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References from Nucleotide Sugar Transporter SLC35 Family Structure and Function. Local targets link to admitted publications; unresolved targets remain external evidence.
Nucleotide sugar transporters of the Golgi apparatus: from basic science to diseases
10.1021/ar0400239 · 2006 · External reference
10.1016/j.febslet.2008.10.016
10.1016/j.febslet.2008.10.016 · External reference
Transporters of nucleotide sugars, nucleotide sulfate and ATP in the Golgi apparatus
10.1016/s0968-0004(97)01053-0 · 1997 · External reference
Mechanisms of glycosylation and sulfation in the Golgi apparatus: evidence for nucleotide sugar/nucleoside monophosphate and nucleotide sulfate/nucleoside monophosphate antiports in the Golgi apparatus membrane
10.1073/pnas.81.22.7051 · 1984 · External reference
Reconstitution into proteoliposomes and partial purification of the Golgi apparatus membrane UDP-galactose, UDP-xylose, and UDP-glucuronic acid transport activities
10.1016/s0021-9258(18)48465-7 · 1992 · External reference
Functional expression of the CMP-sialic acid transporter in Escherichia coli and its identification as a simple mobile carrier
10.1093/glycob/cwj029 · 2006 · External reference
An insight into the orphan nucleotide sugar transporter SLC35A4
10.1016/j.bbamcr.2017.02.002 · 2017 · External reference
SLC35A5 Protein-A Golgi complex member with putative nucleotide sugar transport activity
10.3390/ijms20020276 · 2019 · External reference
Solute carrier family 35 member F2 is indispensable for papillary thyroid carcinoma progression through activation of transforming growth factor-β type I receptor/apoptosis signal-regulating kinase 1/mitogen-activated protein kinase signaling axis
10.1111/cas.13478 · 2017 · External reference
Short N-terminal region of UDP-galactose transporter (SLC35A2) is crucial for galactosylation of N-glycans
10.1016/j.bbrc.2014.10.098 · 2014 · External reference
UDP-galactose (SLC35A2) and UDP-N-acetylglucosamine (SLC35A3) transporters form glycosylation-related complexes with Mannoside Acetylglucosaminyltransferases (Mgats)
10.1074/jbc.m115.636670 · 2015 · External reference
10.1146/annurev.bioeng.8.061505.095745
10.1146/annurev.bioeng.8.061505.095745 · External reference
Lysine at position 329 within a C-terminal dilysine motif is crucial for the ER localization of human SLC35B4
10.1371/journal.pone.0207521 · 2018 · External reference
10.1038/nature24464
10.1038/nature24464 · External reference
Mosaicism of the UDP-galactose transporter SLC35A2 causes a congenital disorder of glycosylation
10.1016/j.ajhg.2013.03.012 · 2013 · External reference
SLC35A2-related congenital disorder of glycosylation: defining the phenotype
10.1016/j.ejpn.2018.08.002 · 2018 · External reference
A new case of UDP-galactose transporter deficiency (SLC35A2-CDG): molecular basis, clinical phenotype, and therapeutic approach
10.1007/s10545-015-9828-6 · 2015 · External reference
10.1002/ana.25243
10.1002/ana.25243 · External reference
Brain somatic mutations in <em>SLC35A2</em> cause intractable epilepsy with aberrant N-glycosylation
10.1212/nxg.0000000000000294 · 2018 · External reference
Clinical, neuroradiological and biochemical features of SLC35A2-CDG patients
10.1002/jimd.12055 · 2019 · External reference
SLC35A2-CDG: Functional characterization, expanded molecular, clinical, and biochemical phenotypes of 30 unreported individuals
2019 · External reference
10.1016/s0021-9258(18)37590-2
10.1016/s0021-9258(18)37590-2 · External reference
Indispensability of transmembrane domains of Golgi UDP-galactose transporter as revealed by analysis of genetic defects in UDP-galactose transporter-deficient murine had-1 mutant cell lines and construction of deletion mutants
10.1093/oxfordjournals.jbchem.a022556 · 1999 · External reference
Point mutations identified in Lec8 Chinese hamster ovary glycosylation mutants that inactivate both the UDP-galactose and CMP-sialic acid transporters
10.1074/jbc.m011124200 · 2001 · External reference
Recessive mutations in SLC35A3 cause early onset epileptic encephalopathy with skeletal defects
10.1002/ajmg.a.38112 · 2017 · External reference
A case of early onset epileptic encephalopathy with de novo mutation in SLC35A2: clinical features and treatment for epilepsy
10.1016/j.braindev.2016.09.009 · 2017 · External reference
10.1136/jmedgenet-2013-101753
10.1136/jmedgenet-2013-101753 · External reference
10.1101/gr.3690506
10.1101/gr.3690506 · External reference
UDP-N-acetylglucosamine transporter and UDP-galactose transporter form heterologous complexes in the Golgi membrane
10.1016/j.febslet.2012.10.016 · 2012 · External reference
N-acetylglucosaminyltransferases and nucleotide sugar transporters form multi-enzyme-multi-transporter assemblies in golgi membranes in vivo
10.1007/s00018-019-03032-5 · 2019 · External reference
Targeting the expression of functional murine CMP-sialic acid transporter to the E. coli inner membrane
10.1016/j.bbrc.2007.08.070 · 2007 · External reference
10.1007/s10529-016-2233-x
10.1007/s10529-016-2233-x · External reference
A vital sugar code for ricin toxicity
10.1038/cr.2017.116 · 2017 · External reference
Medical aspects of toxin weapons
10.1016/j.tox.2005.06.015 · 2005 · External reference
Molecular cloning, sequence characterization, and tissue expression analysis of three water buffalo (Bubalus bubalis;) genes – ST6GAL1, ST8SIA4, SLC35C1
10.5194/aab-59-363-2016 · 2016 · External reference
10.1096/fj.08-123737
10.1096/fj.08-123737 · External reference
AXER is an ATP/ADP exchanger in the membrane of the endoplasmic reticulum
10.1038/s41467-018-06003-9 · 2018 · External reference
Tissue-specific mRNA expression profiles of human solute carrier 35 transporters
10.2133/dmpk.24.91 · 2009 · External reference
SLC35D3 increases autophagic activity in midbrain dopaminergic neurons by enhancing BECN1-ATG14-PIK3C3 complex formation
10.1080/15548627.2016.1179402 · 2016 · External reference
10.1371/journal.pgen.1004124
10.1371/journal.pgen.1004124 · External reference
The Slc35d3 gene, encoding an orphan nucleotide sugar transporter, regulates platelet-dense granules
10.1182/blood-2006-08-040196 · 2007 · External reference
The platelet release reaction: granules' constituents, secretion and functions
10.1080/09537100120068170 · 2001 · External reference
10.1016/s0049-3848(99)00015-8
10.1016/s0049-3848(99)00015-8 · External reference
A new variant of Hermansky-Pudlak syndrome due to mutations in a gene responsible for vesicle formation
10.1016/s0002-9343(99)00436-2 · 2000 · External reference
The human solute carrier gene SLC35B4 encodes a bifunctional nucleotide sugar transporter with specificity for UDP-xylose and UDP-N-acetylglucosamine
10.1074/jbc.m504783200 · 2005 · External reference
Subcellular localization of UDP-GlcNAc, UDP-Gal and SLC35B4 transporters
10.18388/abp.2011_2255 · 2011 · External reference
Characterization of yeast Yea4p, a uridine diphosphate-N-acetylglucosamine transporter localized in the endoplasmic reticulum and required for chitin synthesis
10.1074/jbc.275.18.13580 · 2000 · External reference
10.1074/jbc.m109.016964
10.1074/jbc.m109.016964 · External reference
A novel endocytosis signal related to the KKXX ER-retrieval signal
10.1002/j.1460-2075.1995.tb07219.x · 1995 · External reference
10.1074/jbc.274.21.15080
10.1074/jbc.274.21.15080 · External reference
The C-terminal dilysine motif confers endoplasmic reticulum localization to type I membrane proteins in plants
10.1105/tpc.12.7.1179 · 2000 · External reference
Golgi self-correction generates bioequivalent glycans to preserve cellular homeostasis
10.7554/elife.14814 · 2016 · External reference
10.1016/j.csbj.2014.05.003 · Admitted local publication
Golgi GDP-mannose uptake requires Leishmania LPG2. A member of a eukaryotic family of putative nucleotide-sugar transporters
10.1074/jbc.272.6.3799 · 1997 · External reference
The VRG4 gene is required for GDP-mannose transport into the lumen of the Golgi in the yeast, Saccharomyces cerevisiae
10.1074/jbc.272.50.31908 · 1997 · External reference
10.1074/jbc.m311353200
10.1074/jbc.m311353200 · External reference
Direct investigation of the Aspergillus GDP-mannose transporter by STD NMR spectroscopy
10.1002/cbic.201100483 · 2011 · External reference
10.1002/cbic.200800526
10.1002/cbic.200800526 · External reference
10.1074/jbc.274.13.8779
10.1074/jbc.274.13.8779 · External reference
10.1093/bioinformatics/btr350
10.1093/bioinformatics/btr350 · External reference
10.1002/cpbi.3
10.1002/cpbi.3 · External reference
10.1074/jbc.273.32.20189
10.1074/jbc.273.32.20189 · External reference
10.1093/glycob/cwn080
10.1093/glycob/cwn080 · External reference
10.1038/s41477-017-0022-8
10.1038/s41477-017-0022-8 · External reference
Improving protein disorder prediction by deep bidirectional long short-term memory recurrent neural networks
2016 · External reference
10.1016/s0006-3495(99)77009-8
10.1016/s0006-3495(99)77009-8 · External reference
10.1074/jbc.271.50.32330
10.1074/jbc.271.50.32330 · External reference
10.1073/pnas.94.25.13442
10.1073/pnas.94.25.13442 · External reference
10.1002/cbic.201300298
10.1002/cbic.201300298 · External reference
Amino acid residues important for CMP-sialic acid recognition by the CMP-sialic acid transporter: analysis of the substrate specificity of UDP-galactose/CMP-sialic acid transporter chimeras
10.1093/glycob/cws116 · 2012 · External reference
10.1074/jbc.m010542200
10.1074/jbc.m010542200 · External reference
Substrate recognition by nucleotide sugar transporters-further characterization of substrate recognition regions by analyses of UDP-galactose/CMP-sialic acid transporter chimeras and biochemical analysis of the substrate specificity of parental and chimeric transporters
2003 · External reference
CDG nomenclature: time for a change!
10.1016/j.bbadis.2009.08.005 · 2009 · External reference
Protein-specific glycoprofiling for patient diagnostics
10.1373/clinchem.2015.248518 · 2016 · External reference
Solving glycosylation disorders: fundamental approaches reveal complicated pathways
10.1016/j.ajhg.2013.10.024 · 2014 · External reference
10.1016/j.tig.2018.03.002
10.1016/j.tig.2018.03.002 · External reference
Genetic complementation reveals a novel human congenital disorder of glycosylation of type II, due to inactivation of the Golgi CMP-sialic acid transporter
10.1182/blood-2004-09-3509 · 2005 · External reference
A functional splice variant of the human Golgi CMP-sialic acid transporter
10.1007/s10719-016-9697-8 · 2016 · External reference
10.1016/0301-4622(88)80011-5
10.1016/0301-4622(88)80011-5 · External reference
Intellectual disability and bleeding diathesis due to deficient CMP—sialic acid transport
10.1212/wnl.0b013e3182a08f53 · 2013 · External reference
10.1002/ajmg.a.38412
10.1002/ajmg.a.38412 · External reference
A mutation in the gene coding for the sialic acid transporter SLC35A1 is required for platelet life span but not proplatelet formation
10.3324/haematol.2018.198028 · 2018 · External reference
Structural basis for the delivery of activated sialic acid into Golgi for sialyation
2019 · External reference
Structural basis for mammalian nucleotide sugar transport
10.7554/elife.45221 · 2019 · External reference
Sialic acid concentrations in plants are in the range of inadvertent contamination
10.1007/s00425-005-0206-8 · 2006 · External reference
10.2174/9781608053865113010004
10.2174/9781608053865113010004 · 2013 · External reference
Structure and function of vertebrate CMP–sialic acid synthetases
10.1093/glycob/cwh113 · 2004 · External reference