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VelocityFM: Short-Horizon Protein Trajectory Prediction via Flow Matching in Velocity Space

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Protein dynamics is fundamentally a trajectory prediction problem, but molecular dynamics (MD) simulation remains expensive and static structure predictors do not model time-ordered motion. We present VelocityFM, a short-horizon protein trajectory predictor that applies rectified flow matching in velocity space over residue frames and torsions. The model combines six Invariant Point Attention (IPA) blocks with a two-layer per-residue temporal self-attention encoder, and is trained on 710...

Protein dynamics is fundamentally a trajectory prediction problem, but molecular dynamics (MD) simulation remains expensive and static structure predictors do not model time-ordered motion. We present VelocityFM, a short-horizon protein trajectory predictor that applies rectified flow matching in velocity space over residue frames and torsions. The model combines six Invariant Point Attention (IPA) blocks with a two-layer per-residue temporal self-attention encoder, and is trained on 710 ATLAS proteins comprising 2090 filtered replicate trajectories. At the primary 128-frame rollout horizon, VelocityFM achieves a median TM-score of 0.929 on 72 held out proteins, with 100% of proteins remaining above TM> 0.7 and 100% clash-free generation. Backbone geometry also remains strong, with a median Ramachandran favoured rate of 91.09%, while dynamics calibration is conservative with median RMSF ratio 0.697. These results show that velocity-space geometric learning can generalise short-horizon trajectory prediction to unseen proteins while preserving fold structure and geometric validity within its intended operating regime.
MD (LOCATION) Invariant Point Attention (ORG) IPA (ORG) ATLAS (ORG) VelocityFM (PERSON) Ramachandran (PERSON) RMSF (ORG)
Originally published by bioRxiv Read original →