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抗人 AHCY 抗体对
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抗人 AHCY 抗体对

01AB02781

Adenosylhomocysteinase (AHCY) is a cytosolic, NAD+-dependent enzyme that catalyzes the reversible hydrolysis of S-adenosyl-L-homocysteine (SAH) into adenosine and homocysteine. By removing SAH, which is a potent competitive inhibitor of S-adenosyl-L-methionine-dependent methyltransferases, AHCY serves as a key regulator of cellular methylation potential and one-carbon metabolism. The enzyme functions as a tetramer with a tightly bound NAD cofactor per subunit, acting as a metabolic gatekeeper for redox balance and epigenetic regulation. Pathogenic mutations in AHCY cause AHCY deficiency, a condition characterized by elevated plasma methionine and SAH levels, delayed myelination, myopathy, and psychomotor retardation.

Human
规格起售价
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技术参数

靶点基因名
AHCY
基因别名
SAHH
蛋白别名
adenosylhomocysteinase; AHCY
UniProt
P23526
物种
Human

产品详情

靶点名称
AHCY
蛋白名称
adenosylhomocysteinase
蛋白别名
Adenosylhomocysteinase; AdoHcyase; S-adenosyl-L-homocysteine hydrolase
靶点基因名
AHCY
基因别名
SAHH
UniProt
P23526
来源物种
Homo sapiens (Human)
物种反应性
Human

背景介绍

Adenosylhomocysteinase (AHCY) is a cytosolic, NAD+-dependent enzyme that catalyzes the reversible hydrolysis of S-adenosyl-L-homocysteine (SAH) into adenosine and homocysteine. By removing SAH, which is a potent competitive inhibitor of S-adenosyl-L-methionine-dependent methyltransferases, AHCY serves as a key regulator of cellular methylation potential and one-carbon metabolism. The enzyme functions as a tetramer with a tightly bound NAD cofactor per subunit, acting as a metabolic gatekeeper for redox balance and epigenetic regulation. Pathogenic mutations in AHCY cause AHCY deficiency, a condition characterized by elevated plasma methionine and SAH levels, delayed myelination, myopathy, and psychomotor retardation.