Number of the records: 1
homogentizát 1,2-dioxygenáza
SYS d050560 LBL 00000nx--j22000003--45-- 005 20240119201443.3 100 $a 20050630csloy0103----ba0 152 $b mesh 250 $a homogentizát 1,2-dioxygenáza $x AD $x AE $x AI $x AN $x BI $x BL $x CF $x CH $x CL $x CS $x DE $x DF $x EC $x GE $x HI $x IM $x IP $x ME $x PD $x PH $x PK $x PO $x RE $x SD $x ST $x TO $x TU $x UL $x UR $8 slo 300 1-
$a 2006(1969) $8 eng 300 1-
$a Dioxygenases (1969-2005) $8 eng 330 1-
$a A 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. $8 eng 550 $3 sllk_un_auth*d000474 $Y Alkaptonuria $5 B $a alkaptonúria 550 $3 sllk_un_auth*d000474 $Y Alkaptonuria $5 F $a alkaptonúria 686 $a D08.811.682.690.416.326 750 $a Homogentisate 1,2-Dioxygenase $8 eng 801 -0
$a US $b DNLM $c 20050630 801 -2
$a SK $b BA006 $c 20060605 980 $x M
Number of the records: 1