Arginase, type II is an arginase protein that in humans is encoded by the ARG2 gene.[5]
Arginase catalyzes the hydrolysis of argininetoornithine and urea. At least two isoforms of mammalian arginase exists (types I and II, this enzyme) which differ in their tissue distribution, subcellular localization, immunologic crossreactivity and physiologic function. The type II isoform encoded by this gene, is located in the mitochondria and expressed in extra-hepatic tissues, especially kidney. The physiologic role of this isoform is poorly understood; it is thought to play a role in nitric oxide and polyamine metabolism. Transcript variants of the type II gene resulting from the use of alternative polyadenylation sites have been described.
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
Hydrolases: carbon-nitrogen non-peptide (EC 3.5)
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3.5.1: Linear amides / Amidohydrolases |
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3.5.2: Cyclic amides/ Amidohydrolases |
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3.5.3: Linear amidines/ Ureohydrolases |
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3.5.4: Cyclic amidines/ Aminohydrolases |
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3.5.5: Nitriles/ Aminohydrolases |
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3.5.99: Other |
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Activity |
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Regulation |
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Classification |
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Kinetics |
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Types |
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