The promiscuous binding pocket of SLC35A1 ensures redundant transport of CDP-ribitol to the Golgi
Published 2021 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
The promiscuous binding pocket of SLC35A1 ensures redundant transport of CDP-ribitol to the Golgi
Authors
Keywords
dystroglycan, glycosylation, nucleotide transport, SLC35A1, SLC35A4, sialic acid, ribitol
Journal
JOURNAL OF BIOLOGICAL CHEMISTRY
Volume -, Issue -, Pages 100789
Publisher
Elsevier BV
Online
2021-05-18
DOI
10.1016/j.jbc.2021.100789
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Failure to eliminate a phosphorylated glucose analog leads to neutropenia in patients with G6PT and G6PC3 deficiency
- (2019) Maria Veiga-da-Cunha et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Structural basis for mammalian nucleotide sugar transport
- (2019) Shivani Ahuja et al. eLife
- Structural basis for substrate specificity and regulation of nucleotide sugar transporters in the lipid bilayer
- (2019) Joanne L. Parker et al. Nature Communications
- SWISS-MODEL: homology modelling of protein structures and complexes
- (2018) Andrew Waterhouse et al. NUCLEIC ACIDS RESEARCH
- A mutation in the gene coding for the sialic acid transporter SLC35A1 is required for platelet life span but not proplatelet formation
- (2018) Alexandre Kauskot et al. HAEMATOLOGICA
- Structural basis of nucleotide sugar transport across the Golgi membrane
- (2017) Joanne L. Parker et al. NATURE
- The Muscular Dystrophy GeneTMEM5Encodes a Ribitol β1,4-Xylosyltransferase Required for the Functional Glycosylation of Dystroglycan
- (2016) Hiroshi Manya et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- ISPD produces CDP-ribitol used by FKTN and FKRP to transfer ribitol phosphate onto α-dystroglycan
- (2016) Isabelle Gerin et al. Nature Communications
- Identification of a Post-translational Modification with Ribitol-Phosphate and Its Defect in Muscular Dystrophy
- (2016) Motoi Kanagawa et al. Cell Reports
- The functional O-mannose glycan on α-dystroglycan contains a phospho-ribitol primed for matriglycan addition
- (2016) Jeremy L Praissman et al. eLife
- A Novel Approach to High-Quality Postmortem Tissue Procurement: The GTEx Project
- (2015) Latarsha J. Carithers et al. BIOPRESERVATION AND BIOBANKING
- Matriglycan: a novel polysaccharide that links dystroglycan to the basement membrane
- (2015) T. Yoshida-Moriguchi et al. GLYCOBIOLOGY
- Identification and Characterization of a Golgi-Localized UDP-Xylose Transporter Family from Arabidopsis
- (2015) Berit Ebert et al. PLANT CELL
- Covalent docking using autodock: Two-point attractor and flexible side chain methods
- (2015) Giulia Bianco et al. PROTEIN SCIENCE
- A Novel Approach to High-Quality Postmortem Tissue Procurement: The GTEx Project
- (2015) Latarsha J. Carithers et al. Biopreservation and Biobanking
- Disease mutations in CMP-sialic acid transporter SLC35A1 result in abnormal -dystroglycan O-mannosylation, independent from sialic acid
- (2015) M. Riemersma et al. HUMAN MOLECULAR GENETICS
- Glycobiology of -dystroglycan and muscular dystrophy
- (2014) T. Endo JOURNAL OF BIOCHEMISTRY
- The Golgi localized bifunctional UDP-rhamnose/UDP-galactose transporter family of Arabidopsis
- (2014) C. Rautengarten et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- The glucuronyltransferase B4GAT1 is required for initiation of LARGE-mediated α-dystroglycan functional glycosylation
- (2014) Tobias Willer et al. eLife
- B4GAT1 is the priming enzyme for the LARGE-dependent functional glycosylation of α-dystroglycan
- (2014) Jeremy L Praissman et al. eLife
- Structure and function of nucleotide sugar transporters: Current progress
- (2014) Barbara Hadley et al. Computational and Structural Biotechnology Journal
- Mutations in B3GALNT2 Cause Congenital Muscular Dystrophy and Hypoglycosylation of α-Dystroglycan
- (2013) Elizabeth Stevens et al. AMERICAN JOURNAL OF HUMAN GENETICS
- GTDC2 modifies O-mannosylated α-dystroglycan in the endoplasmic reticulum to generate N-acetyl glucosamine epitopes reactive with CTD110.6 antibody
- (2013) Mitsutaka Ogawa et al. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
- Dissecting the Molecular Basis of the Role of the O-Mannosylation Pathway in Disease: α-Dystroglycan and Forms of Muscular Dystrophy
- (2013) David Live et al. CHEMBIOCHEM
- Genome engineering using the CRISPR-Cas9 system
- (2013) F Ann Ran et al. Nature Protocols
- Intellectual disability and bleeding diathesis due to deficient CMP-sialic acid transport
- (2013) M. Mohamed et al. NEUROLOGY
- SGK196 Is a Glycosylation-Specific O-Mannose Kinase Required for Dystroglycan Function
- (2013) T. Yoshida-Moriguchi et al. SCIENCE
- Deciphering the Glycosylome of Dystroglycanopathies Using Haploid Screens for Lassa Virus Entry
- (2013) L. T. Jae et al. SCIENCE
- An Optimized microRNA Backbone for Effective Single-Copy RNAi
- (2013) Christof Fellmann et al. Cell Reports
- Dystroglycan Function Requires Xylosyl- and Glucuronyltransferase Activities of LARGE
- (2012) K.-i. Inamori et al. SCIENCE
- AutoDock4 and AutoDockTools4: Automated docking with selective receptor flexibility
- (2009) Garrett M. Morris et al. JOURNAL OF COMPUTATIONAL CHEMISTRY
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreCreate your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create Now