二氢蕨酸合酶
磺胺
DHPS公司
酶
化学
药品
抗药性
突变
ATP合酶
生物化学
微生物学
生物
药理学
立体化学
基因
免疫学
突变
乙胺嘧啶
疟疾
恶性疟原虫
作者
Mi‐Kyung Yun,Yinan Wu,Zhenmei Li,Ying Zhao,Michael Brett Waddell,Antonio M. Ferreira,Richard E. Lee Jr.,Donald Bashford,Stephen W. White
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2012-03-01
卷期号:335 (6072): 1110-1114
被引量:262
标识
DOI:10.1126/science.1214641
摘要
The sulfonamide antibiotics inhibit dihydropteroate synthase (DHPS), a key enzyme in the folate pathway of bacteria and primitive eukaryotes. However, resistance mutations have severely compromised the usefulness of these drugs. We report structural, computational, and mutagenesis studies on the catalytic and resistance mechanisms of DHPS. By performing the enzyme-catalyzed reaction in crystalline DHPS, we have structurally characterized key intermediates along the reaction pathway. Results support an S(N)1 reaction mechanism via formation of a novel cationic pterin intermediate. We also show that two conserved loops generate a substructure during catalysis that creates a specific binding pocket for p-aminobenzoic acid, one of the two DHPS substrates. This substructure, together with the pterin-binding pocket, explains the roles of the conserved active-site residues and reveals how sulfonamide resistance arises.
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