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7JLJ

Crystal structure of Bacillus subtilis UppS in complex with clomiphene

7JLJ の概要
エントリーDOI10.2210/pdb7jlj/pdb
関連するPDBエントリー7JLI
分子名称Isoprenyl transferase, Clomifene (3 entities in total)
機能のキーワードundecaprenyl, cis-prenyltransferase, carrier lipid, clomiphene, transferase
由来する生物種Bacillus subtilis
タンパク質・核酸の鎖数1
化学式量合計30220.08
構造登録者
Workman, S.D.,Strynadka, N.C.J. (登録日: 2020-07-29, 公開日: 2021-08-04, 最終更新日: 2023-10-18)
主引用文献Workman, S.D.,Day, J.,Farha, M.A.,El Zahed, S.S.,Bon, C.,Brown, E.D.,Organ, M.G.,Strynadka, N.C.J.
Structural Insights into the Inhibition of Undecaprenyl Pyrophosphate Synthase from Gram-Positive Bacteria.
J.Med.Chem., 64:13540-13550, 2021
Cited by
PubMed Abstract: The polyprenyl lipid undecaprenyl phosphate (CP) is the universal carrier lipid for the biosynthesis of bacterial cell wall polymers. CP is synthesized in its pyrophosphate form by undecaprenyl pyrophosphate synthase (UppS), an essential -prenyltransferase that is an attractive target for antibiotic development. We previously identified a compound (MAC-0547630) that showed promise as a novel class of inhibitor and an ability to potentiate β-lactam antibiotics. Here, we provide a structural model for MAC-0547630's inhibition of UppS and a structural rationale for its enhanced effect on UppS from . We also describe the synthesis of a MAC-0547630 derivative (JPD447), show that it too can potentiate β-lactam antibiotics, and provide a structural rationale for its improved potentiation. Finally, we present an improved structural model of clomiphene's inhibition of UppS. Taken together, our data provide a foundation for structure-guided drug design of more potent UppS inhibitors in the future.
PubMed: 34473495
DOI: 10.1021/acs.jmedchem.1c00941
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (3.1 Å)
構造検証レポート
Validation report summary of 7jlj
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2024-11-06に公開中

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