ACTC1 and PRKCE

  • Number of citations of the paper that reports this interaction (PMID 11968018)
  • 8
  • Data Source:
  • HPRD (in vivo)

ACTC1

PRKCE

Gene Name actin, alpha, cardiac muscle 1 protein kinase C, epsilon
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
  • Prostate cancer (gene x gene interaction) ( 22219177)
  • Refractive error ( 20835239)
Protein-Protein Interactions 35 interactors: ABLIM3 ABRA ACTB ACTN4 ACTR2 AFAP1 ANG BCL11A CAPN1 CFL1 DMD DMTN DYNLL1 EZR FSCN1 GAPDH GC HSPB1 KLHL17 KLHL2 KPTN LASP1 MIB2 MPC1 MYLK PLEC PRKCE SCIN SLC4A1 SYNE1 SYNE2 TNNI3K TWF1 WAS WIPF1 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
Entrez ID 70 5581
HPRD ID 00015 01500
Ensembl ID ENSG00000159251 ENSG00000171132
Uniprot IDs B3KPP5 P68032 L7RTI5 Q02156
PDB IDs 2WH0
Enriched GO Terms of Interacting Partners?
Tagcloud ?
accompany  ach3  ach4  cardiac  cardiomyocytes  cardiomyogenic  cd29  commitment  cscs  elusive  fate  hdac  hdac1  hdac2  hypothesize  indicative  loci  mark  modifications  mscs  myh6  myl2  noticed  possess  sca  stronger  tnni3  tnnt2  trichostatin 
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 
Tagcloud (Difference) ?
accompany  ach3  ach4  cardiac  cardiomyocytes  cardiomyogenic  cd29  commitment  cscs  elusive  fate  hdac  hdac1  hdac2  hypothesize  indicative  loci  mark  modifications  mscs  myh6  myl2  noticed  possess  sca  stronger  tnni3  tnnt2  trichostatin 
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 
Tagcloud (Intersection) ?