Literature DB >> 22225642

Mechanistic studies on the flavin:NADH reductase (PrnF) from Pseudomonas fluorescens involved in arylamine oxygenation.

Manish Kumar Tiwari1, Raushan Kumar Singh, Jung-Kul Lee, Huimin Zhao.   

Abstract

We report the mechanistic studies of a FAD:NADH reductase (PrnF) involved in arylamine oxygenation. PrnF catalyzes the reduction of FAD via a sequential ordered bi-bi mechanism with NADH as the first substrate to bind and FADH(2) as the first product to be released. The residues Asp145 and His146 are proposed as catalytic acid/base residues for PrnF based on pH profile and molecular dynamics simulation studies. These studies provide the first detailed account of the mechanism of the flavin reductase involved in arylamine oxygenation.
Copyright © 2011 Elsevier Ltd. All rights reserved.

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Year:  2011        PMID: 22225642     DOI: 10.1016/j.bmcl.2011.12.078

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  1 in total

1.  Engineered Bacterial Flavin-Dependent Monooxygenases for the Regiospecific Hydroxylation of Polycyclic Phenols.

Authors:  Susann Herrmann; Martin Dippe; Pascal Pecher; Evelyn Funke; Markus Pietzsch; Ludger A Wessjohann
Journal:  Chembiochem       Date:  2022-02-09       Impact factor: 3.461

  1 in total

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