Form of presentation | Articles in international journals and collections |
Year of publication | 2014 |
|
Kotov Nikolay Viktorovich, author
|
Bibliographic description in the original language |
Sadreev II, Chen MZ, Welsh GI, Umezawa Y, Kotov NV, Valeyev NV. A systems model of phosphorylation for inflammatory signaling events.
PLoS One. 2014 Oct 21;9(10):e110913. |
Annotation |
Phosphorylation is a fundamental biochemical reaction that modulates protein activity in cells. While a single phosphorylation event is relatively easy to understand, multisite phosphorylation requires systems approaches for deeper elucidation of the underlying molecular mechanisms. In this paper we develop a mechanistic model for single- and multi-site phosphorylation. The proposed model is compared with previously reported studies. We compare the predictions of our model with experiments published in the literature in the context of inflammatory signaling events in order to provide a mechanistic description of the multisite phosphorylation-mediated regulation of Signal Transducer and Activator of Transcription 3 (STAT3) and Interferon Regulatory Factor 5 (IRF-5) proteins. The presented model makes crucial predictions for transcription factor phosphorylation events in the immune system. The model proposes potential mechanisms for T cell phenotype switching and production of cytokines. |
Keywords |
Systems Model, Phosphorylation, Signaling Events. |
The name of the journal |
PLos ONE
|
URL |
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4205014/ |
Please use this ID to quote from or refer to the card |
https://repository.kpfu.ru/eng/?p_id=93373&p_lang=2 |
Full metadata record |
Field DC |
Value |
Language |
dc.contributor.author |
Kotov Nikolay Viktorovich |
ru_RU |
dc.date.accessioned |
2014-01-01T00:00:00Z |
ru_RU |
dc.date.available |
2014-01-01T00:00:00Z |
ru_RU |
dc.date.issued |
2014 |
ru_RU |
dc.identifier.citation |
Sadreev II, Chen MZ, Welsh GI, Umezawa Y, Kotov NV, Valeyev NV. A systems model of phosphorylation for inflammatory signaling events.
PLoS One. 2014 Oct 21;9(10):e110913. |
ru_RU |
dc.identifier.uri |
https://repository.kpfu.ru/eng/?p_id=93373&p_lang=2 |
ru_RU |
dc.description.abstract |
PLos ONE |
ru_RU |
dc.description.abstract |
Phosphorylation is a fundamental biochemical reaction that modulates protein activity in cells. While a single phosphorylation event is relatively easy to understand, multisite phosphorylation requires systems approaches for deeper elucidation of the underlying molecular mechanisms. In this paper we develop a mechanistic model for single- and multi-site phosphorylation. The proposed model is compared with previously reported studies. We compare the predictions of our model with experiments published in the literature in the context of inflammatory signaling events in order to provide a mechanistic description of the multisite phosphorylation-mediated regulation of Signal Transducer and Activator of Transcription 3 (STAT3) and Interferon Regulatory Factor 5 (IRF-5) proteins. The presented model makes crucial predictions for transcription factor phosphorylation events in the immune system. The model proposes potential mechanisms for T cell phenotype switching and production of cytokines. |
ru_RU |
dc.language.iso |
ru |
ru_RU |
dc.subject |
Systems Model |
ru_RU |
dc.subject |
Phosphorylation |
ru_RU |
dc.subject |
Signaling Events. |
ru_RU |
dc.title |
A systems model of phosphorylation for inflammatory signaling events.
PLoS One. 2014 Oct 21;9(10):e110913. |
ru_RU |
dc.type |
Articles in international journals and collections |
ru_RU |
|