B4GAT1 is the priming enzyme for the LARGE-dependent functional glycosylation of α-dystroglycan
about
The secretory pathway kinasesThe Structure of the T190M Mutant of Murine α-Dystroglycan at High Resolution: Insight into the Molecular Basis of a Primary DystroglycanopathyThe Muscular Dystrophy Gene TMEM5 Encodes a Ribitol β1,4-Xylosyltransferase Required for the Functional Glycosylation of Dystroglycan.The functional O-mannose glycan on α-dystroglycan contains a phospho-ribitol primed for matriglycan additionSecretome analysis identifies novel signal Peptide peptidase-like 3 (Sppl3) substrates and reveals a role of Sppl3 in multiple Golgi glycosylation pathways.Neurons and glia modify receptor protein-tyrosine phosphatase ζ (RPTPζ)/phosphacan with cell-specific O-mannosyl glycans in the developing brain.Ectopic clustering of Cajal-Retzius and subplate cells is an initial pathological feature in Pomgnt2-knockout mice, a model of dystroglycanopathy.Milder forms of muscular dystrophy associated with POMGNT2 mutations.ISPD produces CDP-ribitol used by FKTN and FKRP to transfer ribitol phosphate onto α-dystroglycan.Four-week rapamycin treatment improves muscular dystrophy in a fukutin-deficient mouse model of dystroglycanopathyLARGE2-dependent glycosylation confers laminin-binding ability on proteoglycans.Clear differences in cerebrospinal fluid proteome between women with chronic widespread pain and healthy women - a multivariate explorative cross-sectional study.Matriglycan: a novel polysaccharide that links dystroglycan to the basement membrane.What Have We Learned from Glycosyltransferase Knockouts in Mice?Recent advancements in understanding mammalian O-mannosylation.Differentiation-related glycan epitopes identify discrete domains of the muscle glycocalyx.The evolution of the dystroglycan complex, a major mediator of muscle integrity.3D structural analysis of protein O-mannosyl kinase, POMK, a causative gene product of dystroglycanopathy.Protein O-Linked Mannose β-1,4-N-Acetylglucosaminyl-transferase 2 (POMGNT2) Is a Gatekeeper Enzyme for Functional Glycosylation of α-Dystroglycan.Muscular Dystrophy with Ribitol-Phosphate Deficiency: A Novel Post-Translational Mechanism in Dystroglycanopathy.Expression system for structural and functional studies of human glycosylation enzymes.Rapid screening of sugar-nucleotide donor specificities of putative glycosyltransferases.Overexpression of Mutant FKRP Restores Functional Glycosylation and Improves Dystrophic Phenotype in FKRP Mutant Mice.
P2860
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P2860
B4GAT1 is the priming enzyme for the LARGE-dependent functional glycosylation of α-dystroglycan
description
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2014年の論文
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name
B4GAT1 is the priming enzyme f ...... lycosylation of α-dystroglycan
@ast
B4GAT1 is the priming enzyme f ...... lycosylation of α-dystroglycan
@en
B4GAT1 is the priming enzyme f ...... lycosylation of α-dystroglycan
@en-gb
B4GAT1 is the priming enzyme f ...... lycosylation of α-dystroglycan
@nl
type
label
B4GAT1 is the priming enzyme f ...... lycosylation of α-dystroglycan
@ast
B4GAT1 is the priming enzyme f ...... lycosylation of α-dystroglycan
@en
B4GAT1 is the priming enzyme f ...... lycosylation of α-dystroglycan
@en-gb
B4GAT1 is the priming enzyme f ...... lycosylation of α-dystroglycan
@nl
prefLabel
B4GAT1 is the priming enzyme f ...... lycosylation of α-dystroglycan
@ast
B4GAT1 is the priming enzyme f ...... lycosylation of α-dystroglycan
@en
B4GAT1 is the priming enzyme f ...... lycosylation of α-dystroglycan
@en-gb
B4GAT1 is the priming enzyme f ...... lycosylation of α-dystroglycan
@nl
P2093
P2860
P921
P3181
P356
P1433
P1476
B4GAT1 is the priming enzyme f ...... lycosylation of α-dystroglycan
@en
P2093
Annapoorani Ramiah
David H Live
Jeremy L Praissman
Kelley W Moremen
Lance Wells
Zoeisha S Chinoy
P2860
P3181
P356
10.7554/ELIFE.03943
P407
P577
2014-01-01T00:00:00Z