| First Author | McTamney PM | Year | 2009 |
| Journal | J Am Chem Soc | Volume | 131 |
| Issue | 40 | Pages | 14212-3 |
| PubMed ID | 19777994 | Mgi Jnum | J:322697 |
| Mgi Id | MGI:7260100 | Doi | 10.1021/ja906642n |
| Citation | McTamney PM, et al. (2009) A mammalian reductive deiodinase has broad power to dehalogenate chlorinated and brominated substrates. J Am Chem Soc 131(40):14212-3 |
| abstractText | Iodotyrosine deiodinase is essential for iodide homeostasis and proper thyroid function in mammals. This enzyme promotes a net reductive deiodination of 3-iodotyrosine to form iodide and tyrosine. Such a reductive dehalogenation is uncommon in aerobic organisms, and its requirement for flavin mononucleotide is even more uncommon in catalysis. Reducing equivalents are now shown to transfer directly from the flavin to the halogenated substrate without involvement of other components typically included in the standard enzymatic assay. Additionally, the deiodinase has been discovered to act as a debrominase and a dechlorinase. These new activities expand the possible roles of flavin in biological catalysis and provide a foundation for determining the mechanism of this unusual process. |
