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. 2017 Dec 15;8(70):115420–115433. doi: 10.18632/oncotarget.23271

Table 1. Kinetic parameters of mutant and wild-type forms of FBP1 and FBP2.

kcat [s−1] a ks[μM], F-1,6-BP a kis[μM], F-1,6-BP a n, F-1,6-BP a A50[mM], Mg2+ n, Mg2+ IC50, AMP [μM] a n, AMP a
FBP2 WT 20.9±2.52 3.66±0.07 111±2.3 1.61±0.04 0.88±0.05 1.96±0.21 0.59±0.01 2.04±0.05
FBP2 D187L 15.3±0.56 12.9±0.64 120±12 1.72±0.05 3.22±0.23 2.05±0.27 1.44±0.06 2.29±0.21
FBP2 L190G 23.8±3.19 5.82±0.20 119±3.6 1.99±0.06 1.96±0.09 1.94±0.17 84.4±6.7323300±2520 2.06±0.331.68±0.25
FBP1 b 16.7±0.5 2.2±0.4 157±48 1 0.31±0.01 1.93±0.12 5.06±0.27 1.95±0.16

Data presented as mean±SD

a – determined at Mg2+ concentration of 5 mM for wild-type FBP2, 15 mM for D187L mutant and 10 mM for L190G mutant.

b – as described in [20].