Difference between revisions of "Part:BBa K258001"

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303–476 of TliA.
 
303–476 of TliA.
  
<div align="center" style="padding-left: 66px; padding-top: 8px;"><a href="http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2642768/"><img style="border: 0px solid ; width: 500px; height: 500px;" alt="w6" src="https://static.igem.org/mediawiki/parts/0/03/LARD1.jpg"></a></div>
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<div align="center" style="padding-left: 66px; padding-top: 8px;"><a href="http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2642768/"><img style="border: 0px solid ; width: 500px; height: 500px;" alt="w6" src="https://static.igem.org/mediawiki/parts/0/03/LARD1.jpg"></a></div></html>
  
 
<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here

Revision as of 10:47, 17 October 2009

Lipase ABC transporter recognition domain (LARD 1)

Lard 1 was designed for the secretion of fusion proteins.The LARD 1 included four glycine-rich repeats comprising a β-roll structure, and were added to the C-terminus of test proteins. Either Pro-Gly linker or Factor Xa site can be added between fusion proteins and LARD 1. Upon supplementation of E. coli with ABC transporter from E. chrysanthemi (ABC transporter PrtDEF), which function well in the phylogenetically-neighboring genus E.coli, EGF-LARDs were excreted into the culture supernatant. For LARD1, linkers may be engineered to have a Factor Xa cleavage site. LARD1 also contained residues 303–476 of TliA.

w6

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]