Difference between revisions of "YGR101W"
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| − | |valign="top" nowrap bgcolor="{{SGDblue}}"| '''Systematic name''' || [http:// | + | |valign="top" nowrap bgcolor="{{SGDblue}}"| '''Systematic name''' || [http://www.yeastgenome.org/cgi-bin/locus.pl?dbid=S000003333 YGR101W] |
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|valign="top" nowrap bgcolor="{{SGDblue}}"| '''Gene name''' ||''PCP1 '' | |valign="top" nowrap bgcolor="{{SGDblue}}"| '''Gene name''' ||''PCP1 '' | ||
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|valign="top" nowrap bgcolor="{{SGDblue}}"| '''Coordinates''' | |valign="top" nowrap bgcolor="{{SGDblue}}"| '''Coordinates''' | ||
| − | |nowrap| Chr VII: | + | |nowrap| Chr VII:693363..694403 |
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| − | | | + | |valign="top" nowrap bgcolor="{{SGDblue}}"| '''Primary SGDID''' || S000003333 |
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| − | '''Description of | + | '''Description of YGR101W:''' Mitochondrial serine protease required for the processing of various mitochondrial proteins and maintenance of mitochondrial DNA and morphology; belongs to the rhomboid-GlpG superfamily of intramembrane peptidases<ref name='S000071826'>Esser K, et al. (2002) A novel two-step mechanism for removal of a mitochondrial signal sequence involves the mAAA complex and the putative rhomboid protease Pcp1. J Mol Biol 323(5):835-43 {{SGDpaper|S000071826}} PMID 12417197</ref><ref name='S000073854'>Herlan M, et al. (2003) Processing of Mgm1 by the rhomboid-type protease Pcp1 is required for maintenance of mitochondrial morphology and of mitochondrial DNA. J Biol Chem 278(30):27781-8 {{SGDpaper|S000073854}} PMID 12707284</ref><ref name='S000073216'>McQuibban GA, et al. (2003) Mitochondrial membrane remodelling regulated by a conserved rhomboid protease. Nature 423(6939):537-41 {{SGDpaper|S000073216}} PMID 12774122</ref><ref name='S000074000'>Sesaki H, et al. (2003) Cells lacking Pcp1p/Ugo2p, a rhomboid-like protease required for Mgm1p processing, lose mtDNA and mitochondrial structure in a Dnm1p-dependent manner, but remain competent for mitochondrial fusion. Biochem Biophys Res Commun 308(2):276-83 |
| − | {{SGDpaper| | + | {{SGDpaper|S000074000}} PMID 12901865</ref> |
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==Community Commentary== | ==Community Commentary== | ||
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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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==References== | ==References== | ||
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Latest revision as of 06:45, 23 January 2012
Share your knowledge...Edit this entry! <protect>
| Systematic name | YGR101W |
| Gene name | PCP1 |
| Aliases | MDM37, RBD1 |
| Feature type | ORF, Verified |
| Coordinates | Chr VII:693363..694403 |
| Primary SGDID | S000003333 |
Description of YGR101W: Mitochondrial serine protease required for the processing of various mitochondrial proteins and maintenance of mitochondrial DNA and morphology; belongs to the rhomboid-GlpG superfamily of intramembrane peptidases[1][2][3][4]
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Community Commentary
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Protein Details
Protein Function/Process
Limited proteolysis of Mgm1p generating the short isoform of Mgm1p depends on the mitochondrial rhomboid protease Pcp1p. Lack of Pcp1p can partially be complemented by expression of an artificial variant of the short isoform of Mgm1p. [2] [5]
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References
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- ↑ Esser K, et al. (2002) A novel two-step mechanism for removal of a mitochondrial signal sequence involves the mAAA complex and the putative rhomboid protease Pcp1. J Mol Biol 323(5):835-43 SGD PMID 12417197
- ↑ 2.0 2.1 Herlan M, et al. (2003) Processing of Mgm1 by the rhomboid-type protease Pcp1 is required for maintenance of mitochondrial morphology and of mitochondrial DNA. J Biol Chem 278(30):27781-8 SGD PMID 12707284
- ↑ McQuibban GA, et al. (2003) Mitochondrial membrane remodelling regulated by a conserved rhomboid protease. Nature 423(6939):537-41 SGD PMID 12774122
- ↑ Sesaki H, et al. (2003) Cells lacking Pcp1p/Ugo2p, a rhomboid-like protease required for Mgm1p processing, lose mtDNA and mitochondrial structure in a Dnm1p-dependent manner, but remain competent for mitochondrial fusion. Biochem Biophys Res Commun 308(2):276-83 SGD PMID 12901865
- ↑ submitted by Andreas Reichert on 2003-09-25
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