Journal of Biological Chemistry · 1995 · 182 citations · 28 references
Life SciencesBiochemistryMolecular BiologyCell SignalingProteomicsSignal TransductionEnzyme FunctionPost-translational Regulation14-3-3 DomainsConsensus Motif IdentificationMass Spectrometry ProteomicsPi3k SignalingProtein Kinase InhibitorsRaf SignalingRaf-mek-erk SignalingSequence Motif Discovery
The 14-3-3 protein family has received considerable attention recently in the literature, because of the finding that beta and zeta isoforms interact with and activate Raf. We had previously shown that these 14-3-3 isoforms also exist as phosphorylated forms in mammalian and avian brain. The presence of this modification enhances the activity of 14-3-3 as an inhibitor of protein kinase C nearly 2-fold. In this report we show by a combination of electrospray mass spectrometry and protein microsequencing that alpha and delta are in vivo post-translationally modified forms of beta and zeta, respectively, and the site of phosphorylation, serine 185, is in a consensus sequence motif for proline-directed kinases.
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Binding of 14-3-3 Proteins to the Protein Kinase Raf and Effects on Its Activation
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Activation of Raf-1 by 14-3-3 proteins
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Tohru Ichimura, Toshiaki Isobe, Tsuneo Okuyama et al. · Proceedings of the National Academy of Sciences · 1988 · 339 citations · Full text
14-3-3 Protein Homologs Required for the DNA Damage Checkpoint in Fission Yeast
Jon C. Ford, Fahad Al‐Khodairy, Eleftheria Fotou et al. · Science · 1994 · 339 citations
Stimulatory Effects of Yeast and Mammalian 14-3-3 Proteins on the Raf Protein Kinase
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