Other names published for TIM10: MRS11, YHR005C-A
TIM10 LITERATURE TOPICS
- Curated Literature
- Genetics/Cell Biology
- Cellular Location
- Function/Process
- Genetic Interactions
- Mutants/Phenotypes
- Regulation of
- Nucleic Acid Information
- Gene Product Information
- Related Genes/Proteins
- Research Aids
- Genome-wide Analysis
- Proteome-wide Analysis
- Other Topics
- Additional Information
TIM10 - Mutants/Phenotypes (24)
| Reference | Other Genes Addressed |
|---|---|
| Baker MJ, et al. (2012) Impaired folding of the mitochondrial small TIM chaperones induces clearance by the i-AAA protease. J Mol Biol 424(5):227-39 | |
| Reinhold R, et al. (2012) The channel-forming Sym1 protein is transported by the TIM23 complex in a presequence-independent manner. Mol Cell Biol 32(24):5009-21 | |
| Papic D, et al. (2011) Multispan mitochondrial outer membrane protein Ugo1 follows a unique Mim1-dependent import pathway. J Cell Biol 194(3):397-405 | |
| Hasson SA, et al. (2010) Substrate specificity of the TIM22 mitochondrial import pathway revealed with small molecule inhibitor of protein translocation. Proc Natl Acad Sci U S A 107(21):9578-83 | |
| Baker MJ, et al. (2009) Structural and functional requirements for activity of the Tim9-Tim10 complex in mitochondrial protein import. Mol Biol Cell 20(3):769-79 | |
| Sideris DP, et al. (2009) A novel intermembrane space-targeting signal docks cysteines onto Mia40 during mitochondrial oxidative folding. J Cell Biol 187(7):1007-22 | |
| Breslow DK, et al. (2008) A comprehensive strategy enabling high-resolution functional analysis of the yeast genome. Nat Methods 5(8):711-8 | |
| Ivanova E, et al. (2008) Assembly of the mitochondrial Tim9-Tim10 complex: a multi-step reaction with novel intermediates. J Mol Biol 375(1):229-39 | |
| Wagner K, et al. (2008) The assembly pathway of the mitochondrial carrier translocase involves four preprotein translocases. Mol Cell Biol 28(13):4251-60 | |
| Milenkovic D, et al. (2007) Biogenesis of the essential Tim9-Tim10 chaperone complex of mitochondria: site-specific recognition of cysteine residues by the intermembrane space receptor Mia40. J Biol Chem 282(31):22472-80 | |
| Sideris DP and Tokatlidis K (2007) Oxidative folding of small Tims is mediated by site-specific docking onto Mia40 in the mitochondrial intermembrane space. Mol Microbiol 65(5):1360-73 | |
| Vergnolle MA, et al. (2007) Mutation of Conserved Charged Residues in Mitochondrial TIM10 Subunits Precludes TIM10 Complex Assembly, but Does not Abolish Growth of Yeast Cells. J Mol Biol 371(5):1315-24 | |
| Brandner K, et al. (2005) Taz1, an outer mitochondrial membrane protein, affects stability and assembly of inner membrane protein complexes: implications for Barth Syndrome. Mol Biol Cell 16(11):5202-14 | |
| Vergnolle MA, et al. (2005) Distinct domains of small Tims involved in subunit interaction and substrate recognition. J Mol Biol 351(4):839-49 | |
| Wiedemann N, et al. (2004) Biogenesis of the protein import channel Tom40 of the mitochondrial outer membrane: intermembrane space components are involved in an early stage of the assembly pathway. J Biol Chem 279(18):18188-94 | |
| Allen S, et al. (2003) Juxtaposition of the two distal CX3C motifs via intrachain disulfide bonding is essential for the folding of Tim10. J Biol Chem 278(40):38505-13 | |
| Dunn CD and Jensen RE (2003) Suppression of a defect in mitochondrial protein import identifies cytosolic proteins required for viability of yeast cells lacking mitochondrial DNA. Genetics 165(1):35-45 | |
| Senapin S, et al. (2003) Transcription of TIM9, a new factor required for the petite-positive phenotype of Saccharomyces cerevisiae, is defective in spt7 mutants. Curr Genet 44(4):202-10 | |
| Truscott KN, et al. (2002) Mitochondrial import of the ADP/ATP carrier: the essential TIM complex of the intermembrane space is required for precursor release from the TOM complex. Mol Cell Biol 22(22):7780-9 | |
| Murphy MP, et al. (2001) The essential function of the small Tim proteins in the TIM22 import pathway does not depend on formation of the soluble 70-kilodalton complex. Mol Cell Biol 21(18):6132-8 | |
| Koehler CM, et al. (2000) Tim18p, a new subunit of the TIM22 complex that mediates insertion of imported proteins into the yeast mitochondrial inner membrane. Mol Cell Biol 20(4):1187-93 | |
| Koehler CM, et al. (1999) Human deafness dystonia syndrome is a mitochondrial disease. Proc Natl Acad Sci U S A 96(5):2141-6 | |
| Koehler CM, et al. (1998) Import of mitochondrial carriers mediated by essential proteins of the intermembrane space. Science 279(5349):369-73 | |
| Jarosch E, et al. (1997) A soluble 12-kDa protein of the mitochondrial intermembrane space, Mrs11p, is essential for mitochondrial biogenesis and viability of yeast cells. Mol Gen Genet 255(2):157-65 |




