PTGES3 and AIP

  • Number of citations of the paper that reports this interaction (PMID 11259606)
  • 23
  • Data Source:
  • BioGRID (affinity chromatography technology, affinity chromatography technology, affinity chromatography technology)
  • HPRD (in vitro, in vivo)

PTGES3

AIP

Gene Name prostaglandin E synthase 3 (cytosolic) aryl hydrocarbon receptor interacting protein
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 25 interactors: AHR AIP ARNT CASP3 CASP7 CAV3 CD2AP COPG1 COPG2 DNAJB1 DNMT3A EIF2AK2 ERBB3 ESR1 FES GZMB HSF1 HSP90AA1 HSPA1A NR3C1 NR3C2 STIP1 SURF1 TERT THRA 16 interactors: AHR ARNT CLEC7A CSNK2A1 EGFR GNA13 GNAQ HSP90AA1 IKBKG IRF7 PDE4A PPARA PTGES3 STIP1 TNNI3K TOMM20
Entrez ID 10728 9049
HPRD ID 06138 10408
Ensembl ID ENSG00000110958 ENSG00000110711
Uniprot IDs Q15185 O00170
PDB IDs 1EJF 1LG0 2LKN 4AIF 4APO
Enriched GO Terms of Interacting Partners?
Tagcloud ?
12q13  15q25  15q26  3p22  50k  beadchip  centric  cornell  customized  decile  ecg  heritability  humancvd  illumina  lvh  lyon  nmb  prognostically  qrs  rs2290893  rs2292462  rs4966014  rs6797133  scn5a  sokolow  sum  trait  typed  voltage 
aminolaevulinate  aspect  autosomal  coproporphyria  counterparts  cutanea  decarboxylase  dehydratase  develops  elucidating  hepatoerythropoietic  hereditary  heteroallelic  homo  inherited  intermittent  mutational  overt  pct  porphyria  porphyrias  puberty  rarely  recessive  tarda  uncommon  uroporphyrinogen  variegate  vp 
Tagcloud (Difference) ?
12q13  15q25  15q26  3p22  50k  beadchip  centric  cornell  customized  decile  ecg  heritability  humancvd  illumina  lvh  lyon  nmb  prognostically  qrs  rs2290893  rs2292462  rs4966014  rs6797133  scn5a  sokolow  sum  trait  typed  voltage 
aminolaevulinate  aspect  autosomal  coproporphyria  counterparts  cutanea  decarboxylase  dehydratase  develops  elucidating  hepatoerythropoietic  hereditary  heteroallelic  homo  inherited  intermittent  mutational  overt  pct  porphyria  porphyrias  puberty  rarely  recessive  tarda  uncommon  uroporphyrinogen  variegate  vp 
Tagcloud (Intersection) ?