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6D9F

Protein 60 with aldehyde deformylating oxidase activity from Kitasatospora setae

6D9F の概要
エントリーDOI10.2210/pdb6d9f/pdb
分子名称Putative VlmB homolog, FE (III) ION, SULFATE ION, ... (5 entities in total)
機能のキーワードferritin-like, lyase
由来する生物種Kitasatospora setae (strain ATCC 33774 / DSM 43861 / JCM 3304 / KCC A-0304 / NBRC 14216 / KM-6054) (Streptomyces setae)
タンパク質・核酸の鎖数2
化学式量合計74503.66
構造登録者
Arenas, R.,Wilson, D.K.,Mak, W.S.,Siegel, J.B. (登録日: 2018-04-28, 公開日: 2019-05-08, 最終更新日: 2024-03-13)
主引用文献Mak, W.S.,Wang, X.,Arenas, R.,Cui, Y.,Bertolani, S.,Deng, W.Q.,Tagkopoulos, I.,Wilson, D.K.,Siegel, J.B.
Discovery, Design, and Structural Characterization of Alkane-Producing Enzymes across the Ferritin-like Superfamily.
Biochemistry, 59:3834-3843, 2020
Cited by
PubMed Abstract: To complement established rational and evolutionary protein design approaches, significant efforts are being made to utilize computational modeling and the diversity of naturally occurring protein sequences. Here, we combine structural biology, genomic mining, and computational modeling to identify structural features critical to aldehyde deformylating oxygenases (ADOs), an enzyme family that has significant implications in synthetic biology and chemoenzymatic synthesis. Through these efforts, we discovered latent ADO-like function across the ferritin-like superfamily in various species of Bacteria and Archaea. We created a machine learning model that uses protein structural features to discriminate ADO-like activity. Computational enzyme design tools were then utilized to introduce ADO-like activity into the small subunit of class I ribonucleotide reductase. The integrated approach of genomic mining, structural biology, molecular modeling, and machine learning has the potential to be utilized for rapid discovery and modulation of functions across enzyme families.
PubMed: 32935984
DOI: 10.1021/acs.biochem.0c00665
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.03 Å)
構造検証レポート
Validation report summary of 6d9f
検証レポート(詳細版)ダウンロードをダウンロード

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件を2025-02-05に公開中

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