Affiliation:
1. The University of Manchester Chemistry UNITED KINGDOM OF GREAT BRITAIN AND NORTHERN IRELAND
2. The University of Manchester Chemical Engineering UNITED KINGDOM OF GREAT BRITAIN AND NORTHERN IRELAND
3. The University of Manchester Manchester Institute of Biotechnology 131 Princess Street M1 7DN Manchester UNITED KINGDOM OF GREAT BRITAIN AND NORTHERN IRELAND
Abstract
The nonheme iron dioxygenase capreomycin C (CmnC) hydroxylates a free L‐arginine amino acid regio‐ and stereospe‐cifically at the C3‐position as part of the capreomycin antibiotics biosynthesis. Little is known on its structure, catalytic cycle and substrate specificity and, therefore, a comprehensive computational study was performed. A large QM cluster model of CmnC was created of 297 atoms and the mechanisms for C3−H, C4−H and C5−H hydroxylation and C3−C4 desaturation were investigated. All low‐energy pathways correspond to radical reaction mechanisms with an initial hydrogen atom abstraction followed by OH rebound to form alcohol product complexes. The work is compared to alternative L‐Arg hydroxylating nonheme iron dioxygenases and the differences in active site polarity are compared. We show that a tight hydrogen bonding network in the substrate binding pocket positions the substrate in an ideal orientation for C3−H activation, whereby the polar groups in the substrate binding pocket induce an electric field effect that guides the selectivity