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人 CNDP1 抗体对
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人 CNDP1 抗体对

01AB03049

Carnosine dipeptidase 1 (CNDP1) is a 56.8 kDa homodimeric M20 metalloprotease primarily expressed in the brain, where it functions as the principal human carnosinase. It specifically hydrolyzes Xaa-His dipeptides, exhibiting its highest catalytic activity toward carnosine and anserine using Zn2+ as a cofactor. The enzyme exists in both intracellular and secreted forms, contributing to protein hydrolysis, tissue regeneration, and cell cycle regulation. Structurally, CNDP1 contains a signal peptide and a characteristic beta-strand arrangement. Clinically, mutations in the CNDP1 gene are linked to rare metabolic disorders such as homocarnosinosis and carnosinemia, which are characterized by the accumulation of carnosine and associated neurological symptoms. Additionally, its downregulation has been identified as a poor prognostic indicator in hepatocellular carcinoma and other cancers, suggesting its utility as a potential biomarker for disease progression.

Human
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技术参数

靶点基因名
CNDP1
基因别名
CN1; CPGL2
蛋白别名
carnosine dipeptidase 1; CNDP1
UniProt
Q96KN2
物种
Human

产品详情

靶点名称
CNDP1
蛋白名称
carnosine dipeptidase 1
蛋白别名
Beta-Ala-His dipeptidase; CNDP dipeptidase 1; Carnosine dipeptidase 1; Glutamate carboxypeptidase-like protein 2; Serum carnosinase
靶点基因名
CNDP1
基因别名
CN1; CPGL2
UniProt
Q96KN2
来源物种
Homo sapiens (Human)
物种反应性
Human

背景介绍

Carnosine dipeptidase 1 (CNDP1) is a 56.8 kDa homodimeric M20 metalloprotease primarily expressed in the brain, where it functions as the principal human carnosinase. It specifically hydrolyzes Xaa-His dipeptides, exhibiting its highest catalytic activity toward carnosine and anserine using Zn2+ as a cofactor. The enzyme exists in both intracellular and secreted forms, contributing to protein hydrolysis, tissue regeneration, and cell cycle regulation. Structurally, CNDP1 contains a signal peptide and a characteristic beta-strand arrangement. Clinically, mutations in the CNDP1 gene are linked to rare metabolic disorders such as homocarnosinosis and carnosinemia, which are characterized by the accumulation of carnosine and associated neurological symptoms. Additionally, its downregulation has been identified as a poor prognostic indicator in hepatocellular carcinoma and other cancers, suggesting its utility as a potential biomarker for disease progression.