Comparative assessment of protein large language models for enzyme commission number prediction

dc.commentsCEB58233por
dc.contributor.authorCapela, Joãopor
dc.contributor.authorZimmermann-Kogadeeva, Mariapor
dc.contributor.authorDijk, Aalt D. J. vanpor
dc.contributor.authorde Ridder, Dickpor
dc.contributor.authorDias, Oscarpor
dc.contributor.authorRocha, Miguelpor
dc.date.accessioned2025-03-19T17:02:08Z
dc.date.available2025-03-19T17:02:08Z
dc.date.issued2025
dc.date.updated2025-03-17T14:08:08Z
dc.description.abstractBackground: Protein large language models (LLM) have been used to extract representations of enzyme sequences to predict their function, which is encoded by enzyme commission (EC) numbers. However, a comprehensive comparison of different LLMs for this task is still lacking, leaving questions about their relative performance. Moreover, protein sequence alignments (e.g. BLASTp or DIAMOND) are often combined with machine learning models to assign EC numbers from homologous enzymes, thus compensating for the shortcomings of these models predictions. In this context, LLMs and sequence alignment methods have not been extensively compared as individual predictors, raising unaddressed questions about LLMs performance and limitations relative to the alignment methods. In this study, we set out to assess the performance of ESM2, ESM1b, and ProtBERT language models in their ability to predict EC numbers, comparing them with BLASTp, against each other and against models that rely on one-hot encodings of amino acid sequences. Results: Our findings reveal that combining these LLMs with fully connected neural networks surpasses the performance of deep learning models that rely on one-hot encodings. Moreover, although BLASTp provided marginally better results overall, DL models provide results that complement BLASTps, revealing that LLMs better predict certain EC numbers while BLASTp excels in predicting others. The ESM2 stood out as the best model among the LLMs tested, providing more accurate predictions on difficult annotation tasks and for enzymes without homologs. Conclusions: Crucially, this study demonstrates that LLMs still have to be improved to become the gold standard tool over BLASTp in mainstream enzyme annotation routines. On the other hand, LLMs can provide good predictions for more difficult-to-annotate enzymes, particularly when the identity between the query sequence and the reference database falls below 25%. Our results reinforce the claim that BLASTp and LLM models complement each other and can be more effective when used together. © The Author(s) 2025.por
dc.description.publicationversioninfo:eu-repo/semantics/publishedVersion
dc.description.sponsorshipFCT supported this study under the strategic funding of the UIDB/04469/2020 unit and by LABBELS (LA/P/0029/2020). We also thank FCT for the PhD fellowship to J. Capela (DFA/BD/08789/2021) and funding O. Dias (DOI 10.54499/CEECIND/03425/2018/CP1581/CT0020). J. Capela also acknowledge the European Molecular Biology Laboratory (EMBL) Corporate Partnership Programme for funding a short-term visitor fellowship. M. Zimmermann-Kogadeeva is supported by the EMBL.por
dc.distributioninternationalpor
dc.identifier.citationCapela, J., Zimmermann-Kogadeeva, M., Dijk, A.D.J.v. et al. Comparative Assessment of Protein Large Language Models for Enzyme Commission Number Prediction. BMC Bioinformatics 26, 68 (2025). https://doi.org/10.1186/s12859-025-06081-9por
dc.identifier.doi10.1186/s12859-025-06081-9por
dc.identifier.issn1471-2105por
dc.identifier.pmid40016653por
dc.identifier.urihttps://hdl.handle.net/1822/95041
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherBioMed Central (BMC)por
dc.relationinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB%2F04469%2F2020/PTpor
dc.relationLA/P/0029/2020por
dc.relationDFA/BD/08789/2021por
dc.relationinfo:eu-repo/grantAgreement/FCT/CEEC IND 2018/CEECIND%2F03425%2F2018%2FCP1581%2FCT0020/PTpor
dc.relation.publisherversionhttps://bmcbioinformatics.biomedcentral.com/articles/10.1186/s12859-025-06081-9por
dc.rightsopenAccesspor
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/por
dc.subjectDeep learningpor
dc.subjectEnzyme annotationpor
dc.subjectLarge language modelspor
dc.titleComparative assessment of protein large language models for enzyme commission number predictionpor
dc.typearticle
dspace.entity.typePublicationen
oaire.citationConferencePlaceUnited Kingdom
oaire.citationIssue68por
oaire.citationVolume26por
oaire.versionVoRpor
sdum.journalBMC Bioinformaticspor

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