Utilize este identificador para referenciar este registo: https://hdl.handle.net/10216/117920
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Campo DCValorIdioma
dc.creatorDias, AF-
dc.creatorFrancisco, T-
dc.creatorRodrigues, TA-
dc.creatorGrou, CP-
dc.creatorAzevedo, JE-
dc.date.accessioned2018-12-20T10:07:36Z-
dc.date.available2018-12-20T10:07:36Z-
dc.date.issued2016-
dc.identifier.issn0167-4889-
dc.identifier.urihttps://repositorio-aberto.up.pt/handle/10216/117920-
dc.description.abstractIn the field of intracellular protein sorting, peroxisomes are most famous by their capacity to import oligomeric proteins. The data supporting this remarkable property are abundant and, understandably, have inspired a variety of hypothetical models on how newly synthesized (cytosolic) proteins reach the peroxisome matrix. However, there is also accumulating evidence suggesting that many peroxisomal oligomeric proteins actually arrive at the peroxisome still as monomers. In support of this idea, recent data suggest that PEX5, the shuttling receptor for peroxisomal matrix proteins, is also a chaperone/holdase, binding newly synthesized peroxisomal proteins in the cytosol and blocking their oligomerization. Here we review the data behind these two different perspectives and discuss their mechanistic implications on this protein sorting pathway. This article is part of a Special Issue entitled: Peroxisomes edited by Ralf Erdmann.-
dc.description.sponsorshipThis work was supported by national funds through FCT – Fundação para a Ciência e a Tecnologia/MEC-Ministério da Educação e Ciência and when applicable co-funded by FEDER funds within the partnership agreement PT2020 related with the research unit number 4293; and by the project FCOMP-01-0124-FEDER-019731 (PTDC/BIABCM/118577/2010) funded by national funds through FCT and co-funded by Fundo Europeu de Desenvolvimento Regional (FEDER) through the Operation- alCompetitiveness Programme(COMPETE).A. F.D., T.F., T.A.R. and C. P. G. were supported by FCT, Programa Operacional Potencial Humano (POPH) do Quadro de Referência Estratégico Nacional (QREN), and Fundo Social Europeu (FSE).-
dc.language.isoeng-
dc.publisherElsevier-
dc.relationinfo:eu-repo/grantAgreement/FCT/COMPETE/118577/PT-
dc.relation.ispartofBiochimica et Biophysica Acta - Molecular Cell Research, vol.1863(5), p. 814-820-
dc.rightsopenAccess-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/legalcode-
dc.subject.meshAnimals-
dc.subject.meshEukaryotic Cells/chemistry-
dc.subject.meshEukaryotic Cells/metabolism-
dc.subject.meshGene Expression Regulation-
dc.subject.meshHumans-
dc.subject.meshPeroxisomal Targeting Signal 2 Receptor-
dc.subject.meshPeroxisome-Targeting Signal 1 Receptor-
dc.subject.meshPeroxisomes/chemistry-
dc.subject.meshPeroxisomes/metabolism-
dc.subject.meshPlants/chemistry-
dc.subject.meshPlants/metabolism-
dc.subject.meshProtein Isoforms/chemistry-
dc.subject.meshProtein Isoforms/genetics-
dc.subject.meshProtein Isoforms/metabolism-
dc.subject.meshProtein Multimerization-
dc.subject.meshProtein Structure, Secondary-
dc.subject.meshProtein Structure, Tertiary-
dc.subject.meshProtein Transport-
dc.subject.meshReceptors, Cytoplasmic and Nuclear/chemistry-
dc.subject.meshReceptors, Cytoplasmic and Nuclear/genetics-
dc.subject.meshReceptors, Cytoplasmic and Nuclear/metabolism-
dc.subject.meshSaccharomyces cerevisiae/chemistry-
dc.subject.meshSaccharomyces cerevisiae/metabolism-
dc.subject.meshSignal Transduction-
dc.subject.meshTime Factors-
dc.titleThe first minutes in the life of a peroxisomal matrix protein-
dc.typeArtigo em Revista Científica Internacional-
dc.contributor.uportoInstituto de Investigação e Inovação em Saúde-
dc.identifier.doi10.1016/j.bbamcr.2015.09.025-
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/pii/S0167488915003377?via%3Dihub-
Aparece nas coleções:I3S - Artigo em Revista Científica Internacional

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