Egyszerű nézet

dc.contributor.author Sirokmány, Gábor
dc.contributor.author Geiszt, Miklós
dc.date.accessioned 2019-09-27T09:22:18Z
dc.date.available 2019-09-27T09:22:18Z
dc.date.issued 2019
dc.identifier 85063277271
dc.identifier.citation journalVolume=10;pagination=394, pages: 8;journalTitle=FRONTIERS IN IMMUNOLOGY;journalAbbreviatedTitle=FRONT IMMUNOL;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/7345
dc.identifier.uri doi:10.3389/fimmu.2019.00394
dc.description.abstract Peroxidase enzymes can oxidize a multitude of substrates in diverse biological processes. According to the latest phylogenetic analysis, there are four major heme peroxidase superfamilies. In this review, we focus on certain members of the cyclooxygenase-peroxidase superfamily (also labeled as animal heme peroxidases) and their connection to specific NADPH oxidase enzymes which provide H2O2 for the one-and two-electron oxidation of various peroxidase substrates. The family of NADPH oxidases is a group of enzymes dedicated to the production of superoxide and hydrogen peroxide. There is a handful of known and important physiological functions where one of the seven known human NADPH oxidases plays an essential role. In most of these functions NADPH oxidases provide H2O2 for specific heme peroxidases and the concerted action of the two enzymes is indispensable for the accomplishment of the biological function. We discuss human and other metazoan examples of such cooperation between oxidases and peroxidases and analyze the biological importance of their functional interaction. We also review those oxidases and peroxidases where this kind of partnership has not been identified yet.
dc.relation.ispartof urn:issn:1664-3224
dc.title The Relationship of NADPH Oxidases and Heme Peroxidases: Fallin' in and Out
dc.type Journal Article
dc.date.updated 2019-07-30T10:29:56Z
dc.language.rfc3066 en
dc.rights.holder NULL
dc.identifier.mtmt 30640448
dc.identifier.wos 000460293700001
dc.identifier.pubmed 30891045
dc.contributor.department SE/AOK/I/Élettani Intézet
dc.contributor.department SE/AOK/I/ÉI/MTA-SE Lendület Peroxidáz Enzimek Kutatócsoport
dc.contributor.institution Semmelweis Egyetem


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