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甲基丙二酸血症的一种新变体——培养成纤维细胞中辅酶-脱辅基酶结合缺陷

A new variant of methylmalonic acidemia-defective coenzyme-apoenzyme binding in cultured fibroblasts.

作者信息

Morrow G, Revsin B, Clark R, Lebowitz J, Whelan D T

出版信息

Clin Chim Acta. 1978 Apr 3;85(1):67-72. doi: 10.1016/0009-8981(78)90102-x.

Abstract

Cultured fibroblasts from a patient with methylmalonic acidemia, clinically responsive to vitamin B-12, were studied in vitro. Kinetic analysis revealed abnormal binding of the coenzyme, 5'-deoxyadenosylcobalamin, for its methylmalonyl-CoA carbonylmutase apoenzyme, i.e., KM of 3.8 X 10(-5) M versus control KM of 1.5 X 10(-8) M. These data are interpreted as indicating a structural defect of the apoenzyme at the coenzyme binding site, and represent another variant of this genetic disorder.

摘要

对一名临床上对维生素B-12有反应的甲基丙二酸血症患者的培养成纤维细胞进行了体外研究。动力学分析显示,辅酶5'-脱氧腺苷钴胺素与其甲基丙二酰辅酶A羧基变位酶脱辅酶的结合异常,即其米氏常数(KM)为3.8×10^(-5)M,而对照的KM为1.5×10^(-8)M。这些数据被解释为表明脱辅酶在辅酶结合位点存在结构缺陷,并且代表了这种遗传性疾病的另一种变体。

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