Protein–ligand binding residue prediction enhancement through hybrid deep heterogeneous learning of sequence and structure data

Knowledge of protein-ligand binding residues is important for understanding the functions of proteins and their interaction mechanisms. From experimentally solved protein structures, how to accurately identify its potential binding sites of a specific ligand on the protein is still a challenging problem. Compared with structure-alignment-based methods, machine learning algorithms provide an alternative flexible solution which is less dependent on annotated homogeneous protein structures. Several factors are important for an efficient protein-ligand prediction model, e.g. discriminative feature representation and effective learning architecture to deal with both the large-scale and severely imbalanced data.