Methods for Detecting Critical Residues in Proteins.

In proteins, certain amino acids may play a critical role in determining their structure and function. Examples include flexible regions, which allow domain motions, and highly conserved residues on functional interfaces, which play a role in binding and interaction with other proteins. Detecting these regions facilitates the analysis and simulation of protein rigidity and conformational changes, and aids in characterizing protein-protein binding. We present a protocol that combines graph-theory rigidity analysis and machine-learning-based methods for predicting critical residues in proteins. Our approach combines amino-acid specific information and data obtained by two complementary methods. One method, KINARI, performs graph-based analysis to find rigid clusters of amino acids in a protein, while the other method relies on evolutionary conservation scores to find functional interfaces in proteins. Our machine learning model combines both methods, in addition to amino acid type and solvent-accessible surface area.