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Literature summary for 3.5.3.1 extracted from

  • Joerink, M.; Savelkoul, H.F.; Wiegertjes, G.F.
    Evolutionary conservation of alternative activation of macrophages: structural and functional characterization of arginase 1 and 2 in carp (Cyprinus carpio L.) (2006), Mol. Immunol., 43, 1116-1128.
    View publication on PubMed
Search for more literature for 3.5.3.1

Cloned(Commentary)

Cloned (Comment) Organism
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 Cyprinus carpio

Inhibitors

Inhibitors Comment Organism Structure
Nomega-hydroxy-L-arginine
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 Cyprinus carpio

Organism

Organism UniProt Comment Textmining
Cyprinus carpio Q4A3J0 and highly homologous sequence variants Q4A4U9, Q4A3J1, isoform arginase II; isoform arginase II
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Cyprinus carpio Q4A3J1 and highly homologous sequence variants Q4A4U9, Q4A3J0, isoform arginase II; isoform arginase II
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Cyprinus carpio Q4A3J2 isoform arginase I; isoform arginase I
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Cyprinus carpio Q4A4U9 and highly homologous sequence variants Q4A3J1, Q4A3J0, isoform arginase II; isoform arginase II
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Source Tissue

Source Tissue Comment Organism Textmining
kidney mid kidney, basal enzyme expression Cyprinus carpio
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liver highest expression of all organs examined Cyprinus carpio
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macrophage cultured head-kidney derived macrophages, significant enzyme activity, inhibitable by Nomega-hydroxy-L-arginine and induced by dibutyryl cyclic adenosine Cyprinus carpio
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macrophage cultured head-kidney derived macrophages, significant enzyme activity, inhibitable by Nomega-hydroxy-L-arginine, not inducible by dibutyryl cyclic adenosine Cyprinus carpio
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additional information enzyme found in all organs examined Cyprinus carpio
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