Literature DB >> 20057057

Role of tyrosine 131 in the active site of paAzoR1, an azoreductase with specificity for the inflammatory bowel disease prodrug balsalazide.

Chan-Ju Wang1, Nicola Laurieri, Areej Abuhammad, Edward Lowe, Isaac Westwood, Ali Ryan, Edith Sim.   

Abstract

Azoreductase 1 from Pseudomonas aeruginosa strain PAO1 (paAzoR1) catalyses the activation of the prodrug balsalazide and reduces the azo dye methyl red using reduced nicotinamide adenine dinucleotide cofactor as an electron donor. To investigate the mechanism of the enzyme, a Y131F mutation was introduced and the enzymic properties of the mutant were compared with those of the wild-type enzyme. The crystallographic structure of the mutant with methyl red bound was solved at 2.1 A resolution and compared with the wild-type structure. Tyr131 is important in the architecture of the active site but is not essential for enzymic activity.

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Year:  2009        PMID: 20057057      PMCID: PMC2805523          DOI: 10.1107/S1744309109044741

Source DB:  PubMed          Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun        ISSN: 1744-3091


  26 in total

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  9 in total

1.  Crystallization and preliminary X-ray diffraction analysis of the azoreductase PpAzoR from Pseudomonas putida MET94.

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3.  Effects of Orange II and Sudan III azo dyes and their metabolites on Staphylococcus aureus.

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9.  Mechanistic and Crystallographic Studies of Azoreductase AzoA from Bacillus wakoensis A01.

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  9 in total

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