Difference between revisions of "Part:BBa K4035004"
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<partinfo>BBa_K4035004 short</partinfo> | <partinfo>BBa_K4035004 short</partinfo> | ||
− | + | This protein is made of two yeast copper metallotionein protein, CUP1 (BBa_M45090), linked together by a rigid linker made of seven times the AP 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_K4035011). The (AP)7 linker is a common rigid linker made of several successive Alanin followed by Proline. | |
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+ | ===Characterization=== | ||
+ | |||
+ | ===Sequence and Features=== | ||
<partinfo>BBa_K4035004 SequenceAndFeatures</partinfo> | <partinfo>BBa_K4035004 SequenceAndFeatures</partinfo> | ||
Revision as of 05:58, 13 September 2021
Dimerization of the copper metallothionein 1 : CUP1-(AP)7-CUP1
This protein is made of two yeast copper metallotionein protein, CUP1 (BBa_M45090), linked together by a rigid linker made of seven times the AP 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_K4035011). The (AP)7 linker is a common rigid linker made of several successive Alanin followed by Proline.
Characterization
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal PstI site found at 90
Illegal PstI site found at 312 - 12INCOMPATIBLE WITH RFC[12]Illegal PstI site found at 90
Illegal PstI site found at 312 - 21COMPATIBLE WITH RFC[21]
- 23INCOMPATIBLE WITH RFC[23]Illegal PstI site found at 90
Illegal PstI site found at 312 - 25INCOMPATIBLE WITH RFC[25]Illegal PstI site found at 90
Illegal PstI site found at 312 - 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 306