Difference between revisions of "YGL027C"
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| + | Specifically higher expression in carbon limited chemostat cultures versus carbon excess. | ||
| + | <ref>Boer VM, et al. (2003) The genome-wide transcriptional responses of Saccharomyces cerevisiae grown on glucose in aerobic chemostat cultures limited for carbon, nitrogen, phosphorus, or sulfur. | ||
| + | J Biol Chem 278(5):3265-74</ref> | ||
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Revision as of 13:02, 21 February 2007
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| Systematic name | YGL027C |
| Gene name | CWH41 |
| Aliases | DER7, GLS1 |
| Feature type | ORF, Verified |
| Coordinates | Chr VII:446148..443647 |
Description of YGL027C: Processing alpha glucosidase I, ER type II integral membrane N-glycoprotein involved in assembly of cell wall beta 1,6 glucan and asparagine-linked protein glycosylation; also involved in ER protein quality control and sensing of ER stress[1][2][3][4]
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References
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- ↑ Hitt R and Wolf DH (2004) DER7, encoding alpha-glucosidase I is essential for degradation of malfolded glycoproteins of the endoplasmic reticulum. FEMS Yeast Res 4(8):815-20 SGD PMID 15450188
- ↑ Ram AF, et al. (1994) A new approach for isolating cell wall mutants in Saccharomyces cerevisiae by screening for hypersensitivity to calcofluor white. Yeast 10(8):1019-30 SGD PMID 7992502
- ↑ Jiang B, et al. (1996) CWH41 encodes a novel endoplasmic reticulum membrane N-glycoprotein involved in beta 1,6-glucan assembly. J Bacteriol 178(4):1162-71 SGD PMID 8576053
- ↑ Romero PA, et al. (1997) The yeast CWH41 gene encodes glucosidase I. Glycobiology 7(7):997-1004 SGD PMID 9363442
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