Identifying key residues in intrinsically disordered regions of proteins using machine learning

Abstract

Conserved residues in protein homolog sequence alignments are structurally or functionally important. For intrinsically disordered proteins (IDPs) or proteins with intrinsically disordered regions (IDRs), however, alignment often fails because they lack a steric structure to constrain evolution. Although sequences vary, the physicochemical features of IDRs may be preserved in maintaining function. Therefore, a method to retrieve common IDR features may help identify functionally important residues. We applied un-supervised contrastive learning to train a model with self-attention neuronal networks on human IDR orthologs. During training, parameters were optimized to match sequences in ortholog pairs but not in other IDRs. The trained model successfully identifies previously reported critical residues from experimental studies, especially those with an overall pattern (e.g. multiple aromatic residues or charged blocks) rather than short motifs. This predictive model can therefore be used to identify potentially important residues in other proteins.