Author
Listed:
- Daniel A. Erlanson
(Frontier Medicines Corporation)
- Stephen K. Burley
(RCSB Protein Data Bank
The State University of New Jersey)
- Daren Fearon
(Harwell Science and Innovation Campus)
- James S. Fraser
(University of California San Francisco)
- Dale Kreitler
(NSLS-II)
- Maria Cristina Nonato
(University of São Paulo)
- Naoki Sakai
(Japan Synchrotron Radiation Research Institute)
- Jan Wollenhaupt
(Proteros Biostructures GmbH)
- Manfred S. Weiss
(Macromolecular Crystallography)
Abstract
Fragment screening by crystallography has recently skyrocketed. Multiple synchrotrons have built specialized screening platforms, established workflows, and assembled compound libraries. Crystallographic fragment screening is now widely accessible to groups that had previously not considered the approach. While hundreds of crystallographic fragment-screening campaigns have been conducted in the last few years, most of the underlying data have neither been published nor made publicly accessible. This perspective highlights the importance of establishing effective mechanisms for preserving large and often heterogeneous groups of datasets intrinsic to crystallographic fragment-screening campaigns, thereby ensuring their accessibility for advancing research and enabling applications such as training AI-based models.
Suggested Citation
Daniel A. Erlanson & Stephen K. Burley & Daren Fearon & James S. Fraser & Dale Kreitler & Maria Cristina Nonato & Naoki Sakai & Jan Wollenhaupt & Manfred S. Weiss, 2025.
"Where and how to house big data on small fragments,"
Nature Communications, Nature, vol. 16(1), pages 1-6, December.
Handle:
RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-59233-z
DOI: 10.1038/s41467-025-59233-z
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