PreprintCited by 38RNA and protein synthesis mechanismsProtein Structure and DynamicsMachine Learning in Bioinformatics

RNA3DB: A structurally-dissimilar dataset split for training and benchmarking deep learning models for RNA structure prediction

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Szikszai, Marcell, Magnus, Marcin, Sanghi, Siddhant, Kadyan, Sachin, Bouatta, Nazim, Rivas, Elena·2024·Journal of Molecular Biology

Preprint — published as 10.1016/j.jmb.2024.168552 · Paper page

Abstract

With advances in protein structure prediction thanks to deep learning models like AlphaFold, RNA structure prediction has recently received increased attention from deep learning researchers. RNAs introduce substantial challenges due to the sparser availability and lower structural diversity of the experimentally resolved RNA structures in comparison to protein structures. These challenges are often poorly addressed by the existing literature, many of which report inflated performance due to using training and testing sets with significant structural overlap. Further, the most recent Critical Assessment of Structure Prediction (CASP15) has shown that deep learning models for RNA structure are currently outperformed by traditional methods. In this paper we present RNA3DB, a dataset of structured RNAs, derived from the Protein Data Bank (PDB), that is designed for training and benchmarking deep learning models. The RNA3DB method arranges the RNA 3D chains into distinct groups (Components) that are non-redundant both with regard to sequence as well as structure, providing a robust way of dividing training, validation, and testing sets. Any split of these structurally-dissimilar Components are guaranteed to produce test and validations sets that are distinct by sequence and structure from those in the training set. We provide the RNA3DB dataset, a particular train/test split of the RNA3DB Components (in an approximate 70/30 ratio) that will be updated periodically. We also provide the RNA3DB methodology along with the source-code, with the goal of creating a reproducible and customizable tool for producing structurally-dissimilar dataset splits for structural RNAs. Graphical Abstract: Highlights: While there is a recent surge in applying deep learning to RNA structure prediction, domain experts have raised concerns about generalization and current trends in benchmarking. Many of the concerns primarily relate to how novel RNA families–i.e. families unseen in the training set–are benchmarked, and whether the models are effective at handling such cases. Performance on bench-marks reflective of real-world applications, such as CASP15 and RNA-Puzzles, is poor for RNA deep learning models. We present a dataset–RNA3DB–that is designed for training and bench-marking deep learning models for RNA structure prediction. RNA3DB provides coverage of all RNA chains found in the Protein Data Bank (PDB). RNA3DB is clustered into groups that are both sequentially and structurally non-redundant, providing a robust way of creating training, validation, and testing sets for deep learning models. Along with the dataset, we also provide a transparent methodology as well as the source-code, making our tool both reproducible and customizable.

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Authors
Szikszai, M., Magnus, M., Sanghi, S., Kadyan, S., Bouatta, N., & Rivas, E.
Affiliations
  • Harvard University (US)
  • Columbia University (US)
Venue
Journal of Molecular Biology
Publisher
openRxiv
Published
2024-02-02
Volume
436
Issue
17
Pages
168552-168552
ISSN
0022-2836 (ISSN-L)
OpenAlex
W4393219516
Cited by
38
References
2
Citations by year
2026: 12 · 2025: 16 · 2024: 10
FWCI
5.31
Type
journal article
Language
en
Open access
Licence
cc-by
Locations
  • Journal of Molecular Biology (publishedVersion, cc-by)
  • bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by)
  • PubMed (publishedVersion)
  • Europe PMC (PubMed Central) (acceptedVersion)
  • PubMed Central (acceptedVersion)
  • PubMed Central (submittedVersion, cc-by)
Funders
  • National Institutes of Health (5r21gm148902-02, 1R21GM148902)
  • National Institute of General Medical Sciences (R21 GM148902, R01GM144423)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA and protein synthesis mechanisms
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Structure and Dynamics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Machine Learning in Bioinformatics
Keywords
RNA structure prediction, dataset splits, RNA tertiary structure, Protein Data Bank, CASP15

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