Canonical and kinase activity-independent mechanisms for extracellular signal-regulated kinase 5 (ERK5) nuclear translocation require dissociation of Hsp90 from the ERK5-Cdc37 complex (Q28854310)

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English	Canonical and kinase activity-independent mechanisms for extracellular signal-regulated kinase 5 (ERK5) nuclear translocation require dissociation of Hsp90 from the ERK5-Cdc37 complex	scientific journal article

Statements

scholarly article

1 reference

28 February 2017

Canonical and kinase activity-independent mechanisms for extracellular signal-regulated kinase 5 (ERK5) nuclear translocation require dissociation of Hsp90 from the ERK5-Cdc37 complex (English)

1 reference

28 February 2017

Cell division cycle 37

1 reference

GOA release 2020-03-11

Heat shock protein 90 alpha (cytosolic), class B member 1

1 reference

GOA release 2020-03-11

Mitogen-activated protein kinase 7

1 reference

GOA release 2020-03-11

Jose R. Bayascas

object named as

Jose R. Bayascas

7

1 reference

ORCID Public Data File 2021

author name string

Tatiana Erazo

1

1 reference

28 February 2017

Ana Moreno

2

1 reference

28 February 2017

Gerard Ruiz-Babot

3

1 reference

28 February 2017

Arantza Rodríguez-Asiain

4

1 reference

28 February 2017

Nicholas A. Morrice

5

1 reference

28 February 2017

Josep Espadamala

6

1 reference

28 February 2017

Nestor Gómez

8

1 reference

28 February 2017

Jose M. Lizcano

9

1 reference

28 February 2017

language of work or name

0 references

publication date

1 April 2013

1 reference

28 February 2017

Molecular and Cellular Biology

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28 February 2017

33

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28 February 2017

8

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28 February 2017

1671–1686

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28 February 2017

Pharmacological inhibition of BMK1 suppresses tumor growth through promyelocytic leukemia protein

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Differential regulation and properties of MAPKs

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14-3-3 cooperates with LKB1 to regulate the activity and localization of QSK and SIK

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The heat shock protein 90-CDC37 chaperone complex is required for signaling by types I and II interferons

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Interaction between the 90-kDa heat shock protein and soluble guanylyl cyclase: physiological significance and mapping of the domains mediating binding

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Targeted deletion of mek5 causes early embryonic death and defects in the extracellular signal-regulated kinase 5/myocyte enhancer factor 2 cell survival pathway

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MEK5 and ERK5 are localized in the nuclei of resting as well as stimulated cells, while MEKK2 translocates from the cytosol to the nucleus upon stimulation

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The Mechanism of Hsp90 regulation by the protein kinase-specific cochaperone p50(cdc37)

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Heat-shock protein 90 and Cdc37 interact with LKB1 and regulate its stability

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Components of a new human protein kinase signal transduction pathway

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Primary structure of BMK1: a new mammalian map kinase

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Structure and mechanism of the Hsp90 molecular chaperone machinery

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Mammalian mitogen-activated protein kinase signal transduction pathways activated by stress and inflammation

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ERK5 signalling in prostate cancer promotes an invasive phenotype

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Multisite phosphorylation of Erk5 in mitosis

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Expression of Erk5 in early stage breast cancer and association with disease free survival identifies this kinase as a potential therapeutic target

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Hsp90 regulates the phosphorylation and activity of serum- and glucocorticoid-regulated kinase-1.

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Activation of a C-terminal transcriptional activation domain of ERK5 by autophosphorylation.

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Aberrant expression of extracellular signal-regulated kinase 5 in human prostate cancer

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based on heuristic

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Automated identification and quantification of protein phosphorylation sites by LC/MS on a hybrid triple quadrupole linear ion trap mass spectrometer

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https://pubmed.ncbi.nlm.nih.gov/23428871

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based on heuristic

inferred from PubMed ID database lookup

Erk5 nuclear location is independent on dual phosphorylation, and favours resistance to TRAIL-induced apoptosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/23428871

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of protein SUMOylation in vivo

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1128/MCB.01246-12

1 reference

Consolidated OpenCitations Corpus – April 2017

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OpenCitations bibliographic resource ID

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

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