TADA3 and RARA

  • Number of citations of the paper that reports this interaction (PMID 12235159)
  • 26
  • Data Source:
  • BioGRID (pull down)
  • HPRD (in vivo, in vitro)

TADA3

RARA

Gene Name transcriptional adaptor 3 retinoic acid receptor, alpha
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 27 interactors: ADPGK ANKRD12 AR CCDC101 CCNC EIF3J EP300 ESR1 FAM107B HEXIM2 HIST3H3 HSPA8 ING5 KDM1A MAGEH1 NR1I2 PIAS4 RARA RFX1 RXRA SAP18 TADA2A TP53 TXNRD2 USP5 XRCC6 ZNF7 86 interactors: AKT1 ARID1A ARID5A ARNTL BAG1 BTG1 CCND3 CDK7 CEBPA CLOCK CNOT1 COPS2 E2F1 ESR1 FN1 FOXO1 GADD45G GATA2 HDAC1 HDAC3 HDAC4 HMGA1 HR IRX4 ITGB1BP2 KAT2B KDM5A KLF5 LRIF1 MAPK6 MECR MED1 MED25 MED6 MMS19 NCOA1 NCOA2 NCOA3 NCOA6 NCOR1 NCOR2 NKX2-1 NPAS2 NR0B2 NR1H2 NR1H3 NR2E3 NR3C1 NR4A2 NRBF2 NRIP1 NRIP2 NSD1 PARP1 PHF8 PIN1 PML PNRC2 POU2F1 PRAME PRDX6 PRKCA PSMC5 RAC3 RXRA RXRB RXRG SIRT1 SMARCD3 SMARCE1 SNW1 SP1 SPEN SRC STAT5B TADA3 TEKT4 THRB TNIP1 TOP2B TRIM24 TRIP4 UBE3A UBQLN1 USP7 ZBTB16
Entrez ID 10474 5914
HPRD ID 04252 06769
Ensembl ID ENSG00000171148
Uniprot IDs A8K899 O75528 A8K840 A8MUP8 B4E1J4 F1D8N9 P10276 Q6I9R7
PDB IDs 1DKF 1DSZ 3A9E 3KMR 3KMZ 4DQM
Enriched GO Terms of Interacting Partners?
Tagcloud ?
3p  anomalies  arm  camk1  congenital  creld1  define  deleted  deletion  deletions  features  give  handicap  interstitial  involve  kb  lengths  mb  mtmr14  overlap  presents  prove  respect  rise  seizures  srgap3  syndrome  terminus  typical 
apl  bodies  compartmentalisation  covalently  dependant  disrupted  fits  indirectly  kr  leukaemia  localisation  localises  lys487  lys490  modification  modifies  mutagenesis  named  nd10  phosphoprotein  pic1  pml  pods  promyelocytic  rangap1  subcellular  sumo  translocated  ubc9 
Tagcloud (Difference) ?
3p  anomalies  arm  camk1  congenital  creld1  define  deleted  deletion  deletions  features  give  handicap  interstitial  involve  kb  lengths  mb  mtmr14  overlap  presents  prove  respect  rise  seizures  srgap3  syndrome  terminus  typical 
apl  bodies  compartmentalisation  covalently  dependant  disrupted  fits  indirectly  kr  leukaemia  localisation  localises  lys487  lys490  modification  modifies  mutagenesis  named  nd10  phosphoprotein  pic1  pml  pods  promyelocytic  rangap1  subcellular  sumo  translocated  ubc9 
Tagcloud (Intersection) ?