cardiomyopathy-associated protein 5 (myospryn, Dystrobrevin-binding protein 2, SPRY domain-containing protein 2, tripartite motif- containing protein 76, genethonin-3, CMYA5, C5orf10, DTNBP2, SPRYD2, TRIM76)
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Function
Structure
- amphipathic helix regions act as an anchoring domain for PKA, & appear to be responsible of the interaction between myospryn & PRKAR2A
- contains 1 B30.2/SPRY domain
- contains 2 fibronectin F3 modules
Compartment
- cytoplasm (putative), perinuclear region (putative)
- found predominantly at the periphery of the nucleus but also throughout the cell
- localized at the Z-line costamere connection level of the sarcolemma & in lysosomes (putative)
Expression
- expressed in skeletal muscle; at a strong level & in heart
Pathology
- down-regulated in muscle cell lines derived from patients with Duchenne muscular dystrophy