THE INTERACTION BETWEEN COUMARIN DRUGS AND DNA GYRASE

被引:241
作者
MAXWELL, A
机构
[1] Department of Biochemistry, University of Leicester, Leicester
基金
英国惠康基金;
关键词
D O I
10.1111/j.1365-2958.1993.tb01728.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The coumarin group of antibiotics have as their target the bacterial enzyme DNA gyrase. The drugs bind to the B subunit of gyrase and inhibit DNA supercoiling by blocking the ATPase activity. Recent data show that the binding site for the drugs lies within the N-terminal part of the B protein, and individual amino acids involved in coumarin interaction are being identified. The mode of inhibition of the gyrase ATPase reaction by coumarins is unlikely to be simple competitive inhibition, and the drugs may act by stabilizing a conformation of the enzyme with low affinity for ATP.
引用
收藏
页码:681 / 686
页数:6
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