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Biochemistry|June 19, 2002
A new electron transport mechanism in mitochondrial steroid hydroxylase systems based on structural changes upon the reduction of adrenodoxinDirk Beilke, Roland Weiss, Frank Löhr, et al.
Journal of Biomolecular NMR|March 11, 2009
Intermolecular dynamics studied by paramagnetic taggingXingfu Xu, Peter H J Keizers, Wolfgang Reinle, et al.
The FEBS Journal|October 11, 2014
A natural heme-signature variant of CYP267A1 from Sorangium cellulosum So ce56 executes diverse ω-hydroxylationYogan Khatri, Frank Hannemann, Marco Girhard, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|December 15, 2015
Metabolism of Oral Turinabol by Human Steroid Hormone-Synthesizing Cytochrome P450 EnzymesLina Schiffer, Simone Brixius-Anderko, Frank Hannemann, et al.
Journal of Inorganic Biochemistry|May 4, 2011
Structural and thermodynamic characterization of the adrenodoxin-like domain of the electron-transfer protein Etp1 from Schizosaccharomyces pombeJürgen J Müller, Frank Hannemann, Burkhard Schiffler, et al.
Bioelectrochemistry (Amsterdam, Netherlands)|February 21, 2012
Direct and mediated electrochemical response of the cytochrome P450 106A2 from Bacillus megaterium ATCC 13368Hélène Colas, Kerstin M Ewen, Frank Hannemann, et al.
The FEBS Journal|September 24, 2017
Biochemical and structural characterization of CYP109A2, a vitamin D<sub>3</sub> 25-hydroxylase from Bacillus megateriumAmmar Abdulmughni, Ilona K Jóźwik, Elisa Brill, et al.
The Journal of Steroid Biochemistry and Molecular Biology|April 30, 2016
Biotransformation of the mineralocorticoid receptor antagonists spironolactone and canrenone by human CYP11B1 and CYP11B2: Characterization of the products and their influence on mineralocorticoid receptor transactivationLina Schiffer, Anne-Rose Müller, Anna Hobler, et al.
Journal of the American Chemical Society|April 29, 2008
Dynamics in a pure encounter complex of two proteins studied by solution scattering and paramagnetic NMR spectroscopyXingfu Xu, Wolfgang Reinle, Frank Hannemann, et al.
Molecular Genetics and Metabolism|May 25, 2010
Five novel mutations in CYP11B2 gene detected in patients with aldosterone synthase deficiency type I: Functional characterization and structural analysesHuy-Hoang Nguyen, Frank Hannemann, Michaela F Hartmann, et al.
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