Difference between revisions of "Part:BBa K200008"

 
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__NOTOC__
 
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<partinfo>BBa_K200008 short</partinfo>
 
<partinfo>BBa_K200008 short</partinfo>
  
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Phenylalanine hydroxylase (PAH) is an enzyme used to break down phenylalanine in humans.
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Phenylalanine hydroxylase (PAH) encodes the enzyme phenylalanine hydroxylase that is the rate-limiting step in phenylalanine catabolism. Deficiency of this enzyme activity results in the autosomal recessive disorder phenylketonuria.
  
 
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Revision as of 20:55, 26 August 2009

Phenylalanine hydroxylase

Phenylalanine hydroxylase (PAH) encodes the enzyme phenylalanine hydroxylase that is the rate-limiting step in phenylalanine catabolism. Deficiency of this enzyme activity results in the autosomal recessive disorder phenylketonuria.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 287
    Illegal BamHI site found at 814
    Illegal XhoI site found at 524
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]