Počet záznamov: 1
glutaryl-CoA-dehydrogenáza
SYS d050770 LBL 00000nz--a2200000o--4500 005 20250606214851.5 008 050630|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 065 $a D08.811.682.660.425 066 $a 01 $c 03 150 $a glutaryl-CoA-dehydrogenáza $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 665 $a 2006(1973) $2 eng 665 $a Acyl Coenzyme A (1973-1979) $2 eng 665 $a Coenzymes (1973-1979) $2 eng 665 $a Glutarates (1973-1980) $2 eng 665 $a Oxidoreductases (1983-2003) $2 eng 665 $a Oxidoreductases Acting on CH-CH Group Donors (2004-2005) $2 eng 680 9-
$i A flavoprotein enzyme that is responsible for the catabolism of LYSINE; HYDROXYLYSINE; and TRYPTOPHAN. It catalyzes the oxidation of GLUTARYL-CoA to crotonoyl-CoA using FAD as a cofactor. Glutaric aciduria type I is an inborn error of metabolism due to the deficiency of glutaryl-CoA dehydrogenase. $2 eng 750 -2
$a Glutaryl-CoA Dehydrogenase $2 eng 980 $x M
Počet záznamov: 1