RAB6A and RABAC1

  • Number of citations of the paper that reports this interaction (PMID 10329441)
  • 15
  • Data Source:
  • HPRD (two hybrid)

RAB6A

RABAC1

Gene Name RAB6A, member RAS oncogene family Rab acceptor 1 (prenylated)
Image No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 20 interactors: BICD1 BICD2 CHM CHML DCTN1 ERC1 FKBP2 GDI1 GOLGA1 GOLGA2 GOLGA4 KIF20A OCRL PMM1 RAB7A RABAC1 RABGAP1 RABGGTB SYTL5 TMF1 63 interactors: ADCK3 CMTM3 CREB3 DUSP12 FAM160A2 FXR2 GDI1 HRAS HRG LNX1 MAD2L1 MCF2L MIEF2 NAT14 NDRG4 NIF3L1 NR3C2 NUDT18 PBX3 PLEKHF2 PLK1 RAB17 RAB1A RAB22A RAB33A RAB3A RAB4A RAB4B RAB5A RAB5B RAB5C RAB6A RAB7A RAP1A RASD2 REEP5 RGS2 RHEB RHOA RIC8A RIMS2 RIN3 RPS20 RRAS2 SGK1 SNCA SNX1 SNX10 SNX11 SNX15 SPG21 SYT16 TNIP1 TRIM32 TSHR TUBB2A TXN2 VAMP2 VIM VTA1 WDYHV1 WIPI2 ZFYVE21
Entrez ID 5870 10567
HPRD ID 01543 05375
Ensembl ID ENSG00000175582 ENSG00000105404
Uniprot IDs P20340 Q53ET8 Q9UI14
PDB IDs 1YZQ 2GIL 3BBP 3CWZ 4DKX
Enriched GO Terms of Interacting Partners?
Tagcloud ?
autosomal  axonal  causal  coh1  cohen  constitutively  disability  dystrophy  golgi  gtpase  inactive  integrity  intellectual  interfered  microcephaly  neurite  neuritogenesis  outgrowth  preferentially  preparations  prevents  q72l  recessive  rnai  scaffold  solubilization  t27n  vps13b 
Tagcloud (Difference) ?
autosomal  axonal  causal  coh1  cohen  constitutively  disability  dystrophy  golgi  gtpase  inactive  integrity  intellectual  interfered  microcephaly  neurite  neuritogenesis  outgrowth  preferentially  preparations  prevents  q72l  recessive  rnai  scaffold  solubilization  t27n  vps13b 
Tagcloud (Intersection) ?