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I’ve read both of the papers on Vina v1.2.0 and ADFR, but I still don’t understand the difference.
Are Vina’s flexible docking and ADFR the same thing or not?
They are different in many ways. The receptor sidechain sampling features described in the ADFR paper are exclusive to ADFR. Vina samples sidechain torsions the same way as if they were ligand torsions
As of 2024 which method is better to run docking for rigid-ligand/partially flexible protein?
Dear all,
Upon reading a tutorial on partially protein-flexible docking using Vina, I couldn’t understand how it differs from ADFR.
I’ve read both of the papers on Vina v1.2.0 and ADFR, but I still don’t understand the difference.
Are Vina’s flexible docking and ADFR the same thing or not?
As of 2024 which method is better to run docking for rigid-ligand/partially flexible protein?
Best Regards,
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