| ASAL | arginosuccinic acid lyase |
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| ASL | antistreptolysin; argininosuccinate lyase |
| ICL | idiopathic CD4 T-cell lymphocytopenia; iris-clip lens; isocitrate lyase |
| TPL | third party liability; titanium proximal loading; tumor progression locus; tyrosine phenol-lyase |
| ACA | abnormal coronary artery; acrodermatitis chronica atrophicans; acute cerebellar ataxia; adenocarcino... |
| PAL | L-Phenylalanine ammonia-lyase |
|---|---|
| AMO | Ammonia monooxygenase |
| NAN | Non-ammonia-N |
| NAN | non-ammonia nitrogen |
| ACL | ATP citrate lyase |
| phenylalanine ammonia lyase | <enzyme> An enzyme that catalyses the deamination of l-phenylalanine to form trans-cinnamate and ammonia. It may also act on l-tyrosine. Since the enzyme deprives neoplastic tissue of phenylalanine, it has been used experimentally in the treatment of acute lymphoblastic leukaemia. The enzyme is obtained from many plants and is used as an enzymic marker for lignification and other developmental processes in plant cells. Pharmacological action: antineoplastic agent. Chemical name: L-Phenylalanine ammonia-lyase Registry number: EC 4.3.1.5 (12 Dec 1998) |
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| aspartate ammonia-lyase | <enzyme> An enzyme that catalyses the conversion of aspartic acid to ammonia and fumaric acid in plants and some microorganisms. Chemical name: L-Aspartate ammonia-lyase Registry number: EC 4.3.1.1 (12 Dec 1998) |
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| histidine ammonia-lyase | <enzyme> An enzyme of the lyase class that catalyses the reaction of l-histidine to form urocanate and ammonia. The reaction is the initial step of histidine catabolism. Genetic deficiency of the enzyme, transmitted as an autosomal recessive trait, causes histidinaemia. Chemical name: L-Histidine ammonia-lyase Registry number: EC 4.3.1.3 (12 Dec 1998) |
| diaminopropionate ammonia-lyase | <enzyme> Used for the determination of diaminopropionic acid Registry number: EC 4.3.1.- (26 Jun 1999) |
| ethanolamine ammonia-lyase | <enzyme> An enzyme that catalyses the deamination of ethanolamine to acetaldehyde. Chemical name: Ethanolamine ammonia-lyase Registry number: EC 4.3.1.7 (12 Dec 1998) |
| L-tyrosine ammonia-lyase | <enzyme> Catalyses the conversion of tyrosine to trans-p-coumaric acid and ammonia Registry number: EC 4.3.1.- Synonym: tyrosine ammonia-lyase (26 Jun 1999) |
| phenylalanine | <amino acid> One of the amino acids which the body cannot manufacture itself, but must acquire from food. It is abundant in meats and cheese. Phenylalanine is a precursor of tyrosine and together they lead to the formation of thyroxine or thyroid hormone and of adrenaline and noradrenaline which is converted into a neurotransmitter, a brain chemical which transmits nerve impulses. This neurotransmitter is used by the brain to manufacture noradrenaline which promotes mental alertness, memory, elevates mood and suppresses the appetite very effectively. Along with another amino acid, tryptophan, phenylalanine governs the release of an intestinal hormone called cholecystokinin. Overuse of phenylalanine supplements can cause anxiety, headaches and hypertension and are contraindicated for pregnant woman, those who suffer from anxiety attacks, high blood pressure, PKU, pigmented melanoma or anyone taking an anti-depressant containing monoamine oxidase inhibitors. (15 Oct 1997) |
| phenylalanine 4-hydroxylase | <enzyme> An enzyme that catalyses the oxidation of l-phenylalanine to l-tyrosine with O2 and tetrahydrobiopterin (the latter forming the dihydro derivative) which is reduced by NADPH and a reductase to the active form; a deficiency of either of these enzymes will result in phenylketonuria. Synonym: phenylalanine 4-hydroxylase. (05 Mar 2000) |
| phenylalanine 4-monooxygenase | <enzyme> An enzyme that catalyses the oxidation of l-phenylalanine to l-tyrosine with O2 and tetrahydrobiopterin (the latter forming the dihydro derivative) which is reduced by NADPH and a reductase to the active form; a deficiency of either of these enzymes will result in phenylketonuria. Synonym: phenylalanine 4-hydroxylase. (05 Mar 2000) |
| phenylalanine aminopeptidase | <enzyme> Metalloenzyme from legionella pneumophila; mw: 35,000; pH optimum 8-9.5 Registry number: EC 3.4.11.- (26 Jun 1999) |
| phenylalanine hydroxylase | <enzyme> An enzyme of the oxidoreductase class that catalyses the reaction l-phenylalanine, tetrahydrobiopterin, and oxygen to yield l-tyrosine, dihydrobiopterin, and water, the reaction synthesizing tyrosine from phenylalanine. Chemical name: L-Phenylalanine,tetrahydrobiopterin:oxygen oxidoreductase (4-hydroxylating) Registry number: EC 1.14.16.1 (12 Dec 1998) |
| phenylalanine hydroxylase phosphatase | <enzyme> Catalyses dephosphorylation of phosphorylated phenylalanine hydroxylase Registry number: EC 3.1.3.- Synonym: phe hydroxylase phosphatase (26 Jun 1999) |
| phenylalanine oxidase | <enzyme> Forms phenylpyruvate in the presence of air; consider also phenylalanine dehydrogenase (nad) which requires nad Registry number: EC 1.4.3.- Synonym: phenylalanine desaminase, l-phenylalanine oxidase, phenylalanine dehydrogenase (26 Jun 1999) |
| phenylalanine-trna ligase | <enzyme> An enzyme that activates phenylalanine with its specific transfer RNA. Chemical name: Phenylalanine:tRNA(Phe) ligase (AMP-forming) Registry number: EC 6.1.1.20 (12 Dec 1998) |
| n-formylmethionine leucyl-phenylalanine | <chemical> N-formylmethionyl-leucyl-phenylalanine. A formylated tripeptide originally isolated from bacterial filtrates that is positively chemotactic to polymorphonuclear leucocytes, and causes them to release lysosomal enzymes and become metabolically activated. Chemical name: L-Phenylalanine, N-(N-(N-formyl-L-methionyl)-L-leucyl)- (12 Dec 1998) |
| N-formylmethionyl-leucyl-phenylalanine carboxypeptidase | <enzyme> Human salivary enzyme liberates phenylalanine from the chemotactic peptide n-formylmethionine leucyl-phenylalanine Registry number: EC 3.4.- Synonym: n-formyl-methionine leucyl-phenylalanyl carboxypeptidase, formylmet-leu-phe carboxypeptidase (26 Jun 1999) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|