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9C0M

FphH, Staphylococcus aureus fluorophosphonate-binding serine hydrolases H, apo form 2 at room temperature

9C0M の概要
エントリーDOI10.2210/pdb9c0m/pdb
分子名称Alpha/beta fold hydrolase, CALCIUM ION (3 entities in total)
機能のキーワードfphh, staphylococcus aureus, s. aureus, fluorophosphonate-binding, serine hydrolases, lipase, room temperature, humidity, humidifier, hydrolase
由来する生物種Staphylococcus aureus USA300-CA-263
タンパク質・核酸の鎖数1
化学式量合計28495.93
構造登録者
Fellner, M. (登録日: 2024-05-26, 公開日: 2025-01-08, 最終更新日: 2025-04-16)
主引用文献Fellner, M.,Randall, G.,Bitac, I.R.C.G.,Warrender, A.K.,Sethi, A.,Jelinek, R.,Kass, I.
Similar but Distinct-Biochemical Characterization of the Staphylococcus aureus Serine Hydrolases FphH and FphI.
Proteins, 93:1009-1021, 2025
Cited by
PubMed Abstract: Staphylococcus aureus is a major cause of infections like bacteremia, pneumonia, and endocarditis. These infections are often linked to the ability of S. aureus to form biofilms. Several S. aureus serine hydrolases have previously been identified to be active during biofilm-forming conditions. Here, we present the biochemical characterization of two of these enzymes-fluorophosphonate binding hydrolase H and I (FphH, FphI). Cryogenic and room-temperature X-ray crystallography, enzymatic substrate profiling, small-angle X-ray scattering analysis, and molecular dynamics simulations provide new insights into similarities and differences between these two hydrolase_4 domain family members. We discover that these enzymes share an overall fold, including a flexible lid or cap region above the active site, which can be seen to be mobile in solution. Differences in the active site pocket and lid residues differentiate them and explain speed differences in their carboxyesterase substrate profile toward small unbranched carbon chain ester molecules. The first analysis of FphI is also compared to our previous knowledge of FphH and its association to stress conditions. These results enable the future precise targeting of Fph serine hydrolase family members with a long-term goal to significantly improve the health and wellbeing of individuals and populations worldwide.
PubMed: 39726198
DOI: 10.1002/prot.26785
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.5 Å)
構造検証レポート
Validation report summary of 9c0m
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2026-04-15に公開中

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