6KFB

Hydroxynitrile lyase from the millipede, Chamberlinius hualienensis bound with thiocyanate

6KFB の概要

• エントリーDOI: 10.2210/pdb6kfb/pdb
• 分子名称: Hydroxynitrile lyase, alpha-L-fucopyranose-(1-6)-2-acetamido-2-deoxy-beta-D-glucopyranose, THIOCYANATE ION, ... (4 entities in total)
• 機能のキーワード: hydroxynitrile lyase, lipocalin fold, four disulfide bonds, dimer, lyase
• 由来する生物種: Chamberlinius hualienensis
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 18666.68

構造登録者

Motojima, F.,Izumi, A.,Asano, Y. (登録日: 2019-07-07, 公開日: 2020-07-08, 最終更新日: 2023-11-22)

主引用文献

Motojima, F.,Izumi, A.,Nuylert, A.,Zhai, Z.,Dadashipour, M.,Shichida, S.,Yamaguchi, T.,Nakano, S.,Asano, Y.
R-hydroxynitrile lyase from the cyanogenic millipede, Chamberlinius hualienensis-A new entry to the carrier protein family Lipocalines.
Febs J., 288:1679-1695, 2021

PubMed Abstract: Hydroxynitrile lyases (HNLs) catalyze the cleavage of cyanohydrin into cyanide and the corresponding aldehyde or ketone. Moreover, they catalyze the synthesis of cyanohydrin in the reverse reaction, utilized in industry for preparation of enantiomeric pure pharmaceutical ingredients and fine chemicals. We discovered a new HNL from the cyanogenic millipede, Chamberlinius hualienensis. The enzyme displays several features including a new primary structure, high stability, and the highest specific activity in (R)-mandelonitrile ((R)-MAN) synthesis (7420 U·mg ) among the reported HNLs. In this study, we elucidated the crystal structure and reaction mechanism of natural ChuaHNL in ligand-free form and its complexes with acetate, cyanide ion, and inhibitors (thiocyanate or iodoacetate) at 1.6, 1.5, 2.1, 1.55, and 1.55 Å resolutions, respectively. The structure of ChuaHNL revealed that it belongs to the lipocalin superfamily, despite low amino acid sequence identity. The docking model of (R)-MAN with ChuaHNL suggested that the hydroxyl group forms hydrogen bonds with R38 and K117, and the nitrile group forms hydrogen bonds with R38 and Y103. The mutational analysis showed the importance of these residues in the enzymatic reaction. From these results, we propose that K117 acts as a base to abstract a proton from the hydroxyl group of cyanohydrins and R38 acts as an acid to donate a proton to the cyanide ion during the cleavage reaction of cyanohydrins. The reverse mechanism would occur during the cyanohydrin synthesis. (Photo: Dr. Yuko Ishida) DATABASES: Structural data are available in PDB database under the accession numbers 6JHC, 6KFA, 6KFB, 6KFC, and 6KFD.

PubMed: 32679618
DOI: 10.1111/febs.15490

実験手法

X-RAY DIFFRACTION (1.55 Å)