Difference between revisions of "YDL189W"
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{|{{Prettytable}} align = 'right' width = '200px' | {|{{Prettytable}} align = 'right' width = '200px' | ||
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− | |valign="top" nowrap bgcolor="{{SGDblue}}"| '''Systematic name''' || [http://db.yeastgenome.org/cgi-bin/locus.pl? | + | |valign="top" nowrap bgcolor="{{SGDblue}}"| '''Systematic name''' || [http://db.yeastgenome.org/cgi-bin/locus.pl?dbid=S000002348 YDL189W] |
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|valign="top" nowrap bgcolor="{{SGDblue}}"| '''Gene name''' ||''RBS1 '' | |valign="top" nowrap bgcolor="{{SGDblue}}"| '''Gene name''' ||''RBS1 '' | ||
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|valign="top" nowrap bgcolor="{{SGDblue}}"| '''Coordinates''' | |valign="top" nowrap bgcolor="{{SGDblue}}"| '''Coordinates''' | ||
|nowrap| Chr IV:122217..123590 | |nowrap| Chr IV:122217..123590 | ||
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+ | |valign="top" nowrap bgcolor="{{SGDblue}}"| '''Primary SGDID''' || S000002348 | ||
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<br> | <br> | ||
− | '''Description of | + | '''Description of YDL189W:''' Protein of unknown function, identified as a high copy suppressor of psk1 psk2 mutations that confer temperature-sensitivity for galactose utilization; proposed to bind single-stranded nucleic acids via its R3H domain<ref name='S000072754'>Rutter J, et al. (2002) Coordinate regulation of sugar flux and translation by PAS kinase. Cell 111(1):17-28 |
{{SGDpaper|S000072754}} PMID 12372297</ref> | {{SGDpaper|S000072754}} PMID 12372297</ref> | ||
<br> | <br> | ||
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J Biol Chem 278(5):3265-74</ref> | J Biol Chem 278(5):3265-74</ref> | ||
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<protect> | <protect> |
Revision as of 07:46, 27 February 2007
Share your knowledge...Edit this entry! <protect>
Systematic name | YDL189W |
Gene name | RBS1 |
Aliases | |
Feature type | ORF, Verified |
Coordinates | Chr IV:122217..123590 |
Primary SGDID | S000002348 |
Description of YDL189W: Protein of unknown function, identified as a high copy suppressor of psk1 psk2 mutations that confer temperature-sensitivity for galactose utilization; proposed to bind single-stranded nucleic acids via its R3H domain[1]
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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. [2] [3]
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References
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