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. 2010 Apr 21;95(7):3418–3427. doi: 10.1210/jc.2010-0058

Table 2.

Kinetic analysis of the POR mutant p.Y607C according to yeast microsomal coexpression assays of either WT or mutant POR with human CYP17A1, CYP21A2, and CYP19A1

CYP17A1
CYP21A2
CYP19A1
17α-Hydroxylase Prog → 17OHP 17,20-Lyase (classic) 17Preg → DHEA 17,20-Lyase (alternative) 5pdiolone → An 21-Hydroxylase Prog → DOC Aromatase A → E1
Vmax (pmol/μg · min)
 WT 0.24 ± 0.02 0.22 ± 0.00 0.27 ± 0.01 0.30 ± 0.02 0.014 ± 0.001
 p.Y607C 0.21 ± 0.02 0.13 ± 0.01 0.16 ± 0.00 0.27 ± 0.02 0.010 ± 0.001
Kmm)
 WT 0.26 ± 0.10 0.71 ± 0.04 0.85 ± 0.14 0.24 ± 0.08 180 ± 44
 p.Y607C 0.41 ± 0.13 0.95 ± 0.11 0.75 ± 0.06 0.27 ± 0.10 262 ± 54
Catalytic efficiency Vmax/Km (% WT)
 p.Y607C 56 ± 3 44 ± 4 66 ± 3 79 ± 2 56 ± 3

All assays were carried out in three independent triplicate experiments; results are presented as means ± sem. For CYP17A1, both 17α-hdyroxylase and 17,20-lyase activities within the classic and alternative androgen pathway were determined. Prog, Progesterone; 17Preg, 17-hydroxypregnenolone; 5pdiolone, 5-pregnanediolone; DOC, 11-deoxycortiocosterone; A, androstenedione; E1, estrone.