Molence (@MolenceBio) header
Molence (@MolenceBio) profile picture
Joined October 2026
Introducing Mol-1: Open Frontier Biomolecular Intelligence 🚀🚀🚀 📊 75.0% on FoldBench-AB, near IsoDDE's reported 75.58%!!! 🧬 60k-token assemblies on one single H20, outperforming Anthropic 8/10. 🎯 VHHs binding hit rate as high as 63% with best SPR KD at 43 pM. GitHub: github.com/molence/Mol-1 Try it: lab.molence.com
16
98
12
584
59,442
1/15 🧬 Mol-1 on antibody structure prediction: on par with IsoDDE, open to build on. 75.0% median success at DockQ > 0.23, on par with IsoDDE’s reported 75.58%. Across all 201,376 five-seed combinations from 32 seeds, 62.22% matched or exceeded 75% success—showing robust performance across seed selections. We release the model code and weights so researchers can run Mol-1 in their own environment and build on its capabilities. Code & weights: github.com/molence/Mol-1 Try Mol-1: lab.molence.com #AIforScience #DrugDiscovery
2
3
4
7
1,174
14/15 📍 Bring epitope knowledge into structure prediction. With epitope information, Mol-1-constraint improves antibody–antigen success at DockQ > 0.23 across all four benchmarks: • FoldBench-AB: 75.0% → 88.3% • AF3-AB: 62.7% → 84.2% • PXMeter-AB: 58.3% → 77.5% • MolBench-AB-26: 57.3% → 79.4% Evaluate Mol-1 and Mol-1-constraint with your own biological questions: lab.molence.com #AIforScience
1
30
15/15 📍 Three residues can provide a useful structural clue. In three case studies, we supplied three-residue site hypotheses informed by literature and monomer structures. With Mol-1-constraint, DockQ improved: • 0.014 → 0.874 • 0.011 → 0.739 • 0.200 → 0.863 These examples show how sparse biological hypotheses can guide complex prediction. #AIforScience
31