UGCG: A Promising Drug Target for Various Diseases (G7357)
UGCG: A Promising Drug Target for Various Diseases
UGCG, or Urolucin, is a drug target (or biomarker) that has been identified and characterized for its role in various diseases, including cancer, diabetes, and neurodegenerative disorders. Its unique structure and function make it an attractive target for drug development, with potential applications in treating a wide range of diseases.
UGCG is a small molecule that is expressed in various tissues and organs, including the brain, pancreas, and gastrointestinal tract. It is a potent inhibitor of the enzyme PKA, which is involved in the phosphorylation of many intracellular proteins. PKA is a key regulator of cell signaling and is involved in many important cellular processes, including cell growth, differentiation, and survival.
The inhibition of PKA by UGCG has been shown to have a variety of therapeutic effects. For example, it has been shown to be a potent inhibitor of cancer cell proliferation and has been used in various clinical trials as a potential treatment for pancreatic cancer. In addition, UGCG has also been shown to be a potent inhibitor of neurodegenerative disorders, such as Alzheimer's disease and Parkinson's disease.
UGCG's unique structure and function make it an attractive target for drug development due to its ability to selectively target PKA-phosphorylated proteins. This allows for the development of small molecules that can specifically inhibit PKA and have a more targeted and effective effect on disease processes.
UGCG has also been shown to have a variety of other therapeutic effects, including its ability to protect against neurotoxins, such as glutamate, a neurotransmitter that is involved in many important cellular processes, including learning and memory. In addition, UGCG has also been shown to have a variety of other physiological effects, including its ability to regulate blood sugar levels and its role in the regulation of sleep-wake cycles.
The potential applications of UGCG are vast and continue to be explored by researchers. Its ability to selectively target PKA-phosphorylated proteins makes it an attractive target for the development of small molecules that can treat a wide range of diseases, including cancer, diabetes, and neurodegenerative disorders. As research continues to advance, the potential applications of UGCG will continue to emerge, and it will be an exciting and promising area of research for the future.
Protein Name: UDP-glucose Ceramide Glucosyltransferase
Functions: Participates in the initial step of the glucosylceramide-based glycosphingolipid/GSL synthetic pathway at the cytosolic surface of the Golgi (PubMed:8643456, PubMed:1532799). Catalyzes the transfer of glucose from UDP-glucose to ceramide to produce glucosylceramide/GlcCer (such as beta-D-glucosyl-(1<->1')-N-acylsphing-4-enine) (PubMed:1532799, PubMed:8643456). GlcCer is the core component of glycosphingolipids/GSLs, amphipathic molecules consisting of a ceramide lipid moiety embedded in the outer leaflet of the membrane, linked to one of hundreds of different externally oriented oligosaccharide structures (PubMed:8643456). Glycosphingolipids are essential components of membrane microdomains that mediate membrane trafficking and signal transduction, implicated in many fundamental cellular processes, including growth, differentiation, migration, morphogenesis, cell-to-cell and cell-to-matrix interactions (By similarity). They are required for instance in the proper development and functioning of the nervous system (By similarity). As an example of their role in signal transduction, they regulate the leptin receptor/LEPR in the leptin-mediated signaling pathway (By similarity). They also play an important role in the establishment of the skin barrier regulating keratinocyte differentiation and the proper assembly of the cornified envelope (By similarity). The biosynthesis of GSLs is also required for the proper intestinal endocytic uptake of nutritional lipids (By similarity). Catalyzes the synthesis of xylosylceramide/XylCer (such as beta-D-xylosyl-(1<->1')-N-acylsphing-4-enine) using UDP-Xyl as xylose donor (PubMed:33361282)
More Common Targets
UGDH | UGDH-AS1 | UGGT1 | UGGT2 | UGP2 | UGT1A1 | UGT1A10 | UGT1A3 | UGT1A4 | UGT1A5 | UGT1A6 | UGT1A7 | UGT1A8 | UGT1A9 | UGT2A1 | UGT2A2 | UGT2A3 | UGT2B10 | UGT2B11 | UGT2B15 | UGT2B17 | UGT2B27P | UGT2B28 | UGT2B29P | UGT2B4 | UGT2B7 | UGT3A1 | UGT3A2 | UGT8 | UHMK1 | UHRF1 | UHRF2 | UICLM | UIMC1 | ULBP1 | ULBP2 | ULBP3 | ULK1 | ULK2 | ULK3 | ULK4 | ULK4P1 | ULK4P2 | ULK4P3 | UMAD1 | UMLILO | UMOD | UMODL1 | UMODL1-AS1 | UMPS | UNC119 | UNC119-myristate complex | UNC119B | UNC13A | UNC13B | UNC13C | UNC13D | UNC45A | UNC45B | UNC50 | UNC5A | UNC5B | UNC5B-AS1 | UNC5C | UNC5CL | UNC5D | UNC79 | UNC80 | UNC93A | UNC93B1 | UNC93B2 | UNC93B3 | UNC93B5 | Uncharactered LOC400863 | Uncharacterized FLJ44790 | Uncharacterized LOC101927121, transcript variant X1 | Uncharacterized LOC101928822, transcript variant X1 | Uncharacterized LOC101929670, transcript variant X1 | Uncharacterized LOC102723888, transcript variant X1 | Uncharacterized LOC102724782, transcript variant X2 | Uncharacterized LOC102724946, transcript variant X3 | Uncharacterized LOC105371833, transcript variant X2 | Uncharacterized LOC105372229, transcript variant X1 | Uncharacterized LOC105373166, transcript variant X2 | Uncharacterized LOC105373806, transcript variant X1 | Uncharacterized LOC105374567, transcript variant X2 | Uncharacterized LOC105374812, transcript variant X2 | Uncharacterized LOC105375163, transcript variant X1 | Uncharacterized LOC105376875, transcript variant X2 | Uncharacterized protein BC001742 | Uncharacterized protein FLJ23867 | Uncharacterized protein MGC16142 | Uncharacterized protein MGC27345 | UNCX | UNG | Uniplex complex | UNK | UNKL | UNQ9370 | UOX