EPM2A and PPP1R3D

  • Number of citations of the paper that reports this interaction (PMID 23624058)
  • 1
  • Data Source:
  • BioGRID (fluorescent resonance energy transfer)

EPM2A

PPP1R3D

Gene Name epilepsy, progressive myoclonus type 2A, Lafora disease (laforin) protein phosphatase 1, regulatory subunit 3D
Image No pdb structure No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 7 interactors: EPM2AIP1 NFU1 NHLRC1 PPP1R3D PRKAA1 PRKAA2 PRKAB2 3 interactors: EPM2A PPP1CA PPP1CC
Entrez ID 7957 5509
HPRD ID 06345 04507
Ensembl ID ENSG00000112425 ENSG00000132825
Uniprot IDs O95278 O95685 Q86X09
PDB IDs
Enriched GO Terms of Interacting Partners?
Tagcloud ?
arms  autophago  biogenesis  branched  chop  defects  disposal  encode  epilepsy  epm2b  glycogen  hyperphosphorylated  insoluble  knock  lafora  laforin  laforinmalin  lamp1  lc3  lysosomal  malin  myoclonus  overaccumulation  proteasomal  s6  slight  speculate  starvation  ubiquitinated 
allows  autophagic  biosynthesis  dephosphorylates  downregulated  downregulates  e3  enhancement  epilepsy  excess  fatal  glucan  glycogen  glycogenic  interacts  lafora  laforin  ligase  malin  myoclonus  neuron  phosphatase  physically  r6  recruited  subunits  targeting  ubiquitination 
Tagcloud (Difference) ?
arms  autophago  biogenesis  branched  chop  defects  disposal  encode  epm2b  hyperphosphorylated  insoluble  knock  laforinmalin  lamp1  lc3  lysosomal  overaccumulation  proteasomal  s6  slight  speculate  starvation  ubiquitinated 
allows  autophagic  biosynthesis  dephosphorylates  downregulated  downregulates  e3  enhancement  excess  fatal  glucan  glycogenic  interacts  ligase  neuron  phosphatase  physically  r6  recruited  subunits  targeting  ubiquitination 
Tagcloud (Intersection) ?
epilepsy  glycogen  lafora  laforin  malin  myoclonus