GSDMB and AGT

  • Number of citations of the paper that reports this interaction (PMID 21988832)
  • 14
  • Data Source:
  • BioGRID (two hybrid)

GSDMB

AGT

Gene Name gasdermin B angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 7 interactors: AGT APP HIVEP1 IGFBP2 ORM1 PEBP1 SERPINA1 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 55876 183
HPRD ID 17082 00106
Ensembl ID ENSG00000073605 ENSG00000135744
Uniprot IDs Q8TAX9 B0ZBE2 B2R5S1 P01019
PDB IDs 1N9U 1N9V 2JP8 2WXW 2X0B 4AA1 4APH 4FYS
Enriched GO Terms of Interacting Partners?
Tagcloud ?
17q12  african  americans  ancestry  asthma  asthmatic  beadchip  caribbeans  ethnic  european  explain  grasp  harbouring  heritability  humanexome  illumina  latino  latinos  loci  maf  missense  missing  mthfr  parent  representing  reveals  robustly  trios  variants 
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) ?
17q12  african  americans  ancestry  asthma  asthmatic  beadchip  caribbeans  ethnic  european  explain  grasp  harbouring  heritability  humanexome  illumina  latino  latinos  loci  maf  missense  missing  mthfr  parent  representing  reveals  robustly  trios  variants 
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) ?