Source:
Generated By: https://synbiohub.org/public/igem/igem2sbol/1
Created by: James DiCarlo
Date created: 2009-10-20 11:00:00
Date modified: 2015-05-08 01:11:46
3L.3_23.C1.06
| Types | DnaRegion |
| Roles | Other sequence_feature |
| Sequences | BBa_K277067_sequence (Version 1) |
Description
3L.3_23.C1.06 is 801 bases long and is cloned into the pGem-T vector.3L.3_23.C1.06 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.C1.06 is a constituent of 3L.3_23.C1 (along with 3L.3_23.C1.01, 3L.3_23.C1.02, 3L.3_23.C1.03, 3L.3_23.C1.04, 3L.3_23.C1.05, 3L.3_23.C1.07, 3L.3_23.C1.08, and 3L.3_23.C1.09.)
This part contains at least part of the following features (positions offset from first base of sequence):
kind and name offset notes
gene YCL036W (263..+1963) Protein of unknown function%2C identified as a high-copy suppressor of a dbp5 mutation
mutation_affecting_coding_sequence YCL036W_re_remove_BglI (689..700) removal of BglI
forward_primer YCL036W_tagf1v1 (400..427)
Sequence (corresponds to coordinates 49239..50039 in synthetic chromosome yeast_chr3_3_23)