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4DBX

Crystal structure of aminoglycoside phosphotransferase APH(2")-ID/APH(2")-IVA

3R7Z」から置き換えられました3LZH」から置き換えられました
4DBX の概要
エントリーDOI10.2210/pdb4dbx/pdb
関連するPDBエントリー4DE4 4DFB 4DFU
分子名称APH(2")-ID (2 entities in total)
機能のキーワードstructural genomics, mcsg, midwest center for structural genomics, eukaryotic protein kinase-like fold, aminoglycoside phosphotransferase, kinase, transferase, aminoglycosides, intracellular, psi-biology
由来する生物種Enterococcus casseliflavus
タンパク質・核酸の鎖数1
化学式量合計38279.04
構造登録者
主引用文献Shakya, T.,Stogios, P.J.,Waglechner, N.,Evdokimova, E.,Ejim, L.,Blanchard, J.E.,McArthur, A.G.,Savchenko, A.,Wright, G.D.
A small molecule discrimination map of the antibiotic resistance kinome.
Chem.Biol., 18:1591-1601, 2011
Cited by
PubMed Abstract: Kinase-mediated resistance to antibiotics is a significant clinical challenge. These enzymes share a common protein fold characteristic of Ser/Thr/Tyr protein kinases. We screened 14 antibiotic resistance kinases against 80 chemically diverse protein kinase inhibitors to map resistance kinase chemical space. The screens identified molecules with both broad and narrow inhibition profiles, proving that protein kinase inhibitors offer privileged chemical matter with the potential to block antibiotic resistance. One example is the flavonol quercetin, which inhibited a number of resistance kinases in vitro and in vivo. This activity was rationalized by determination of the crystal structure of the aminoglycoside kinase APH(2″)-IVa in complex with quercetin and its antibiotic substrate kanamycin. Our data demonstrate that protein kinase inhibitors offer chemical scaffolds that can block antibiotic resistance, providing leads for co-drug design.
PubMed: 22195561
DOI: 10.1016/j.chembiol.2011.10.018
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.004 Å)
構造検証レポート
Validation report summary of 4dbx
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2026-02-04に公開中

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