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5UXA

Crystal structure of macrolide 2'-phosphotransferase MphB from Escherichia coli

5UXA の概要
エントリーDOI10.2210/pdb5uxa/pdb
関連するPDBエントリー5UXB 5UXC 5UXD
分子名称Macrolide 2'-phosphotransferase II, CALCIUM ION (3 entities in total)
機能のキーワードantibiotic resistance, macrolide, phosphotransferase, kinase, structural genomics, center for structural genomics of infectious diseases, csgid, national institute of allergy and infectious diseases, niaid, transferase
由来する生物種Escherichia coli
タンパク質・核酸の鎖数1
化学式量合計34647.44
構造登録者
主引用文献Pawlowski, A.C.,Stogios, P.J.,Koteva, K.,Skarina, T.,Evdokimova, E.,Savchenko, A.,Wright, G.D.
The evolution of substrate discrimination in macrolide antibiotic resistance enzymes.
Nat Commun, 9:112-112, 2018
Cited by
PubMed Abstract: The production of antibiotics by microbes in the environment and their use in medicine and agriculture select for existing and emerging resistance. To address this inevitability, prudent development of antibiotic drugs requires careful consideration of resistance evolution. Here, we identify the molecular basis for expanded substrate specificity in MphI, a macrolide kinase (Mph) that does not confer resistance to erythromycin, in contrast to other known Mphs. Using a combination of phylogenetics, drug-resistance phenotypes, and in vitro enzyme assays, we find that MphI and MphK phosphorylate erythromycin poorly resulting in an antibiotic-sensitive phenotype. Using likelihood reconstruction of ancestral sequences and site-saturation combinatorial mutagenesis, supported by Mph crystal structures, we determine that two non-obvious mutations in combination expand the substrate range. This approach should be applicable for studying the functional evolution of any antibiotic resistance enzyme and for evaluating the evolvability of resistance enzymes to new generations of antibiotic scaffolds.
PubMed: 29317655
DOI: 10.1038/s41467-017-02680-0
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.95 Å)
構造検証レポート
Validation report summary of 5uxa
検証レポート(詳細版)ダウンロードをダウンロード

246905

件を2025-12-31に公開中

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