MOTIVATION: Protein engineering methods are commonly employed to decipher the folding mechanism of proteins and enzymes. However, such experiments are exceedingly time and resource intensive. It would therefore be advantageous to develop a simple computational tool to predict changes in folding rates upon mutations. Such a method should be able to rapidly provide the sequence position and chemical nature to modulate through mutation, to effect a particular change in rate. This can be of importance in protein folding, function or mechanistic studies. RESULTS: We have developed a robust knowledge-based methodology to predict the changes in folding rates upon mutations formulated from amino and acid properties using multiple linear regression approach. We benchmarked this method against an experimental database of 790 point mutations from 26 two-state proteins. Mutants were first classified according to secondary structure, accessible surface area and position along the primary sequence. Three prime amino acid features eliciting the best relationship with folding rates change were then shortlisted for each class along with an optimized window length. We obtained a self-consistent mean absolute error of 0.36 s(-1) and a mean Pearson correlation coefficient (PCC) of 0.81. Jack-knife test resulted in a MAE of 0.42 s(-1) and a PCC of 0.73. Moreover, our method highlights the importance of outlier(s) detection and studying their implications in the folding mechanism. AVAILABILITY AND IMPLEMENTATION: A web server 'Folding RaCe' has been developed and is available at http://www.iitm.ac.in/bioinfo/proteinfolding/foldingrace.html. CONTACT: gromiha@iitm.ac.in SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
MOTIVATION: Protein engineering methods are commonly employed to decipher the folding mechanism of proteins and enzymes. However, such experiments are exceedingly time and resource intensive. It would therefore be advantageous to develop a simple computational tool to predict changes in folding rates upon mutations. Such a method should be able to rapidly provide the sequence position and chemical nature to modulate through mutation, to effect a particular change in rate. This can be of importance in protein folding, function or mechanistic studies. RESULTS: We have developed a robust knowledge-based methodology to predict the changes in folding rates upon mutations formulated from amino and acid properties using multiple linear regression approach. We benchmarked this method against an experimental database of 790 point mutations from 26 two-state proteins. Mutants were first classified according to secondary structure, accessible surface area and position along the primary sequence. Three prime amino acid features eliciting the best relationship with folding rates change were then shortlisted for each class along with an optimized window length. We obtained a self-consistent mean absolute error of 0.36 s(-1) and a mean Pearson correlation coefficient (PCC) of 0.81. Jack-knife test resulted in a MAE of 0.42 s(-1) and a PCC of 0.73. Moreover, our method highlights the importance of outlier(s) detection and studying their implications in the folding mechanism. AVAILABILITY AND IMPLEMENTATION: A web server 'Folding RaCe' has been developed and is available at http://www.iitm.ac.in/bioinfo/proteinfolding/foldingrace.html. CONTACT: gromiha@iitm.ac.in SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Authors: Marta Nadal; Stefan Prekovic; Nerea Gallastegui; Christine Helsen; Montserrat Abella; Karolina Zielinska; Marina Gay; Marta Vilaseca; Marta Taulès; Adriaan B Houtsmuller; Martin E van Royen; Frank Claessens; Pablo Fuentes-Prior; Eva Estébanez-Perpiñá Journal: Nat Commun Date: 2017-02-06 Impact factor: 14.919
Authors: Rosalyn C Zimmermann; Mihaela E Sardiu; Christa A Manton; Md Sayem Miah; Charles A S Banks; Mark K Adams; Devin C Koestler; Douglas R Hurst; Mick D Edmonds; Michael P Washburn; Danny R Welch Journal: PLoS One Date: 2021-11-17 Impact factor: 3.752