Skip to main content
. 2011 May 13;16(6):899–912. doi: 10.1007/s00775-011-0789-4

Fig. 1.

Fig. 1

Structures and reactions of substrates used to characterize the CYP102A1 mutants. a Alkoxyresorufin O-dealkylation: R is: H (methoxyresorufin), CH3 (ethoxyresorufin), C2H5 (n-propoxyresorufin), C3H7 (n-butoxyresorufin), C4H9 (n-pentoxyresorufin), C5H11 (n-hexoxyresorufin), C6H13 (n-heptoxyresorufin), C7H15 (n-octoxyresorufin), C6H5 (benzyloxyresorufin). b Testosterone hydroxylation: arrows indicate identified positions of hydroxylation