We here create a kinetic model for a single enzyme within the T. brucei trypanothione synthesis pathway, the enzyme trypanothione synthetase based on the insights from the laboratory experiments
SEEK ID: https://fairdomhub.org/assays/244
Modelling analysis
Projects: SilicoTryp
Investigation: Kinetic understanding of the T. brucei trypanothione synthesis pathway
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Biological problem addressed: Enzymology
Organisms: No organisms
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Created: 31st Jul 2014 at 08:26
Last updated: 8th Nov 2017 at 14:21
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Projects: SilicoTryp, IMOMESIC
Institutions: University of Groningen, VU University Amsterdam
SysMO is a European transnational funding and research initiative on "Systems Biology of Microorganisms".
The goal pursued by SysMO was to record and describe the dynamic molecular processes going on in unicellular microorganisms in a comprehensive way and to present these processes in the form of computerized mathematical models.
Systems biology will raise biomedical and biotechnological research to a new quality level and contribute markedly to progress in understanding. Pooling European research ...
Projects: BaCell-SysMO, COSMIC, SUMO, KOSMOBAC, SysMO-LAB, PSYSMO, SCaRAB, MOSES, TRANSLUCENT, STREAM, SulfoSys, SysMO DB, SysMO Funders, SilicoTryp, Noisy-Strep
Web page: http://sysmo.net/
The SilicoTryp project aims at the creation of a “Silicon Trypanosome”, a comprehensive, experiment-based, multi-scale mathematical model of trypanosome physiology. Trypanosomes are blood-stream parasites transmitted by tsetse flies; they cause African sleeping sickness in humans and livestock. Currently available drugs have severe side effects, and the parasites are rapidly developing resistance. In this project, we collect a wide range of new experimental data on the parasite in its various ...
Programme: SysMO
Public web page: http://silicotryp.ibls.gla.ac.uk/wiki/Main_Page
Organisms: Trypanosoma brucei
Aim. To provide critical quantitative parameter information and to model redox balance by determining the cellular concentration of all enzymes involved in the trypanothione-dependent hydroperoxide detoxification system of trypanosomes and by performing the kinetic characterization of the involved enzymes under pseudo-physiological conditions.
Submitter: Alejandro Leroux
Studies: Determination of the redox state and the total concentration of the tryp..., Kinetic characterization of trypanothione-dependent enzymes, Kinetic modelling of Trypanothione Synthetase to elucidate the enzyme me...
Assays: Creating kinetic model of Trypanothione Synthetase, Trypanothione synthetase ATP consumption steady state data, Trypanothione synthetase Gsp and T(SH)2 production measured by HPLC
Snapshots: No snapshots
The enzyme Trypanothione Synthetase (TryS) is a complex enzyme that catalyses the two step reaction that forms trypanothione from 2 molecules of GSH and 1 molecule of Spd and the use of ATP
Submitter: Jurgen Haanstra
Investigation: Kinetic understanding of the T. brucei trypanot...
Snapshots: No snapshots
All datapoints that were measured are displayed together with the accompanying simulations by the computational model
Creators: Jurgen Haanstra, Alejandro Leroux
Submitter: Jurgen Haanstra
Relationship type: Simulation results
TbTryS activity was measured at 37°C in the in vivo-like buffer. All substrate stock solutions were prepared in the in vivo-like buffer and the pH was adjusted to 7.0. The assays were performed in a final volume of 2 ml and contained 0.2 mM NADH, 1 mM phosphoenolpyruvate, 4 units pyruvate kinase, 4 units L-lactate dehydrogenase, 0.17 µM TbTryS, 2.1 mM ATP and varying amounts of GSH, and Spd.
An extended model description of the TryS model
Creators: Jurgen Haanstra, Alejandro Leroux
Submitter: Jurgen Haanstra
Relationship type: Not specified
The file contains the initial rate measurements of TbTryS obtained under different substrate and product initial concentrations.
Mechanistical model of the catalytic cycle of Trypanothione Synthetase
Creators: Jurgen Haanstra, Alejandro Leroux
Submitter: Jurgen Haanstra
Model type: Linear equations
Model format: Copasi
Environment: Copasi
Organism: Trypanosoma brucei
Investigations: Kinetic understanding of the T. brucei trypanot...
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Date Published: 3rd Jul 2013
Publication Type: Not specified
PubMed ID: 23814051
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