MME and AGT

  • Number of citations of the paper that reports this interaction (PMID 15283675)
  • 54
  • Data Source:
  • BioGRID (enzymatic study)

MME

AGT

Gene Name membrane metallo-endopeptidase angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 16 interactors: ADCYAP1 ADM AGT CSNK2A1 CSNK2B EDN1 EDN2 GAST LYN NDRG1 NPPA NPPC PIK3CB PIK3R1 SHC1 VIP 22 interactors: ACE2 AGTR1 AGTR2 ATP6AP2 CMA1 CTSG DNPEP ECE1 ENPEP EWSR1 GRB2 GSDMB ITSN2 KNG1 MAS1 MEP1A MME PRCP PREP PRG2 REN TP53
Entrez ID 4311 183
HPRD ID 00392 00106
Ensembl ID ENSG00000196549 ENSG00000135744
Uniprot IDs P08473 B0ZBE2 B2R5S1 P01019
PDB IDs 1DL9 1DMT 1QVD 1R1H 1R1I 1R1J 1Y8J 2QPJ 2YB9 1N9U 1N9V 2JP8 2WXW 2X0B 4AA1 4APH 4FYS
Enriched GO Terms of Interacting Partners?
Tagcloud ?
adh  alb  albinism  arbitrarily  assortment  backcrossing  constitution  duplicate  electrophoretically  fumarate  glo  glucosephosphate  glyoxalase  gpd  homeologous  hydratase  intersubspecies  isocitrate  malic  mannosephosphate  midh  mpi  numbered  phosphorylase  provisionally  sme  sorbitol  sord  ssod 
agc  alleles  amplified  autophosphorylation  berardinelli  changing  coding  codon  exons  heterozygous  iinsulin  inheritance  insulin  lesion  lipodystrophic  lipodystrophy  mellitus  outside  pathogenetic  polymorphism  polymorphisms  recessive  seip  sequenced  ser339  silent  substitution  unlikely  val 
Tagcloud (Difference) ?
adh  alb  albinism  arbitrarily  assortment  backcrossing  constitution  duplicate  electrophoretically  fumarate  glo  glucosephosphate  glyoxalase  gpd  homeologous  hydratase  intersubspecies  isocitrate  malic  mannosephosphate  midh  mpi  numbered  phosphorylase  provisionally  sme  sorbitol  sord  ssod 
agc  alleles  amplified  autophosphorylation  berardinelli  changing  coding  codon  exons  heterozygous  iinsulin  inheritance  insulin  lesion  lipodystrophic  lipodystrophy  mellitus  outside  pathogenetic  polymorphism  polymorphisms  recessive  seip  sequenced  ser339  silent  substitution  unlikely  val 
Tagcloud (Intersection) ?