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. 2012 Aug 2;3:148. doi: 10.3389/fphar.2012.00148

Table 3.

Kinetic constants of AKR1B toward 4-hydroxynonenal, isocaproaldehyde, and prostaglandin H2.

Substrates 4-Hydroxynonenal
Isocaproaldehyde
Prostaglandin H2e
Km (μM) Kcat (s−1) Km (μM) Kcat (s−1) Km (μM) Vmax (nmol/min/mg)
HUMAN
AKR1B1 716a 0.84a 1b 0.66b 1.9 44
AKR1B10 31a 2.01a 330c 0.72c No activity
AKR1B15 n.d. n.d. n.d. n.d. n.d.
MOUSE
Akr1b3 665a 0.82a 62d 1.3d 9.3 26
Akr1b7 256a 0.1a 320d 0.38d 3.8 53.4
Akr1b8 230a 3.18a 71d 0.03d No activity
Akr1b16 n.d. n.d. n.d. n.d. n.d.
RAT
Akr1b4 33f 0.23f n.d. n.d. n.d.
r-Akr1b10 1.6g 0.05g 11g 0.03g n.d.
Akr1b13 30f 0.18f n.d. n.d. n.d.
Akr1b14 7.6h 0.02h 16h 0.03h n.d.

n.d., not determined.

References (for comparison data were converted in μM for the Km and in s−1 for the Kcat): aJoshi et al. (2010), bMatsuura et al. (1996), cMartin and Maser (2009), dMartinez et al. (2001), eKabututu et al. (2009), fEndo et al. (2009a), gEndo et al. (2010b), hEndo et al. (2010a).