Difference between revisions of "Part:BBa K1729002"
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Branda, Steven S ''et al''. "Prediction and Identification of New Natural Substrates of the Yeast Mitochondrial Intermediate Peptidase." J Biol Chem 270 (1995): 27366-73. | Branda, Steven S ''et al''. "Prediction and Identification of New Natural Substrates of the Yeast Mitochondrial Intermediate Peptidase." J Biol Chem 270 (1995): 27366-73. | ||
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+ | <b> Uses </b> | ||
Used in part BBa_K2077002. When connected to a fluorescent protein by a GS linker, mls targets fluorescence to yeast mitochondria even in strains with defunct mitochondria lacking ribosomal protein mRPS12, which is necessary for yeast mitochondria to translate their genome and make electron transport proteins needed to generate a membrane potential. | Used in part BBa_K2077002. When connected to a fluorescent protein by a GS linker, mls targets fluorescence to yeast mitochondria even in strains with defunct mitochondria lacking ribosomal protein mRPS12, which is necessary for yeast mitochondria to translate their genome and make electron transport proteins needed to generate a membrane potential. |
Revision as of 01:10, 22 October 2016
Yeast MRPS12 mitochondrial localization signal
This translational start sequence includes the Kozak and codon-optimized sequence for the mitochondrial localization signal of Saccharomyces cerevisiae mitochondrial ribosomal protein [http://www.yeastgenome.org/locus/S000005319/overview MRPS12]. The cleavage site was predicted based on identification of an R-10 motif (RxFxxTxxxx), which is typical of precursors cleaved sequentially by the yeast mitochondrial processing peptidase and mitochondrial intermediate peptidase (Branda et al.).
The part sequence corresponds to nucleotides 694840-694739 on chromosome XIV of the S. cerevisiae S288C reference genome. See also BBa_K1729001
References
Branda, Steven S et al. "Prediction and Identification of New Natural Substrates of the Yeast Mitochondrial Intermediate Peptidase." J Biol Chem 270 (1995): 27366-73.
Uses
Used in part BBa_K2077002. When connected to a fluorescent protein by a GS linker, mls targets fluorescence to yeast mitochondria even in strains with defunct mitochondria lacking ribosomal protein mRPS12, which is necessary for yeast mitochondria to translate their genome and make electron transport proteins needed to generate a membrane potential.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]