PPM1A and CACNA1A

  • Number of citations of the paper that reports this interaction (PMID 15728831)
  • 6
  • Data Source:
  • HPRD (in vivo, in vitro)

PPM1A

CACNA1A

Gene Name protein phosphatase, Mg2+/Mn2+ dependent, 1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
Image
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 19 interactors: AKT1 CACNA1A CACNA1B CACNA1C CTNNB1 DVL1 DVL2 DVL3 EEF2 FGFR2 GRM3 HSPB1 MSN NR4A1 PIK3R1 PRKCD RPLP0 SMAD2 SMAD3 92 interactors: ABCA2 ABI1 ACTN1 AGRN ALDOA AMIGO2 AP2M1 ARHGAP22 ASNA1 BTG3 BZRAP1 C1QTNF1 CABP1 CACNB1 CACNB4 CALM2 CALM3 CKAP5 CRIM1 CRMP1 CSNK2B CYSRT1 DNAJB5 EFEMP1 EFEMP2 EHMT2 EIF3A FBLN1 GNB1 GOLGA6L5P GRN HECW1 HHATL HIVEP1 HSPG2 IP6K1 JAG2 KALRN KHDRBS3 KIAA1191 LAMB1 LLGL1 LPHN1 LRP1 LTBP1 LTBP3 LTBP4 MANBAL MATK MATN2 MEGF6 MEGF8 MIA3 MOAP1 NDUFB8 NELFCD NELL1 NELL2 NOTCH1 NOXA1 OLIG1 PCSK5 PCSK6 PMM1 PPIG PPM1A PPP1R12C PTGDS PUF60 RBM12B RIMBP2 RPL31 RPS17 SCP2 SPRY1 SRRM4 SRSF1 SUMF2 SYT1 TAF15 TELO2 TSC22D1 TSPAN7 TUBB2B UQCRC2 VARS VPS52 VWF WBP1 YLPM1 ZCCHC17 ZNF233
Entrez ID 5494 773
HPRD ID 16199 03004
Ensembl ID ENSG00000100614 ENSG00000141837
Uniprot IDs B2R8E4 P35813 B5TYJ1 O00555 Q9NS89
PDB IDs 1A6Q 3FXJ 3FXK 3FXL 3FXM 3FXO 3BXK
Enriched GO Terms of Interacting Partners?
Tagcloud ?
agt  card4  casp1  csf2  csf3  curcuma  f2r  icam1  ifng  ikbkb  ikbke  il10  il1a  il1b  il8  impressive  irak2  longa  map3k1  nfkb1  nfkb2  nfkbia  raf1  relb  ticam1  ticam2  tnfalphaip3  tnfrsf7  tnfsf10 
acetazolamide  ataxia  attacks  autosomal  causative  causing  coincidence  confutes  defect  dysarthria  dystonia  ea  ea2  encodes  episodes  episodic  gait  gated  heterogeneous  inherited  migraine  mim  nonsense  oculomotor  paroxysmal  q  varied  voltage 
Tagcloud (Difference) ?
agt  card4  casp1  csf2  csf3  curcuma  f2r  icam1  ifng  ikbkb  ikbke  il10  il1a  il1b  il8  impressive  irak2  longa  map3k1  nfkb1  nfkb2  nfkbia  raf1  relb  ticam1  ticam2  tnfalphaip3  tnfrsf7  tnfsf10 
acetazolamide  ataxia  attacks  autosomal  causative  causing  coincidence  confutes  defect  dysarthria  dystonia  ea  ea2  encodes  episodes  episodic  gait  gated  heterogeneous  inherited  migraine  mim  nonsense  oculomotor  paroxysmal  q  varied  voltage 
Tagcloud (Intersection) ?