US 2025/0029680 A1 · DRUGGABILITY SCORE-BASED RANKING AND LIGAND TYPE CLASSIFICATION OF PROTEIN-LIGAND BINDING SITES

Abstract

The present invention enables the prediction of both the ligand type for protein-ligand binding sites and their druggability scores. The invention provides a computational method to investigate the ligand type and druggability of protein-ligand binding sites. The invention has two distinct training sets for two different prediction methods. The method leverages attention-based deep learning models for both ligand type and druggability prediction tasks. Deep learning models incorporate both channel-based and spatial-based attention mechanisms. The training phase focuses on the coordinates of known ligand binding sites to enhance the accuracy of druggability prediction. The method also provides the capability to update the training set with new data, thereby ensuring continued improvement in the prediction performance. The invention also details a computer device with a memory and processor, storing a computer program to implement the method. The device processes input in the PDB format, performs the necessary cleaning steps, and utilizes the trained models to predict ligand binding site's types and their respective druggability scores. The results are integrated into a table representation and presented to the user, offering an efficient way to understand and apply the predictions.

Claims8

Dependent claims

A method for a druggability score-based ranking and ligand type classification of protein-ligand binding sites (RCLigand), comprising:

creating a first training set for classifying ligand binding sites of proteins according to ligand types, wherein the first training set includes different types of ligand labels and their known binding sites on a target molecule;
creating a second training set for calculating a druggability score of protein-binding sites, wherein the second training set includes pocket and non-pocket coordinates;
identifying the position of the pocket coordinates associated with the binding of a known ligand type and assigning a corresponding ligand label to one or more regions defined;
detection of protein-ligand binding sites that tend to bind with more than one ligand type and not be included in the training process;
analyzing the regions for a first deep learning model in a calculation of a pocket druggability score, wherein said analyzing provides enhanced druggability score accuracy;
performing a deep learning process to a second deep learning model to classify one or more pockets, wherein the second deep learning model is configured to predict one or more ligand binding sites based on the ligand type;
and
providing the predicted ligand type associated with the binding sites and predicting the druggability score of these regions as an output.

5 more elements

A computer device comprising a memory and a processor, wherein the memory stores a computer program and is characterized in that when executing the computer program, the processor implements steps of a method comprising:

obtaining a ligand type labeled training set, wherein
the training set includes protein-ligand binding sites' cartesian coordinates and atom types, and wherein
a first deep learning model is trained, and utilizes a set of weighted parameters that enable the first deep learning model to make predictions;
obtaining the training set being annotated with labels distinguishing between pocket and non-pocket regions, wherein
the training set includes protein-ligand binding sites' cartesian coordinates and atom types, and wherein
a second deep learning model is trained, and utilizes a set of weighted parameters that enable the second deep learning model to make predictions;
a molecular file is created with coordinate and type data, and a file is created by including different protein attributes without number limit for each protein;
a Protein Data Bank (PDB) file is received as an input, then processed by preserving atom-related headers while removing all other non-essential header information;
and
utilizing the trained model to create a druggability score prediction for each ligand binding site.

7 more elements

Dependencies are inferred from the claim text.

Druggability score-based ranking and ligand type classification of protein-ligand binding sites

Life of this patent

Druggability score-based ranking and ligand type classification of protein-ligand binding sites

Life of this patent

Abstract

Claims8