TY - JOUR T1 - Convert Your Favorite Protein Modeling Program Into A Mutation Predictor: “MODICT” JF - bioRxiv DO - 10.1101/038992 SP - 038992 AU - Ibrahim Tanyalcin AU - Katrien Stouffs AU - Dorien Daneels AU - Carla Al Assaf AU - Danny Coomans AU - Willy Lissens AU - Anna Jansen AU - Alexander Gheldof Y1 - 2016/01/01 UR - http://biorxiv.org/content/early/2016/02/06/038992.abstract N2 - Motivation: Predict whether a mutation is deleterious based on the custom 3D model of a protein.Methods: We have developed modiot, a mutation prediction tool which is based on per residue RMSD (root mean square deviation) values of superimposed 3D protein models. Our mathematical algorithm was tested for 42 described mutations in multiple genes including renin, beta-tubulin, biotinidase, sphingomyelin phosphodiesterase-1, phenylalanine hydroxylase and medium chain Acyl-Coa dehydrogenase. Moreover, modiot scores corresponded to experimentally verified residual enzyme activities in mutated biotinidase, phenylalanine hydroxylase and medium chain Acyl-CoA dehydrogenase. Several commercially available prediction algorithms were tested and results were compared. The modiot PERL package and the manual can be downloaded from https://github.com/MODICT/MODICT.Conclusion: We show here that modiot is capable tool for mutation effect prediction at the protein level, using superimposed 3D protein models instead of sequence based algorithms used by POLYPHEN and SIFT. ER -