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SNP2Structure: A Public and Versatile Resource for Mapping and Three-Dimensional Modeling of Missense SNPs on Human Protein Structures
One of the long-standing challenges in biology is to understand how non-synonymous single nucleotide polymorphisms (nsSNPs) change protein structure and further affect their function. While it is impractical to solve all the mutated protein structures experimentally, it is quite feasible to model th...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Research Network of Computational and Structural Biotechnology
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4759123/ https://www.ncbi.nlm.nih.gov/pubmed/26949480 http://dx.doi.org/10.1016/j.csbj.2015.09.002 |
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author | Wang, Difei Song, Lei Singh, Varun Rao, Shruti An, Lin Madhavan, Subha |
author_facet | Wang, Difei Song, Lei Singh, Varun Rao, Shruti An, Lin Madhavan, Subha |
author_sort | Wang, Difei |
collection | PubMed |
description | One of the long-standing challenges in biology is to understand how non-synonymous single nucleotide polymorphisms (nsSNPs) change protein structure and further affect their function. While it is impractical to solve all the mutated protein structures experimentally, it is quite feasible to model the mutated structures in silico. Toward this goal, we built a publicly available structure database resource (SNP2Structure, https://apps.icbi.georgetown.edu/snp2structure) focusing on missense mutations, msSNP. Compared with web portals with similar aims, SNP2Structure has the following major advantages. First, our portal offers direct comparison of two related 3D structures. Second, the protein models include all interacting molecules in the original PDB structures, so users are able to determine regions of potential interaction changes when a protein mutation occurs. Third, the mutated structures are available to download locally for further structural and functional analysis. Fourth, we used Jsmol package to display the protein structure that has no system compatibility issue. SNP2Structure provides reliable, high quality mapping of nsSNPs to 3D protein structures enabling researchers to explore the likely functional impact of human disease-causing mutations. |
format | Online Article Text |
id | pubmed-4759123 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Research Network of Computational and Structural Biotechnology |
record_format | MEDLINE/PubMed |
spelling | pubmed-47591232016-03-04 SNP2Structure: A Public and Versatile Resource for Mapping and Three-Dimensional Modeling of Missense SNPs on Human Protein Structures Wang, Difei Song, Lei Singh, Varun Rao, Shruti An, Lin Madhavan, Subha Comput Struct Biotechnol J Research Article One of the long-standing challenges in biology is to understand how non-synonymous single nucleotide polymorphisms (nsSNPs) change protein structure and further affect their function. While it is impractical to solve all the mutated protein structures experimentally, it is quite feasible to model the mutated structures in silico. Toward this goal, we built a publicly available structure database resource (SNP2Structure, https://apps.icbi.georgetown.edu/snp2structure) focusing on missense mutations, msSNP. Compared with web portals with similar aims, SNP2Structure has the following major advantages. First, our portal offers direct comparison of two related 3D structures. Second, the protein models include all interacting molecules in the original PDB structures, so users are able to determine regions of potential interaction changes when a protein mutation occurs. Third, the mutated structures are available to download locally for further structural and functional analysis. Fourth, we used Jsmol package to display the protein structure that has no system compatibility issue. SNP2Structure provides reliable, high quality mapping of nsSNPs to 3D protein structures enabling researchers to explore the likely functional impact of human disease-causing mutations. Research Network of Computational and Structural Biotechnology 2015-09-30 /pmc/articles/PMC4759123/ /pubmed/26949480 http://dx.doi.org/10.1016/j.csbj.2015.09.002 Text en © 2015 Wang et al. Published by Elsevier B.V. on behalf of the Research Network of Computational and Structural Biotechnology. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Research Article Wang, Difei Song, Lei Singh, Varun Rao, Shruti An, Lin Madhavan, Subha SNP2Structure: A Public and Versatile Resource for Mapping and Three-Dimensional Modeling of Missense SNPs on Human Protein Structures |
title | SNP2Structure: A Public and Versatile Resource for Mapping and Three-Dimensional Modeling of Missense SNPs on Human Protein Structures |
title_full | SNP2Structure: A Public and Versatile Resource for Mapping and Three-Dimensional Modeling of Missense SNPs on Human Protein Structures |
title_fullStr | SNP2Structure: A Public and Versatile Resource for Mapping and Three-Dimensional Modeling of Missense SNPs on Human Protein Structures |
title_full_unstemmed | SNP2Structure: A Public and Versatile Resource for Mapping and Three-Dimensional Modeling of Missense SNPs on Human Protein Structures |
title_short | SNP2Structure: A Public and Versatile Resource for Mapping and Three-Dimensional Modeling of Missense SNPs on Human Protein Structures |
title_sort | snp2structure: a public and versatile resource for mapping and three-dimensional modeling of missense snps on human protein structures |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4759123/ https://www.ncbi.nlm.nih.gov/pubmed/26949480 http://dx.doi.org/10.1016/j.csbj.2015.09.002 |
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