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p-T,Y-MAPK8 translocates from the cytosol to the nucleoplasm
Stable Identifier
R-HSA-9673322
Type
Reaction [transition]
Species
Homo sapiens
Compartment
cytosol
,
nucleoplasm
ReviewStatus
5/5
Locations in the PathwayBrowser
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Disease (Homo sapiens)
Infectious disease (Homo sapiens)
Parasitic Infection Pathways (Homo sapiens)
Leishmania infection (Homo sapiens)
Killing mechanisms (Homo sapiens)
WNT5:FZD7-mediated leishmania damping (Homo sapiens)
p-T,Y-MAPK8 translocates from the cytosol to the nucleoplasm (Homo sapiens)
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The layout of this reaction may differ from that in the pathway view due to the constraints in pathway layout
NRAGE, NRIF, NADE, TRAF6 mediate, through unclear mechanisms, MAPK8 (aka JNK) activation by threonine and tyrosine phosphorylation. While active (phosphorylated) MAPK8 moves to the nucleus and phosphorylates transcription factors such as c-JUN and ATF2, these have not been implicated in p75-mediated cell death. p75 activates the intrinsic caspase pathway (involving mitochondrial release of cytochrome c, Apaf-1, and caspases-9) rather than the extrinsic (caspase-8) pathway activated by most other death receptors (Troy et al. 2002).
Literature References
PubMed ID
Title
Journal
Year
12097334
Mechanisms of p75-mediated death of hippocampal neurons. Role of caspases
Friedman, JE
,
Friedman, WJ
,
Troy, CM
J Biol Chem
2002
Participants
Input
p-T,Y-MAPK8 [cytosol]
(Homo sapiens)
Output
p-T,Y-MAPK8 [nucleoplasm]
(Homo sapiens)
Participates
as an event of
WNT5:FZD7-mediated leishmania damping (Homo sapiens)
Authored
Jassal, B (2020-01-07)
Murillo, JI (2019-10-22)
Reviewed
Gregory, DJ (2020-02-04)
Created
Murillo, JI (2020-01-07)
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