2.4.1.265: dolichyl-P-Glc:Glc1Man9GlcNAc2-PP-dolichol alpha-1,3-glucosyltransferase
This is an abbreviated version!
For detailed information about dolichyl-P-Glc:Glc1Man9GlcNAc2-PP-dolichol alpha-1,3-glucosyltransferase, go to the full flat file.
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Synonyms
ALG8, Dol-P-Glc:Glc1-Man9-GlcNAc2-P-P-Dol glucosyltransferase, dolichyl-P-Glc:Glc1 Man9GlcNAc2-PP-dolichyl alpha1,3-glucosyltransferase, dolichyl-P-Glc:Glc1Man9GlcNAc2-PP-dolichyl alpha1,3-glucosyltransferase, dolichyl-P-glucose:Glc1Man9GlcNAc2-PP-dolichyl alpha3-glucosyltransferase, hALG8, hALG8p
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Reference
Reference on EC 2.4.1.265 - dolichyl-P-Glc:Glc1Man9GlcNAc2-PP-dolichol alpha-1,3-glucosyltransferase
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Runge, K.W.
Robbins, P.W.: A new yeast mutation in the glucosylation steps of the asparagine-linked glycosylation pathway. Formation of a novel asparagine-linked oligosaccharide containing two glucose residues
J. Biol. Chem.
261
15582-15590
1986
Saccharomyces cerevisiae (P40351)
Chantret, I.; Dancourt, J.; Dupre, T.; Delenda, C.; Bucher, S.; Vuillaumier-Barrot, S.; Ogier de Baulny, H.; Peletan, C.; Danos, O.; Seta, N.; Durand, G.; Oriol, R.; Codogno, P.; Moore, S.E.
A deficiency in dolichyl-P-glucose:Glc1Man9GlcNAc2-PP-dolichyl alpha3-glucosyltransferase defines a new subtype of congenital disorders of glycosylation
J. Biol. Chem.
278
9962-9971
2003
Homo sapiens (Q9BVK2)
Vesela, K.; Honzik, T.; Hansikova, H.; Haeuptle, M.A.; Semberova, J.; Stranak, Z.; Hennet, T.; Zeman, J.
A new case of ALG8 deficiency (CDG Ih)
J. Inherit. Metab. Dis.
32
259264
2009
Homo sapiens
Schollen, E.; Frank, C.G.; Keldermans, L.; Reyntjens, R.; Grubenmann, C.E.; Clayton, P.T.; Winchester, B.G.; Smeitink, J.; Wevers, R.A.; Aebi, M.; Hennet, T.; Matthijs, G.
Clinical and molecular features of three patients with congenital disorders of glycosylation type Ih (CDG-Ih) (ALG8 deficiency)
J. Med. Genet.
41
550-556
2004
Homo sapiens (Q9BVK2)
St๖lting, T.; Omran, H.; Erlekotte, A.; Denecke, J.; Reunert, J.; Marquardt, T.
Novel ALG8 mutations expand the clinical spectrum of congenital disorder of glycosylation type Ih
Mol. Genet. Metab.
98
305-309
2009
Homo sapiens (Q9BVK2), Homo sapiens
Stagljar, I.; te Heesen, S.; Aebi, M.
New phenotype of mutations deficient in glucosylation of the lipid-linked oligosaccharide: cloning of the ALG8 locus
Proc. Natl. Acad. Sci. USA
91
5977-5981
1994
Saccharomyces cerevisiae (P40351)
Diaz-Barrera, A.; Soto, E.; Altamirano, C.
Alginate production and alg8 gene expression by Azotobacter vinelandii in continuous cultures
J. Ind. Microbiol. Biotechnol.
39
613-621
2012
Azotobacter vinelandii
Rehman, Z.U.; Wang, Y.; Moradali, M.F.; Hay, I.D.; Rehm, B.H.
Insights into the assembly of the alginate biosynthesis machinery in Pseudomonas aeruginosa
Appl. Environ. Microbiol.
79
3264-3272
2013
Pseudomonas aeruginosa
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