Difference between revisions of "Part:BBa K533006:Design"

 
(→‎Design Notes)
Line 1: Line 1:
−
 
 
__NOTOC__
 
__NOTOC__
 
<partinfo>BBa_K533006 short</partinfo>
 
<partinfo>BBa_K533006 short</partinfo>
Line 7: Line 6:
  
 
===Design Notes===
 
===Design Notes===
−
proline rich sequence is much longer than the length required for SH3 binding, for easier binding to SH3 domain.
+
The coding sequence is driven by T7 promoter.
  
 +
We added his tag to the N-terminal to facilitate purification of the expressed protein. Proline rich sequence put here is much longer than the length required for SH3 binding, for tighter binding to SH3 domain.
  
 +
Proline rich sequence PVPPPVPPRRRP is from the structure of SH3 complexed with a proline rich peptide solved by Wittekind, ''et al''. The Kd value is determined by them to be 3.57uM.
  
 
===Source===
 
===Source===

Revision as of 16:08, 5 October 2011

Multi-Proline-mCherry


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 109
    Illegal BamHI site found at 908
    Illegal XhoI site found at 113
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


Design Notes

The coding sequence is driven by T7 promoter.

We added his tag to the N-terminal to facilitate purification of the expressed protein. Proline rich sequence put here is much longer than the length required for SH3 binding, for tighter binding to SH3 domain.

Proline rich sequence PVPPPVPPRRRP is from the structure of SH3 complexed with a proline rich peptide solved by Wittekind, et al. The Kd value is determined by them to be 3.57uM.

Source

mCherry sequence is from Clontech plasmid pmCherry-N1 and multi-proline sequence is synthesized from a consensus sequence of SH3 binding sequence.

References