A gene on chromosome 3q27.1 that encodes an enzyme that catalyses the addition of the first dol-P-Man-derived mannose in an alpha 1,3 linkage to Man5GlcNAc2-PP-Dol. Molecular pathologyALG3 is mutated in congenital disorder of glycosylation type Id (CDGId). Segen's Medical Dictionary. ...
(1996) The isolation of a Dol-P-Man synthase from Ustilago maydis that functions in Saccharomyces cerevisiae. Yeast, 12, 765- 771.Zimmermann, J. W., C. A. Specht, B. X. Cazares, and P. W. Robbins. 1996. The isolation of a Dol-P-Man synthase from Ustilago maydis that ...
产品名称ALG12 (Dol-P-Man:Man(7)GlcNAc(2)-PP-Dol alpha-1,6-mannosyltransferase, Asparagine-linked Glycosylation Protein 12 Homolog, Dolichyl-P-Man:Man(7)GlcNAc(2)-PP-dolichyl-alpha-1,6-mannosyltransferase, Man 产品货号MBS6009241 产品价格现货询价,电话:010-67529703 ...
2004. Functional analysis of the ALG3 gene encoding the Dol-P-Man: Man5GlcNAc2-PP-Dol mannosyl- transferase enzyme of P. pastoris. Glycobiology. 14(5):399-407.Davidson RC, Nett JH, Renfer E, Li H, Stadheim TA, Miller BJ, Miele RG, Hamilton SR...
Deficiency of Dol-P-Man synthase subunit DPM3 bridges the congenital disorders of glycosylation with the dystroglycanopathies. Am J Hum Genet 2009;85:76-86.Lefeber DJ, Schonberger J, Morava E, Guillard M, Huyben KM, et al. (2009) Deficiency of Dol-P-Man synthase subunit DPM3 bridges ...
Lehle, 2001 Biosynthesis of lipid- linked oligosaccharides in yeast: the ALG3 gene encodes the Dol-P-Man:Man5GlcNAc2-PP-Dol mannosyltransferase. Biol. Chem. 382: 321-328.Sharma CB , Knauer R , Lehle L . 2001 . Biosynthesis of lipid-linked oligosaccharides in yeast...
Deficiency of Dol-P-Man synthase subunit DPM3 bridges the congenital disorders of glycosylation with the dystroglycanopathies. Am J Hum Genet. 2009; 85 :76–86.Lefeber DJ, Scho¨nberger J, Morava E, Guillard M, Huyben KM, et al. (2009) Deficiency of Dol-P-Man synthase subunit DPM3 ...