7DN1

Hetero-oligomers of SCR-SCR2 crystal structure with NADPH

7DN1 の概要

• エントリーDOI: 10.2210/pdb7dn1/pdb
• 分子名称: Carbonyl Reductase, (S)-specific carbonyl reductase, NADPH DIHYDRO-NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE, ... (4 entities in total)
• 機能のキーワード: rossman fold, tetramer, tag-free, wild type with nadph, oxidoreductase
• 由来する生物種: Candida parapsilosis (Yeast); 詳細
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 61804.57

構造登録者

Li, Y.H.,Zhang, R.Z.,Forouhar, F.,Wang, C.,Montelione, G.T.,Szyperski, T.,Xu, Y.,Hunt, J.F. (登録日: 2020-12-08, 公開日: 2022-04-06, 最終更新日: 2023-11-29)

主引用文献

Li, Y.,Zhang, R.,Wang, C.,Forouhar, F.,Clarke, O.B.,Vorobiev, S.,Singh, S.,Montelione, G.T.,Szyperski, T.,Xu, Y.,Hunt, J.F.
Oligomeric interactions maintain active-site structure in a noncooperative enzyme family.
Embo J., 41:e108368-e108368, 2022

PubMed Abstract: The evolutionary benefit accounting for widespread conservation of oligomeric structures in proteins lacking evidence of intersubunit cooperativity remains unclear. Here, crystal and cryo-EM structures, and enzymological data, demonstrate that a conserved tetramer interface maintains the active-site structure in one such class of proteins, the short-chain dehydrogenase/reductase (SDR) superfamily. Phylogenetic comparisons support a significantly longer polypeptide being required to maintain an equivalent active-site structure in the context of a single subunit. Oligomerization therefore enhances evolutionary fitness by reducing the metabolic cost of enzyme biosynthesis. The large surface area of the structure-stabilizing oligomeric interface yields a synergistic gain in fitness by increasing tolerance to activity-enhancing yet destabilizing mutations. We demonstrate that two paralogous SDR superfamily enzymes with different specificities can form mixed heterotetramers that combine their individual enzymological properties. This suggests that oligomerization can also diversify the functions generated by a given metabolic investment, enhancing the fitness advantage provided by this architectural strategy.

PubMed: 35801308
DOI: 10.15252/embj.2021108368

実験手法

X-RAY DIFFRACTION (1.74 Å)