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. 2020 Nov 27;477(22):4425–4441. doi: 10.1042/BCJ20200656

Table 3. Summary of effects of various modulators of PFK activity on each human PFK isoform.

Metabolite PFK-M PFK-L PFK-P
AMP (1200 µM) kcatATP/K0.5ATP (s−1 µM−1) −12% +9% +220%
kcatF6P/K0.5F6P (s−1 µM−1) −25% +766% +162%
ADP (600 µM) kcatATP/K0.5ATP (s−1 µM−1) −52% −47% +39%
kcatF6P/K0.5F6P (s−1 µM−1) −13% +157% +129%
GDP (1100 µM) kcatATP/K0.5ATP (s−1 µM−1) +4.3% −48% −0.2%
kcatF6P/K0.5F6P (s−1 µM−1) ND ND ND
F26BP (10 µM) kcatATP/K0.5ATP (s−1 µM−1) −7.4% +6.5% +88%
kcatF6P/K0.5F6P (s−1 µM−1) +82% +148% +111%
Citrate (600 µM) kcatATP/K0.5ATP (s−1 µM−1) +5% +28% +136%
kcatF6P/K0.5F6P (s−1 µM−1) −36% +2% −78%
PEP (1100 µM) kcatATP/K0.5ATP (s−1 µM−1) −11% +1% −40%
kcatF6P/K0.5F6P (s−1 µM−1) −7% +92% +9%

Effect of modulators with respect to ATP and F6P, as measured by percentage changes in specificity constants compared with control PFK without modulator (absolute values in Table 2).