5NY5
The apo structure of 3,4-dihydroxybenzoic acid decarboxylases from Enterobacter cloacae
Summary for 5NY5
Entry DOI | 10.2210/pdb5ny5/pdb |
Descriptor | 3,4-dihydroxybenzoate decarboxylase, GLYCEROL (3 entities in total) |
Functional Keywords | ubid-family, carboxylation, catechols, prenylated fmn, hydrolase |
Biological source | Enterobacter cloacae |
Total number of polymer chains | 2 |
Total formula weight | 108602.22 |
Authors | Dordic, A.,Gruber, K.,Payer, S.,Glueck, S.,Pavkov-Keller, T.,Marshall, S.,Leys, D. (deposition date: 2017-05-11, release date: 2017-09-13, Last modification date: 2020-11-18) |
Primary citation | Payer, S.E.,Marshall, S.A.,Barland, N.,Sheng, X.,Reiter, T.,Dordic, A.,Steinkellner, G.,Wuensch, C.,Kaltwasser, S.,Fisher, K.,Rigby, S.E.J.,Macheroux, P.,Vonck, J.,Gruber, K.,Faber, K.,Himo, F.,Leys, D.,Pavkov-Keller, T.,Glueck, S.M. Regioselective para-Carboxylation of Catechols with a Prenylated Flavin Dependent Decarboxylase. Angew. Chem. Int. Ed. Engl., 56:13893-13897, 2017 Cited by PubMed Abstract: The utilization of CO as a carbon source for organic synthesis meets the urgent demand for more sustainability in the production of chemicals. Herein, we report on the enzyme-catalyzed para-carboxylation of catechols, employing 3,4-dihydroxybenzoic acid decarboxylases (AroY) that belong to the UbiD enzyme family. Crystal structures and accompanying solution data confirmed that AroY utilizes the recently discovered prenylated FMN (prFMN) cofactor, and requires oxidative maturation to form the catalytically competent prFMN species. This study reports on the in vitro reconstitution and activation of a prFMN-dependent enzyme that is capable of directly carboxylating aromatic catechol substrates under ambient conditions. A reaction mechanism for the reversible decarboxylation involving an intermediate with a single covalent bond between a quinoid adduct and cofactor is proposed, which is distinct from the mechanism of prFMN-associated 1,3-dipolar cycloadditions in related enzymes. PubMed: 28857436DOI: 10.1002/anie.201708091 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.501 Å) |
Structure validation
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