Modulation of F-actin rearrangement by the cyclic AMP/cAMP-dependent protein kinase (PKA) pathway is mediated by MAPK-activated protein kinase 5 and requires PKA-induced nuclear export of MK5. (Q45345894)

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scientific article published on 17 October 2007

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English	Modulation of F-actin rearrangement by the cyclic AMP/cAMP-dependent protein kinase (PKA) pathway is mediated by MAPK-activated protein kinase 5 and requires PKA-induced nuclear export of MK5.	scientific article published on 17 October 2007

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scholarly article

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Europe PubMed Central

PubMed publication ID

13 December 2017

Modulation of F-actin rearrangement by the cyclic AMP/cAMP-dependent protein kinase (PKA) pathway is mediated by MAPK-activated protein kinase 5 and requires PKA-induced nuclear export of MK5. (English)

1 reference

Europe PubMed Central

PubMed publication ID

13 December 2017

6

object named as

Ugo Moens

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Europe PubMed Central

PubMed publication ID

13 December 2017

Sergiy Kostenko

3

object named as

Sergiy Kostenko

1 reference

Europe PubMed Central

PubMed publication ID

13 December 2017

Mona Johannessen

5

object named as

Mona Johannessen

1 reference

Europe PubMed Central

PubMed publication ID

13 December 2017

1

object named as

Nancy Gerits

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Europe PubMed Central

PubMed publication ID

13 December 2017

author name string

Theresa Mikalsen

2

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Europe PubMed Central

PubMed publication ID

13 December 2017

Alexey Shiryaev

4

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Europe PubMed Central

PubMed publication ID

13 December 2017

language of work or name

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publication date

17 October 2007

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Europe PubMed Central

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13 December 2017

number of pages

12

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based on heuristic

inferred from page(s)

Journal of Biological Chemistry

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Europe PubMed Central

PubMed publication ID

13 December 2017

282

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Europe PubMed Central

PubMed publication ID

13 December 2017

51

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Europe PubMed Central

PubMed publication ID

13 December 2017

37232-37243

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Europe PubMed Central

PubMed publication ID

13 December 2017

MAP kinases and cell migration

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ERK and p38 MAPK-activated protein kinases: a family of protein kinases with diverse biological functions

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Regulatory mechanisms and functions of MAP kinase signaling pathways.

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Functions of the MAPK family in vertebrate-development

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The protein kinase complement of the human genome

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MAPKAPK5, a novel mitogen-activated protein kinase (MAPK)-activated protein kinase, is a substrate of the extracellular-regulated kinase (ERK) and p38 kinase

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Distinct cellular functions of MK2.

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Serine/Threonine kinases 3pK and MAPK-activated protein kinase 2 interact with the basic helix-loop-helix transcription factor E47 and repress its transcriptional activity

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MAPKAP kinase 3pK phosphorylates and regulates chromatin association of the polycomb group protein Bmi1

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Elimination of protein kinase MK5/PRAK activity by targeted homologous recombination

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Scaffolding by ERK3 regulates MK5 in development

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Activation of MK5/PRAK by the atypical MAP kinase ERK3 defines a novel signal transduction pathway

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Characterization of the atypical MAPK ERK4 and its activation of the MAPK-activated protein kinase MK5

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Regulation of MAPK-activated protein kinase 5 activity and subcellular localization by the atypical MAPK ERK4/MAPK4.

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PRAK is essential for ras-induced senescence and tumor suppression

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Crosstalk between cAMP and MAP kinase signaling in the regulation of cell proliferation

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Regulation of actin-based cell migration by cAMP/PKA.

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Crosstalk between cAMP-dependent kinase and MAP kinase through a protein tyrosine phosphatase

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The cAMP signalling pathway activates CREB through PKA, p38 and MSK1 in NIH 3T3 cells

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Cyclic AMP selectively uncouples mitogen-activated protein kinase cascades from activating signals

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Subcellular localization and biological actions of activated RSK1 are determined by its interactions with subunits of cyclic AMP-dependent protein kinase

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Both binding and activation of p38 mitogen-activated protein kinase (MAPK) play essential roles in regulation of the nucleocytoplasmic distribution of MAPK-activated protein kinase 5 by cellular stress

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Role of basic region leucine zipper transcription factors cyclic AMP response element binding protein (CREB), CREB2, activating transcription factor 2 and CAAT/enhancer binding protein alpha in cyclic AMP response element-mediated transcription.

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Transcriptional regulation by cyclic AMP.

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Identifiers

10.1074/JBC.M704873200

1 reference

Europe PubMed Central

PubMed publication ID

13 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

13 December 2017

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