Schizosaccharomyces pombe Git1 Is a C2
... obvious homologs in other eukaryotes, Git1 is only distantly related to a conserved fungal protein family of unknown function as well as the UNC-13/Munc13 protein family involved in synaptic vesicle exocytosis. All of these proteins contain a similar C2 domain near their carboxy-terminus, along with ...
... obvious homologs in other eukaryotes, Git1 is only distantly related to a conserved fungal protein family of unknown function as well as the UNC-13/Munc13 protein family involved in synaptic vesicle exocytosis. All of these proteins contain a similar C2 domain near their carboxy-terminus, along with ...
Xenopus laevis Stromal Cell-Derived Factor 1
... growth-related oncogene; cSDF-1, cat SDF-1; mSDF-1, mouse SDF-1. ...
... growth-related oncogene; cSDF-1, cat SDF-1; mSDF-1, mouse SDF-1. ...
ii. synthetic analogues to target the membrane ci-m6pr - HAL
... and the deduced amino acid sequence for the CI-M6PR, were reported to be strikingly similar (99.4% identical in the amino acid sequence) to those reported for the human insulin-like growth factor II (IGFII) receptor from HepG2 hepatoma cells [23]. These findings supported the suggestion that CI-M6PR ...
... and the deduced amino acid sequence for the CI-M6PR, were reported to be strikingly similar (99.4% identical in the amino acid sequence) to those reported for the human insulin-like growth factor II (IGFII) receptor from HepG2 hepatoma cells [23]. These findings supported the suggestion that CI-M6PR ...
VLDL receptor
The very-low-density-lipoprotein receptor (VLDLR) is a transmembrane lipoprotein receptor of the low-density-lipoprotein (LDL) receptor family. VLDLR shows considerable homology with the members of this lineage. Discovered in 1992 by T. Yamamoto, VLDLR is widely distributed throughout the tissues of the body, including the heart, skeletal muscle, adipose tissue, and the brain, but is absent from the liver. This receptor has an important role in cholesterol uptake, metabolism of apoprotein-E-containing triacylglycerol-rich lipoproteins, and neuronal migration in the developing brain. In humans, VLDLR is encoded by the VLDLR gene. Mutations of this gene may lead to a variety of symptoms and diseases, which include type I lissencephaly, cerebellar hypoplasia, and atherosclerosis.