RHEB and ATR

  • Number of citations of the paper that reports this interaction (PMID 15854902)
  • 168
  • Data Source:
  • BioGRID (affinity chromatography technology)
  • HPRD (in vitro)

RHEB

ATR

Gene Name Ras homolog enriched in brain ATR serine/threonine kinase
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 22 interactors: A2M APOE ARIH2 ATM ATR BNIP3 BNIP3L BRAF ECSIT FKBP8 MTOR NCAM1 PDE6D PLD1 PSEN1 PSEN2 RABAC1 RAF1 RPS6KB1 RPTOR TSC1 TSC2 47 interactors: AATF ABL1 AP1B1 AP2A2 ARHGEF1 ATM ATRIP BLM BRCA1 BRCA2 CDKN2C CEP164 CHD4 CHEK1 CHEK2 CLSPN CREB1 DCLRE1C DTL E2F1 E4F1 EEF1E1 EP300 FANCA FANCD2 FLT1 H2AFX KDR LIG4 MCM2 MRE11A MSH2 NBN PA2G4 PIK3CA POLD1 POLN PPP2R2A PTS RAD17 RHEB TP53 TREX1 UPF1 VPRBP XPA XRCC5
Entrez ID 6009 545
HPRD ID 03188 08369
Ensembl ID ENSG00000106615 ENSG00000175054
Uniprot IDs Q15382 Q13535
PDB IDs 1XTQ 1XTR 1XTS 3SEA 3T5G
Enriched GO Terms of Interacting Partners?
Tagcloud ?
abovementioned  altogether  amls  angiomyolipomas  carry  chronically  comparative  deficient  diminished  farnesylthiosalicylic  fts  indeed  irf7  lam  lymphangioleiomyomatosis  mimicked  mtorc1  neoplasms  pathologies  phenomena  rapamycin  salirasib  sirolimus  sporadic  trans  tsc  tsc2  tuberous  yielded 
activators  breakage  broad  chromatin  chromosome  comprises  concept  defect  discuss  emerging  exert  heterochromatin  hybrid  inherited  mediate  member  modulating  mr  numerous  observations  remodelling  repair  retardation  seems  segregation  snf2  somehow  thalaessemia  xnp 
Tagcloud (Difference) ?
abovementioned  altogether  amls  angiomyolipomas  carry  chronically  comparative  deficient  diminished  farnesylthiosalicylic  fts  indeed  irf7  lam  lymphangioleiomyomatosis  mimicked  mtorc1  neoplasms  pathologies  phenomena  rapamycin  salirasib  sirolimus  sporadic  trans  tsc  tsc2  tuberous  yielded 
activators  breakage  broad  chromatin  chromosome  comprises  concept  defect  discuss  emerging  exert  heterochromatin  hybrid  inherited  mediate  member  modulating  mr  numerous  observations  remodelling  repair  retardation  seems  segregation  snf2  somehow  thalaessemia  xnp 
Tagcloud (Intersection) ?