8JKU

Ancestral imine reductase N559

8JKU の概要

• エントリーDOI: 10.2210/pdb8jku/pdb
• 分子名称: Ancestral imine reductase N559, NADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE (3 entities in total)
• 機能のキーワード: ancestral protein, nadph-dependent oxidoreductase, de novo protein
• 由来する生物種: synthetic construct
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 63208.43

構造登録者

Zhu, X.X.,Zheng, G.W. (登録日: 2023-06-01, 公開日: 2023-08-09, 最終更新日: 2024-12-11)

主引用文献

Zhu, X.X.,Zheng, W.Q.,Xia, Z.W.,Chen, X.R.,Jin, T.,Ding, X.W.,Chen, F.F.,Chen, Q.,Xu, J.H.,Kong, X.D.,Zheng, G.W.
Evolutionary insights into the stereoselectivity of imine reductases based on ancestral sequence reconstruction.
Nat Commun, 15:10330-10330, 2024

PubMed Abstract: The stereoselectivity of enzymes plays a central role in asymmetric biocatalytic reactions, but there remains a dearth of evolution-driven biochemistry studies investigating the evolutionary trajectory of this vital property. Imine reductases (IREDs) are one such enzyme that possesses excellent stereoselectivity, and stereocomplementary members are pervasive in the family. However, the regulatory mechanism behind stereocomplementarity remains cryptic. Herein, we reconstruct a panel of active ancestral IREDs and trace the evolution of stereoselectivity from ancestors to extant IREDs. Combined with coevolution analysis, we reveal six historical mutations capable of recapitulating stereoselectivity evolution. An investigation of the mechanism with X-ray crystallography shows that they collectively reshape the substrate-binding pocket to regulate stereoselectivity inversion. In addition, we construct an empirical fitness landscape and discover that epistasis is prevalent in stereoselectivity evolution. Our findings emphasize the power of ASR in circumventing the time-consuming large-scale mutagenesis library screening for identifying mutations that change functions and support a Darwinian premise from a molecular perspective that the evolution of biological functions is a stepwise process.

PubMed: 39609402
DOI: 10.1038/s41467-024-54613-3

実験手法

X-RAY DIFFRACTION (2.57 Å)