Journal
CHEMICAL COMMUNICATIONS
Volume 49, Issue 41, Pages 4694-4696Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c3cc39076d
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- RWTH Aachen University (Germany)
- Kohat University of Science and Technology (Pakistan) through the HRD scholarship
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Solved crystal structures of P450 BM3 variants in complex with styrene provide on the molecular level a first explanation of how a positively charged surface residue inverts the enantiopreference of styrene epoxidation. The obtained insights into productive and non-productive styrene binding modes deepened our understanding of enantioselective epoxidation with P450 BM3.
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