- ALG1
Asparagine-linked glycosylation 1 homolog (S. cerevisiae, beta-1,4-mannosyltransferase), also known as ALG1, is a human
gene .cite web | title = Entrez Gene: ALG1 asparagine-linked glycosylation 1 homolog (S. cerevisiae, beta-1,4-mannosyltransferase)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=56052| accessdate = ]PBB_Summary
section_title =
summary_text = The biosynthesis of lipid-linked oligosaccharides is highly conserved among eukaryotes and is catalyzed by 14 glycosyltransferases in an ordered stepwise manner. Mannosyltransferase I (MT I) catalyzes the first mannosylation step in this process. [supplied by OMIM] cite web | title = Entrez Gene: ALG1 asparagine-linked glycosylation 1 homolog (S. cerevisiae, beta-1,4-mannosyltransferase)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=56052| accessdate = ]References
Further reading
PBB_Further_reading
citations =
*cite journal | author=Otsuki T, Ota T, Nishikawa T, "et al." |title=Signal sequence and keyword trap in silico for selection of full-length human cDNAs encoding secretion or membrane proteins from oligo-capped cDNA libraries. |journal=DNA Res. |volume=12 |issue= 2 |pages= 117-26 |year= 2007 |pmid= 16303743 |doi= 10.1093/dnares/12.2.117
*cite journal | author=Gerhard DS, Wagner L, Feingold EA, "et al." |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121-7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504
*cite journal | author=Kranz C, Denecke J, Lehle L, "et al." |title=Congenital disorder of glycosylation type Ik (CDG-Ik): a defect of mannosyltransferase I. |journal=Am. J. Hum. Genet. |volume=74 |issue= 3 |pages= 545-51 |year= 2004 |pmid= 14973782 |doi= 10.1086/382493
*cite journal | author=Schwarz M, Thiel C, Lübbehusen J, "et al." |title=Deficiency of GDP-Man:GlcNAc2-PP-dolichol mannosyltransferase causes congenital disorder of glycosylation type Ik. |journal=Am. J. Hum. Genet. |volume=74 |issue= 3 |pages= 472-81 |year= 2004 |pmid= 14973778 |doi= 10.1086/382492
*cite journal | author=Grubenmann CE, Frank CG, Hülsmeier AJ, "et al." |title=Deficiency of the first mannosylation step in the N-glycosylation pathway causes congenital disorder of glycosylation type Ik. |journal=Hum. Mol. Genet. |volume=13 |issue= 5 |pages= 535-42 |year= 2004 |pmid= 14709599 |doi= 10.1093/hmg/ddh050
*cite journal | author=Clark HF, Gurney AL, Abaya E, "et al." |title=The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment. |journal=Genome Res. |volume=13 |issue= 10 |pages= 2265-70 |year= 2003 |pmid= 12975309 |doi= 10.1101/gr.1293003
*cite journal | author=Strausberg RL, Feingold EA, Grouse LH, "et al." |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899-903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899
*cite journal | author=Takahashi T, Honda R, Nishikawa Y |title=Cloning of the human cDNA which can complement the defect of the yeast mannosyltransferase I-deficient mutant alg 1. |journal=Glycobiology |volume=10 |issue= 3 |pages= 321-7 |year= 2000 |pmid= 10704531 |doi=PBB_Controls
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