Difference between revisions of "YGR181W"
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| − | '''Description of YGR181W:''' Mitochondrial intermembrane space protein, forms a complex with Tim8p that | + | '''Description of YGR181W:''' Mitochondrial intermembrane space protein, forms a complex with Tim8p that delivers a subset of hydrophobic proteins to the TIM22 complex for insertion into the inner membrane<ref name='S000043156'>Koehler CM, et al. (1999) Human deafness dystonia syndrome is a mitochondrial disease. Proc Natl Acad Sci U S A 96(5):2141-6 {{SGDpaper|S000043156}} PMID 10051608</ref><ref name='S000047441'>Leuenberger D, et al. (1999) Different import pathways through the mitochondrial intermembrane space for inner membrane proteins. EMBO J 18(17):4816-22 {{SGDpaper|S000047441}} PMID 10469659</ref><ref name='S000064131'>Kurz M, et al. (1999) Biogenesis of Tim proteins of the mitochondrial carrier import pathway: differential targeting mechanisms and crossing over with the main import pathway. Mol Biol Cell 10(7):2461-74 {{SGDpaper|S000064131}} PMID 10397776</ref><ref name='S000071489'>Curran SP, et al. (2002) The role of the Tim8p-Tim13p complex in a conserved import pathway for mitochondrial polytopic inner membrane proteins. J Cell Biol 158(6):1017-27 {{SGDpaper|S000071489}} PMID 12221072</ref><ref name='S000131707'>Davis AJ, et al. (2007) The Tim9p/10p and Tim8p/13p complexes bind to specific sites on Tim23p during mitochondrial protein import. Mol Biol Cell 18(2):475-86 |
| − | {{SGDpaper| | + | {{SGDpaper|S000131707}} PMID 17122363</ref> |
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Revision as of 14:05, 21 October 2009
Share your knowledge...Edit this entry! <protect>
| Systematic name | YGR181W |
| Gene name | TIM13 |
| Aliases | |
| Feature type | ORF, Verified |
| Coordinates | Chr VII:858292..858609 |
| Primary SGDID | S000003413 |
Description of YGR181W: Mitochondrial intermembrane space protein, forms a complex with Tim8p that delivers a subset of hydrophobic proteins to the TIM22 complex for insertion into the inner membrane[1][2][3][4][5]
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References
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- ↑ Koehler CM, et al. (1999) Human deafness dystonia syndrome is a mitochondrial disease. Proc Natl Acad Sci U S A 96(5):2141-6 SGD PMID 10051608
- ↑ Leuenberger D, et al. (1999) Different import pathways through the mitochondrial intermembrane space for inner membrane proteins. EMBO J 18(17):4816-22 SGD PMID 10469659
- ↑ Kurz M, et al. (1999) Biogenesis of Tim proteins of the mitochondrial carrier import pathway: differential targeting mechanisms and crossing over with the main import pathway. Mol Biol Cell 10(7):2461-74 SGD PMID 10397776
- ↑ Curran SP, et al. (2002) The role of the Tim8p-Tim13p complex in a conserved import pathway for mitochondrial polytopic inner membrane proteins. J Cell Biol 158(6):1017-27 SGD PMID 12221072
- ↑ Davis AJ, et al. (2007) The Tim9p/10p and Tim8p/13p complexes bind to specific sites on Tim23p during mitochondrial protein import. Mol Biol Cell 18(2):475-86 SGD PMID 17122363
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