Title : Expression and post-translational modification of human 4-hydroxy-phenylpyruvate dioxygenase.

Pub. Date : 2002

PMID : 12127941






5 Functional Relationships(s)
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Sentence
Compound Name
Protein Name
Organism
1 4-hydroxyphenylpyruvate dioxygenase (HPD) (EC 1.13.11.27) is a key enzyme involved in tyrosine catabolism. Tyrosine 4-hydroxyphenylpyruvate dioxygenase Homo sapiens
2 4-hydroxyphenylpyruvate dioxygenase (HPD) (EC 1.13.11.27) is a key enzyme involved in tyrosine catabolism. Tyrosine 4-hydroxyphenylpyruvate dioxygenase Homo sapiens
3 The severe type I tyrosinemia, caused by a deficiency of fumarylacetoacetate hydrolase which functions downstream of HPD in the tyrosine degradation pathway, is often associated with decreased expression of HPD, and interestingly, inhibition of HPD activity seems to ameliorate the clinical symptoms of type I tyrosinemia. Tyrosine 4-hydroxyphenylpyruvate dioxygenase Homo sapiens
4 The severe type I tyrosinemia, caused by a deficiency of fumarylacetoacetate hydrolase which functions downstream of HPD in the tyrosine degradation pathway, is often associated with decreased expression of HPD, and interestingly, inhibition of HPD activity seems to ameliorate the clinical symptoms of type I tyrosinemia. Tyrosine 4-hydroxyphenylpyruvate dioxygenase Homo sapiens
5 The severe type I tyrosinemia, caused by a deficiency of fumarylacetoacetate hydrolase which functions downstream of HPD in the tyrosine degradation pathway, is often associated with decreased expression of HPD, and interestingly, inhibition of HPD activity seems to ameliorate the clinical symptoms of type I tyrosinemia. Tyrosine 4-hydroxyphenylpyruvate dioxygenase Homo sapiens