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Mannosyltransferases

Known as: Mannosyltransferases [Chemical/Ingredient] 
Enzymes that catalyze the transfer of mannose from a nucleoside diphosphate mannose to an acceptor molecule which is frequently another carbohydrate… Expand
National Institutes of Health

Papers overview

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Highly Cited
2013
Highly Cited
2013
Congenital muscular dystrophies with hypoglycosylation of α-dystroglycan (α-DG) are a heterogeneous group of disorders often… Expand
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Highly Cited
2012
Highly Cited
2012
We performed bottom-up engineering of a synthetic pathway in Escherichia coli for the production of eukaryotic trimannosyl… Expand
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2008
2008
Biosynthesis of phosphatidylinositol (PI)-containing lipoarabinomannan (LAM) and lipomannan (LM) of Mycobacterium spp. follows a… Expand
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2006
2006
The biosynthesis of asparagine-linked glycoproteins utilizes a dolichylpyrophosphate-linked glycosyl donor (Dol-PP-GlcNAc(2)Man(9… Expand
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Highly Cited
2005
Highly Cited
2005
Protein O-mannosylation is an essential and evolutionarily conserved post-translational modification among eukaryotes. This form… Expand
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Highly Cited
2004
Highly Cited
2004
Defects in O-mannosylation of alpha-dystroglycan are thought to cause certain types of congenital muscular dystrophies with… Expand
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Highly Cited
2004
Highly Cited
2004
Protein O-mannosyltransferases (Pmt proteins) initiate O-mannosylation of secretory proteins. The PMT gene family of the human… Expand
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Highly Cited
2003
Highly Cited
2003
Protein O-mannosyltransferases (PMTs) initiate the assembly of O-mannosyl glycans, an essential protein modification. Since PMTs… Expand
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Highly Cited
2001
Highly Cited
2001
Attachment of the cationic sugar 4-amino-4-deoxy-l-arabinose (l-Ara4N) to lipid A is required for the maintenance of polymyxin… Expand
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Highly Cited
1997
Highly Cited
1997
S. cerevisiae contains at least six genes (PMT1-6) for dolicholphosphate-D-mannose: protein-O-D-mannosyltransferases. The in vivo… Expand
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