Models

Dataset Information

0

ODea2007_IkappaB


ABSTRACT: O'Dea, E.L., Barken, D., Peralta, R.Q., Tran K.T., Werner, S.L., Kearns, J.D., Levchenko, A., Hoffmann, A. A homeostatic model of IkB metabolism to control constitutive activity. Molecular Systems Biology, 3:111, pp. 1-7. 2007 Questions concerning the paper should be addressed to the corresponding author. Alexander Hoffmann (ahoffmann@ucsd.edu) The original model was written and simulated within MathWorks MatLab 2006a using the ode15s (stiff/NDF) solver. It is highly recommended that those wanting to model this system use the MatLab version which we will freely provide upon request. As always, simulation results vary according to the numerical solver used. Translation to SBML Level 2.1 was performed via reconstruction of the model within MathWorks SimBiology Desktop (version 2.1) followed by an Export to SBML. Please address questions about this SBML model to Jeff Kearns (jkearns@ucsd.edu). BioModels DB curation: The model reproduces the values of diffferent species depicted in Fig 3A and 3B (wt) of the paper corresponding to Model1.1. To depict the the total IkB alpha, beta epsilon species, three additional parameters and their corresponding assignment rules have been introduced in this model by the creator. Model succesfully tested on MathSBML. This model originates from BioModels Database: A Database of Annotated Published Models. It is copyright (c) 2005-2010 The BioModels Team.For more information see the terms of use.To cite BioModels Database, please use Le Novère N., Bornstein B., Broicher A., Courtot M., Donizelli M., Dharuri H., Li L., Sauro H., Schilstra M., Shapiro B., Snoep J.L., Hucka M. (2006) BioModels Database: A Free, Centralized Database of Curated, Published, Quantitative Kinetic Models of Biochemical and Cellular Systems Nucleic Acids Res., 34: D689-D691.

SUBMITTER: Molecular Systems Biology  

PROVIDER: BIOMD0000000147 | BioModels | 2024-09-02

REPOSITORIES: BioModels

altmetric image

Publications

A homeostatic model of IkappaB metabolism to control constitutive NF-kappaB activity.

O'Dea Ellen L EL   Barken Derren D   Peralta Raechel Q RQ   Tran Kim T KT   Werner Shannon L SL   Kearns Jeffrey D JD   Levchenko Andre A   Hoffmann Alexander A  

Molecular systems biology 20070508


Cellular signal transduction pathways are usually studied following administration of an external stimulus. However, disease-associated aberrant activity of the pathway is often due to misregulation of the equilibrium state. The transcription factor NF-kappaB is typically described as being held inactive in the cytoplasm by binding its inhibitor, IkappaB, until an external stimulus triggers IkappaB degradation through an IkappaB kinase-dependent degradation pathway. Combining genetic, biochemica  ...[more]

Similar Datasets

2019-08-27 | MODEL1908270002 | BioModels
2005-01-01 | MODEL8478881246 | BioModels
2009-05-01 | GSE13599 | GEO
2018-04-21 | GSE102190 | GEO
2020-06-27 | GSE101495 | GEO
2020-09-01 | GSE146654 | GEO
2020-09-01 | GSE146652 | GEO
2023-04-12 | GSE215383 | GEO
| PRJNA330745 | ENA
| PRJNA87721 | ENA