Sounds interesting. Since there is already Alphafold, I would assume that your solution concentrates on Alphafold's main weakness: the restriction on cristal structures and steady state, i.e. a single structure snapshot in an unrealistic environment. I would assume that an MD based solution like yours would be able to simulate the movement of structure parts and its interaction with a specific environment. The major challenge of MD so far (as far as I remember) was the computability of decently large proteins in reasonable time. Can you please explain how your solution improves on this? Do you have publications?