| 1. | It is characterized by lowered activity of arginase in hepatic cells.
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| 2. | Arginase catalyzes the hydrolysis of arginine to ornithine and urea.
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| 3. | Arginase transcript variants encoding different isoforms have been found for this gene.
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| 4. | Specifically, arginase converts L-arginine into L-ornithine and urea.
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| 5. | Mammalian arginase is active as a trimer, but some bacterial arginases are hexameric.
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| 6. | Arginase's active site is extraordinarily specific.
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| 7. | Arginase deficiency, unlike other urea cycle disorders, does not entirely prevent ureagenesis.
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| 8. | There are several arginase isozymes that differ in catalytic, molecular and immunological properties.
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| 9. | Ammonia and arginine are thought to cause neurological problems and other symptoms of arginase deficiency.
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| 10. | Arginase is about the enzyme reaction and has links back to both ARG1 and ARG2.
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