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dc.contributor.authorOverton, I M
dc.contributor.authorvan Niekerk, C A
dc.contributor.authorCarter, L G
dc.contributor.authorDawson, A
dc.contributor.authorMartin, D M
dc.contributor.authorCameron, S
dc.contributor.authorMcMahon, S A
dc.contributor.authorWhite, Malcolm F
dc.contributor.authorHunter, W N
dc.contributor.authorNaismith, Jim
dc.contributor.authorBarton, G J
dc.date.accessioned2010-10-14T10:42:53Z
dc.date.available2010-10-14T10:42:53Z
dc.date.issued2008-07
dc.identifier.citationOverton , I M , van Niekerk , C A , Carter , L G , Dawson , A , Martin , D M , Cameron , S , McMahon , S A , White , M F , Hunter , W N , Naismith , J & Barton , G J 2008 , ' TarO : a target optimisation system for structural biology ' , Nucleic Acids Research , vol. 36 , no. suppl 2 , pp. W190-W196 . https://doi.org/10.1093/nar/gkn141en
dc.identifier.issn0305-1048
dc.identifier.otherPURE: 425098
dc.identifier.otherPURE UUID: 006f4299-1cf0-42f5-81d3-66c2655722c5
dc.identifier.otherWOS: 000258142300037
dc.identifier.otherScopus: 48449093586
dc.identifier.otherORCID: /0000-0003-1543-9342/work/47136100
dc.identifier.urihttps://hdl.handle.net/10023/1028
dc.descriptionThis work was funded by the UK Biotechnology and Biological Sciences Research Council (BBSRC) Structural Proteomics of Rational Targets (SPoRT) initiative, (Grant BBS/B/14434). Funding to pay the Open Access publication charges for this article was provided by BBSRC.en
dc.description.abstractTarO (http://www.compbio.dundee.ac.uk/taro) offers a single point of reference for key bioinformatics analyses relevant to selecting proteins or domains for study by structural biology techniques. The protein sequence is analysed by 17 algorithms and compared to 8 databases. TarO gathers putative homologues, including orthologues, and then obtains predictions of properties for these sequences including crystallisation propensity, protein disorder and post-translational modifications. Analyses are run on a high-performance computing cluster, the results integrated, stored in a database and accessed through a web-based user interface. Output is in tabulated format and in the form of an annotated multiple sequence alignment (MSA) that may be edited interactively in the program Jalview. TarO also simplifies the gathering of additional annotations via the Distributed Annotation System, both from the MSA in Jalview and through links to Dasty2. Routes to other information gateways are included, for example to relevant pages from UniProt, COG and the Conserved Domains Database. Open access to TarO is available from a guest account with private accounts for academic use available on request. Future development of TarO will include further analysis steps and integration with the Protein Information Management System (PIMS), a sister project in the BBSRC Structural Proteomics of Rational Targets initiative.
dc.format.extent7
dc.language.isoeng
dc.relation.ispartofNucleic Acids Researchen
dc.rights© 2008 The Author(s) This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.en
dc.subjectSecondary structure Predictionen
dc.subjectMultiple sequence Alignmenten
dc.subjectProtein sequencesen
dc.subjectHigh-throughputen
dc.subjectGenomicsen
dc.subjectDatabaseen
dc.subjectDisorderen
dc.subjectProteomicsen
dc.subjectEvolutionen
dc.subjectSelectionen
dc.subjectQH426 Geneticsen
dc.subject.lccQH426en
dc.titleTarO : a target optimisation system for structural biologyen
dc.typeJournal articleen
dc.contributor.sponsorBBSRCen
dc.description.versionPublisher PDFen
dc.contributor.institutionUniversity of St Andrews. School of Biologyen
dc.contributor.institutionUniversity of St Andrews. Biomedical Sciences Research Complexen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.identifier.doihttps://doi.org/10.1093/nar/gkn141
dc.description.statusPeer revieweden
dc.identifier.urlhttp://www.scopus.com/inward/record.url?scp=48449093586&partnerID=8YFLogxKen
dc.identifier.grantnumberBBS/B/14426en


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