The nuclear localization of ERK2 occurs by mechanisms both independent of and dependent on energy (Q50734500)

18 March 2018

title

The nuclear localization of ERK2 occurs by mechanisms both independent of and dependent on energy (English)

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18 March 2018

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18 March 2018

author name string

Aarati Ranganathan

series ordinal

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18 March 2018

Mustafa N Yazicioglu

series ordinal

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18 March 2018

language of work or name

English

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publication date

4 April 2006

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18 March 2018

Journal of Biological Chemistry

published in

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18 March 2018

volume

281

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issue

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page(s)

15645-15652

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Nuclear localization and regulation of erk- and rsk-encoded protein kinases

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Growth factors induce nuclear translocation of MAP kinases (p42mapk and p44mapk) but not of their activator MAP kinase kinase (p45mapkk) in fibroblasts

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Serum-induced translocation of mitogen-activated protein kinase to the cell surface ruffling membrane and the nucleus

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Phosphorylation of the MAP kinase ERK2 promotes its homodimerization and nuclear translocation

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Growth factor-induced p42/p44 MAPK nuclear translocation and retention requires both MAPK activation and neosynthesis of nuclear anchoring proteins

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Calponin and Mitogen-activated Protein Kinase Signaling in Differentiated Vascular Smooth Muscle

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Stimulus-coupled spatial restriction of extracellular signal-regulated kinase 1/2 activity contributes to the specificity of signal-response pathways

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Identification of novel point mutations in ERK2 that selectively disrupt binding to MEK1

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Evidence for existence of a nuclear pore complex-mediated, cytosol-independent pathway of nuclear translocation of ERK MAP kinase in permeabilized cells

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ERK2 enters the nucleus by a carrier-independent mechanism

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Live Cell Imaging of ERK and MEK: simple binding equilibrium explains the regulated nucleocytoplasmic distribution of ERK.

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Nuclear export of MAP kinase (ERK) involves a MAP kinase kinase (MEK)-dependent active transport mechanism

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The death effector domain protein PEA-15 prevents nuclear entry of ERK2 by inhibiting required interactions

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Non-regulated and stimulated mechanisms cooperate in the nuclear accumulation of MEK1.

21 January 2018

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MEKK1 phosphorylates MEK1 and MEK2 but does not cause activation of mitogen-activated protein kinase

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Nucleocytoplasmic shuttling factors including Ran and CRM1 mediate nuclear export of NFAT In vitro

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Reconstitution of biochemically altered nuclear pores: transport can be eliminated and restored

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CRM1 is responsible for intracellular transport mediated by the nuclear export signal

21 January 2018

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Active MAP kinase in mitosis: localization at kinetochores and association with the motor protein CENP-E

21 January 2018

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Extracellular signal-regulated kinase activates topoisomerase IIalpha through a mechanism independent of phosphorylation

21 January 2018

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Docking domains and substrate-specificity determination for MAP kinases

21 January 2018

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Regulated nucleo/cytoplasmic exchange of HOG1 MAPK requires the importin beta homologs NMD5 and XPO1.

21 January 2018

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21 January 2018

Identifiers

DOI

10.1074/JBC.M513866200

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18 March 2018

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18 March 2018