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VarSite: Disease variants and protein structure
VarSite is a web server mapping known disease‐associated variants from UniProt and ClinVar, together with natural variants from gnomAD, onto protein 3D structures in the Protein Data Bank. The analyses are primarily image‐based and provide both an overview for each human protein, as well as a report...
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Published in: | Protein science 2020-01, Vol.29 (1), p.111-119 |
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creator | Laskowski, Roman A. Stephenson, James D. Sillitoe, Ian Orengo, Christine A. Thornton, Janet M. |
description | VarSite is a web server mapping known disease‐associated variants from UniProt and ClinVar, together with natural variants from gnomAD, onto protein 3D structures in the Protein Data Bank. The analyses are primarily image‐based and provide both an overview for each human protein, as well as a report for any specific variant of interest. The information can be useful in assessing whether a given variant might be pathogenic or benign. The structural annotations for each position in the protein include protein secondary structure, interactions with ligand, metal, DNA/RNA, or other protein, and various measures of a given variant's possible impact on the protein's function. The 3D locations of the disease‐associated variants can be viewed interactively via the 3dmol.js JavaScript viewer, as well as in RasMol and PyMOL. Users can search for specific variants, or sets of variants, by providing the DNA coordinates of the base change(s) of interest. Additionally, various agglomerative analyses are given, such as the mapping of disease and natural variants onto specific Pfam or CATH domains. The server is freely accessible to all at: https://www.ebi.ac.uk/thornton-srv/databases/VarSite. |
doi_str_mv | 10.1002/pro.3746 |
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The analyses are primarily image‐based and provide both an overview for each human protein, as well as a report for any specific variant of interest. The information can be useful in assessing whether a given variant might be pathogenic or benign. The structural annotations for each position in the protein include protein secondary structure, interactions with ligand, metal, DNA/RNA, or other protein, and various measures of a given variant's possible impact on the protein's function. The 3D locations of the disease‐associated variants can be viewed interactively via the 3dmol.js JavaScript viewer, as well as in RasMol and PyMOL. Users can search for specific variants, or sets of variants, by providing the DNA coordinates of the base change(s) of interest. Additionally, various agglomerative analyses are given, such as the mapping of disease and natural variants onto specific Pfam or CATH domains. 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Protein Science published by Wiley Periodicals, Inc. on behalf of The Protein Society.</rights><rights>2019. This article is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5046-1d8872d1d3a16e3b2e5b50695a681c0d3678f3c44d83e9a41a575bff48efb4003</citedby><cites>FETCH-LOGICAL-c5046-1d8872d1d3a16e3b2e5b50695a681c0d3678f3c44d83e9a41a575bff48efb4003</cites><orcidid>0000-0001-5528-0087</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6933866/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6933866/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31606900$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Laskowski, Roman A.</creatorcontrib><creatorcontrib>Stephenson, James D.</creatorcontrib><creatorcontrib>Sillitoe, Ian</creatorcontrib><creatorcontrib>Orengo, Christine A.</creatorcontrib><creatorcontrib>Thornton, Janet M.</creatorcontrib><title>VarSite: Disease variants and protein structure</title><title>Protein science</title><addtitle>Protein Sci</addtitle><description>VarSite is a web server mapping known disease‐associated variants from UniProt and ClinVar, together with natural variants from gnomAD, onto protein 3D structures in the Protein Data Bank. The analyses are primarily image‐based and provide both an overview for each human protein, as well as a report for any specific variant of interest. The information can be useful in assessing whether a given variant might be pathogenic or benign. The structural annotations for each position in the protein include protein secondary structure, interactions with ligand, metal, DNA/RNA, or other protein, and various measures of a given variant's possible impact on the protein's function. The 3D locations of the disease‐associated variants can be viewed interactively via the 3dmol.js JavaScript viewer, as well as in RasMol and PyMOL. Users can search for specific variants, or sets of variants, by providing the DNA coordinates of the base change(s) of interest. Additionally, various agglomerative analyses are given, such as the mapping of disease and natural variants onto specific Pfam or CATH domains. 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Stephenson, James D. ; Sillitoe, Ian ; Orengo, Christine A. ; Thornton, Janet M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5046-1d8872d1d3a16e3b2e5b50695a681c0d3678f3c44d83e9a41a575bff48efb4003</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>3D protein structure</topic><topic>Annotations</topic><topic>CATH</topic><topic>ClinVar</topic><topic>Cloud Computing</topic><topic>Computational Biology</topic><topic>Databases, Genetic</topic><topic>Deoxyribonucleic acid</topic><topic>disease variants</topic><topic>DNA</topic><topic>Domains</topic><topic>Genetic Predisposition to Disease</topic><topic>Genetic Variation</topic><topic>gnomAD</topic><topic>Humans</topic><topic>Internet</topic><topic>Models, Molecular</topic><topic>molecular interactions</topic><topic>natural variants</topic><topic>PDB</topic><topic>Peptide mapping</topic><topic>Pfam</topic><topic>Protein Conformation</topic><topic>Protein structure</topic><topic>Proteins</topic><topic>Proteins - chemistry</topic><topic>Proteins - genetics</topic><topic>Ribonucleic acid</topic><topic>RNA</topic><topic>schematic diagrams</topic><topic>Secondary structure</topic><topic>Servers</topic><topic>Tools for Protein Science</topic><topic>UniProt</topic><topic>User-Computer Interface</topic><topic>VarMap</topic><topic>VarSite</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Laskowski, Roman A.</creatorcontrib><creatorcontrib>Stephenson, James D.</creatorcontrib><creatorcontrib>Sillitoe, Ian</creatorcontrib><creatorcontrib>Orengo, Christine A.</creatorcontrib><creatorcontrib>Thornton, Janet M.</creatorcontrib><collection>Wiley Open Access</collection><collection>Wiley Online Library website</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Protein science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Laskowski, Roman A.</au><au>Stephenson, James D.</au><au>Sillitoe, Ian</au><au>Orengo, Christine A.</au><au>Thornton, Janet M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>VarSite: Disease variants and protein structure</atitle><jtitle>Protein science</jtitle><addtitle>Protein Sci</addtitle><date>2020-01</date><risdate>2020</risdate><volume>29</volume><issue>1</issue><spage>111</spage><epage>119</epage><pages>111-119</pages><issn>0961-8368</issn><eissn>1469-896X</eissn><abstract>VarSite is a web server mapping known disease‐associated variants from UniProt and ClinVar, together with natural variants from gnomAD, onto protein 3D structures in the Protein Data Bank. The analyses are primarily image‐based and provide both an overview for each human protein, as well as a report for any specific variant of interest. The information can be useful in assessing whether a given variant might be pathogenic or benign. The structural annotations for each position in the protein include protein secondary structure, interactions with ligand, metal, DNA/RNA, or other protein, and various measures of a given variant's possible impact on the protein's function. The 3D locations of the disease‐associated variants can be viewed interactively via the 3dmol.js JavaScript viewer, as well as in RasMol and PyMOL. Users can search for specific variants, or sets of variants, by providing the DNA coordinates of the base change(s) of interest. Additionally, various agglomerative analyses are given, such as the mapping of disease and natural variants onto specific Pfam or CATH domains. The server is freely accessible to all at: https://www.ebi.ac.uk/thornton-srv/databases/VarSite.</abstract><cop>Hoboken, USA</cop><pub>John Wiley & Sons, Inc</pub><pmid>31606900</pmid><doi>10.1002/pro.3746</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-5528-0087</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 3D protein structure Annotations CATH ClinVar Cloud Computing Computational Biology Databases, Genetic Deoxyribonucleic acid disease variants DNA Domains Genetic Predisposition to Disease Genetic Variation gnomAD Humans Internet Models, Molecular molecular interactions natural variants PDB Peptide mapping Pfam Protein Conformation Protein structure Proteins Proteins - chemistry Proteins - genetics Ribonucleic acid RNA schematic diagrams Secondary structure Servers Tools for Protein Science UniProt User-Computer Interface VarMap VarSite |
title | VarSite: Disease variants and protein structure |
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