MOTIVATION: Protein-protein interactions underpin many cellular processes and their disruption due to mutations can lead to diseases. With the evolution of protein structure prediction methods like AlphaFold2 and the availability of extensive experimental affinity data, there is a pressing need for updated computational tools that can efficiently predict changes in binding affinity caused by mutations in protein-protein complexes. RESULTS: We developed a deep ensemble model that leverages protein sequences, predicted structure-based features, and protein functional classes to accurately predict the change in binding affinity due to mutations. The model achieved a correlation of 0.97 and a mean absolute error (MAE) of 0.35 kcal/mol on the training dataset, and maintained robust performance on the test set with a correlation of 0.72 and a MAE of 0.83 kcal/mol. Further validation using Leave-One-Out Complex (LOOC) cross-validation exhibited a correlation of 0.83 and a MAE of 0.51 kcal/mol, indicating consistent performance. AVAILABILITY AND IMPLEMENTATION: https://web.iitm.ac.in/bioinfo2/DeepPPAPredMut/index.html.

MOTIVATION: Machine learning techniques require various descriptors from protein and nucleic acid sequences to understand/predict their structure and function as well as distinguishing between disease and neutral mutations. Hence, availability of a feature extraction tool is necessary to bridge the gap. RESULTS: We developed a comprehensive web-based tool, Seq2Feature, which computes 252 protein and 41 DNA sequence-based descriptors. These features include physicochemical, energetic and conformational properties of proteins, mutation matrices and contact potentials as well as nucleotide composition, physicochemical and conformational properties of DNA. We propose that Seq2Feature could serve as an effective tool for extracting protein and DNA sequence-based features as applicable inputs to machine learning algorithms. AVAILABILITY AND IMPLEMENTATION: https://www.iitm.ac.in/bioinfo/SBFE/index.html. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.