FANCA and ATR

  • Number of citations of the paper that reports this interaction (PMID 19109555)
  • 23
  • Data Source:
  • BioGRID (enzymatic study)

FANCA

ATR

Gene Name Fanconi anemia, complementation group A ATR serine/threonine kinase
Image No pdb structure No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 46 interactors: AKT1 ALDOA ATP5B ATR AZIN1 BRCA1 CAPN1 CCT3 CD79A CDK1 CENPE DAXX DDX39B DNAJB1 DUS4L ENO1 FANCC FANCE FANCF FANCG GNB2 HES1 HPRT1 HSP90AA1 IFIT3 IKBKB KRT1 LIPG MKNK1 MX1 NAMPT NUB1 PRPF31 PSMA5 RPL18 SGK1 SMARCA4 SMARCC1 SMARCD3 SNX5 SPTAN1 TAF10 TCERG1 TCP1 TPT1 ZNF24 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 2175 545
HPRD ID 06186 08369
Ensembl ID ENSG00000187741 ENSG00000175054
Uniprot IDs H3BSR5 O15360 Q86U55 Q13535
PDB IDs
Enriched GO Terms of Interacting Partners?
Tagcloud ?
aml  anemia  aplastic  autosomal  brca2  collaborate  complicated  cumulative  cure  decision  fancd1  fanconi  fancq  genotypes  gynecologic  head  inherited  neck  preemptive  prone  recessive  risks  solid  squamous  subset  transplant  usually  wilms 
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) ?
aml  anemia  aplastic  autosomal  brca2  collaborate  complicated  cumulative  cure  decision  fancd1  fanconi  fancq  genotypes  gynecologic  head  neck  preemptive  prone  recessive  risks  solid  squamous  subset  transplant  usually  wilms 
activators  breakage  broad  chromatin  chromosome  comprises  concept  defect  discuss  emerging  exert  heterochromatin  hybrid  mediate  member  modulating  mr  numerous  observations  remodelling  repair  retardation  seems  segregation  snf2  somehow  thalaessemia  xnp 
Tagcloud (Intersection) ?
inherited