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homogentizát 1,2-dioxygenáza

  1. Record numberd050560
    Date06.06.2025
    TypeM
    Topical termhomogentizát 1,2-dioxygenáza
    See also(Later heading) alkaptonúria
    (Skutočné meno) alkaptonúria
    UDCD08.811.682.690.416.326
    NoteA mononuclear Fe(II)-dependent oxygenase, this enzyme catalyzes the conversion of homogentisate to 4-maleylacetoacetate, the third step in the pathway for the catabolism of TYROSINE. Deficiency in the enzyme causes ALKAPTONURIA, an autosomal recessive disorder, characterized by homogentisic aciduria, OCHRONOSIS and ARTHRITIS. This enzyme was formerly characterized as EC 1.13.1.5 and EC 1.99.2.5.
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