Aviso: para depositar documentos, por favor, inicia sesión e identifícate con tu cuenta de correo institucional de la UCM con el botón MI CUENTA UCM. No emplees la opción AUTENTICACIÓN CON CONTRASEÑA
 

Carboxy terminal extended phytocystatins are bifunctional inhibitors of papain and legumain cysteine proteinases

dc.contributor.authorMartinez, Manuel
dc.contributor.authorDíaz Mendoza, María Mercedes
dc.contributor.authorCarrillo, Laura
dc.contributor.authorDiaz, Isabel
dc.date.accessioned2024-01-22T11:35:59Z
dc.date.available2024-01-22T11:35:59Z
dc.date.issued2007
dc.descriptionThe financial support from the Ministerio de Educación y Ciencia (BFU2005-00603) and from the Universidad Politécnica de Madrid (AL07-PID-008) is gratefully acknowledged.
dc.description.abstractPlant legumains are cysteine proteinases putatively involved in processing endogenous proteins. Phytocystatins (PhyCys) have been described as plant inhibitors of papain-like cysteine proteinases. Some PhyCys contain a carboxy terminal extension with an amino acid motif (SNSL) similar to that involved in the inhibition of legumain-like proteins by human cystatins. The role of these carboxy terminal extended PhyCys as inhibitors of legumain-like cysteine proteinases is here shown by in vitro inhibition of human legumain and legumain-like activities from barley extracts. Moreover, site-directed mutagenesis has demonstrated that the asparagine of the SNSL motif is essential in this inhibition. We prove for first time the existence of legumain inhibitors in plants.
dc.description.departmentDepto. de Bioquímica y Biología Molecular
dc.description.facultyFac. de Ciencias Biológicas
dc.description.refereedTRUE
dc.description.sponsorshipMinisterio de Educación y Ciencia (España)
dc.description.sponsorshipUniversidad Politécnica de Madrid
dc.description.statuspub
dc.identifier.citationMartinez, Manuel, et al. «Carboxy Terminal Extended Phytocystatins Are Bifunctional Inhibitors of Papain and Legumain Cysteine Proteinases». FEBS Letters, vol. 581, n.o 16, junio de 2007, pp. 2914-18. https://doi.org/10.1016/j.febslet.2007.05.042.
dc.identifier.doi10.1016/j.febslet.2007.05.042
dc.identifier.essn1873-3468
dc.identifier.issn0014-5793
dc.identifier.officialurlhttps://doi.org/10.1016/j.febslet.2007.05.042
dc.identifier.urihttps://hdl.handle.net/20.500.14352/94326
dc.journal.titleFEBS Letters
dc.language.isoeng
dc.page.final2918
dc.page.initial2914
dc.publisherFEBS Press
dc.rights.accessRightsopen access
dc.subject.cdu577.112
dc.subject.keywordPhyCys
dc.subject.keywordPhytocystatins
dc.subject.keywordBarley
dc.subject.keywordCystatin
dc.subject.keywordCysteine proteinase inhibitor
dc.subject.keywordLegumain
dc.subject.keywordPapain
dc.subject.ucmBiotecnología
dc.subject.unesco2306 Química Orgánica
dc.titleCarboxy terminal extended phytocystatins are bifunctional inhibitors of papain and legumain cysteine proteinases
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number581
dspace.entity.typePublication
relation.isAuthorOfPublicationecb86508-86f5-4719-beed-e6870a1a8732
relation.isAuthorOfPublication.latestForDiscoveryecb86508-86f5-4719-beed-e6870a1a8732

Download

Original bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
Carboxy_terminal_extended_phytocystatins.pdf
Size:
1.02 MB
Format:
Adobe Portable Document Format

Collections