Part:BBa_K277041
3L.3_23.B2.01
3L.3_23.B2.01 is 757 bases long and is cloned into the pGem-T vector.
3L.3_23.B2.01 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. 3L.3_23.B2.01 is a constituent of 3L.3_23.B2 (along with 3L.3_23.B2.02, 3L.3_23.B2.03, 3L.3_23.B2.04, 3L.3_23.B2.05, 3L.3_23.B2.06, 3L.3_23.B2.07, 3L.3_23.B2.08, 3L.3_23.B2.09, 3L.3_23.B2.10, 3L.3_23.B2.11, and 3L.3_23.B2.12.)
This part contains at least part of the following features (positions offset from first base of sequence):
kind and name offset notes
forward_primer YCL049C_tagf1v1 (648..675)
gene YCL049C (417..+1355) Protein of unknown function%3B localizes to membrane fraction%3B YCL049C is not an essential gene%3B
mutation_affecting_coding_sequence YCL049C_re_remove_MmeI (594..605) removal of MmeI
Sequence (the first 757 bases correspond to coordinates 29641..30397 in synthetic chromosome yeast_chr3_3_23)
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 387
None |