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3V4E

Crystal Structure of the galactoside O-acetyltransferase in complex with CoA

3V4E の概要
エントリーDOI10.2210/pdb3v4e/pdb
関連するPDBエントリー3FTT
分子名称Galactoside O-acetyltransferase, DI(HYDROXYETHYL)ETHER, TRIETHYLENE GLYCOL, ... (6 entities in total)
機能のキーワードstructural genomics, center for structural genomics of infectious diseases, csgid, galactoside o-acetyltransferase, coa, transferase
由来する生物種Staphylococcus aureus subsp. aureus
タンパク質・核酸の鎖数3
化学式量合計69906.34
構造登録者
主引用文献Luo, H.B.,Knapik, A.A.,Petkowski, J.J.,Demas, M.,Shumilin, I.A.,Zheng, H.,Chruszcz, M.,Minor, W.
Biophysical analysis of the putative acetyltransferase SACOL2570 from methicillin-resistant Staphylococcus aureus.
J.Struct.Funct.Genom., 14:97-108, 2013
Cited by
PubMed Abstract: Methicillin-resistant Staphylococcus aureus (MRSA) is a major cause of a myriad of insidious and intractable infections in humans, especially in patients with compromised immune systems and children. Here, we report the apo- and CoA-bound crystal structures of a member of the galactoside acetyltransferase superfamily from methicillin-resistant S. aureus SACOL2570 which was recently shown to be down regulated in S. aureus grown in the presence of fusidic acid, an antibiotic used to treat MRSA infections. SACOL2570 forms a homotrimer in solution, as confirmed by small-angle X-ray scattering and dynamic light scattering. The protein subunit consists of an N-terminal alpha-helical domain connected to a C-terminal LβH domain. CoA binds in the active site formed by the residues from adjacent LβH domains. After determination of CoA-bound structure, molecular dynamics simulations were performed to model the binding of AcCoA. Binding of both AcCoA and CoA to SACOL2570 was verified by isothermal titration calorimetry. SACOL2570 most likely acts as an acetyltransferase, using AcCoA as an acetyl group donor and an as-yet-undetermined chemical moiety as an acceptor. SACOL2570 was recently used as a scaffold for mutations that lead the generation of cage-like assemblies, and has the potential to be used for the generation of more complex nanostructures.
PubMed: 23963951
DOI: 10.1007/s10969-013-9158-6
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 3v4e
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2026-04-08に公開中

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