Source:http://linkedlifedata.com/resource/pubmed/id/17191976
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2006-12-28
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pubmed:abstractText |
The potential of the cellular-automata (CA) method for modeling biological networks is demonstrated for the mitogen-activated protein kinase (MAPK) signaling cascade. The models derived reproduced the high signal amplification through the cascade and the deviation of the cascade enzymes from the Michaelis-Menten kinetics, evidencing cooperativity effects. The patterns of pathway change upon varying substrate concentrations and enzyme efficiencies were identified and used to show the ways for controlling pathway processes. Guidance in the selection of enzyme inhibition targets with minimum side effects is one outcome of the study.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
1612-1880
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
2
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
233-43
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:17191976-Automation,
pubmed-meshheading:17191976-Computer Simulation,
pubmed-meshheading:17191976-MAP Kinase Signaling System,
pubmed-meshheading:17191976-Mitogen-Activated Protein Kinases,
pubmed-meshheading:17191976-Models, Biological,
pubmed-meshheading:17191976-Substrate Specificity
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pubmed:year |
2005
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pubmed:articleTitle |
Modeling biochemical networks: a cellular-automata approach.
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pubmed:affiliation |
Center for the Study of Biological Complexity, Virginia Commonwealth University, P.O. Box 842030, Richmond, VA 23284-2030, USA. lbkier@vcu.edu
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pubmed:publicationType |
Journal Article,
Research Support, N.I.H., Extramural
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