SNAP predicts effect of mutations on protein function
Open Access
- 30 August 2008
- journal article
- research article
- Published by Oxford University Press (OUP) in Bioinformatics
- Vol. 24 (20) , 2397-2398
- https://doi.org/10.1093/bioinformatics/btn435
Abstract
Summary: Many non-synonymous single nucleotide polymor-phisms (nsSNPs) in humans are suspected to impact protein function. Here, we present a publicly available server implementation of the method SNAP (screening for non-acceptable polymorphisms) that predicts the functional effects of single amino acid substitutions. SNAP identifies over 80% of the non-neutral mutations at 77% accuracy and over 76% of the neutral mutations at 80% accuracy at its default threshold. Each prediction is associated with a reliability index that correlates with accuracy and thereby enables experimentalists to zoom into the most promising predictions. Availability: Web-server: http://www.rostlab.org/services/SNAP; downloadable program available upon request. Contact:bromberg@rostlab.org Supplementary information: Supplementary data are available at Bioinformatics online.Keywords
This publication has 24 references indexed in Scilit:
- Comprehensive in silico mutagenesis highlights functionally important residues in proteinsBioinformatics, 2008
- SNAP: predict effect of non-synonymous polymorphisms on functionNucleic Acids Research, 2007
- The Pfam protein families databaseNucleic Acids Research, 2004
- SIFT: predicting amino acid changes that affect protein functionNucleic Acids Research, 2003
- The SWISS-PROT protein sequence database and its supplement TrEMBL in 2000Nucleic Acids Research, 2000
- Characterization of single-nucleotide polymorphisms in coding regions of human genesNature Genetics, 1999
- Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasisNature Genetics, 1999
- The Protein Mutant DatabaseNucleic Acids Research, 1999
- Gapped BLAST and PSI-BLAST: a new generation of protein database search programsNucleic Acids Research, 1997
- A mutation in the B chain coding region is associated with impaired proinsulin conversion in a family with hyperproinsulinemia.Proceedings of the National Academy of Sciences, 1987