Interaction of a spin-labelled cholesterol derivative with the cytochrome P-450SCC active site
Author:
Publisher
Wiley
Subject
Biochemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1432-1033.1988.tb13872.x/fullpdf
Reference36 articles.
1. Intermediates in the conversion of cholesterol to pregnenolone: Kinetics and mechanism
2. Cytochrome P450 in adrenocortical mitochondria
3. Hydroperoxysterols as a probe for the mechanism of cytochrome P-450scc-mediated hydroxylation. Homolytic versus heterolytic oxygen-oxygen bond scission.
4. Spectroscopic evidence for the formation of a transient species during cytochrome P-450SCC induced hydroperoxysterol-glycol conversions
5. Proximity of the substrate binding site and the heme-iron catalytic site in cytochrome P-450scc.
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2. Stereoselective reactions of (20R)-3,20-dihydroxy-(3′,4′-dihydro-2′H-pyranyl)-5-pregnene derivatives form 27-nor-3,20,23,26-tetrahydroxy-cholesten-22-ones and related bromo ketones;Steroids;2004-01
3. Accessibility of Tyrosine Residues in Cytochrome P-450scc (CYP11A1);Collection of Czechoslovak Chemical Communications;1998
4. A Central Role for Water in the Control of the Spin State of Cytochrome P-450scc;European Journal of Biochemistry;1997-12
5. Dynamics of Carbon Monoxide Binding with Cytochromes P-450;Biochemistry;1997-08-01
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