STX11 and SNAP25

  • Number of citations of the paper that reports this interaction (PMID 16189514)
  • 699
  • Data Source:
  • BioGRID (two hybrid, two hybrid)
  • HPRD (two hybrid)

STX11

SNAP25

Gene Name syntaxin 11 synaptosomal-associated protein, 25kDa
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 62 interactors: AES APP BLOC1S6 BYSL C1orf109 CARD9 CCBE1 CCDC184 CCDC33 CCNK CDCA7L CTBP2 CWF19L2 EIF1AD FAM110A FAM161A FAM74A4 FAM90A1 FARS2 FHL5 GOLGA8EP GOLGA8F HAUS1 IKBKG IKZF3 KAT5 KCTD9 KDM1A KLC3 KXD1 LENG1 LONRF1 MBIP MEOX2 MFAP1 MID2 NDC80 PPP1R18 PRKAB2 PRPF31 PSMA3 PSMC3 RUNX1T1 SH2D4A SLC38A2 SMARCE1 SNAP23 SNAP25 SNX3 STXBP1 SUV39H1 TAF6L TBK1 TCF4 TNFRSF21 USHBP1 VAMP2 VPS52 WDYHV1 ZCCHC10 ZNF417 ZNF587 34 interactors: APP CCDC53 CENPF CPLX1 DNM1 GOSR1 HGS ITSN1 KCNB1 KIF5B NAPA PRKACA PRKCA PRRT2 RIMS1 SCAMP1 SNAPIN SRCIN1 STX11 STX12 STX1A STX2 STX3 STX4 STX5 STXBP6 SYT1 SYT3 SYT9 TRIM9 VAMP2 VAMP7 VAMP8 ZDHHC17
Entrez ID 8676 6616
HPRD ID 09231 02637
Ensembl ID ENSG00000132639
Uniprot IDs O75558 P60880
PDB IDs 1KIL 1XTG 3RK2 3RK3 3RL0 3ZUR
Enriched GO Terms of Interacting Partners?
Tagcloud ?
autosomal  characterised  defect  done  dysregulation  familial  families  fhl  haemophagocytic  harbour  harbouring  killer  leukaemia  lymphohistiocytosis  milder  mutational  myelogenous  nonsense  perforin  periods  prf1  psychomotor  recessive  retardation  segregation  syntaxin  uncommon  undertaken  unrelated 
anterograde  axonal  axons  blunt  breakdown  bulbous  bulbs  caudate  circumscribed  disorganized  immunocytochemical  immunoreactivity  insult  map5  mca  neurofilament  nf68kd  nonischemic  occlusion  permeating  precedes  reminiscent  roughened  sequalae  subcortical  swellings  synaptosomal  territory  tracts 
Tagcloud (Difference) ?
autosomal  characterised  defect  done  dysregulation  familial  families  fhl  haemophagocytic  harbour  harbouring  killer  leukaemia  lymphohistiocytosis  milder  mutational  myelogenous  nonsense  perforin  periods  prf1  psychomotor  recessive  retardation  segregation  syntaxin  uncommon  undertaken  unrelated 
anterograde  axonal  axons  blunt  breakdown  bulbous  bulbs  caudate  circumscribed  disorganized  immunocytochemical  immunoreactivity  insult  map5  mca  neurofilament  nf68kd  nonischemic  occlusion  permeating  precedes  reminiscent  roughened  sequalae  subcortical  swellings  synaptosomal  territory  tracts 
Tagcloud (Intersection) ?