FBP1 and DYNC1I1

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

FBP1

DYNC1I1

Gene Name fructose-1,6-bisphosphatase 1 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 20 interactors: ACTN1 ASCC2 ASL ATP5J2 BCL2L1 BIN1 CSNK1E DYNC1I1 FBP2 FXR2 HDAC6 HSPA8 KLRC2 LNX1 PARK2 PCNXL4 POT1 PTK2 RNF183 TERF1 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 2203 1780
HPRD ID 01973 04798
Ensembl ID ENSG00000165140 ENSG00000158560
Uniprot IDs P09467 Q2TU34 A4D1I7 B4DME3 F5H050 G5E9K1 O14576 Q8N542 Q8TBF7
PDB IDs 1FTA 2FHY 2FIE 2FIX 2JJK 2VT5 2WBB 2WBD 2Y5K 2Y5L 3A29 3KBZ 3KC0 3KC1
Enriched GO Terms of Interacting Partners?
Tagcloud ?
abundantly  albeit  antagonizes  bccip  fuse  hepatocellular  hypothesize  impairing  implication  interacted  interacts  knockdown  oncogene  p21  p53  physically  proapoptotic  protein1  proto  radiation  restored  stably  suppresses  tctp  transactivation  transactivator  tumorigenesis  undifferentiated 
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) ?
abundantly  albeit  antagonizes  bccip  fuse  hepatocellular  hypothesize  impairing  implication  interacted  interacts  knockdown  oncogene  p21  p53  physically  proapoptotic  protein1  proto  radiation  restored  stably  suppresses  tctp  transactivation  transactivator  tumorigenesis  undifferentiated 
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) ?