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I kappa B proteins: structure, function and regulation.

Authors: S T, Whiteside; A, Israël;

I kappa B proteins: structure, function and regulation.

Abstract

The Rel/NF-kappa B transcription factors represent the paradigm of regulation of transcriptional activation through sub-cellular localization. In unstimulated cells, NK-kappa B exists in an inactive state in the cytoplasm complexed to the inhibitory I kappa B molecules. Upon stimulation, I kappa B is rapidly degraded, freeing NF-kappa B to translocate to the nucleus and to activate the expression of its target genes. In this chapter, we will summarize what is known about the structure of I kappa B molecules, their functions, the mechanisms of I kappa B degradation, and the most common upstream signaling pathway (that is, serine phosphorylation) that leads to I kappa B degradation. Finally, we will discuss alternative mechanisms for induction of NF-kappa B through regulation of I kappa B activity.

Keywords

Protein Conformation, Phosphotransferases, Transcription Factor RelB, NF-kappa B, Structure-Activity Relationship, Proto-Oncogene Proteins, Animals, Humans, Phosphorylation, Signal Transduction, Transcription Factors

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Powered by OpenAIRE graph
Found an issue? Give us feedback
selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
327
Top 10%
Top 1%
Top 1%
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