3WI7

Crystal Structure of the Novel Haloalkane Dehalogenase DatA from Agrobacterium tumefaciens C58

3WI7 の概要

• エントリーDOI: 10.2210/pdb3wi7/pdb
• 関連するPDBエントリー: 3WIB
• 分子名称: Haloalkane dehalogenase, 2-[N-CYCLOHEXYLAMINO]ETHANE SULFONIC ACID, GLYCEROL, ... (4 entities in total)
• 機能のキーワード: haloalkane dehalogenase, hydrolase fold family, hydrolase
• 由来する生物種: Agrobacterium tumefaciens
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 69667.89

構造登録者

Guan, L.J.,Yabuki, H.,Okai, M.,Ohtsuka, J.,Tanokura, M. (登録日: 2013-09-06, 公開日: 2014-07-23, 最終更新日: 2024-05-29)

主引用文献

Guan, L.,Yabuki, H.,Okai, M.,Ohtsuka, J.,Tanokura, M.
Crystal structure of the novel haloalkane dehalogenase DatA from Agrobacterium tumefaciens C58 reveals a special halide-stabilizing pair and enantioselectivity mechanism.
Appl.Microbiol.Biotechnol., 98:8573-8582, 2014

PubMed Abstract: A novel haloalkane dehalogenase DatA from Agrobacterium tumefaciens C58 belongs to the HLD-II subfamily and hydrolyzes brominated and iodinated compounds, leading to the generation of the corresponding alcohol, a halide ion, and a proton. Because DatA possesses a unique Asn-Tyr pair instead of the Asn-Trp pair conserved among the subfamily members, which was proposed to keep the released halide ion stable, the structural basis for its reaction mechanism should be elucidated. Here, we determined the crystal structures of DatA and its Y109W mutant at 1.70 and 1.95 Å, respectively, and confirmed the location of the active site by using its novel competitive inhibitor. The structural information from these two crystal structures and the docking simulation suggested that (i) the replacement of the Asn-Tyr pair with the Asn-Trp pair increases the binding affinity for some halogenated compounds, such as 1,3-dibromopropane, mainly due to the electrostatic interaction between Trp109 and halogenated compounds and the change of substrate-binding mode caused by the interaction and (ii) the primary halide-stabilizing residue is only Asn43 in the wild-type DatA, while Tyr109 is a secondary halide-stabilizing residue. Furthermore, docking simulation using the crystal structures of DatA indicated that its enantioselectivity is determined by the large and small spaces around the halogen-binding site.

PubMed: 24770384
DOI: 10.1007/s00253-014-5751-2

実験手法

X-RAY DIFFRACTION (1.7 Å)