Difference between revisions of "Part:BBa K2443007"
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<partinfo>BBa_K2443007 short</partinfo> | <partinfo>BBa_K2443007 short</partinfo> | ||
− | Glycine tRNA synthetase responsible for attaching glycine onto its tRNA to form an aminoacyl-tRNA. Codon optimized for use in <i>Escherichia coli</i>. Contains a C-terminal hexahistidine tag with a serine glycine linker. Under the regulation of T7 Promoter, RBS and double terminator. | + | Glycine tRNA synthetase responsible for attaching glycine onto its tRNA to form an aminoacyl-tRNA. Codon optimized for use in <i>Escherichia coli</i>. Contains a C-terminal hexahistidine tag with a serine glycine linker. Under the regulation of T7 Promoter, RBS and double terminator. The expected size of GlyRS Alpha subunit is 36 kDa, which closely corresponds to the size observed from the overexpression (lane 5 below). Protein was expressed according to the overexpression protocol on the lethbridge iGEM 2017 wiki (http://2017.igem.org/Team:Lethbridge/Experiments) |
+ | https://static.igem.org/mediawiki/parts/d/d4/Lethbridge_2017_Oct_10_gel_2.png | ||
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Revision as of 17:56, 1 November 2017
GlyRS Alpha subunit optimized for expression in E. coli
Glycine tRNA synthetase responsible for attaching glycine onto its tRNA to form an aminoacyl-tRNA. Codon optimized for use in Escherichia coli. Contains a C-terminal hexahistidine tag with a serine glycine linker. Under the regulation of T7 Promoter, RBS and double terminator. The expected size of GlyRS Alpha subunit is 36 kDa, which closely corresponds to the size observed from the overexpression (lane 5 below). Protein was expressed according to the overexpression protocol on the lethbridge iGEM 2017 wiki (http://2017.igem.org/Team:Lethbridge/Experiments)
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 370
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]