Difference between revisions of "Part:BBa K4140009"
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<partinfo>BBa_K4140009 short</partinfo> | <partinfo>BBa_K4140009 short</partinfo> | ||
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| + | ==Part Description== | ||
Coding sequence for an enzyme that causes phenylalanine to be hydroxylated in order to produce tyrosine. PAH is a hydroxylase that needs biopterin. | Coding sequence for an enzyme that causes phenylalanine to be hydroxylated in order to produce tyrosine. PAH is a hydroxylase that needs biopterin. | ||
Phenylketonuria is a metabolic condition that can occur in humans due to abnormalities in the gene that codes for it | Phenylketonuria is a metabolic condition that can occur in humans due to abnormalities in the gene that codes for it | ||
| + | ==Usage== | ||
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| + | ==Literature Characterization== | ||
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| + | [[File:T--AFCM-EGYPT--CAS2.PNG|thumb|Right|Figure 1.Substrate RNA cleavage assay using wild-type and mutant target RNAs. ]] | ||
| + | <br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br><br> | ||
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| + | ==References== | ||
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here | ||
Revision as of 09:55, 28 September 2022
Phenylalanine hydroxylase (PAH)
Part Description
Coding sequence for an enzyme that causes phenylalanine to be hydroxylated in order to produce tyrosine. PAH is a hydroxylase that needs biopterin. Phenylketonuria is a metabolic condition that can occur in humans due to abnormalities in the gene that codes for it
Usage
Literature Characterization
References
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]