The growing VAO flavoprotein family
- PMID: 18280246
- DOI: 10.1016/j.abb.2008.01.027
The growing VAO flavoprotein family
Abstract
The VAO flavoprotein family is a rapidly growing family of oxidoreductases that favor the covalent binding of the FAD cofactor. In this review we report on the catalytic properties of some newly discovered VAO family members and their mode of flavin binding. Covalent binding of the flavin is a self-catalytic post-translational modification primarily taking place in oxidases. Covalent flavinylation increases the redox potential of the cofactor and thus its oxidation power. Recent findings have revealed that some members of the VAO family anchor the flavin via a dual covalent linkage (6-S-cysteinyl-8alpha-N1-histidyl FAD). Some VAO-type aldonolactone oxidoreductases favor the non-covalent binding of the flavin cofactor. These enzymes act as dehydrogenases, using cytochrome c as electron acceptor.
Similar articles
-
Covalent flavinylation of vanillyl-alcohol oxidase is an autocatalytic process.FEBS J. 2008 Oct;275(20):5191-200. doi: 10.1111/j.1742-4658.2008.06649.x. Epub 2008 Sep 11. FEBS J. 2008. PMID: 18793324
-
l-Galactono-gamma-lactone dehydrogenase from Arabidopsis thaliana, a flavoprotein involved in vitamin C biosynthesis.FEBS J. 2008 Feb;275(4):713-26. doi: 10.1111/j.1742-4658.2007.06233.x. Epub 2008 Jan 10. FEBS J. 2008. PMID: 18190525
-
Characterization of Two VAO-Type Flavoprotein Oxidases from Myceliophthora thermophila.Molecules. 2018 Jan 5;23(1):111. doi: 10.3390/molecules23010111. Molecules. 2018. PMID: 29303991 Free PMC article.
-
Flavoenzymes: diverse catalysts with recurrent features.Trends Biochem Sci. 2000 Mar;25(3):126-32. doi: 10.1016/s0968-0004(99)01533-9. Trends Biochem Sci. 2000. PMID: 10694883 Review.
-
Covalent attachment of flavin adenine dinucleotide (FAD) and flavin mononucleotide (FMN) to enzymes: the current state of affairs.Protein Sci. 1998 Jan;7(1):7-20. doi: 10.1002/pro.5560070102. Protein Sci. 1998. PMID: 9514256 Free PMC article. Review.
Cited by
-
Biosynthesis of Nature-Inspired Unnatural Cannabinoids.Molecules. 2021 May 14;26(10):2914. doi: 10.3390/molecules26102914. Molecules. 2021. PMID: 34068935 Free PMC article. Review.
-
Heterologous expression of two FAD-dependent oxidases with (S)-tetrahydroprotoberberine oxidase activity from Arge mone mexicana and Berberis wilsoniae in insect cells.Planta. 2011 Jun;233(6):1185-97. doi: 10.1007/s00425-011-1357-4. Epub 2011 Feb 15. Planta. 2011. PMID: 21327819
-
Genetic and biochemical strategies for regulation of L-ascorbic acid biosynthesis in plants through the L-galactose pathway.Front Plant Sci. 2023 Mar 15;14:1099829. doi: 10.3389/fpls.2023.1099829. eCollection 2023. Front Plant Sci. 2023. PMID: 37021310 Free PMC article. Review.
-
Biocatalytic Properties and Structural Analysis of Eugenol Oxidase from Rhodococcus jostii RHA1: A Versatile Oxidative Biocatalyst.Chembiochem. 2016 Jul 15;17(14):1359-66. doi: 10.1002/cbic.201600148. Epub 2016 Jun 7. Chembiochem. 2016. PMID: 27123962 Free PMC article.
-
Structural basis of inhibition of Mycobacterium tuberculosis DprE1 by benzothiazinone inhibitors.Proc Natl Acad Sci U S A. 2012 Jul 10;109(28):11354-9. doi: 10.1073/pnas.1205735109. Epub 2012 Jun 25. Proc Natl Acad Sci U S A. 2012. PMID: 22733761 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources