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RAB36, member RAS oncogene family

Rab36
Top mentioned proteins: Rab5, CAN, BCR, ARF6, GST
Papers on Rab36
Rab35 promotes the recruitment of Rab8, Rab13 and Rab36 to recycling endosomes through MICAL-L1 during neurite outgrowth.
Fukuda et al., Sendai, Japan. In Biol Open, 2013
Here we report that Rab35 and MICAL-L1 promote the recruitment of Rab8, Rab13, and Rab36 to Arf6-positive recycling endosomes during neurite outgrowth.
The Rab interacting lysosomal protein (RILP) homology domain functions as a novel effector domain for small GTPase Rab36: Rab36 regulates retrograde melanosome transport in melanocytes.
GeneRIF
Fukuda et al., Sendai, Japan. In J Biol Chem, 2012
Rab36 mediates retrograde melanosome transport in melanocytes through interaction with RILP.
RUTBC2 protein, a Rab9A effector and GTPase-activating protein for Rab36.
GeneRIF
Pfeffer et al., Stanford, United States. In J Biol Chem, 2012
These data show that RUTBC2 can act as a Rab36 GAP in cells and suggest that RUTBC2 links Rab9A function to Rab36 function in the endosomal system.
The first case of myoclonic epilepsy in a child with a de novo 22q11.2 microduplication.
Corsello et al., Palermo, Italy. In Am J Med Genet A, 2011
Emphasizing that this rare association could be one of the many unrecognized aspects underlying this new emerging syndrome and once again its clinical heterogeneity, we suggest further investigation of the function of the RAB36 gene and propose that in the screening of individuals with developmental delay, minor behavioral problems mild dysmorphology and seizures, investigation of 22q11.2
Comprehensive screening for novel rab-binding proteins by GST pull-down assay using 60 different mammalian Rabs.
Fukuda et al., Sendai, Japan. In Traffic, 2010
Three of the 21 Rab-binding proteins we identified, mKIAA1055/TBC1D2B (Rab22-binding protein), GAPCenA/TBC1D11 (Rab36-binding protein) and centaurin beta2/ACAP2 (Rab35-binding protein), are GTPase-activating proteins (GAPs) for Rab or Arf.
Rab36 regulates the spatial distribution of late endosomes and lysosomes through a similar mechanism to Rab34.
GeneRIF
Wang et al., Xiamen, China. In Mol Membr Biol, 2010
Rab36 may regulate the spatial distribution of late endosomes and lysosomes through a similar mechanism to Rab34.
BCR expression is decreased in meningiomas showing loss of heterozygosity of 22q within a new minimal deletion region.
Rieske et al., Łódź, Poland. In Cancer Genet Cytogenet, 2008
The new minimal deletion region (MDR) included the following genes: BCR (breakpoint cluster region), RAB36 (a member of RAS oncogene family), GNAZ [guanine nucleotide binding protein (G protein), alpha-z polypeptide], and RTDR1 (rhabdoid tumor deletion region gene 1).
Isolation of genes from the rhabdoid tumor deletion region in chromosome band 22q11.2.
Biegel et al., Philadelphia, United States. In Gene, 2000
Two genes, RTDR1 and RAB36, were cloned from this portion of 22q11, which is heterozygously or homozygously deleted in pediatric rhabdoid tumors of the brain, kidney and soft tissues.
Cloning and characterization of a novel Rab-family gene, Rab36, within the region at 22q11.2 that is homozygously deleted in malignant rhabdoid tumors.
Inazawa et al., Tokyo, Japan. In Biochem Biophys Res Commun, 1999
As it showed a high degree of sequence homology to genes of the Rab family, we designated it Rab36.
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