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5NY5

The apo structure of 3,4-dihydroxybenzoic acid decarboxylases from Enterobacter cloacae

Summary for 5NY5
Entry DOI10.2210/pdb5ny5/pdb
Descriptor3,4-dihydroxybenzoate decarboxylase, GLYCEROL (3 entities in total)
Functional Keywordsubid-family, carboxylation, catechols, prenylated fmn, hydrolase
Biological sourceEnterobacter cloacae
Total number of polymer chains2
Total formula weight108602.22
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 citationPayer, 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: 28857436
DOI: 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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数据于2024-11-06公开中

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