PRKCE and KRT18

  • Number of citations of the paper that reports this interaction (PMID 7523419)
  • 25
  • Data Source:
  • HPRD (in vitro)

PRKCE

KRT18

Gene Name protein kinase C, epsilon keratin 18, type I
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 57 interactors: ACTA1 ACTC1 ADAP1 AFAP1 AKAP9 ATF2 BRAF BTK CFTR CHAT CNN1 COPB1 COPB2 DSP ELAVL1 FYN GAD1 GAD2 GJA1 GNA12 GNA13 GNB2L1 GRIN1 GRIN2D GRM5 HIST1H1A HK2 IKBKB ITGB1 ITGB2 KEAP1 KRT1 KRT18 MAP4K4 MAPK1 MAPK3 MARK2 MYH2 NANOG NUMB OPRD1 PDLIM5 PDPK1 PECAM1 PIK3CB PPP1R14A PRKD1 RAF1 RASGRP3 RPS6KB2 SLC25A4 SLC4A3 SNCA SRC TIAM1 TRPV1 VDAC1 73 interactors: BBS1 BBS2 BBS4 BBS7 CAMK2A CASP3 CASP6 CASP7 CASP8 CBL CCDC146 CCDC85B CCNI CDC5L CDK1 COL17A1 DEDD DNAJB6 EGFR EP300 EXOC8 FRAT1 GIT2 GOLGA2 GRN HAUS1 HGS HRAS HSPA1A HSPA4 HSPA5 IKBKG KPNA2 KRT15 KRT5 KRT72 KRT8 LDOC1 MAPK14 NME7 ORC5 PDE4DIP PIAS4 PKD1 PKP2 PKP3 PNN POT1 PRKCA PRKCE RAF1 RHPN2 RPS6KA3 SERPINE1 SHC1 SMARCD1 SUMO1 SVIL TCHP TNFRSF1B TRADD TUBG1 TUBGCP4 TXN2 TXNDC11 UPF2 USH2A YTHDC1 YWHAB YWHAE YWHAG YWHAH YWHAZ
Entrez ID 5581 3875
HPRD ID 01500 01020
Ensembl ID ENSG00000171132 ENSG00000111057
Uniprot IDs L7RTI5 Q02156 P05783
PDB IDs 2WH0
Enriched GO Terms of Interacting Partners?
Tagcloud ?
16p11  acgh  actually  appreciating  brwd3  cnv  cnvs  comorbidity  debated  disrupt  duplication  electroclinical  epilepsies  epileptic  grin2a  inheritance  inherited  kcnc3  microdeletions  microduplications  neurodevelopmental  novo  prrt2  re  res  rolandic  shank1  speech  tspan7 
actg2  adenomatous  archived  b4ganlt2  bank  casp3  cdx1  cdx2  classifier  cnn1  col1a1  custom  ezr  fsp1  genomelab  hcellmarkerplex  house  hybridisation  incorporates  lgr5  ms4a12  muc2  mucin  nox1  ntn1  polyp  signatures  slc9a2  vwf 
Tagcloud (Difference) ?
16p11  acgh  actually  appreciating  brwd3  cnv  cnvs  comorbidity  debated  disrupt  duplication  electroclinical  epilepsies  epileptic  grin2a  inheritance  inherited  kcnc3  microdeletions  microduplications  neurodevelopmental  novo  prrt2  re  res  rolandic  shank1  speech  tspan7 
actg2  adenomatous  archived  b4ganlt2  bank  casp3  cdx1  cdx2  classifier  cnn1  col1a1  custom  ezr  fsp1  genomelab  hcellmarkerplex  house  hybridisation  incorporates  lgr5  ms4a12  muc2  mucin  nox1  ntn1  polyp  signatures  slc9a2  vwf 
Tagcloud (Intersection) ?