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3I8A

Staphylococcus aureus H30N, F98Y Dihydrofolate Reductase complexed with NADPH and 2,4-diamino-5-(3-(2,5-dimethoxyphenyl)prop-1-ynyl)-6-ethylpyrimidine (UCP120B)

3I8A の概要
エントリーDOI10.2210/pdb3i8a/pdb
関連するPDBエントリー3FQ0 3FQO
分子名称Dihydrofolate reductase, 5-[3-(2,5-dimethoxyphenyl)prop-1-yn-1-yl]-6-ethylpyrimidine-2,4-diamine, NADPH DIHYDRO-NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE, ... (4 entities in total)
機能のキーワードnadph, one-carbon metabolism, oxidoreductase-oxidoreductase inhibitor complex, oxidoreductase/oxidoreductase inhibitor
由来する生物種Staphylococcus aureus
タンパク質・核酸の鎖数1
化学式量合計19065.30
構造登録者
Frey, K.M.,Lombardo, M.N.,Anderson, A.C. (登録日: 2009-07-09, 公開日: 2010-02-09, 最終更新日: 2023-09-06)
主引用文献Frey, K.M.,Lombardo, M.N.,Wright, D.L.,Anderson, A.C.
Towards the understanding of resistance mechanisms in clinically isolated trimethoprim-resistant, methicillin-resistant Staphylococcus aureus dihydrofolate reductase.
J.Struct.Biol., 170:93-97, 2010
Cited by
PubMed Abstract: Resistance to therapeutics such as trimethoprim-sulfamethoxazole has become an increasing problem in strains of methicillin-resistant Staphylococcus aureus (MRSA). Clinically isolated trimethoprim-resistant strains reveal a double mutation, H30N/F98Y, in dihydrofolate reductase (DHFR). In order to develop novel and effective therapeutics against these resistant strains, we evaluated a series of propargyl-linked antifolate lead compounds for inhibition of the mutant enzyme. For the propargyl-linked antifolates, the F98Y mutation generates minimal (between 1.2- and 6-fold) losses of affinity and the H30N mutation generates greater losses (between 2.4- and 48-fold). Conversely, trimethoprim affinity is largely diminished by the F98Y mutation (36-fold) and is not affected by the H30N mutation. In order to elucidate a mechanism of resistance, we determined a crystal structure of a complex of this double mutant with a lead propargyl-linked antifolate. This structure suggests a resistance mechanism consistent both for the propargyl-linked class of antifolates and for trimethoprim that is based on the loss of a conserved water-mediated hydrogen bond.
PubMed: 20026215
DOI: 10.1016/j.jsb.2009.12.011
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.41 Å)
構造検証レポート
Validation report summary of 3i8a
検証レポート(詳細版)ダウンロードをダウンロード

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件を2024-10-30に公開中

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