YGR181W

From SGD-Wiki
(Redirected from TIM13)
Jump to: navigation, search

Share your knowledge...Edit this entry! <protect>

Systematic name YGR181W
Gene name TIM13
Aliases
Feature type ORF, Verified
Coordinates Chr VII:858287..858604
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]




</protect>

Community Commentary

About Community Commentary. Please share your knowledge!




<protect>

References

See Help:References on how to add references

  1. 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
  2. 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
  3. 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
  4. 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
  5. 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

See Help:Categories on how to add the wiki page for this gene to a Category </protect>