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GNINA rescoring of AutoDock-GPU poses (AutoDock-GNINA) emerged as the strongest single method with a median EF1% of 2.14. DiffDock-based approaches underperformed relative to AutoDock-GNINA, particularly on challenging targets such as OPRK1. Carefully designed consensus ranking improved robustness but did not surpass the best single scorer. Supervised ML re-ranking delivered the largest gains, achieving a median EF1% of 4.49 (+110% over AutoDock-GNINA).
Our results highlight that even the best classical+ML hybrid workflows provide only modest early enrichment on realistic benchmarks. We conclude that no single docking method dominates across targets and that rigorously validated, cost-effective combinations with supervised re-ranking currently offer the most practical value for virtual screening.
| Subjects: | Machine Learning (cs.LG); Biomolecules (q-bio.BM) |
| Cite as: | arXiv:2605.01681 [cs.LG] |
| (or arXiv:2605.01681v1 [cs.LG] for this version) | |
| https://doi.org/10.48550/arXiv.2605.01681 arXiv-issued DOI via DataCite (pending registration) |
From: Youssef Abo-Dahab [view email]
[v1]
Sun, 3 May 2026 02:38:21 UTC (1,051 KB)
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