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Utrn interacts with a complex purified with an anti-periaxin antibody
Stable Identifier
R-MMU-9619682
Type
Reaction [omitted]
Species
Mus musculus
Compartment
plasma membrane
,
cytosol
,
extracellular region
ReviewStatus
5/5
General
SBML
|
BioPAX
Level 2
Level 3
|
PDF
SVG
|
PNG
Low
Medium
High
|
PPTX
|
SBGN
Drp2 and L-Prx interact in mouse cells as part of a dystrophin glycoprotein complex (DGC) at the plasma membrane that also includes dystroglycan. Antibodies against L-Prx identify the dystrophin-related protein utrophin (Utrn) as part of the same complex, although L-Prx and Utrn do not interact directly. This suggests a model where alternate DGC complexs with varied dystrophin-family members may interact (Sherman et al, 2001).
Literature References
PubMed ID
Title
Journal
Year
11430802
Specific disruption of a schwann cell dystrophin-related protein complex in a demyelinating neuropathy
Gillespie, CS
,
Fabrizi, C
,
Brophy, PJ
,
Sherman, DL
Neuron
2001
Participants
Input
L-Prx:Drp2:dystroglycan:laminin-211 [plasma membrane]
(Mus musculus)
Utrn [cytosol]
(Mus musculus)
Output
L-prx dimer:Drp2:dystroglycan:laminin-211:Utrn [plasma membrane]
(Mus musculus)
Orthologous Events
L-PRX:DRP:DGC:laminin-211 interacts with UTRN (Homo sapiens)
Authored
Rothfels, K (2019-08-16)
Reviewed
Aletta, J M (2020-01-17)
Created
Rothfels, K (2018-09-18)
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