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5FBT

Crystal structure of rifampin phosphotransferase RPH-Lm from Listeria monocytogenes in complex with rifampin

5FBT の概要
エントリーDOI10.2210/pdb5fbt/pdb
関連するPDBエントリー5FBS 5FBU
分子名称Phosphoenolpyruvate synthase, Rifampin, CHLORIDE ION, ... (4 entities in total)
機能のキーワードantibiotic resistance, rifamycins, rifampin, phosphotransferase, atp grasp domain, phosphohistidine domain, structural genomics, center for structural genomics of infectious diseases, csgid, transferase-antibiotic complex, transferase/antibiotic
由来する生物種Listeria monocytogenes serotype 4b str. F2365
タンパク質・核酸の鎖数1
化学式量合計99012.50
構造登録者
主引用文献Stogios, P.J.,Cox, G.,Spanogiannopoulos, P.,Pillon, M.C.,Waglechner, N.,Skarina, T.,Koteva, K.,Guarne, A.,Savchenko, A.,Wright, G.D.
Rifampin phosphotransferase is an unusual antibiotic resistance kinase.
Nat Commun, 7:11343-11343, 2016
Cited by
PubMed Abstract: Rifampin (RIF) phosphotransferase (RPH) confers antibiotic resistance by conversion of RIF and ATP, to inactive phospho-RIF, AMP and Pi. Here we present the crystal structure of RPH from Listeria monocytogenes (RPH-Lm), which reveals that the enzyme is comprised of three domains: two substrate-binding domains (ATP-grasp and RIF-binding domains); and a smaller phosphate-carrying His swivel domain. Using solution small-angle X-ray scattering and mutagenesis, we reveal a mechanism where the swivel domain transits between the spatially distinct substrate-binding sites during catalysis. RPHs are previously uncharacterized dikinases that are widespread in environmental and pathogenic bacteria. These enzymes are members of a large unexplored group of bacterial enzymes with substrate affinities that have yet to be fully explored. Such an enzymatically complex mechanism of antibiotic resistance augments the spectrum of strategies used by bacteria to evade antimicrobial compounds.
PubMed: 27103605
DOI: 10.1038/ncomms11343
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.702 Å)
構造検証レポート
Validation report summary of 5fbt
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2025-12-31に公開中

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