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MutDB services: interactive structural analysis of mutation data

Non-synonymous single nucleotide polymorphisms (SNPs) and mutations have been associated with human phenotypes and disease. As more and more SNPs are mapped to phenotypes, understanding how these variations affect the function and expression of genes and gene products becomes an important endeavor....

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Detalles Bibliográficos
Autores principales: Dantzer, Jessica, Moad, Charles, Heiland, Randy, Mooney, Sean
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1160165/
https://www.ncbi.nlm.nih.gov/pubmed/15980479
http://dx.doi.org/10.1093/nar/gki404
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author Dantzer, Jessica
Moad, Charles
Heiland, Randy
Mooney, Sean
author_facet Dantzer, Jessica
Moad, Charles
Heiland, Randy
Mooney, Sean
author_sort Dantzer, Jessica
collection PubMed
description Non-synonymous single nucleotide polymorphisms (SNPs) and mutations have been associated with human phenotypes and disease. As more and more SNPs are mapped to phenotypes, understanding how these variations affect the function and expression of genes and gene products becomes an important endeavor. We have developed a set of tools to aid in the understanding of how amino acid substitutions affect protein structures. To do this, we have annotated SNPs in dbSNP and amino acid substitutions in Swiss-Prot with protein structural information, if available. We then developed a novel web interface to this data that allows for visualization of the location of these substitutions. We have also developed a web service interface to the dataset and developed interactive plugins for UCSF's Chimera structural modeling tool and PyMOL that integrate our annotations with these sophisticated structural visualization and modeling tools. The web services portal and plugins can be downloaded from and the web interface is at .
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spelling pubmed-11601652005-06-29 MutDB services: interactive structural analysis of mutation data Dantzer, Jessica Moad, Charles Heiland, Randy Mooney, Sean Nucleic Acids Res Article Non-synonymous single nucleotide polymorphisms (SNPs) and mutations have been associated with human phenotypes and disease. As more and more SNPs are mapped to phenotypes, understanding how these variations affect the function and expression of genes and gene products becomes an important endeavor. We have developed a set of tools to aid in the understanding of how amino acid substitutions affect protein structures. To do this, we have annotated SNPs in dbSNP and amino acid substitutions in Swiss-Prot with protein structural information, if available. We then developed a novel web interface to this data that allows for visualization of the location of these substitutions. We have also developed a web service interface to the dataset and developed interactive plugins for UCSF's Chimera structural modeling tool and PyMOL that integrate our annotations with these sophisticated structural visualization and modeling tools. The web services portal and plugins can be downloaded from and the web interface is at . Oxford University Press 2005-07-01 2005-06-27 /pmc/articles/PMC1160165/ /pubmed/15980479 http://dx.doi.org/10.1093/nar/gki404 Text en © The Author 2005. Published by Oxford University Press. All rights reserved
spellingShingle Article
Dantzer, Jessica
Moad, Charles
Heiland, Randy
Mooney, Sean
MutDB services: interactive structural analysis of mutation data
title MutDB services: interactive structural analysis of mutation data
title_full MutDB services: interactive structural analysis of mutation data
title_fullStr MutDB services: interactive structural analysis of mutation data
title_full_unstemmed MutDB services: interactive structural analysis of mutation data
title_short MutDB services: interactive structural analysis of mutation data
title_sort mutdb services: interactive structural analysis of mutation data
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1160165/
https://www.ncbi.nlm.nih.gov/pubmed/15980479
http://dx.doi.org/10.1093/nar/gki404
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