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人 MGMT 抗体对
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人 MGMT 抗体对

01AB00314

O-6-methylguanine-DNA methyltransferase (MGMT) is a DNA repair enzyme that directly reverses alkylation damage at the O-6 position of guanine, preventing mutagenic mismatches during replication. This monomeric protein (21.7 kDa) employs a suicide mechanism, transferring alkyl groups to its active site cysteine residue (Cys145), irreversibly inactivating itself. Expressed ubiquitously, particularly in the liver and brain, MGMT safeguards genomic integrity by mitigating G:C to A:T mutations. In cancer, epigenetic silencing via promoter methylation reduces MGMT expression, a hallmark of gliomas, glioblastomas, and other malignancies. Tumors with methylated MGMT promoters exhibit heightened sensitivity to alkylating agents like temozolomide, as impaired repair leads to lethal DNA damage accumulation. Conversely, unmethylated promoters correlate with therapeutic resistance, making MGMT status a critical biomarker for predicting chemotherapy efficacy.

Human
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技术参数

靶点基因名
MGMT
蛋白别名
O-6-methylguanine-DNA methyltransferase; MGMT
UniProt
P16455
物种
Human

产品详情

靶点名称
MGMT
蛋白名称
O-6-methylguanine-DNA methyltransferase
蛋白别名
Methylated-DNA--protein-cysteine methyltransferase; 6-O-methylguanine-DNA methyltransferase; MGMT; O-6-methylguanine-DNA-alkyltransferase
靶点基因名
MGMT
UniProt
P16455
来源物种
Homo sapiens (Human)
物种反应性
Human

背景介绍

O-6-methylguanine-DNA methyltransferase (MGMT) is a DNA repair enzyme that directly reverses alkylation damage at the O-6 position of guanine, preventing mutagenic mismatches during replication. This monomeric protein (21.7 kDa) employs a suicide mechanism, transferring alkyl groups to its active site cysteine residue (Cys145), irreversibly inactivating itself. Expressed ubiquitously, particularly in the liver and brain, MGMT safeguards genomic integrity by mitigating G:C to A:T mutations. In cancer, epigenetic silencing via promoter methylation reduces MGMT expression, a hallmark of gliomas, glioblastomas, and other malignancies. Tumors with methylated MGMT promoters exhibit heightened sensitivity to alkylating agents like temozolomide, as impaired repair leads to lethal DNA damage accumulation. Conversely, unmethylated promoters correlate with therapeutic resistance, making MGMT status a critical biomarker for predicting chemotherapy efficacy.