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4FEW

Crystal structure of the aminoglycoside phosphotransferase APH(3')-Ia, with substrate kanamycin and small molecule inhibitor pyrazolopyrimidine PP2

4FEW の概要
エントリーDOI10.2210/pdb4few/pdb
関連するPDBエントリー4EJ7 4feu 4fev 4fex 4GKH 4GKI
分子名称Aminoglycoside 3'-phosphotransferase AphA1-IAB, KANAMYCIN A, 1-TERT-BUTYL-3-(4-CHLORO-PHENYL)-1H-PYRAZOLO[3,4-D]PYRIMIDIN-4-YLAMINE, ... (8 entities in total)
機能のキーワードpyrazolopyrimidine, pp2, protein kinase inhibitor, center for structural genomics of infectious diseases, csgid, niaid, national institute of allergy and infectious diseases, eukaryotic protein kinase-like fold, alpha/beta protein, transferase, phosphotransferase, aminoglycoside phosphotransferase, antibiotic resistance, aminoglycosides, kanamycin, gtp, intracellular, transferase-transferase inhibitor complex, transferase/transferase inhibitor
由来する生物種Acinetobacter baumannii
タンパク質・核酸の鎖数6
化学式量合計193589.00
構造登録者
主引用文献Stogios, P.J.,Spanogiannopoulos, P.,Evdokimova, E.,Egorova, O.,Shakya, T.,Todorovic, N.,Capretta, A.,Wright, G.D.,Savchenko, A.
Structure-guided optimization of protein kinase inhibitors reverses aminoglycoside antibiotic resistance.
Biochem.J., 454:191-200, 2013
Cited by
PubMed: 23758273
DOI: 10.1042/BJ20130317
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.98 Å)
構造検証レポート
Validation report summary of 4few
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2024-10-02に公開中

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