaed. The data used to test SPAED</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Oct</publication><modification>2026-06-04T13:47:53.802Z</modification><creation>2026-05-09T03:11:28.134Z</creation></dates><accession>S-EPMC12518921</accession><cross_references><pubmed>40991341</pubmed><doi>10.1093/bioinformatics/btaf531</doi></cross_references></HashMap>