ALG1
From Wikipedia, the free encyclopedia
| ALG1, chitobiosyldiphosphodolichol beta-mannosyltransferase | |||
|---|---|---|---|
| Identifiers | |||
| Symbols | ALG1; CDG1K; HMAT1; HMT-1; HMT1; MT-1; Mat-1; hMat-1 | ||
| External IDs | OMIM: 605907 MGI: 2384774 HomoloGene: 5387 GeneCards: ALG1 Gene | ||
| EC number | 2.4.1.142 | ||
| Orthologs | |||
| Species | Human | Mouse | |
| Entrez | 56052 | 208211 | |
| Ensembl | ENSG00000033011 | ENSMUSG00000039427 | |
| UniProt | Q9BT22 | Q921Q3 | |
| RefSeq (mRNA) | NM_019109 | NM_145362 | |
| RefSeq (protein) | NP_061982 | NP_663337 | |
| Location (UCSC) | Chr 16: 5.08 – 5.14 Mb | Chr 16: 5.23 – 5.24 Mb | |
| PubMed search | |||
Chitobiosyldiphosphodolichol beta-mannosyltransferase is an enzyme that is encoded by the ALG1 gene [1] whose structure and function has been conserved from yeast to man.[2][3]
Function
The biosynthesis of lipid-linked oligosaccharides is highly conserved among eukaryotes and is catalyzed by 14 glycosyltransferases in an ordered stepwise manner. The Alg1 mannosyltransferase I (MT I) catalyzes the first mannosylation step in this process.[2]
References
- ↑ Couto JR, Huffaker TC, Robbins PW title = Cloning and expression in Escherichia coli of a yeast mannosyltransferase from the asparagine-linked glycosylation pathway (1984). J.Biol. Chem 259 (1): 378–82. PMID 21915450.
- ↑ 2.0 2.1 "Entrez Gene: ALG1 asparagine-linked glycosylation 1 homolog (S. cerevisiae, beta-1,4-mannosyltransferase)".
- ↑ Takahashi T, Honda R, Nishikawa Y (Mar 2000). "Cloning of the human cDNA which can complement the defect of the yeast mannosyltransferase I-deficient mutant alg 1". Glycobiology 10 (3): 321–7. doi:10.1093/glycob/10.3.321. PMID 10704531.
Further reading
- Couto JR, Huffaker TC, Robbins PW (January 1984). "Cloning and expression in Escherichia coli of a yeast mannosyltransferase from the asparagine-linked glycosylation pathway". J. Biol. Chem. 259 (1): 378–82. PMID 6368538.
- Gao XD, Nishikawa A, Dean N (June 2004). "Physical interactions between the Alg1, Alg2, and Alg11 mannosyltransferases of the endoplasmic reticulum". Glycobiology 14 (6): 559–70. doi:10.1093/glycob/cwh072. PMID 15044395.
- Otsuki T, Ota T, Nishikawa T, et al. (2007). "Signal sequence and keyword trap in silico for selection of full-length human cDNAs encoding secretion or membrane proteins from oligo-capped cDNA libraries.". issue= 2: 117–26. doi:10.1093/dnares/12.2.117. PMID 16303743.
- Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
- Kranz C, Denecke J, Lehle L, et al. (2004). "Congenital Disorder of Glycosylation Type Ik (CDG-Ik): A Defect of Mannosyltransferase I". Am. J. Hum. Genet. 74 (3): 545–51. doi:10.1086/382493. PMC 1182267. PMID 14973782.
- Schwarz M, Thiel C, Lübbehusen J, et al. (2004). "Deficiency of GDP-Man:GlcNAc2-PP-Dolichol Mannosyltransferase Causes Congenital Disorder of Glycosylation Type Ik". Am. J. Hum. Genet. 74 (3): 472–81. doi:10.1086/382492. PMC 1182261. PMID 14973778.
- Grubenmann CE, Frank CG, Hülsmeier AJ, et al. (2004). "Deficiency of the first mannosylation step in the N-glycosylation pathway causes congenital disorder of glycosylation type Ik". Hum. Mol. Genet. 13 (5): 535–42. doi:10.1093/hmg/ddh050. PMID 14709599.
- Clark HF, Gurney AL, Abaya E, et al. (2003). "The Secreted Protein Discovery Initiative (SPDI), a Large-Scale Effort to Identify Novel Human Secreted and Transmembrane Proteins: A Bioinformatics Assessment". Genome Res. 13 (10): 2265–70. doi:10.1101/gr.1293003. PMC 403697. PMID 12975309.
- Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
External links
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