Difference between revisions of "Part:BBa K1969006"
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+ | __NOTOC__ | ||
+ | <partinfo>BBa_K1969006 short</partinfo> | ||
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+ | It is a modified version of nucleotide binding alpha subunit of the heterotrimeric G protein (Gpa2), which originally interacts with the receptor Gpr1p and has signaling role in response to nutrients. it required for the recruitment of Ras-GTP at the plasma membrane and in the nucleus. This modified version is aimed for improving signal transduction downstream heterologously expressed G protein coupled receptor in Saccharomyces cerevisiae. The original sequence of 5 amino acids at C terminus of Gpa2 is replaced by the corresponding sequence in human G alpha protein S1. | ||
+ | |||
+ | <!-- Add more about the biology of this part here | ||
+ | ===Usage and Biology=== | ||
+ | |||
+ | <!-- --> | ||
+ | <span class='h3bb'>Sequence and Features</span> | ||
+ | <partinfo>BBa_K1969006 SequenceAndFeatures</partinfo> | ||
+ | |||
+ | |||
+ | <!-- Uncomment this to enable Functional Parameter display | ||
+ | ===Functional Parameters=== | ||
+ | <partinfo>BBa_K1969006 parameters</partinfo> | ||
+ | <!-- --> |
Latest revision as of 16:10, 14 October 2016
S. cerevisiae GPA2 with 5 amino acids from human G(s) alpha-subunit
It is a modified version of nucleotide binding alpha subunit of the heterotrimeric G protein (Gpa2), which originally interacts with the receptor Gpr1p and has signaling role in response to nutrients. it required for the recruitment of Ras-GTP at the plasma membrane and in the nucleus. This modified version is aimed for improving signal transduction downstream heterologously expressed G protein coupled receptor in Saccharomyces cerevisiae. The original sequence of 5 amino acids at C terminus of Gpa2 is replaced by the corresponding sequence in human G alpha protein S1.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 4