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人 KYAT1 抗体对
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人 KYAT1 抗体对

01AB01750

Kynurenine aminotransferase 1 (KYAT1) is a cytosolic, pyridoxal 5'-phosphate (PLP)-dependent enzyme that plays a central role in the tryptophan catabolic pathway. It catalyzes the irreversible transamination of L-kynurenine to produce kynurenic acid, a neuroactive metabolite that modulates glutamatergic neurotransmission. Additionally, KYAT1 exhibits beta-lyase activity toward sulfur- and selenium-containing cysteine conjugates, a process that can generate reactive intermediates linked to nephrotoxicity. Structurally, the enzyme functions as a dimer with a well-defined active site containing key catalytic residues such as Lys247 and Glu27. Clinically, KYAT1 is associated with hydroxykynureninuria and schizophrenia, as dysregulation of kynurenic acid homeostasis is implicated in various neuropsychiatric and neurodegenerative conditions.

Human
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技术参数

靶点基因名
KYAT1
基因别名
CCBL1
蛋白别名
kynurenine aminotransferase 1; KYAT1
UniProt
Q16773
物种
Human

产品详情

靶点名称
KYAT1
蛋白名称
kynurenine aminotransferase 1
蛋白别名
Kynurenine--oxoglutarate transaminase 1; Cysteine-S-conjugate beta-lyase; Glutamine transaminase K; GTK; Glutamine--phenylpyruvate transaminase; Kynurenine aminotransferase 1; Kynurenine aminotransferase I; KATI; Kynurenine--oxoglutarate transaminase I
靶点基因名
KYAT1
基因别名
CCBL1
UniProt
Q16773
来源物种
Homo sapiens (Human)
物种反应性
Human

背景介绍

Kynurenine aminotransferase 1 (KYAT1) is a cytosolic, pyridoxal 5'-phosphate (PLP)-dependent enzyme that plays a central role in the tryptophan catabolic pathway. It catalyzes the irreversible transamination of L-kynurenine to produce kynurenic acid, a neuroactive metabolite that modulates glutamatergic neurotransmission. Additionally, KYAT1 exhibits beta-lyase activity toward sulfur- and selenium-containing cysteine conjugates, a process that can generate reactive intermediates linked to nephrotoxicity. Structurally, the enzyme functions as a dimer with a well-defined active site containing key catalytic residues such as Lys247 and Glu27. Clinically, KYAT1 is associated with hydroxykynureninuria and schizophrenia, as dysregulation of kynurenic acid homeostasis is implicated in various neuropsychiatric and neurodegenerative conditions.