| Literature DB >> 22308069 |
Michael A Schätzle1, Stephan Flemming, Syed Masood Husain, Michael Richter, Stefan Günther, Michael Müller.
Abstract
In reduced circumstances: tetrahydroxynaphthalene reductase shows a broad substrate range including alternate phenolic compounds and cyclic ketones. Structural modeling reveals major enzyme-substrate interactions; C-terminal truncation of the enzyme causes an altered substrate preference, in accordance with stabilization of the substrate by the C-terminal carboxylate. This effect allows the identification of a homologous enzyme.Entities:
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Year: 2012 PMID: 22308069 DOI: 10.1002/anie.201107695
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336