Difference between revisions of "Part:BBa K4035003"
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<partinfo>BBa_K4035003 short</partinfo> | <partinfo>BBa_K4035003 short</partinfo> | ||
− | + | This protein is made of two yeast copper metallotionein protein, CUP1 ((BBa_M45090), linked together by a flexible linker made of four times the GGGGS amino acid sequence. | |
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===Usage and Biology=== | ===Usage and Biology=== | ||
− | + | Copper metallotionein CUP1 (BBa_M45090) is a protein responsible for copper binding protein in the yeast Saccharomyces cerevisiae. In order to increase the copper retrieval efficiency, two copies of CUP1 were linked together and expressed at the outter surface of S. cerevisiae (BBa_K4035010). The GGGGS linker is a common flexible linker. | |
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+ | ===Characterization=== | ||
+ | |||
+ | ===Sequence and Features=== | ||
<partinfo>BBa_K4035003 SequenceAndFeatures</partinfo> | <partinfo>BBa_K4035003 SequenceAndFeatures</partinfo> | ||
Revision as of 05:39, 13 September 2021
Dimerization of the copper metallothionein 1 : CUP1-(GGGGS)4-CUP1
This protein is made of two yeast copper metallotionein protein, CUP1 ((BBa_M45090), linked together by a flexible linker made of four times the GGGGS amino acid sequence.
Usage and Biology
Copper metallotionein CUP1 (BBa_M45090) is a protein responsible for copper binding protein in the yeast Saccharomyces cerevisiae. In order to increase the copper retrieval efficiency, two copies of CUP1 were linked together and expressed at the outter surface of S. cerevisiae (BBa_K4035010). The GGGGS linker is a common flexible linker.
Characterization
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal PstI site found at 90
Illegal PstI site found at 408 - 12INCOMPATIBLE WITH RFC[12]Illegal PstI site found at 90
Illegal PstI site found at 408 - 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 235
- 23INCOMPATIBLE WITH RFC[23]Illegal PstI site found at 90
Illegal PstI site found at 408 - 25INCOMPATIBLE WITH RFC[25]Illegal PstI site found at 90
Illegal PstI site found at 408 - 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 84