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May I ask how to use multimer parameters for predicting complexes in the AF2 initial guess section after designing the sequence for ProteinMPPNN. Why do some proteins with poor plddt_binder (=50) and pae_interaction (=27) predicted by AlphaFold3 have high iptm and ptm scores and small PAE when I use AlphaFold3 for prediction?
The text was updated successfully, but these errors were encountered:
May I ask how to use multimer parameters for predicting complexes in the AF2 initial guess section after designing the sequence for ProteinMPPNN. Why do some proteins with poor plddt_binder (=50) and pae_interaction (=27) predicted by AlphaFold3 have high iptm and ptm scores and small PAE when I use AlphaFold3 for prediction?
The text was updated successfully, but these errors were encountered: