SMARCA4 and STK11

  • Number of citations of the paper that reports this interaction (PMID 14676191)
  • 42
  • Data Source:
  • BioGRID (affinity chromatography technology)
  • HPRD (in vitro, in vivo)

SMARCA4

STK11

Gene Name SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 serine/threonine kinase 11
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 73 interactors: ACTB ACTL6A AHR AR ARID1A ARID1B ARID2 BRCA1 BRWD1 CARM1 CBX5 CCNE1 CDK19 CDK8 CDKN2A CDX2 CEBPA CEBPB CHD4 CHMP5 CIITA CREB1 CTNNB1 DPF3 ESR1 ETS2 FANCA GATA1 GMNN H2AFX H3F3A HIST1H3A HIST1H4F HIST2H2BE HIST2H3C HSF1 HSF4 IKZF1 KLF1 MBD3 MDM2 MED17 MED6 MKL1 MPHOSPH6 MPP6 MYC MYOCD NR3C1 NR4A2 PABPN1 PAX6 PBRM1 PHB RAP1A RB1 RBL1 RBL2 RELB RFXAP SIN3A SIN3B SMARCB1 SMARCC1 SMARCE1 SS18 SS18L1 STAT2 STAT3 STK11 TMF1 TP53 ZMYND11 29 interactors: APP ATM CAB39 CDC37 ETV4 MAPRE1 MARK1 MARK2 MARK4 MOB4 PARD3 PRKAA1 PRKAA2 PRKACA PTEN RPS6KA3 RPS6KA5 RPS6KB1 SIK1 SIRT1 SMARCA4 SNRK SPDEF STK11IP STRADA STRADB TNIP2 TP53 UBE2D2
Entrez ID 6597 6794
HPRD ID 04459 03740
Ensembl ID ENSG00000127616 ENSG00000118046
Uniprot IDs A7E2E1 B3KNW7 P51532 Q9HBD4 Q15831
PDB IDs 2GRC 2H60 3UVD 2WTK
Enriched GO Terms of Interacting Partners?
Tagcloud ?
abnormality  arid1a  coinactivation  copyright  fish  frame  harboring  heterozygous  infancy  insights  malignancies  missense  monoploid  mrts  pbrm1  protected  remodeling  reserved  rhabdoid  rights  screened  sense  snf  subunits  swi  trisomy  truncating 
alleles  atm  brca1  brca2  brip1  cdh1  chek2  confer  contributing  contributive  fashion  hereditary  influences  lifetime  offers  otherwise  palb2  penetrance  penetrant  personal  polygenic  predisposing  predisposition  quite  snp  suggestive  suspicion  unlikely  venue 
Tagcloud (Difference) ?
abnormality  arid1a  coinactivation  copyright  fish  frame  harboring  heterozygous  infancy  insights  malignancies  missense  monoploid  mrts  pbrm1  protected  remodeling  reserved  rhabdoid  rights  screened  sense  snf  subunits  swi  trisomy  truncating 
alleles  atm  brca1  brca2  brip1  cdh1  chek2  confer  contributing  contributive  fashion  hereditary  influences  lifetime  offers  otherwise  palb2  penetrance  penetrant  personal  polygenic  predisposing  predisposition  quite  snp  suggestive  suspicion  unlikely  venue 
Tagcloud (Intersection) ?