Cargando…
Thio-Linked UDP–Peptide Conjugates as O-GlcNAc Transferase Inhibitors
[Image: see text] O-GlcNAc transferase (OGT) is an essential glycosyltransferase that installs the O-GlcNAc post-translational modification on the nucleocytoplasmic proteome. We report the development of S-linked UDP–peptide conjugates as potent bisubstrate OGT inhibitors. These compounds were assem...
Autores principales: | Rafie, Karim, Gorelik, Andrii, Trapannone, Riccardo, Borodkin, Vladimir S., van Aalten, Daan M. F. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2018
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6016062/ https://www.ncbi.nlm.nih.gov/pubmed/29723473 http://dx.doi.org/10.1021/acs.bioconjchem.8b00194 |
Ejemplares similares
-
Bisubstrate UDP–peptide conjugates as human O-GlcNAc transferase inhibitors
por: Borodkin, Vladimir S., et al.
Publicado: (2014) -
Proteolysis of HCF-1 by Ser/Thr glycosylation-incompetent O-GlcNAc transferase:UDP-GlcNAc complexes
por: Kapuria, Vaibhav, et al.
Publicado: (2016) -
Recognition of a glycosylation substrate by the O-GlcNAc transferase TPR repeats
por: Rafie, Karim, et al.
Publicado: (2017) -
Nucleocytoplasmic human O-GlcNAc transferase is sufficient for O-GlcNAcylation of mitochondrial proteins
por: Trapannone, Riccardo, et al.
Publicado: (2016) -
Substrate and product analogues as human O-GlcNAc transferase inhibitors
por: Dorfmueller, Helge C., et al.
Publicado: (2010)