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. Author manuscript; available in PMC: 2016 Dec 14.
Published in final edited form as: Methods Mol Biol. 2011;734:173–200. doi: 10.1007/978-1-61779-086-7_9

Table 5.

Sensitivity of the kinetic orders on the metabolite concentrations and fluxes of the model in Fig. 2. The largest negative influence is on l-Dopamine (l-DOPA) concentration, X3. This metabolite responds to a change in the kinetic order associate to degradation h3,11; increase its concentration when this parameter decreases. Additionally, S(X4, g4,11) indicates an increase in melanin concentration, X4 when its own synthesis increases

Metabolite concentration
Flux of metabolite
Independent variable X 1 X 2 X 3 X 4 V(X1) V(X2) V(X3) V(X4)
Phytoceramide X 5 0.26 0.26 −0.71 0.26 0.26

PIa X 6 0.52 0.52 −1.41 0.52 0.52

Ipc1b X 7 1.00 1.00 −2.70 1.00 1.00

Pkc1c X 8 −2.70

l-DOPA-extd X 9 0.84 0.31 0.31 0.31

Transport X 10 2.70 1.00 1.00 1.00

Laccase X 11 −2.70
a

Phosphatidylinositol

b

Inositol phosphoryl ceramide synthase 1

c

Protein kinase C 1

d

l-Dopamine extracellular