| MC | 1) Musculo-Cutaneous 2) Mixed Cellularity |
|---|---|
| MCTD | Mixed Connective Tissue Disease |
| MLC | 1) Minimal Lethal Concentration 2) Mixed Lymphocyte Culture |
| NMLH | Nodular Mixed Lymphocytic Histocytic |
| TAE | Trans-Arterial(-Catheter) Embolization Angiography와 동시에 Gel Form과 CTx Agent의 Mixed m... |
| polyvinyl alcohol oxidase | <enzyme> Membrane-bound enzyme in pseudomonas sp.; leads to formation of hydrogen peroxide; does not use pyrroloquinoline quinone Registry number: EC 1.1.3.- (26 Jun 1999) |
|---|---|
| cysteine conjugate S-oxidase | <enzyme> Converts s-benzyl-l-cysteine to s-benzyl-l-cysteine sulfoxide; uses o2 and NADPH; may be a flavin-containing monooxygenase Registry number: EC 1.13.12- (26 Jun 1999) |
| cytochrome-c oxidase | <enzyme> An enzyme complex of the inner mitochondrial membrane that catalyses the reaction between ferrocytochrome c and oxygen to yield ferricytochrome c and water. It is associated with the pumping of protons and the resultant phosphorylation of ADP to ATP. The reaction is the terminal event in the electron transport scheme by which oxygen is used for fuel combustion. It is a part of Complex IV of the respiratory chain. A deficiency of one or more of the polypeptides of this complex results in neuronal loss in brain leading to psychomotor retardation and neurodegenerative disease. Synonym: cytochrome aa3, indophenol oxidase, indophenolase. Chemical name: Ferricytochrome-c:oxygen oxidoreductase Registry number: EC 1.9.3.1 (12 Dec 1998) |
| cytochrome oxidase | <enzyme> Terminal enzyme of the electron transport chain that accepts electrons from (i.e. Oxidizes) cytochrome C and transfers electrons to molecular oxygen. (18 Nov 1997) |
| cytochrome P-450 oxidase | <enzyme> Oxidises NADPH with formation of hydrogen peroxide Registry number: EC 1.6.2.- Synonym: NADPH-p450 reductase, NADPH-cytochrome p450 reductase, cytochrome p450 reductase, cpra gene product (26 Jun 1999) |
| cytokinin oxidase | <enzyme> Isopentenyladenosine to adenosine Registry number: EC 1.- (26 Jun 1999) |
| saccharopine oxidase | <enzyme> Flavoenzyme which catalyses the oxidative cleavage of saccharopine to delta-1-piper9deine-6-carboxylate, glutamate and h2o2 Registry number: EC 1.5.3.- (26 Jun 1999) |
| pristanoyl-CoA oxidase | <enzyme> Pristanoic acid undergoes beta-oxidation giving alternatively rise to acetyl-CoA or propionyl-CoA and h2o2 Registry number: EC 1.3.3.- Synonym: 2,6,10,14-tetramethylpentadecanoyl-CoA oxidase, 2-methylpalmitoyl-CoA oxidase, pristanyl-CoA oxidase (26 Jun 1999) |
| proline oxidase | <enzyme> The first enzyme of the proline degradative pathway. It catalyses the oxidation of proline to pyrroline-5-carboxylic acid in the presence of oxygen and water. The action is not reversible. The specific activity of proline oxidase increases with age. Registry number: EC 1.5.3.- (12 Dec 1998) |
| sarcosine oxidase | <enzyme> Catalyses the oxidative demethylation of sarcosine to glycine Registry number: EC 1.5.3.1 Synonym: sarcosine-oxygen oxidoreductase (demethylating) (26 Jun 1999) |
| propionate-3-nitronate oxidase | <enzyme> From penicillium atrovenetum; flavoprotein; catalyses the oxidation of propionate 3-nitronate in the presence of oxygen to yield malonate saemialdehyde, no2, no3 and h2o2 Registry number: EC 1.7.3.- Synonym: 3-nitropropionate oxidase (26 Jun 1999) |
| protein-lysine 6-oxidase | <enzyme> An enzyme oxidizing peptidyl-lysyl-peptide in the presence of water & molecular oxygen to yield peptidyl-allysyl-peptide plus ammonia & hydrogen peroxide. Chemical name: Protein-L-lysine:oxygen 6-oxidoreductase (deaminating) Registry number: EC 1.4.3.13 (12 Dec 1998) |
| protoporphyrinogen type III oxidase | A mitochondrial enzyme that uses O2 to convert protoporphyrinogen type III to protoporphyrin type III in haem biosynthesis; a deficiency of this enzyme is associated with variegate porphyria. (05 Mar 2000) |
| xanthine oxidase | <enzyme> Dehydrogenases involved in conversion of hypoxanthine to xanthine and xanthine to uric acid, as the final catabolism of purines. Deficient in the human disease xanthinuria. (18 Nov 1997) |
| hexobarbital oxidase | <enzyme> Hexobarbital is oxidised to ketohexobarbital Registry number: EC 1.1.- (26 Jun 1999) |