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tryptophan synthase <enzyme> An enzyme that catalyses the conversion of l-serine and 1-(indol-3-yl)glycerol 3-phosphate to l-tryptophan and glyceraldehyde 3-phosphate. It is a pyridoxal phosphate protein that also catalyses the conversion of serine and indole into tryptophan and water and of indoleglycerol phosphate into indole and glyceraldehyde phosphate.
Chemical name: L-Serine hydro-lyase (adding indoleglycerol-phosphate)
Registry number: EC 4.2.1.20
(12 Dec 1998)
tryptophan synthetase <enzyme> An enzyme that catalyses the conversion of l-serine and 1-(indol-3-yl)glycerol 3-phosphate to l-tryptophan and glyceraldehyde 3-phosphate. It is a pyridoxal phosphate protein that also catalyses the conversion of serine and indole into tryptophan and water and of indoleglycerol phosphate into indole and glyceraldehyde phosphate.
Chemical name: L-Serine hydro-lyase (adding indoleglycerol-phosphate)
Registry number: EC 4.2.1.20
(12 Dec 1998)
tryptophan-trna ligase <enzyme> An enzyme that activates tryptophan with its specific transfer RNA.
Chemical name: L-Tryptophan:tRNA(Trp) ligase (AMP-forming)
Registry number: EC 6.1.1.2
(12 Dec 1998)
tryptophanase <enzyme> An enzyme that catalyses the conversion of l-tryptophan and water to indole, pyruvate, and ammonia. It is a pyridoxal-phosphate protein, requiring k+. It also catalyses 2,3-elimination and beta-replacement reactions of some indole-substituted tryptophan analogs of l-cysteine, l-serine, and other 3-substituted amino acids.
Chemical name: L-Tryptophan indole-lyase (deaminating)
Registry number: EC 4.1.99.1
(12 Dec 1998)
tryptophanuria Enhanced urinary excretion of tryptophan.
Tryptophanuria with dwarfism, a syndrome of dwarfism, mental defect, cutaneous photosensitivity, and gait disturbance associated with tryptophanuria; autosomal recessive inheritance.
(05 Mar 2000)
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