Publication:
APPRIS: selecting functionally important isoforms.

dc.contributor.authorRodriguez, Jose Manuel
dc.contributor.authorPozo, Fernando
dc.contributor.authorCerdán-Vélez, Daniel
dc.contributor.authorDi Domenico, Tomás
dc.contributor.authorVazquez, Jesus
dc.contributor.authorTress, Michael L
dc.contributor.funderNIH - National Human Genome Research Institute (NHGRI) (Estados Unidos)es_ES
dc.contributor.funderInstituto de Salud Carlos IIIes_ES
dc.contributor.funderMinisterio de Ciencia, Innovación y Universidades (España)es_ES
dc.contributor.funderFundación La Caixaes_ES
dc.date.accessioned2023-03-16T14:42:54Z
dc.date.available2023-03-16T14:42:54Z
dc.date.issued2022-01-07
dc.description.abstractAPPRIS (https://appris.bioinfo.cnio.es) is a well-established database housing annotations for protein isoforms for a range of species. APPRIS selects principal isoforms based on protein structure and function features and on cross-species conservation. Most coding genes produce a single main protein isoform and the principal isoforms chosen by the APPRIS database best represent this main cellular isoform. Human genetic data, experimental protein evidence and the distribution of clinical variants all support the relevance of APPRIS principal isoforms. APPRIS annotations and principal isoforms have now been expanded to 10 model organisms. In this paper we highlight the most recent updates to the database. APPRIS annotations have been generated for two new species, cow and chicken, the protein structural information has been augmented with reliable models from the EMBL-EBI AlphaFold database, and we have substantially expanded the confirmatory proteomics evidence available for the human genome. The most significant change in APPRIS has been the implementation of TRIFID functional isoform scores. TRIFID functional scores are assigned to all splice isoforms, and APPRIS uses the TRIFID functional scores and proteomics evidence to determine principal isoforms when core methods cannot.es_ES
dc.description.peerreviewedes_ES
dc.description.sponsorshipNational Human Genome Research Institute of the National Institutes of Health [2 U41 HG007234]; Spanish Ministry of Science, Innovation and Universities [PGC2018-097019-B-I00]; Carlos III Institute of Health-Fondo de Investigacion Sanitaria [PRB3 ´ (IPT17/0019––ISCIII-SGEFI/ERDF, ProteoRed]; ‘la Caixa’ Banking Foundation [HR17-00247]. Funding for open access charge: National Human Genome Research Institute.es_ES
dc.format.numberD1es_ES
dc.format.pageD54es_ES
dc.format.volume50es_ES
dc.identifier.citationNucleic Acids Res. 2022 Jan 7;50(D1):D54-D59es_ES
dc.identifier.doi10.1093/nar/gkab1058es_ES
dc.identifier.e-issn1362-4962es_ES
dc.identifier.journalNucleic acids researches_ES
dc.identifier.pubmedID34755885es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/15658
dc.language.isoenges_ES
dc.publisherOxford University Presses_ES
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/ES/PGC2018-097019-B-I00es_ES
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/ES/IPT17/0019es_ES
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/ES/HR17-00247es_ES
dc.relation.publisherversion10.1093/nar/gkab1058es_ES
dc.repisalud.institucionCNICes_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subject.meshDatabases, Proteines_ES
dc.subject.meshProteomicses_ES
dc.subject.meshAnimalses_ES
dc.subject.meshCattlees_ES
dc.subject.meshChickenses_ES
dc.subject.meshHumanses_ES
dc.subject.meshProtein Conformationes_ES
dc.subject.meshProtein Isoformses_ES
dc.subject.meshProteinses_ES
dc.titleAPPRIS: selecting functionally important isoforms.es_ES
dc.typejournal articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
relation.isAuthorOfPublication63e55d34-c1c9-439c-bc46-f5b9830e538a
relation.isAuthorOfPublication9743763b-919c-4fa9-a53c-57c41be5e0ac
relation.isAuthorOfPublication.latestForDiscovery63e55d34-c1c9-439c-bc46-f5b9830e538a

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