Difference between revisions of "Part:BBa K422010"
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<partinfo>BBa_K422010 short</partinfo> | <partinfo>BBa_K422010 short</partinfo> | ||
− | + | ===Biological Background=== | |
+ | The ribosome binding domain of the trigger factor trigA binds to the large subunit of the ribosome [1]. | ||
+ | |||
+ | ===Cloning strategy=== | ||
+ | BBF RFC28: A method for combinatorial multi-part assembly based on the Type IIs restriction enzyme AarI. '''CheB-A''' is an A-part compatible for N-Terminal fusion. For more information see [http://2010.igem.org/Team:ETHZ_Basel/Biology/Cloning]. | ||
+ | |||
+ | ===References=== | ||
+ | [1] Hesterkamp, Deuerling and Bukau: The Amino-terminal 118 amino acids of Escherichia coli Trigger factor constitute a domain that is necessary and sufficient for binding to ribosomes. The Journal of Biologcial Chemistry. 1997; 272:35. | ||
+ | |||
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Revision as of 08:49, 25 October 2010
trig (AarI A-part)
Biological Background
The ribosome binding domain of the trigger factor trigA binds to the large subunit of the ribosome [1].
Cloning strategy
BBF RFC28: A method for combinatorial multi-part assembly based on the Type IIs restriction enzyme AarI. CheB-A is an A-part compatible for N-Terminal fusion. For more information see [http://2010.igem.org/Team:ETHZ_Basel/Biology/Cloning].
References
[1] Hesterkamp, Deuerling and Bukau: The Amino-terminal 118 amino acids of Escherichia coli Trigger factor constitute a domain that is necessary and sufficient for binding to ribosomes. The Journal of Biologcial Chemistry. 1997; 272:35.
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal PstI site found at 364
- 12INCOMPATIBLE WITH RFC[12]Illegal PstI site found at 364
- 21COMPATIBLE WITH RFC[21]
- 23INCOMPATIBLE WITH RFC[23]Illegal PstI site found at 364
- 25INCOMPATIBLE WITH RFC[25]Illegal PstI site found at 364
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 88