DYNC1I1 and DYNLL1

  • Number of citations of the paper that reports this interaction (PMID 20921139)
  • 48
  • Data Source:
  • BioGRID (affinity chromatography technology, unspecified method)
  • HPRD (in vitro)

DYNC1I1

DYNLL1

Gene Name dynein, cytoplasmic 1, intermediate chain 1 dynein, light chain, LC8-type 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 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 77 interactors: ACTB ACTC1 ACTG1 ALDOA AMBRA1 AMOTL2 B3GALT4 BCAS1 BCL2L11 BMF C14orf1 CA2 CACNB1 CCDC36 CLIP2 CS DAZ1 DLG4 DLGAP1 DNAJB9 DNM2 DNM3 DNMT1 DYNC1H1 DYNC1I1 EEF1A1 GAPDH GLUD1 GLUL GNB2L1 GPHN GRIN3A HIP1R HSPA8 INPP1 IQUB KANK2 LDHA MAP1B MARK3 MAST2 ME2 MTA1 MTR MYO10 MYO5A NDUFA4L2 NFKBIA NOS1 NRF1 NTRK1 NTRK2 NTRK3 PAK1 PAN2 PARD3 PAX6 PFKM PFKP PKIA PKIB PKIG POLH RAB4A RGS2 SHROOM3 TERT THAP8 TNFRSF14 TP53BP1 TUBA3C TUBB TXNDC17 VIM ZHX1 ZMYND11 ZNF354A
Entrez ID 1780 8655
HPRD ID 04798 03334
Ensembl ID ENSG00000158560 ENSG00000088986
Uniprot IDs A4D1I7 B4DME3 F5H050 G5E9K1 O14576 Q8N542 Q8TBF7 P63167 Q6FGH9
PDB IDs 1CMI 3ZKE 3ZKF
Enriched GO Terms of Interacting Partners?
Tagcloud ?
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 
1inq53a  250viqd  52gqvd  adapter  attempt  capsid  defective  dynein  hiv  immunodeficiency  integrase  interaction  kd  ma  motifs  mutational  p150glued  particulate  predicts  proper  q252a  replication  requirement  reverse  steps  tctex  transcriptase  uncoating 
Tagcloud (Difference) ?
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 
1inq53a  250viqd  52gqvd  adapter  attempt  capsid  defective  dynein  hiv  immunodeficiency  integrase  interaction  kd  ma  motifs  mutational  p150glued  particulate  predicts  proper  q252a  replication  requirement  reverse  steps  tctex  transcriptase  uncoating 
Tagcloud (Intersection) ?