Computational modeling without structural validation can lead to compound design dead-ends. HYPERFOCUS^TM combines real experimental data with fragment libraries and virtual screening to refine and confirm our predictions.

HYPERFOCUS^TM enables us to create detailed structural models of potential drug pockets and show where candidate compounds bind to proteins, offering valuable insight into how these compounds affect protein structures and interactions.

HYPERFOCUS^TM leverages computational predictions against cryo-EM data to generate a comprehensive picture of how binding affects protein structures and their interactions beyond what is possible with conventional computational methods alone.