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- Table of Contents
Facts about E3 ubiquitin-protein ligase NHLRC1.
In complex with EPM2A/laforin and HSP70, suppresses the cellular toxicity of misfolded proteins by promoting their degradation during the ubiquitin-proteasome system (UPS). Ubiquitinates the glycogen-targeting protein phosphatase subunits PPP1R3C/PTG and PPP1R3D at a laforin-dependent manner and targets for proteasome-dependent degradation, thus decreasing glycogen accumulation.
Mouse | |
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Gene Name: | Nhlrc1 |
Uniprot: | Q8BR37 |
Entrez: | 105193 |
Belongs to: |
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No superfamily |
bA204B7.2; E3 ubiquitin-protein ligase NHLRC1; EC 6.3.2.-; EPM2A; EPM2BMGC119264; MALIN; MGC119262; MGC119265; NHL repeat containing 1; NHL repeat-containing protein 1
Mass (kDA):
42.69 kDA
Mouse | |
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Location: | 13|13 A5 |
Sequence: | 13; |
PMID: 12958597 by Chan E.M., et al. Mutations in NHLRC1 cause progressive myoclonus epilepsy.
PMID: 19036738 by Garyali P., et al. The malin-laforin complex suppresses the cellular toxicity of misfolded proteins by promoting their degradation through the ubiquitin-proteasome system.