Carboxy terminal extended phytocystatins are bifunctional inhibitors of papain and legumain cysteine proteinases
dc.contributor.author | Martinez, Manuel | |
dc.contributor.author | Díaz Mendoza, María Mercedes | |
dc.contributor.author | Carrillo, Laura | |
dc.contributor.author | Diaz, Isabel | |
dc.date.accessioned | 2024-01-22T11:35:59Z | |
dc.date.available | 2024-01-22T11:35:59Z | |
dc.date.issued | 2007 | |
dc.description | The 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.abstract | Plant 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.department | Depto. de Bioquímica y Biología Molecular | |
dc.description.faculty | Fac. de Ciencias Biológicas | |
dc.description.refereed | TRUE | |
dc.description.sponsorship | Ministerio de Educación y Ciencia (España) | |
dc.description.sponsorship | Universidad Politécnica de Madrid | |
dc.description.status | pub | |
dc.identifier.citation | Martinez, 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.doi | 10.1016/j.febslet.2007.05.042 | |
dc.identifier.essn | 1873-3468 | |
dc.identifier.issn | 0014-5793 | |
dc.identifier.officialurl | https://doi.org/10.1016/j.febslet.2007.05.042 | |
dc.identifier.uri | https://hdl.handle.net/20.500.14352/94326 | |
dc.journal.title | FEBS Letters | |
dc.language.iso | eng | |
dc.page.final | 2918 | |
dc.page.initial | 2914 | |
dc.publisher | FEBS Press | |
dc.rights.accessRights | open access | |
dc.subject.cdu | 577.112 | |
dc.subject.keyword | PhyCys | |
dc.subject.keyword | Phytocystatins | |
dc.subject.keyword | Barley | |
dc.subject.keyword | Cystatin | |
dc.subject.keyword | Cysteine proteinase inhibitor | |
dc.subject.keyword | Legumain | |
dc.subject.keyword | Papain | |
dc.subject.ucm | Biotecnología | |
dc.subject.unesco | 2306 Química Orgánica | |
dc.title | Carboxy terminal extended phytocystatins are bifunctional inhibitors of papain and legumain cysteine proteinases | |
dc.type | journal article | |
dc.type.hasVersion | VoR | |
dc.volume.number | 581 | |
dspace.entity.type | Publication | |
relation.isAuthorOfPublication | ecb86508-86f5-4719-beed-e6870a1a8732 | |
relation.isAuthorOfPublication.latestForDiscovery | ecb86508-86f5-4719-beed-e6870a1a8732 |
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