PARK2 and ATXN3

  • Number of citations of the paper that reports this interaction (PMID 22081612)
  • 13
  • Data Source:
  • BioGRID (pull down, affinity chromatography technology, x-ray crystallography)

PARK2

ATXN3

Gene Name parkin RBR E3 ubiquitin protein ligase ataxin 3
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 77 interactors: AIMP2 ARR3 ARRB2 ATXN3 BAG5 CASK CASP1 CASP8 CDK5 CHPF CRX CSNK1A1 CUL1 DLG1 DLX2 DNM1L DYT10 EPS15 FAM46C FBP1 FBXO7 FBXW7 GPR37 GRIN2B HEXDC IKBKG MEOX1 MEOX2 MFN1 NDUFA4L2 PAFAH1B2 PDCD2 PICK1 PRKACA PSMA1 PSMA7 PSMC5 PSMD4 RAC1 RAD1 RAD23A RANBP2 RBCK1 REL RGS2 RGS3 SEPT4 SEPT5 SIM2 SNCA SNCAIP STUB1 SYT11 TCF4 TOMM40 TOMM70A TRIP13 TUBA4A TUBB UBASH3A UBASH3B UBB UBC UBE2D2 UBE2D3 UBE2E1 UBE2G1 UBE2G2 UBE2J1 UBE2L3 UBE2L6 UBE2M UBE2N UBE2V1 UCHL1 YWHAH ZNF746 43 interactors: ANXA7 APP ARHGAP19 ARHGDIA ASIC1 C16orf70 CASP1 CDKN1A CSNK2B DNM2 EWSR1 GSK3B HDAC6 KAT2B MKNK1 NCOR1 PARK2 PICK1 PJA1 PSMD7 RAD23A RAD23B RFFL RPS6KA1 SQSTM1 STUB1 SUMO1 TEX11 TK1 TRAF6 TRIM54 TRIM55 TRIM63 TUBA1A TUBB UBB UBC UBE2L3 UBE2S UBE4B UBQLN1 USP21 VCP
Entrez ID 5071 4287
HPRD ID 03967 06131
Ensembl ID ENSG00000185345 ENSG00000066427
Uniprot IDs O60260 Q5VVX4 P54252
PDB IDs 1IYF 2JMO 4BM9 4I1F 4I1H 1YZB 2AGA 2DOS 2JRI 2KLZ
Enriched GO Terms of Interacting Partners?
Tagcloud ?
ataxin  atp13a2  atxn3  b12  cag  cgg  chediak  coexist  cytopathies  fmr1  fragile  gaucher  gba  glucocerebrosidase  hereditary  higashi  idiopathic  joseph  kufor  levodopa  lyst  machado  parkin  parkinsonism  pn  polg1  premutation  rakeb  tremor 
14q32  amplifies  ataxia  atm  atnx3  break  breaks  cag  deposited  eventually  expansions  glutamine  inactivated  inefficient  joseph  machado  mjd  neurodegeneration  nonetheless  pnkp  polymorphic  polynucleotide  polyq  sca3  spinocerebellar  strand  telangiectasia  tri  untreatable 
Tagcloud (Difference) ?
ataxin  atp13a2  b12  cgg  chediak  coexist  cytopathies  fmr1  fragile  gaucher  gba  glucocerebrosidase  hereditary  higashi  idiopathic  kufor  levodopa  lyst  parkin  parkinsonism  pn  polg1  premutation  rakeb  tremor 
14q32  amplifies  ataxia  atm  atnx3  break  breaks  deposited  eventually  expansions  glutamine  inactivated  inefficient  mjd  neurodegeneration  nonetheless  pnkp  polymorphic  polynucleotide  polyq  sca3  spinocerebellar  strand  telangiectasia  tri  untreatable 
Tagcloud (Intersection) ?
atxn3  cag  joseph  machado