I-MUTANT Suite
I-MUTANT Suite predicts the effects of single point mutations on protein stability using support vector machine (SVM) algorithms, providing both sign predictions (increase/decrease) and quantitative ΔΔG estimates from protein sequence or structure.
Key Features:
- Core component: I-Mutant2.0 implements support vector machine (SVM) models to predict stability changes upon single point mutations.
- Dual input capability: Predictions can be generated from either protein sequence or protein structure input.
- Predictive modes: Operates as a classifier to predict stability sign (increase/decrease) and as a regression estimator to predict ΔΔG values.
- Training and validation: Models were trained and validated using ProTherm, the thermodynamic experimental database of protein stability changes due to mutations.
- Accuracy metrics: Classifier accuracy is 80% with structural information and 77% with sequence information; ΔΔG prediction correlation coefficients are 0.71 (structure, standard error 1.30 kcal/mol) and 0.62 (sequence, standard error 1.45 kcal/mol).
Scientific Applications:
- Protein engineering and design: Provides stability impact data for rational design of proteins with altered stability profiles.
- Therapeutic and industrial protein development: Supports selection and prioritization of single point mutations for proteins intended for therapeutic or industrial applications.
Methodology:
Predictions are produced by SVM models (I‑Mutant2.0) trained and validated on ProTherm, accepting sequence or structure input and outputting classification of stability sign and regression estimates of ΔΔG (kcal/mol).
Topics
Collections
Details
- Maturity:
- Mature
- Cost:
- Free of charge
- Tool Type:
- web application
- Operating Systems:
- Linux, Windows, Mac
- Programming Languages:
- Python
- Added:
- 1/22/2015
- Last Updated:
- 11/24/2024
Operations
Data Inputs & Outputs
Protein structure analysis
Outputs
Publications
Capriotti E, Fariselli P, Casadio R. I-Mutant2.0: predicting stability changes upon mutation from the protein sequence or structure. Nucleic Acids Research. 2005;33(Web Server):W306-W310. doi:10.1093/nar/gki375. PMID:15980478. PMCID:PMC1160136.