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@@ -111,7 +111,8 @@ prank predict -c alphafold test.ds # use alphafold config and model (confi
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mapping to predicted pockets, and a calibrated probability of being a ligand-binding residue
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* PyMol and ChimeraX visualizations in `visualizations/` directory (`.pml` and `.cxc` scripts with data files in `data/`)
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* generating visualizations can be turned off by `-visualizations 0` parameter
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* coordinates of the SAS points can be found in `visualizations/data/<struct_file>_points.pdb.gz`. There the "Residue sequence number" (23-26 of HETATM record)
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*`-vis_renderers 'pymol,chimerax'` parameter can be used to turn individual visualization renderers on/off
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* coordinates of SAS points can be found in `visualizations/data/<struct_file>_points.pdb.gz`. There the "Residue sequence number" (23-26 of HETATM record)
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corresponds to the rank of the corresponding pocket (points with value 0 don't belong to any pocket)
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*`-vis_copy_proteins 0` parameter can be used to turn off copying of protein structures to the visualizations directory (faster but visualizations won't be portable)
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@@ -163,20 +164,22 @@ are supported at the moment).
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Rescoring output:
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*`<struct_file>_rescored.csv`: list of pockets sorted by the new score
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*`<struct_file>_predictions.csv`: same as with `prank predict` (since 2.5)
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* Note: probability column is calibrated for rescoring fpocket predictions
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* visualizations
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Note: probability column in `predictions.csv` is calibrated for rescoring fpocket predictions.
prank rescore fpocket.ds -c rescore_2024 # use a new experimental rescoring model
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prank rescore fpocket.ds -c rescore_2024 # use new experimental rescoring model (recommended for alphafold models)
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prank eval-rescore fpocket.ds # evaluate rescoring model on a dataset with known ligands
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~~~
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For rescoring the dataset file needs to have a specific 2-column format. See examples in `test_data/`: `fpocket.ds`, `concavity.ds`, `puresnet.ds`.
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New experimental rescoring model `-c rescore_2024` shows promising result but hasn't been fully evaluated yet. It is recommended for AlphaFold models, NMR and cryo-EM structures since it doesn't depend on b-factor as a feature.
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