Difference between revisions of "YER008C"
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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. | ||
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Revision as of 13:02, 21 February 2007
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Systematic name | YER008C |
Gene name | SEC3 |
Aliases | PSL1 |
Feature type | ORF, Verified |
Coordinates | Chr V:171817..167807 |
Description of YER008C: Non-essential subunit of the exocyst complex (Sec3p, Sec5p, Sec6p, Sec8p, Sec10p, Sec15p, Exo70p, Exo84p) which mediates targeting of post-Golgi vesicles to sites of active exocytosis; Sec3p specifically is a spatial landmark for secretion[1][2][3]
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Protein Details
Protein Modification
Modification(s): Phosphorylation
Identified as an efficient substrate of Clb2-Cdk1-as1 in a screen of a proteomic GST-fusion library. [4] [5]
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References
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- ↑ TerBush DR, et al. (1996) The Exocyst is a multiprotein complex required for exocytosis in Saccharomyces cerevisiae. EMBO J 15(23):6483-94 SGD PMID 8978675
- ↑ Finger FP, et al. (1998) Sec3p is a spatial landmark for polarized secretion in budding yeast. Cell 92(4):559-71 SGD PMID 9491896
- ↑ Finger FP and Novick P (1998) Spatial regulation of exocytosis: lessons from yeast. J Cell Biol 142(3):609-12 SGD PMID 9700152
- ↑ Ubersax JA, et al. (2003) Targets of the cyclin-dependent kinase Cdk1. Nature 425(6960):859-64 SGD PMID 14574415
- ↑ submitted by Jeff Ubersax on 2004-01-27
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