| Literature DB >> 23674349 |
Abstract
The carboxy terminal tail of epidermal growth factor receptor (EGFR) plays a critical role in the regulation of the enzyme activity of the kinase. There is a good structural model for the mechanism by which the C-terminal tail proximal to the kinase domain contributes to the negative regulation of the activity. Its conformation in the active state, conversely, has remained elusive due to its dynamic nature. A recently published structure of EGFR kinase domain shows the conformation of the proximal C-terminal tail in the active kinase. Analysis of this conformational state of the C-terminal tail is presented, and some of the mutagenesis data is revisited.Entities:
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Year: 2013 PMID: 23674349 PMCID: PMC3719092 DOI: 10.1002/pro.2283
Source DB: PubMed Journal: Protein Sci ISSN: 0961-8368 Impact factor: 6.725