DPCexplorer: A Django Web Application for Interactive Exploration of DPCfam and DPCstruct Protein Domain Classifications
Abstract
This is the accepted, camera-ready version of the manuscript, submitted for publication in the Proceedings of the 22nd IEEE International Conference on eScience (eScience 2026), Naples, Italy, September 2026. It reflects the revisions made in response to peer review, including the implementation of the REST API described in Section VI.E. © 2026 IEEE. Personal use of this material is permitted. Permission from IEEE must be obtained for all other uses, in any current or future media, including reprinting/republishing this material for advertising or promotional purposes, creating new collective works, for resale or redistribution to servers or lists, or reuse of any copyrighted component of this work in other works. The rapid growth of protein sequence and structure databases has created a significant annotation gap that manual curation alone cannot bridge. Two recent computational biology methods, DPCfam and DPCstruct, address this by applying the Density Peak Clustering (DPC) algorithm to automatically group millions of protein domains into putative families called metaclusters. This process yielded 81,384 sequence-based and 28,246 structure-based families with no manual curation, many of which have no counterpart in Pfam, CATH, or SCOP and form the "dark matter" of the protein universe. We present DPCexplorer, a unified Django web application that closes the access gap. Raw archives were preprocessed on the ORFEO HPC cluster and loaded into a PostgreSQL database optimised with B-Tree, GIN trigram, and functional indexes. Built on the Model-View-Template pattern, the platform accepts four query types (DPCfam MCID, DPCstruct MCID, Pfam ID, and UniProt accession) and returns paginated metadata tables, per-protein domain-architecture diagrams, and downloadable biological files (FASTA, MSA, HMM, PDB). For DPCstruct metaclusters it integrates the PDBe-Molstar (Mol*) 3D viewer to render AlphaFold2-predicted structures coloured by per-residue pLDDT confidence directly in the browser. DPCexplorer is fully reproducible from its GitHub repository and the associated Zenodo data deposit.
Fields of Study & Subjects
Protein Structure and Dynamics
Enzyme Structure and Function
Bioinformatics and Genomic Networks
Publication details
- Journal / source
- Zenodo (CERN European Organization for Nuclear Research)
- Publication date
- 7 August 2026
- Language
- EN
- Document type
- Preprint