Other

Part:BBa_K277086

Designed by: James DiCarlo   Group: iGEM09_Johns_Hopkins-BAG   (2009-10-21)


3L.3_23.C3.07


3L.3_23.C3.07 is 749 bases long and is cloned into the pGem-T vector.

3L.3_23.C3.07 was designed as a piece of synthetic chromosome 3 with the goal of minimizing and stabilizing that chromosome and to that end has had any tRNAs, introns, repeat regions, and transposons that were present in the wildtype chromosome removed. In addition a very few gene sequences were slightly recoded to add or remove restriction enzyme recognition sites to facilitate assembly; most gene sequences were slightly recoded to introduce unique primers for diagnostic PCR amplification, and some gene sequences were slightly recoded to address the distribution of stop codon usage. The whole synthetic chromosome may be viewed at http://macbeth.clark.jhu.edu/cgi-bin/gbrowse 3L.3_23.C3.07 is a constituent of 3L.3_23.C3 (along with 3L.3_23.C3.01, 3L.3_23.C3.02, 3L.3_23.C3.03, 3L.3_23.C3.04, 3L.3_23.C3.05, 3L.3_23.C3.06, 3L.3_23.C3.08, 3L.3_23.C3.09, 3L.3_23.C3.10, 3L.3_23.C3.11, 3L.3_23.C3.12, 3L.3_23.C3.13, and 3L.3_23.C3.14.)

This part contains at least part of the following features (positions offset from first base of sequence):

kind and name offset notes

forward_primer YCL027W_tagf1v1 (63..90)

reverse_primer YCL027W_tagr1v1 (534..561)

gene YCL027W (-236..+1302) Membrane protein localized to the shmoo tip%2C required for cell fusion%3B expression regulated by mating pheromone%3B proposed to coordinate signaling%2C fusion%2C and polarization events required for fusion%3B potential Cdc28p substrate

Sequence (corresponds to coordinates 62719..63467 in synthetic chromosome yeast_chr3_3_23)

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal EcoRI site found at 57
    Illegal EcoRI site found at 174
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal EcoRI site found at 57
    Illegal EcoRI site found at 174
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal EcoRI site found at 57
    Illegal EcoRI site found at 174
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal EcoRI site found at 57
    Illegal EcoRI site found at 174
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal EcoRI site found at 57
    Illegal EcoRI site found at 174
  • 1000
    COMPATIBLE WITH RFC[1000]


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