| LOX | lysyl oxidase |
|---|---|
| LOXL | lysyl oxidase-like |
| LH | Lysyl hydroxylase |
|---|---|
| LO | Lysyl oxidase |
| LOX | Lysyl oxidase |
| L-BK | Lysyl-bradykinin |
| LysRS | Lysyl-tRNA synthetase |
| lysyl | The univalent radical of lysine. (05 Mar 2000) |
|---|---|
| lysyl 2-oxoglutarate dioxygenase | <enzyme> An enzyme that acts on specific lysyl residues in certain proteins (e.g., collagens) with alpha-ketoglutarate and O2 to produce d-hydroxylysyl residues, succinate, and CO2; this enzyme, which requires Fe2+ and ascorbate, is deficient in Ehlers-Danlos syndrome type VI. Synonym: lysyl 2-oxoglutarate dioxygenase. (05 Mar 2000) |
| lysyl endopeptidase | <enzyme> Alkaline protease with bacteriolytic acitvity from achromobacter lyticus; cleaves carboxyl bond of lysine residues Registry number: EC 3.4.21.50 Synonym: achromobacter protease I, achromopeptidase, lysyl endoprotease (26 Jun 1999) |
| lysyl hydroxylase | <enzyme> An enzyme that acts on specific lysyl residues in certain proteins (e.g., collagens) with alpha-ketoglutarate and O2 to produce d-hydroxylysyl residues, succinate, and CO2; this enzyme, which requires Fe2+ and ascorbate, is deficient in Ehlers-Danlos syndrome type VI. Synonym: lysyl 2-oxoglutarate dioxygenase. (05 Mar 2000) |
| lysyl oxidase | <enzyme> Extracellular enzyme that deaminates lysine and hydroxylysine residues in collagen or elastin to form aldehydes, that then interact with each other or with other lysyl side chains to form crosslinks. (18 Nov 1997) |
| lysyl-bradykinin | <protein> Decapeptide (lysyl bradykinin, amino acid sequence KRPPGFSPFR) produced in kidney. Like bradykinin, an inflammatory mediator (a kinin), causes dilation of renal blood vessels and increased water excretion. (18 Nov 1997) |
| lysyl |
the acyl radical of lysine.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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|---|---|
| lysyl hydroxylase |
an enzyme of the oxidoreductase class that catalyzes the hydroxylation of specific lysine residues in nascent procollagen chains; the hydroxylysine residues act as sites of attachment for disaccharide prosthetic groups and are involved in the formation of strong interchain crosslinks in collagen. The enzyme requires Fe2+, ascorbate, and α-ketoglutarate for activity. Deficiency of enzyme activity, an autosomal recessive trait, results in Ehlers-Danlos syndrome, type VI. In EC nomenclature, called procollagen-lysine 5-dioxygenase.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|
| lysyl oxidase |
an enzyme of the oxidoreductase class that catalyzes the oxidative deamination of lysine and hydroxylysine residues to the corresponding aldehydes, a step in the formation of covalent crosslinks in collagens and elastins. The reaction requires pyridoxal phosphate and Cu2+; the deficiency of enzyme activity and attendant physiological consequences occurring in Ehlers-Danlos syndrome, type IX (X-linked cutis laxa) and Menkes' syndrome appear to be secondary to deficiencies in copper metabolism or transport.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| lysyl-b. |
older name for kallidin.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|