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M dimer gets exported from nucleus
Stable Identifier
R-HSA-9831677
Type
Reaction [uncertain]
Species
Homo sapiens
Related Species
Human respiratory syncytial virus A
Compartment
cytosol
,
nucleoplasm
ReviewStatus
5/5
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Disease (Homo sapiens)
Infectious disease (Homo sapiens)
Viral Infection Pathways (Homo sapiens)
Respiratory Syncytial Virus Infection Pathway (Homo sapiens)
Respiratory syncytial virus (RSV) genome replication, transcription and translation (Homo sapiens)
Maturation of hRSV A proteins (Homo sapiens)
M dimer gets exported from nucleus (Homo sapiens)
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In order to fulfill its role as a scaffold in virus assembly, which takes place in the periplasmic region of the host cell, protein M localizes to cytosol. Nuclear export is dependent on exportin-1 (XPO1, CRM1), a component of nuclear export receptor complexes, that associates with a nuclear export signal (NES) within residues 194 to 206 of M (Ghildyal et al, 2009).
Literature References
PubMed ID
Title
Journal
Year
19297465
The respiratory syncytial virus matrix protein possesses a Crm1-mediated nuclear export mechanism
Bardin, PG
,
Teng, MN
,
Ghildyal, R
,
Tran, KC
,
Soegiyono, L
,
Ho, A
,
Jans, DA
,
Dias, M
J Virol
2009
Participants
Input
p-M dimer [nucleoplasm]
(Human respiratory syncytial virus A)
Output
p-M dimer [cytosol]
(Human respiratory syncytial virus A)
Participates
as an event of
Maturation of hRSV A proteins (Homo sapiens)
This event is regulated
Positively by
Regulator
XPO1 [nucleoplasm]
(Homo sapiens)
Disease
Name
Identifier
Synonyms
respiratory syncytial virus infectious disease
DOID:1273
Authored
Stephan, R (2023-03-22)
Reviewed
Bergeron, HC (2023-11-03)
Created
Stephan, R (2023-03-24)
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