CoCoNat: a novel method based on deep learning for coiled-coil prediction
Open accessPublished version of a preprint
Abstract
Motivation: Coiled-coil domains (CCD) are widespread in all organisms and perform several crucial functions. Given their relevance, the computational detection of CCD is very important for protein functional annotation. State-of-the-art prediction methods include the precise identification of CCD boundaries, the annotation of the typical heptad repeat pattern along the coiled-coil helices as well as the prediction of the oligomerization state. Results: In this article, we describe CoCoNat, a novel method for predicting coiled-coil helix boundaries, residue-level register annotation, and oligomerization state. Our method encodes sequences with the combination of two state-of-the-art protein language models and implements a three-step deep learning procedure concatenated with a Grammatical-Restrained Hidden Conditional Random Field for CCD identification and refinement. A final neural network predicts the oligomerization state. When tested on a blind test set routinely adopted, CoCoNat obtains a performance superior to the current state-of-the-art both for residue-level and segment-level CCD. CoCoNat significantly outperforms the most recent state-of-the-art methods on register annotation and prediction of oligomerization states. Availability and implementation: CoCoNat web server is available at https://coconat.biocomp.unibo.it. Standalone version is available on GitHub at https://github.com/BolognaBiocomp/coconat.
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More recently, deep learning methods have been employed to distinguish dimers, trimers and tetramers.
“More recently, deep learning methods have been employed to distinguish dimers, trimers and tetramers.43−45”
From Assessment of the Topology and Oligomerisation States of Coiled Coils Using Metadynamics with Conformational Restraints (2025) · cites this paper as [44]
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“The input of this network is built based on a well-known biophysical feature: the oligomeric state of canonical CCD is largely determined by the nature of hydrophobic residues in the heptad repeat pattern, namely, residues labelled with registers a and d (see Woolfson, 2023).”
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“2009), MARCOIL (Delorenzi and Speed 2002), Multicoil2 (Trigg et al. 2011), CoCoPRED (Feng et al.”
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- Authors
- Madeo, G., Savojardo, C., Manfredi, M., Martelli, P. L., & Casadio, R.
- Affiliations
- University of Bologna (IT)
- Corresponding author
- Martelli, Pier Luigi
- Venue
- Bioinformatics
- Publisher
- Oxford University Press (OUP)
- Published
- 2023-08-01
- Volume
- 39
- Issue
- 8
- ISSN
- 1367-4803 (ISSN-L)
- 1367-4811
- PMC
- PMC10425188
- OpenAlex
- W4385564477
- Cited by
- 38
- References
- 9
- Citations by year
- 2026: 17 · 2025: 8 · 2024: 13
- FWCI
- 3.39
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Bioinformatics (publishedVersion, cc-by)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Archivio istituzionale della ricerca (Alma Mater Studiorum Università di Bologna) (submittedVersion, cc-by)
- Funders
- Ministry of University and Research
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Machine Learning in Bioinformatics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Structure and Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
- Keywords
- coiled-coil domain, heptad repeat, protein language models, hidden conditional random fields, protein structure prediction
- MeSH terms
- Protein Domains, Deep Learning, Proteins, Neural Networks, Computer, Molecular Sequence Annotation
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