9LF7
A PAE-hydrolyse Poc14
9LF7 の概要
| エントリーDOI | 10.2210/pdb9lf7/pdb |
| 分子名称 | Poc14_A, 2-(N-MORPHOLINO)-ETHANESULFONIC ACID (3 entities in total) |
| 機能のキーワード | esterase, pae-hydrolyzing, hydrolysis, alpha/beita hydrolyse, hydrolase |
| 由来する生物種 | Erythrobacter cryptus DSM 12079 |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 71872.47 |
| 構造登録者 | |
| 主引用文献 | Rong, Z.,Hong, L.G.,Huo, Y.Y.,Li, J.,Zheng, D.Q.,Ha, Y.,Fan, J.,Xu, X.W.,Wu, Y.H. Molecular Insight Into the Hydrolysis of Phthalate Esters by a Family IV Esterase. Environ.Microbiol., 27:e70134-e70134, 2025 Cited by PubMed Abstract: Phthalate esters (PAEs) are prevalent environmental contaminants, with their biodegradation efficiently driven by microorganisms through ester bond hydrolysis. This study investigates the mechanism of Poc14, a novel family IV esterase, using x-ray crystallography, bioinformatics, biochemistry and site-directed mutagenesis. Phylogenetic analysis classifies Poc14 as a family IV esterase with conserved catalytic motifs crucial for its activity. Poc14 retains over 80% activity at 50°C for 4 h and tolerates up to 5% methanol or DMF, though surfactants like Tweens inhibit its function. Poc14 activity is independent of metal ions, and the addition of EDTA further enhances its activity by approximately 130%. The 1.8 Å crystal structure reveals a CAP domain and two substrate channels. Enzyme assays show Poc14 hydrolyses short-chain diethyl phthalate (DEP) (K = 0.068 mM, V = 9975 μM/min/mg) but not long-chain di(2-ethylhexyl) phthalate (DEHP) due to steric hindrance. Molecular docking assessed Poc14's potential to hydrolyse DEP and DEHP after residue mutations, resulting in the Poc14-AAG variant. Poc14-AAG could hydrolyse one bond of DEHP and diester bonds of DEP. Our study positions Poc14 as a promising enzyme for environmental remediation, with potential for optimising DEHP degradation and exploring dimerisation effects. PubMed: 40600832DOI: 10.1111/1462-2920.70134 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.8 Å) |
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