Biology:ALG11
From HandWiki
Short description: Protein-coding gene in the species Homo sapiens
 Generic protein structure example |
Asparagine-linked glycosylation protein 11 is an enzyme encoded by the ALG11 gene.[1]
See also
- Congenital disorder of glycosylation
References
- ↑ "Entrez Gene: asparagine-linked glycosylation 11". https://www.ncbi.nlm.nih.gov/gene?Db=gene&Cmd=ShowDetailView&TermToSearch=440138.
- ↑ Cipollo, JF; Trimble, RB; Chi, JH; Yan, Q; Dean, N (2001). "The yeast ALG11 gene specifies addition of the terminal alpha 1,2-Man to the Man5GlcNAc2-PP-dolichol N-glycosylation intermediate formed on the cytosolic side of the endoplasmic reticulum". J. Biol. Chem. 276 (24): 21828–40. doi:10.1074/jbc.m010896200. PMID 11278778.
- ↑ Gao, XD; Nishikawa, A; Dean, N. (Jun 2004). "Physical interactions between the Alg1, Alg2, and Alg11 mannosyltransferases of the endoplasmic reticulum. 2004". Glycobiology 14 (6): 559–70. doi:10.1093/glycob/cwh072. PMID 15044395.
External links
- Human ALG11 genome location and ALG11 gene details page in the UCSC Genome Browser.
Further reading
- "UTP14c is a recently acquired retrogene associated with spermatogenesis and fertility in man.". Biol. Reprod. 74 (4): 644–51. 2006. doi:10.1095/biolreprod.105.046698. PMID 16354793.
- "A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip.". Hum. Mol. Genet. 19 (8): 1413–24. 2010. doi:10.1093/hmg/ddq016. PMID 20080937.
- "Large-scale mapping of human protein-protein interactions by mass spectrometry.". Mol. Syst. Biol. 3 (1): 89. 2007. doi:10.1038/msb4100134. PMID 17353931.
- "The yeast ALG11 gene specifies addition of the terminal alpha 1,2-Man to the Man5GlcNAc2-PP-dolichol N-glycosylation intermediate formed on the cytosolic side of the endoplasmic reticulum". J. Biol. Chem. 276 (24): 21828–40. June 2001. doi:10.1074/jbc.M010896200. PMID 11278778.
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