DIPS-Plus: The enhanced database of interacting protein structures for interface prediction

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Abstract
In this work, we expand on a dataset recently introduced for protein interface prediction (PIP), the Database of Interacting Protein Structures (DIPS), to present DIPS-Plus, an enhanced, feature-rich dataset of 42,112 complexes for machine learning of protein interfaces. While the original DIPS dataset contains only the Cartesian coordinates for atoms contained in the protein complex along with their types, DIPS-Plus contains multiple residue-level features including surface proximities, half-sphere amino acid compositions, and new profile hidden Markov model (HMM)-based sequence features for each amino acid, providing researchers a curated feature bank for training protein interface prediction methods. We demonstrate through rigorous benchmarks that training an existing state-of-the-art (SOTA) model for PIP on DIPS-Plus yields new SOTA results, surpassing the performance of some of the latest models trained on residue-level and atom-level encodings of protein complexes to date.
Funding Information
  • Foundation for the National Institutes of Health (R01GM093123, R01GM146340, R01GM093123, R01GM146340, R01GM093123, R01GM146340)
  • U.S. Department of Energy (DE-AR0001213, DE-SC0020400, DE-SC0021303, DE-AR0001213, DE-SC0020400, DE-SC0021303, DE-AR0001213, DE-SC0020400, DE-SC0021303)
  • National Science Foundation (DBI1759934, IIS1763246, DBI1759934, IIS1763246, DBI1759934, IIS1763246)

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