| Literature DB >> 27364382 |
F Hafna Ahmed1, A Elaaf Mohamed1, Paul D Carr1, Brendon M Lee1, Karmen Condic-Jurkic1, Megan L O'Mara1, Colin J Jackson1.
Abstract
Bilirubin is a potent antioxidant that is produced from the reduction of the heme degradation product biliverdin. In mammalian cells and Cyanobacteria, NADH/NADPH-dependent biliverdin reductases (BVRs) of the Rossmann-fold have been shown to catalyze this reaction. Here, we describe the characterization of Rv2074 from Mycobacterium tuberculosis, which belongs to a structurally and mechanistically distinct family of F420 H2 -dependent BVRs (F-BVRs) that are exclusively found in Actinobacteria. We have solved the crystal structure of Rv2074 bound to its cofactor, F420 , and used this alongside molecular dynamics simulations, site-directed mutagenesis and NMR spectroscopy to elucidate its catalytic mechanism. The production of bilirubin by Rv2074 could exploit the anti-oxidative properties of bilirubin and contribute to the range of immuno-evasive mechanisms that have evolved in M. tuberculosis to allow persistent infection.Entities:
Keywords: F420; Mycobacterium tuberculosis; bilirubin; biliverdin; biliverdin reductase; enzyme catalysis; flavin/deazaflavin oxidoreductase; mycobacteria
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Year: 2016 PMID: 27364382 PMCID: PMC5338246 DOI: 10.1002/pro.2975
Source DB: PubMed Journal: Protein Sci ISSN: 0961-8368 Impact factor: 6.725