Difference between revisions of "Part:BBa K4765002"

(Introduction)
(Introduction)
Line 7: Line 7:
 
__TOC__
 
__TOC__
 
===Introduction===
 
===Introduction===
Ag1 is a corresponding antigen of [https://parts.igem.org/Part:BBa_K4765003 BBa_K4765003(Nb1)]<ref>Glass, D. S., & Riedel-Kruse, I. H. (2018). A Synthetic Bacterial Cell-Cell Adhesion Toolbox for Programming Multicellular Morphologies and Patterns. ''Cell, 174''(3), 649-658.e16. https://doi.org/10.1016/j.cell.2018.06.041</ref>. The interaction between Ag-Nb can mediate specific adhesion between ''E.coli''.
+
Ag1 is a corresponding antigen of [https://parts.igem.org/Part:BBa_K4765003 BBa_K4765003(Nb1)]<ref>Glass, D. S., & Riedel-Kruse, I. H. (2018). A Synthetic Bacterial Cell-Cell Adhesion Toolbox for Programming Multicellular Morphologies and Patterns. ''Cell, 174''(3), 649-658.e16. https://doi.org/10.1016/j.cell.2018.06.041</ref>. The interaction between Ag-Nb can mediate specific binding between ''E.coli''.
  
 
===Usage and Biology===
 
===Usage and Biology===

Revision as of 15:12, 12 October 2023


Ag1, Akt3PH from 10.1016/j.cell.2018.06.041

contributed by Fudan iGEM 2023

Introduction

Ag1 is a corresponding antigen of BBa_K4765003(Nb1)[1]. The interaction between Ag-Nb can mediate specific binding between E.coli.

Usage and Biology

The combination of Ag1's single-domain structure and the intimin surface display system allows the entirety of a highly specific, cell surface-bound adhesin to be encoded as a single fusion protein.

Characterization

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
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI.rc site found at 340


Reference

  1. Glass, D. S., & Riedel-Kruse, I. H. (2018). A Synthetic Bacterial Cell-Cell Adhesion Toolbox for Programming Multicellular Morphologies and Patterns. Cell, 174(3), 649-658.e16. https://doi.org/10.1016/j.cell.2018.06.041