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Post-translational modification of indoleamine 2,3-dioxygenase: N-terminal modification and nitration

✍ Scribed by Hidetsugu Fujigaki; Kanako Takahashi; Suwako Fujigaki; Junichi Masuda; Osamu Takikawa; Sanford P. Markey; Mitsuru Seishima; Kuniaki Saito

Book ID
119258023
Publisher
Elsevier Science
Year
2007
Tongue
English
Weight
268 KB
Volume
1304
Category
Article
ISSN
0531-5131

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✍ Lene Aarenstrup; Anne-Marie Falch; Kirsten K Jakobsen; SΓΈren Neve; Linda Ø Henri πŸ“‚ Article πŸ“… 2002 πŸ› Elsevier Science 🌐 English βš– 434 KB

## Abstract 4‐hydroxyphenylpyruvate dioxygenase (HPD) (EC 1.13.11.27) is a key enzyme involved in tyrosine catabolism. Congenital HPD deficiency is a rare, relatively benign condition known as hereditary type III tyrosinemia. The severe type I tyrosinemia, caused by a deficiency of fumarylacetoacet