Difference between revisions of "YKL134C"
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− | '''Description of YKL134C:''' Mitochondrial intermediate peptidase, cleaves N-terminal residues of a subset of proteins upon import, after their cleavage by mitochondrial processing peptidase (Mas1p-Mas2p); may contribute to mitochondrial iron homeostasis<ref name=' | + | '''Description of YKL134C:''' Mitochondrial intermediate peptidase, cleaves N-terminal residues of a subset of proteins upon import, after their cleavage by mitochondrial processing peptidase (Mas1p-Mas2p); may contribute to mitochondrial iron homeostasis<ref name='S000051417'>Branda SS, et al. (1999) Mitochondrial intermediate peptidase and the yeast frataxin homolog together maintain mitochondrial iron homeostasis in Saccharomyces cerevisiae. Hum Mol Genet 8(6):1099-110 {{SGDpaper|S000051417}} PMID 10332043</ref><ref name='S000057577'>Isaya G, et al. (1994) MIP1, a new yeast gene homologous to the rat mitochondrial intermediate peptidase gene, is required for oxidative metabolism in Saccharomyces cerevisiae. Mol Cell Biol 14(8):5603-16 |
− | {{SGDpaper| | + | {{SGDpaper|S000057577}} PMID 8035833</ref> |
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Revision as of 03:40, 18 December 2008
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Systematic name | YKL134C |
Gene name | OCT1 |
Aliases | |
Feature type | ORF, Verified |
Coordinates | Chr XI:191441..189129 |
Primary SGDID | S000001617 |
Description of YKL134C: Mitochondrial intermediate peptidase, cleaves N-terminal residues of a subset of proteins upon import, after their cleavage by mitochondrial processing peptidase (Mas1p-Mas2p); may contribute to mitochondrial iron homeostasis[1][2]
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References
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- ↑ Branda SS, et al. (1999) Mitochondrial intermediate peptidase and the yeast frataxin homolog together maintain mitochondrial iron homeostasis in Saccharomyces cerevisiae. Hum Mol Genet 8(6):1099-110 SGD PMID 10332043
- ↑ Isaya G, et al. (1994) MIP1, a new yeast gene homologous to the rat mitochondrial intermediate peptidase gene, is required for oxidative metabolism in Saccharomyces cerevisiae. Mol Cell Biol 14(8):5603-16 SGD PMID 8035833
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