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PreprintCC BYbioRxiv

RNAbridge: a database of extended and non-canonical helices

  1. 1Institute of Computing Science, Poznan University of Technology

Abstract

RNA function is dictated by 3D architecture. Although 2D structural models based on canonical Watson-Crick base pairs are widely used, they often fail to capture the non-canonical interactions, tertiary contacts, and coaxial stacking important for biological activity. We have developed RNAbridge, a comprehensive database and web application that systematically identifies, quantifies, and visualizes extended non-canonical helices and multi-way junctions. Using a geometry- and stacking-based pipeline, we analyzed the Protein Data Bank and compiled a catalog of 135,541 structural motifs. RNAbridge includes a user-friendly interface with interactive filters, synchronized 2D and 3D visualizations, and detailed structural data, including helical bend angles and stacking paths. By connecting simplified 2D topologies with complex 3D structures, RNAbridge serves as a valuable resource for structural biologists and lays the foundation for future machine learning applications in RNA structure prediction. The database, available at https://rnabridge.cs.put.poznan.pl/, is automatically updated once a week.

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BibTeX
@misc{zakrzewski2026rnabridge,
  title = {{RNAbridge: a database of extended and non-canonical helices}},
  author = {D. Zakrzewski and M. Antczak and T. Zok},
  howpublished = {bioRxiv},
  year = {2026},
  month = sep,
  doi = {10.64898/2026.09.15.751775},
  url = {https://www.biorxiv.org/content/10.64898/2026.09.15.751775v1},
  note = {CC BY},
}
RIS
TY  - UNPB
TI  - RNAbridge: a database of extended and non-canonical helices
AU  - D. Zakrzewski
AU  - M. Antczak
AU  - T. Zok
PY  - 2026
DA  - 2026/09/15
PB  - bioRxiv
DO  - 10.64898/2026.09.15.751775
UR  - https://www.biorxiv.org/content/10.64898/2026.09.15.751775v1
AB  - RNA function is dictated by 3D architecture. Although 2D structural models based on canonical Watson-Crick base pairs are widely used, they often fail to capture the non-canonical interactions, tertiary contacts, and coaxial stacking important for biological activity. We have developed RNAbridge, a comprehensive database and web application that systematically identifies, quantifies, and visualizes extended non-canonical helices and multi-way junctions. Using a geometry- and stacking-based pipeline, we analyzed the Protein Data Bank and compiled a catalog of 135,541 structural motifs. RNAbridge includes a user-friendly interface with interactive filters, synchronized 2D and 3D visualizations, and detailed structural data, including helical bend angles and stacking paths. By connecting simplified 2D topologies with complex 3D structures, RNAbridge serves as a valuable resource for structural biologists and lays the foundation for future machine learning applications in RNA structure prediction. The database, available at https://rnabridge.cs.put.poznan.pl/, is automatically updated once a week.
ER  -