Das Suchergebnis hat sich seit Ihrer Suchanfrage verändert. Eventuell werden Dokumente in anderer Reihenfolge angezeigt.
  • Treffer 3 von 20693
Zurück zur Trefferliste

Evolution, expression, and substrate specificities of aldehyde oxidase enzymes in eukaryotes

  • Aldehyde oxidases (AOXs) are a small group of enzymes belonging to the larger family of molybdo-flavoenzymes, along with the well-characterized xanthine oxidoreductase. The two major types of reactions that are catalyzed by AOXs are the hydroxylation of heterocycles and the oxidation of aldehydes to their corresponding carboxylic acids. Different animal species have different complements of AOX genes. The two extremes are represented in humans and rodents; whereas the human genome contains a single active gene (AOX1), those of rodents, such as mice, are endowed with four genes (Aox1-4), clustering on the same chromosome, each encoding a functionally distinct AOX enzyme. It still remains enigmatic why some species have numerous AOX enzymes, whereas others harbor only one functional enzyme. At present, little is known about the physiological relevance of AOX enzymes in humans and their additional forms in other mammals. These enzymes are expressed in the liver and play an important role in the metabolisms of drugs and other xenobiotics.Aldehyde oxidases (AOXs) are a small group of enzymes belonging to the larger family of molybdo-flavoenzymes, along with the well-characterized xanthine oxidoreductase. The two major types of reactions that are catalyzed by AOXs are the hydroxylation of heterocycles and the oxidation of aldehydes to their corresponding carboxylic acids. Different animal species have different complements of AOX genes. The two extremes are represented in humans and rodents; whereas the human genome contains a single active gene (AOX1), those of rodents, such as mice, are endowed with four genes (Aox1-4), clustering on the same chromosome, each encoding a functionally distinct AOX enzyme. It still remains enigmatic why some species have numerous AOX enzymes, whereas others harbor only one functional enzyme. At present, little is known about the physiological relevance of AOX enzymes in humans and their additional forms in other mammals. These enzymes are expressed in the liver and play an important role in the metabolisms of drugs and other xenobiotics. In this review, we discuss the expression, tissue-specific roles, and substrate specificities of the different mammalian AOX enzymes and highlight insights into their physiological roles.zeige mehrzeige weniger

Metadaten exportieren

Weitere Dienste

Suche bei Google Scholar Statistik - Anzahl der Zugriffe auf das Dokument
Metadaten
Verfasserangaben:Mineko TeraoORCiD, Enrico GarattiniORCiD, Maria João RomãoORCiD, Silke LeimkühlerORCiDGND
DOI:https://doi.org/10.1074/jbc.REV119.007741
ISSN:0021-9258
ISSN:1083-351X
Titel des übergeordneten Werks (Englisch):The journal of biological chemistry
Verlag:American Society for Biochemistry and Molecular Biology
Verlagsort:Rockville
Publikationstyp:Wissenschaftlicher Artikel
Sprache:Englisch
Datum der Erstveröffentlichung:06.03.2020
Erscheinungsjahr:2020
Datum der Freischaltung:03.05.2024
Freies Schlagwort / Tag:2Fe-2S cluster; aldehyde oxidase (AOX); drug metabolism; enzyme evolution; flavin adenine dinucleotide (FAD); flavoprotein; iron-sulfur protein; metal-containing enzyme; metalloenzyme; molybdenum; molybdenum cofactor (Moco); molybdo-flavoenzyme; mouse; oxidase; oxygen radicals; xenobiotic
Band:295
Ausgabe:16
Seitenanzahl:13
Erste Seite:5377
Letzte Seite:5389
Fördernde Institution:Deutsche ForschungsgemeinschaftGerman Research Foundation (DFG); [Le1171/8-3]; FCT-MCTES, research unit UCIBIO [UID/Multi/04378/2019,; PTDC/BBB-BEP/1185/2014]; Fondazione Italo Monzino; Associazione per la; Ricerca sul Cancro (AIRC)Fondazione AIRC per la ricerca sul cancro
Organisationseinheiten:Mathematisch-Naturwissenschaftliche Fakultät / Institut für Biochemie und Biologie
DDC-Klassifikation:5 Naturwissenschaften und Mathematik / 57 Biowissenschaften; Biologie / 570 Biowissenschaften; Biologie
Peer Review:Referiert
Publikationsweg:Open Access / Hybrid Open-Access
Lizenz (Deutsch):License LogoCC-BY - Namensnennung 4.0 International
Verstanden ✔
Diese Webseite verwendet technisch erforderliche Session-Cookies. Durch die weitere Nutzung der Webseite stimmen Sie diesem zu. Unsere Datenschutzerklärung finden Sie hier.