AbstractO-linked β-N-acetylglucosamine (O-GlcNAc) is a dynamic nucleocytoplasmic post-translational modification more analogous to phosphorylation than to classical complex O-glycosylation. A large number of nuclear and cytosolic proteins are modified by O-GlcNAc. Proteins modified by O-GlcNAc include transcription factors, signaling components, and metabolic enzymes. While the modification has been known for almost 20 years, functions for the monosaccharide modification are just now emerging. In this review, we will focus on the cycling enzymes and emerging roles for this post-translational modification in regulating signal transduction and transcription. Finally, we will discuss future directions and the working model of O-GlcNAc serving ...
Protein glycosylation is one of the most abundant posttransla-tional modifications and plays a funda...
O-GlcNAcylation is dynamic and a ubiquitous post-translational modification. O-GlcNAcylated proteins...
The covalent attachment of O-linked beta-N-acetylglucosamine (O-GlcNAc) to Ser/Thr residues of prote...
Protein modification by O-linked -N-acetyl glucosamine (O-GlcNAc) has rapidly emerged as a major cel...
C REB controls gene expression programs that underlie diverse neuronal processes, ranging from neura...
The dynamic posttranslational modification of proteins by O-linked-β-N-acetylglucosamine (O-GlcNAc g...
Abstract Post-translational modification of proteins at serine and threonine side chains by β-N-acet...
The concepts of both protein glycosylation and cellular signaling have been influenced by O-linked-β...
The cycling (addition and removal) of O-linked N-acetylglucosamine (O-GlcNAc) on serine or threonine...
Hundreds post-translational modifications (PTM) were characterized among which a large variety of gl...
The addition and removal of N-acetylglucosamine (GlcNAc) molecules on serine or threonine residues o...
Within higher eukaryotes, hundreds of nucleocytoplasmic proteins are modified by an N-acetylglucosam...
AbstractSer(Thr)-O-linked β-N-acetylglucosamine (O-GlcNAc) is a ubiquitous modification of nucleocyt...
The nutrient sensor, O-linked N-acetylglucosamine (O-GlcNAc), cycles on and off nuclear and cytosoli...
2018-10-24Functional diversity of transcribed proteins is exponentially expanded with the addition o...
Protein glycosylation is one of the most abundant posttransla-tional modifications and plays a funda...
O-GlcNAcylation is dynamic and a ubiquitous post-translational modification. O-GlcNAcylated proteins...
The covalent attachment of O-linked beta-N-acetylglucosamine (O-GlcNAc) to Ser/Thr residues of prote...
Protein modification by O-linked -N-acetyl glucosamine (O-GlcNAc) has rapidly emerged as a major cel...
C REB controls gene expression programs that underlie diverse neuronal processes, ranging from neura...
The dynamic posttranslational modification of proteins by O-linked-β-N-acetylglucosamine (O-GlcNAc g...
Abstract Post-translational modification of proteins at serine and threonine side chains by β-N-acet...
The concepts of both protein glycosylation and cellular signaling have been influenced by O-linked-β...
The cycling (addition and removal) of O-linked N-acetylglucosamine (O-GlcNAc) on serine or threonine...
Hundreds post-translational modifications (PTM) were characterized among which a large variety of gl...
The addition and removal of N-acetylglucosamine (GlcNAc) molecules on serine or threonine residues o...
Within higher eukaryotes, hundreds of nucleocytoplasmic proteins are modified by an N-acetylglucosam...
AbstractSer(Thr)-O-linked β-N-acetylglucosamine (O-GlcNAc) is a ubiquitous modification of nucleocyt...
The nutrient sensor, O-linked N-acetylglucosamine (O-GlcNAc), cycles on and off nuclear and cytosoli...
2018-10-24Functional diversity of transcribed proteins is exponentially expanded with the addition o...
Protein glycosylation is one of the most abundant posttransla-tional modifications and plays a funda...
O-GlcNAcylation is dynamic and a ubiquitous post-translational modification. O-GlcNAcylated proteins...
The covalent attachment of O-linked beta-N-acetylglucosamine (O-GlcNAc) to Ser/Thr residues of prote...