SGK196 is a glycosylation-specific O-mannose kinase required for dystroglycan function

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SGK196 is a glycosylation-specific O-mannose kinase required for dystroglycan function is …
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scholarly articleQ13442814

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P819ADS bibcode2013Sci...341..896Y
P356DOI10.1126/SCIENCE.1239951
P3181OpenCitations bibliographic resource ID1509859
P932PMC publication ID3848040
P698PubMed publication ID23929950
P5875ResearchGate publication ID255716224

P50authorLiping YuQ55189535
Kevin P CampbellQ58144660
Stanley F NelsonQ90679187
Takako Yoshida-MoriguchiQ105623621
P2093author name stringMary E Anderson
Hane Lee
Tobias Willer
Francesco Muntoni
David Venzke
Tamieka Whyte
P2860cites workMissense mutations in β-1,3-N-acetylglucosaminyltransferase 1 (B3GNT1) cause Walker-Warburg syndrome.Q36731388
Deciphering the glycosylome of dystroglycanopathies using haploid screens for lassa virus entryQ37572562
Structures of sialylated O-linked oligosaccharides of bovine peripheral nerve alpha-dystroglycan. The role of a novel O-mannosyl-type oligosaccharide in the binding of alpha-dystroglycan with lamininQ38349218
Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophiesQ42524150
Editing of H2BC NMR spectraQ46687439
LARGE can functionally bypass alpha-dystroglycan glycosylation defects in distinct congenital muscular dystrophies.Q47375901
Presenilin 1 regulates the processing of beta-amyloid precursor protein C-terminal fragments and the generation of amyloid beta-protein in endoplasmic reticulum and GolgiQ48334621
Dystroglycan function requires xylosyl- and glucuronyltransferase activities of LARGEQ24301093
Demonstration of mammalian protein O-mannosyltransferase activity: coexpression of POMT1 and POMT2 required for enzymatic activityQ24303491
ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndromeQ24316024
Mutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of α-dystroglycanQ24321692
The protein kinase complement of the human genomeQ24324497
A novel human beta1,3-N-acetylgalactosaminyltransferase that synthesizes a unique carbohydrate structure, GalNAcbeta1-3GlcNAcQ28511795
Improved spectral resolution in cosy 1H NMR spectra of proteins via double quantum filteringQ29618846
O-mannosyl phosphorylation of alpha-dystroglycan is required for laminin binding.Q34090655
Like-acetylglucosaminyltransferase (LARGE)-dependent modification of dystroglycan at Thr-317/319 is required for laminin binding and arenavirus infection.Q34223029
Glycomic analyses of mouse models of congenital muscular dystrophyQ35065134
Dystroglycan: from biosynthesis to pathogenesis of human disease.Q36367346
Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause of Walker-Warburg syndromeQ36439344
Identification of mutations in TMEM5 and ISPD as a cause of severe cobblestone lissencephalyQ36451494
P433issue6148
P407language of work or nameEnglishQ1860
P921main subjectglycosylationQ898365
carbohydrate phosphorylationQ14863084
Beta-1,3-N-acetylgalactosaminyltransferase 2Q21109542
Protein O-mannose kinaseQ21121418
Protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-)Q21123155
Protein-O-mannose kinaseQ21986759
Protein O-linked mannose beta 1,4-N-acetylglucosaminyltransferase 2Q21990911
P304page(s)896-899
P577publication date2013-08-08
P1433published inScienceQ192864
P1476titleSGK196 is a glycosylation-specific O-mannose kinase required for dystroglycan function
P478volume341

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cites work (P2860)
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