Info! This is a derivative of the model smallbone15

penkler1

vPFvALD

vPFvALD

f16bpPF = gapPF + dhapPF

vPFvATPASE

vPFvATPASE

atpPF = adpPF

vPFvENO

vPFvENO

p2gPF = pepPF

vPFvG3PDH

vPFvG3PDH

dhapPF + nadhPF = nadPF + g3pPF

vPFvGAPDH

vPFvGAPDH

nadPF + gapPF = b13pgPF + nadhPF

vPFvGLCtr

vPFvGLCtr

glcEX = glcPF

vPFvGLYtr

vPFvGLYtr

g3pPF = glyEX

vPFvHK

vPFvHK

glcPF + atpPF = g6pPF + adpPF

vPFvLACtr

vPFvLACtr

lacPF = lacEX

vPFvLDH

vPFvLDH

pyrPF + nadhPF = nadPF + lacPF

vPFvPFK

vPFvPFK

f6pPF + atpPF = f16bpPF + adpPF

vPFvPGI

vPFvPGI

g6pPF = f6pPF

vPFvPGK

vPFvPGK

b13pgPF + adpPF = p3gPF + atpPF

vPFvPGM

vPFvPGM

p3gPF = p2gPF

vPFvPK

vPFvPK

pepPF + adpPF = pyrPF + atpPF

vPFvPYRtr

vPFvPYRtr

pyrPF = pyrEX

vPFvTPI

vPFvTPI

dhapPF = gapPF

Global parameters

Assignment rules

hPF = pHConversionFactor / pow(10, phPF)

hEX = pHConversionFactor / pow(10, phEX)

Function definitions

Note that constraints are not enforced in simulations. It remains the responsibility of the user to verify that simulation results satisfy these constraints.


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Construction and validation of a detailed kinetic model of glycolysis in Plasmodium falciparum.

  • Gerald Penkler
  • Francois du Toit
  • Waldo Adams
  • Marina Rautenbach
  • Daniel C Palm
  • David D van Niekerk
  • Jacky L Snoep
FEBS J. 2015; 282 (8): 1481-1511
Abstract
UNLABELLED: The enzymes in the Embden-Meyerhof-Parnas pathway of Plasmodium falciparum trophozoites were kinetically characterized and their integrated activities analyzed in a mathematical model. For validation of the model, we compared model predictions for steady-state fluxes and metabolite concentrations of the hexose phosphates with experimental values for intact parasites. The model, which is completely based on kinetic parameters that were measured for the individual enzymes, gives an accurate prediction of the steady-state fluxes and intermediate concentrations. This is the first detailed kinetic model for glucose metabolism in P. falciparum, one of the most prolific malaria-causing protozoa, and the high predictive power of the model makes it a strong tool for future drug target identification studies. The modelling workflow is transparent and reproducible, and completely documented in the SEEK platform, where all experimental data and model files are available for download.
DATABASE: The mathematical models described in the present study have been submitted to the JWS Online Cellular Systems Modelling Database (http://jjj.bio.vu.nl/database/penkler). The investigation and complete experimental data set is available on SEEK (10.15490/seek.1.
INVESTIGATION: 56).

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