Difference between revisions of "Part:BBa K842006"
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Cloning and Uses | Cloning and Uses | ||
This part was generated via PCR from the E. coli strain DH5α and cloned into the vector pSB1C3. It is to be used with other chemotaxis genes to form a complete regulatory pathway that controls the response system in MCP and the direction of rotation in flagella. | This part was generated via PCR from the E. coli strain DH5α and cloned into the vector pSB1C3. It is to be used with other chemotaxis genes to form a complete regulatory pathway that controls the response system in MCP and the direction of rotation in flagella. | ||
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<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here | ||
===Usage and Biology=== | ===Usage and Biology=== |
Latest revision as of 01:12, 4 October 2012
cheA
CheA is a regulatory protein that becomes activated when the methyl-accepting chemotaxis protein (MCP) is not bound to any attractant. The activated cheA self-phosphorylates itself by hydrolyzing ATP in order to gain a phosphate group. CheA then donates its phosphate group to activate cheB or cheA.
Used for researcher control of signaling mechanisms that influence flagella function.
Cloning and Uses
This part was generated via PCR from the E. coli strain DH5α and cloned into the vector pSB1C3. It is to be used with other chemotaxis genes to form a complete regulatory pathway that controls the response system in MCP and the direction of rotation in flagella.
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 1286
- 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 1286
- 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 1286
- 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 1286
- 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 1286
Illegal NgoMIV site found at 1636 - 1000COMPATIBLE WITH RFC[1000]