肉碱
酰基转移酶
肉碱O-棕榈酰转移酶
辅酶A
化学
活动站点
转移酶
生物化学
肉碱棕榈酰转移酶I
乙酰肉碱
酶
乙酰转移酶
氧阴离子孔
立体化学
生物合成
β氧化
还原酶
乙酰化
基因
作者
G. Jogl,Yu‐Shan Hsiao,Liang Tong
标识
DOI:10.1196/annals.1320.002
摘要
A bstract : Carnitine acyltransferases catalyze the exchange of acyl groups between carnitine and coenzyme A (CoA). These enzymes include carnitine acetyltransferase (CrAT), carnitine octanoyltransferase (CrOT), and carnitine palmitoyltransferases (CPTs). CPT‐I and CPT‐II are crucial for the β‐oxidation of long‐chain fatty acids in the mitochondria by enabling their transport across the mitochondrial membrane. The activity of CPT‐I is inhibited by malonyl‐CoA, a crucial regulatory mechanism for fatty acid oxidation. Mutation or dysregulation of the CPT enzymes has been linked to many serious, even fatal human diseases, and these enzymes are promising targets for the development of therapeutic agents against type 2 diabetes and obesity. We have determined the crystal structures of murine CrAT, alone and in complex with its substrate carnitine or CoA. The structure contains two domains. Surprisingly, these two domains share the same backbone fold, which is also similar to that of chloramphenicol acetyltransferase and dihydrolipoyl transacetylase. The active site is located at the interface between the two domains, in a tunnel that extends through the center of the enzyme. Carnitine and CoA are bound in this tunnel, on opposite sides of the catalytic His343 residue. The structural information provides a molecular basis for understanding the catalysis by carnitine acyltransferases and for designing their inhibitors. In addition, our structural information suggests that the substrate carnitine may assist the catalysis by stabilizing the oxyanion in the reaction intermediate.
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