Difference between revisions of "YGL058W"
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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 12:02, 21 February 2007
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| Systematic name | YGL058W |
| Gene name | RAD6 |
| Aliases | UBC2 |
| Feature type | ORF, Verified |
| Coordinates | Chr VII:393992..394510 |
Description of YGL058W: Ubiquitin-conjugating enzyme (E2), involved in postreplication repair (with Rad18p), sporulation, telomere silencing, and ubiquitin-mediated N-end rule protein degradation (with Ubr1p)[1][2][3]
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References
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- ↑ Broomfield S, et al. (2001) DNA postreplication repair and mutagenesis in Saccharomyces cerevisiae. Mutat Res 486(3):167-84 SGD PMID 11459630
- ↑ Bailly V, et al. (1997) Yeast DNA repair proteins Rad6 and Rad18 form a heterodimer that has ubiquitin conjugating, DNA binding, and ATP hydrolytic activities. J Biol Chem 272(37):23360-5 SGD PMID 9287349
- ↑ Jentsch S, et al. (1987) The yeast DNA repair gene RAD6 encodes a ubiquitin-conjugating enzyme. Nature 329(6135):131-4 SGD PMID 3306404
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