Počet záznamov: 1
homogentizát 1,2-dioxygenáza
SYS d050560 LBL 00000nz--a2200000o--4500 005 20250606214938.4 008 050630|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 065 $a D08.811.682.690.416.326 066 $a 01 $c 03 150 $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 $2 slo 550 $7 sllk_us_auth*d000474 $Y Alkaptonuria $w b $a alkaptonúria 550 $7 sllk_us_auth*d000474 $Y Alkaptonuria $w p $a alkaptonúria 665 $a 2006(1969) $2 eng 665 $a Dioxygenases (1969-2005) $2 eng 680 9-
$i 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. $2 eng 750 -2
$a Homogentisate 1,2-Dioxygenase $2 eng 980 $x M
Počet záznamov: 1