The metabolic origins of mannose in glycoproteins

scientific article published on 09 January 2014

The metabolic origins of mannose in glycoproteins is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1074/JBC.M113.544064
P932PMC publication ID3945336
P698PubMed publication ID24407290

P50authorHudson H. FreezeQ38320794
P2093author name stringDavid A Scott
Marie-Estelle Losfeld
Mie Ichikawa
P2860cites workCarbohydrate-deficient glycoprotein syndrome type Ib. Phosphomannose isomerase deficiency and mannose therapyQ24564669
Derivatization in Mass Spectrometry—1. SilylationQ30930859
Determination of metabolic flux ratios from 13C-experiments and gas chromatography-mass spectrometry data: protocol and principlesQ31065954
Deletion of genes encoding cytochrome oxidases and quinol monooxygenase blocks the aerobic-anaerobic shift in Escherichia coli K-12 MG1655.Q34177720
Mannose efflux from the cells: a potential source of mannose in bloodQ34695595
Phosphomannose isomerase inhibitors improve N-glycosylation in selected phosphomannomutase-deficient fibroblastsQ35604388
Comparative metabolic flux profiling of melanoma cell lines: beyond the Warburg effectQ35605096
Enzyme-to-enzyme channeling in the early steps of glycolysis in rat pancreatic isletsQ35878499
Stimulation of N-linked glycosylation and lipid-linked oligosaccharide synthesis by stress responses in metazoan cellsQ36440729
Mass isotopomer analysis of metabolically labeled nucleotide sugars and N- and O-glycans for tracing nucleotide sugar metabolismsQ37160924
Mannose corrects altered N-glycosylation in carbohydrate-deficient glycoprotein syndrome fibroblastsQ37353246
Endoplasmic reticulum-to-cytosol transport of free polymannose oligosaccharides in permeabilized HepG2 cells.Q37626046
Failure of short-term mannose therapy of patients with carbohydrate-deficient glycoprotein syndrome type 1A.Q38333419
Activation of glycogen phosphorylase with 5-aminoimidazole-4-carboxamide riboside (AICAR). Assessment of glycogen as a precursor of mannosyl residues in glycoconjugatesQ38345859
Human fibroblasts prefer mannose over glucose as a source of mannose for N-glycosylation. Evidence for the functional importance of transported mannoseQ41091656
Glycogen: a carbohydrate source for GLUT-1 glycosylation during glucose deprivation of 3T3-L1 adipocytesQ42814443
Rapid activation of glycogen phosphorylase by the endoplasmic reticulum unfolded protein responseQ44132514
Correcting mass isotopomer distributions for naturally occurring isotopesQ44153792
Oral mannose therapy persistently corrects the severe clinical symptoms and biochemical abnormalities of phosphomannose isomerase deficiencyQ44218677
Acylic sugar derivatives for GC/MS analysis of 13C-enrichment during carbohydrate metabolismQ45147529
Compartmentation of lactate originating from glycogen and glucose in cultured astrocytesQ46845563
A comparison of three methods of glycogen measurement in tissuesQ48532632
Functional characterisation of human SGLT-5 as a novel kidney-specific sodium-dependent sugar transporterQ50337162
Successful prenatal mannose treatment for congenital disorder of glycosylation-Ia in mice.Q50776761
Mannose 6-Phosphate: Anomeric Form Used by Phosphomannose Isomerase and Its l-Epimerization by Phosphoglucose IsomeraseQ55061500
Mannose supplementation in carbohydrate-deficient glycoprotein syndrome type I and phosphomannomutase deficiencyQ74827807
P433issue10
P407language of work or nameEnglishQ1860
P921main subjectmannoseQ10809118
P304page(s)6751-6761
P577publication date2014-01-09
P1433published inJournal of Biological ChemistryQ867727
P1476titleThe metabolic origins of mannose in glycoproteins
P478volume289

Reverse relations

cites work (P2860)
Q38290461A mouse model of a human congenital disorder of glycosylation caused by loss of PMM2.
Q34462529Biallelic mutations in CAD, impair de novo pyrimidine biosynthesis and decrease glycosylation precursors
Q92619790Characterization of Cell Glycocalyx with Mass Spectrometry Methods
Q93271890D-mannose attenuates bone loss in mice via Treg cell proliferation and gut microbiota-dependent anti-inflammatory effects
Q38795724Enterocyte glycosylation is responsive to changes in extracellular conditions: implications for membrane functions
Q27311626Glycomic Characterization of Induced Pluripotent Stem Cells Derived from a Patient Suffering from Phosphomannomutase 2 Congenital Disorder of Glycosylation (PMM2-CDG)
Q58721374Mannose Alters Gut Microbiome, Prevents Diet-Induced Obesity, and Improves Host Metabolism
Q46217441Mannose and fructose metabolism in red blood cells during cold storage in SAGM.
Q34615237Mannose metabolism: more than meets the eye.
Q64250347Metabolic Reprogramming of the Host Cell by Human Adenovirus Infection
Q47106452Oral D-galactose supplementation in PGM1-CDG.
Q42272453Perhaps a wee bit of sugar would help
Q92007890SLC35A2-CDG: Functional characterization, expanded molecular, clinical, and biochemical phenotypes of 30 unreported Individuals
Q90533932Unveiling the metabolic fate of monosaccharides in cell membranes with glycomic and glycoproteomic analyses

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