| 1. | The overall reaction of catechol 1, 2-dioxygenase.
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| 2. | 1-Methyltryptophan inhibits indoleamine dioxygenase, but is also a very slow substrate.
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| 3. | The most prominent class of inhibitor of NO dioxygenase to date is imidazole antibiotics.
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| 4. | It is a synthetic 4-hydroxyphenylpyruvate dioxygenase.
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| 5. | Subsequent oxidation is followed by a proposed dioxygenase mechanism that leads to epoxide formation.
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| 6. | Examples include the non-heme dioxygenase enzymes and JmjC-family histone demethylases.
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| 7. | Structure based development of phenylimidazole-derived inhibitors of indoleamine 2, 3-dioxygenase.
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| 8. | This enzyme is also called "'4-hydroxyphenylpyruvate dioxygenase II " '.
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| 9. | This enzyme is also called "'linoleate dioxygenase, manganese lipoxygenase " '.
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| 10. | The latter reaction is a remnant activity of the more ancient nitric oxide dioxygenase function of globins.
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