PID1 and THAP1

  • Number of citations of the paper that reports this interaction (PMID 25416956)
  • 0
  • Data Source:
  • BioGRID (two hybrid)

PID1

THAP1

Gene Name phosphotyrosine interaction domain containing 1 THAP domain containing, apoptosis associated protein 1
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 13 interactors: ADAMTSL4 BANP CCDC33 CRX GOLGA2 GOPC KRTAP10-1 LRP1 MDFI NME1 NOTCH2NL SPERT THAP1 58 interactors: ACOT7 AKAP17A AKAP9 AP2B1 ARL6IP4 BAG5 BMS1P5 BYSL C11orf57 C1orf35 C7orf50 CHD2 CSNK2A1 DCAF8 DVL2 FAM124A FAM133A FXR2 GPATCH2L HNRNPLL KLF12 KRTAP10-7 LASP1 MORF4L1 MORF4L2 MRPL11 NKAP NUP62 PAWR PHF1 PID1 POLR2L POLR2M PPIG PRKAA1 PRR20A QKI RALYL RBM39 RIPPLY1 RP9P RPS25 SAP30BP SERF2 SLU7 STRBP TCEA2 TPM3 TRAF5 TRIM26 TTLL10 TXN2 U2AF2 WDYHV1 YES1 ZCCHC10 ZNF385C ZNF408
Entrez ID 55022 55145
HPRD ID 07944 15496
Ensembl ID ENSG00000153823 ENSG00000131931
Uniprot IDs Q7Z2X4 Q9NVV9
PDB IDs 2JTG 2KO0 2L1G
Enriched GO Terms of Interacting Partners?
Tagcloud ?
adaptor  apla  associates  augmented  changed  confocal  depending  developmentally  disrupted  e3  est  fe65  ligase  localization  motif  nedd4  originally  phosphotyrosine  pid2  pplp  pull  putative  subcellular  tag  ubiquitin  ubiquitinated  ubiquitylation  w243kp245k  ww 
assembled  childhood  compatible  confirms  contiguous  definite  deletions  distinctive  dystonia  dyt1  eighty  gch1  imprinted  ireland  laxity  maternally  microcephaly  myoclonus  nineteen  nkx2  phenotypically  probable  probands  progressing  sequenced  sgce  stature  uk  upper 
Tagcloud (Difference) ?
adaptor  apla  associates  augmented  changed  confocal  depending  developmentally  disrupted  e3  est  fe65  ligase  localization  motif  nedd4  originally  phosphotyrosine  pid2  pplp  pull  putative  subcellular  tag  ubiquitin  ubiquitinated  ubiquitylation  w243kp245k  ww 
assembled  childhood  compatible  confirms  contiguous  definite  deletions  distinctive  dystonia  dyt1  eighty  gch1  imprinted  ireland  laxity  maternally  microcephaly  myoclonus  nineteen  nkx2  phenotypically  probable  probands  progressing  sequenced  sgce  stature  uk  upper 
Tagcloud (Intersection) ?