Coding
Part:BBa_K200008
Designed by: Charles Fracchia, Royah Vaezi, Tianyi Wang, Nuri Purswani Group: iGEM09_Imperial College London (2009-08-12)
Phenylalanine hydroxylase
[http://en.wikipedia.org/wiki/Phenylalanine_hydroxylase Phenylalanine hydroxylase (PAH)] is the enzyme that determines the rate-limiting step in phenylalanine catabolism. Deficiency of this enzyme activity results in the autosomal recessive disorder phenylketonuria.#PAH1
As part of the Imperial 2009 iGEM E.ncapsulator project, E.coli was engineered to synthesise PAH to a tunable threshold, and successfully coat and protect it through the stomach, until release in the small intestine.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 287
Illegal BamHI site found at 814
Illegal XhoI site found at 524 - 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
References
[http://www.ncbi.nlm.nih.gov/nuccore/NM_000277.1?report=fasta Sequence from NCBI] <biblio>#PAH1 pmid = 2014036 </biblio>
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Categories
Parameters
None |