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ERK7 Is an Autoactivated Member of the MAPK Family

Abe, Mark K. ; Kahle, Kristopher T. ; Saelzler, Matthew P. ; Orth, Kim ; Dixon, Jack E. ; Rosner, Marsha R.

The Journal of biological chemistry, 2001-06, Vol.276 (24), p.21272-21279 [Periódico revisado por pares]

United States: Elsevier Inc

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Título:
ERK7 Is an Autoactivated Member of the MAPK Family
Autor: Abe, Mark K. ; Kahle, Kristopher T. ; Saelzler, Matthew P. ; Orth, Kim ; Dixon, Jack E. ; Rosner, Marsha R.
Assuntos: Adenosine Triphosphate - metabolism ; Amino Acid Sequence ; Animals ; Butadienes - pharmacology ; Cell Line ; Chlorocebus aethiops ; COS Cells ; Enzyme Activation ; Enzyme Inhibitors - pharmacology ; Extracellular Signal-Regulated MAP Kinases ; MAP Kinase Signaling System - physiology ; Mice ; Mitogen-Activated Protein Kinase 1 - metabolism ; Mitogen-Activated Protein Kinase Kinases - metabolism ; Mitogen-Activated Protein Kinases - chemistry ; Mitogen-Activated Protein Kinases - metabolism ; Molecular Sequence Data ; Nitriles - pharmacology ; Phosphorylation ; Rats ; Recombinant Proteins - metabolism ; Substrate Specificity ; Transfection
É parte de: The Journal of biological chemistry, 2001-06, Vol.276 (24), p.21272-21279
Notas: ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
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Descrição: Extracellular signal-regulated kinase 7 (ERK7) shares significant sequence homology with other members of the ERK family of signal transduction proteins, including the signature TEY activation motif. However, ERK7 has several distinguishing characteristics. Unlike other ERKs, ERK7 has been shown to have significant constitutive activity in serum-starved cells, which is not increased further by extracellular stimuli that typically activate other members of the mitogen-activated protein kinase (MAPK) family. On the other hand, ERK7's activation state and kinase activity appear to be regulated by its ability to utilize ATP and the presence of its extended C-terminal region. In this study, we investigated the mechanism of ERK7 activation. The results suggest that 1) MAPK kinase (MEK) inhibitors do not suppress ERK7 kinase activity; 2) intramolecular autophosphorylation is sufficient for activation of ERK7 in the absence of an upstream MEK; and 3) multiple regions of the C-terminal domain of ERK7 regulate its kinase activity. Taken together, these results indicate that autophosphorylation is sufficient for ERK7 activation and that the C-terminal domain regulates its kinase activity through multiple interactions.
Editor: United States: Elsevier Inc
Idioma: Inglês

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ERK7 Is an Autoactivated Member of the MAPK Family

Abe, Mark K. ; Kahle, Kristopher T. ; Saelzler, Matthew P. ; Orth, Kim ; Dixon, Jack E. ; Rosner, Marsha R.

United States: Elsevier Inc

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