نتایج جستجو برای: ماژور ژن glcnac

تعداد نتایج: 19786  

2014
Alice Boulanger Claudine Zischek Martine Lautier Stevie Jamet Pauline Rival Sébastien Carrère Matthieu Arlat Emmanuelle Lauber

UNLABELLED N-Acetylglucosamine (GlcNAc), the main component of chitin and a major constituent of bacterial peptidoglycan, is present only in trace amounts in plants, in contrast to the huge amount of various sugars that compose the polysaccharides of the plant cell wall. Thus, GlcNAc has not previously been considered a substrate exploited by phytopathogenic bacteria during plant infection. Xan...

Journal: :American journal of physiology. Cell physiology 2006
Tamas Nagy Voraratt Champattanachai Richard B Marchase John C Chatham

We previously reported that glucosamine and hyperglycemia attenuate the response of cardiomyocytes to inositol 1,4,5-trisphosphate-generating agonists such as ANG II. This appears to be related to an increase in flux through the hexosamine biosynthesis pathway (HBP) and decreased Ca2+ entry into the cells; however, a direct link between HBP and intracellular Ca2+ homeostasis has not been establ...

Journal: :The Biochemical journal 2004
Yuji Honda Motomitsu Kitaoka Kiyoshi Hayashi

A family 36 glycosyltransferase gene was cloned from Vibrio proteolyticus. The deduced amino acid sequence showed a high degree of identity with ChBP (chitobiose phosphorylase) from another species, Vibrio furnissii. The recombinant enzyme catalysed the reversible phosphorolysis of (GlcNAc)2 (chitobiose) to form 2-acetamide-2-deoxy-alpha-D-glucose 1-phosphate [GlcNAc-1-P] and GlcNAc, but showed...

Journal: :The Biochemical journal 2001
A S Opat F Houghton P A Gleeson

The steady-state localization of medial-Golgi enzymes is likely to involve retrograde transport pathways; however, the trafficking of these resident enzymes through the Golgi stack is unclear. To investigate if the medial-Golgi enzyme beta-1,2-N-acetylglucosaminyltransferase I (GlcNAc-TI) is transported to the late Golgi, a modified GlcNAc-TI bearing an N-glycan site on the C-terminus was const...

Journal: :Journal of the American Chemical Society 2008
Peter M Clark Jessica F Dweck Daniel E Mason Courtenay R Hart Suzanne B Buck Eric C Peters Brian J Agnew Linda C Hsieh-Wilson

We report an advanced chemoenzymatic strategy for the direct fluorescence detection, proteomic analysis, and cellular imaging of O-GlcNAc-modified proteins. O-GlcNAc residues are selectively labeled with fluorescent or biotin tags using an engineered galactosyltransferase enzyme and [3 + 2] azide-alkyne cycloaddition chemistry. We demonstrate that this approach can be used for direct in-gel det...

Journal: :Glycobiology 2016
Amélie Saumonneau Elise Champion Pauline Peltier-Pain Dora Molnar-Gabor Johann Hendrickx Vinh Tran Markus Hederos Gyula Dekany Charles Tellier

Human milk oligosaccharides (HMOs) are recognized as benefiting breast-fed infants in multiple ways. As a result, there is growing interest in the synthesis of HMOs mimicking their natural diversity. Most HMOs are fucosylated oligosaccharides. α-l-Fucosidases catalyze the hydrolysis of α-l-fucose from the non-reducing end of a glucan. They fall into the glycoside hydrolase GH29 and GH95 familie...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2012
Seok-Ho Yu Michael Boyce Amberlyn M Wands Michelle R Bond Carolyn R Bertozzi Jennifer J Kohler

O-linked β-N-acetylglucosamine (O-GlcNAc) is a reversible posttranslational modification found on hundreds of nuclear and cytoplasmic proteins in higher eukaryotes. Despite its ubiquity and essentiality in mammals, functional roles for the O-GlcNAc modification remain poorly defined. Here we develop a combined genetic and chemical approach that enables introduction of the diazirine photocrossli...

Journal: :American journal of physiology. Heart and circulatory physiology 2009
Gladys A Ngoh Tariq Hamid Sumanth D Prabhu Steven P Jones

We previously demonstrated that the O-linked beta-N-acetylglucosamine (O-GlcNAc) posttranslational modification confers cardioprotection at least partially through mitochondrial-dependent mechanisms, but it remained unclear if O-GlcNAc signaling interfered with other mechanisms of cell death. Because ischemia/hypoxia causes endoplasmic reticulum (ER) stress, we ascertained whether O-GlcNAc sign...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2002
Keith Vosseller Lance Wells M Daniel Lane Gerald W Hart

Increased flux of glucose through the hexosamine biosynthetic pathway (HSP) is believed to mediate hyperglycemia-induced insulin resistance in diabetes. The end product of the HSP, UDP beta-N-acetylglucosamine (GlcNAc), is a donor sugar nucleotide for complex glycosylation in the secretory pathway and for O-linked GlcNAc (O-GlcNAc) addition to nucleocytoplasmic proteins. Cycling of the O-GlcNAc...

2012
Luis Izquierdo Angela Mehlert Michael AJ Ferguson

We recently presented a model for site-specific protein N-glycosylation in Trypanosoma brucei whereby the TbSTT3A oligosaccharyltransferase (OST) first selectively transfers biantennary Man(5)GlcNAc(2) from the lipid-linked oligosaccharide (LLO) donor Man(5)GlcNAc(2)-PP-Dol to N-glycosylation sequons in acidic to neutral peptide sequences and TbSTT3B selectively transfers triantennary Man(9)Glc...

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