RAP1GAP and DYNC1I1

  • Number of citations of the paper that reports this interaction (PMID 21900206)
  • 27
  • Data Source:
  • BioGRID (two hybrid)

RAP1GAP

DYNC1I1

Gene Name RAP1 GTPase activating protein dynein, cytoplasmic 1, intermediate chain 1
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
  • Immune reponse to smallpox (secreted IL-10) ( 22610502)
  • Obesity-related traits ( 23251661)
Protein-Protein Interactions 15 interactors: BRAF CDK1 CSNK1G2 DYNC1I1 GNAZ MAP1LC3B MAPK6 MEX3B MLLT4 PFN2 PLK1 PRKACA RALGDS RAP1A ZBTB12 31 interactors: ANXA7 BICD1 C2orf44 CADM4 CDKN1A DNM2 DYNLL1 DYNLL2 DYNLRB1 DYNLT1 DYNLT3 EMILIN1 FAM110A FAM83D FBP1 GRB7 GSK3B KAT7 MCC NAGK NUDT21 PIN1 RAP1GAP RCC1 RUNDC3B SMN1 STAU1 TAOK1 TK1 TRIM58 UBC
Entrez ID 5909 1780
HPRD ID 02609 04798
Ensembl ID ENSG00000076864 ENSG00000158560
Uniprot IDs P47736 A4D1I7 B4DME3 F5H050 G5E9K1 O14576 Q8N542 Q8TBF7
PDB IDs 1SRQ 3BRW
Enriched GO Terms of Interacting Partners?
Tagcloud ?
autophosphorylated  burst  c3g  crk  detrimental  fascin  filamentous  forced  gradual  gtpase  guanine  holds  hyperactivation  imperative  irrespective  labile  microspikes  motile  n17rap1  presumed  protrusions  recruits  releasing  reverses  sh3  unidentified  v12rap1 
10q24  17p13  cgh  cnvs  congenital  deletions  dlx5  duplications  eexons  encompassing  enhancer  enhancers  exonic  exons  families  foot  fourth  hearing  hs1642  kb  malformation  microdeletions  shfm  shfm1  split  syndromic  telomeric  tp63  unrelated 
Tagcloud (Difference) ?
autophosphorylated  burst  c3g  crk  detrimental  fascin  filamentous  forced  gradual  gtpase  guanine  holds  hyperactivation  imperative  irrespective  labile  microspikes  motile  n17rap1  presumed  protrusions  recruits  releasing  reverses  sh3  unidentified  v12rap1 
10q24  17p13  cgh  cnvs  congenital  deletions  dlx5  duplications  eexons  encompassing  enhancer  enhancers  exonic  exons  families  foot  fourth  hearing  hs1642  kb  malformation  microdeletions  shfm  shfm1  split  syndromic  telomeric  tp63  unrelated 
Tagcloud (Intersection) ?