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9U01

De novo TIM barrel with Kemp eliminase activity - KempTIM1 (apo)

9U01 の概要
エントリーDOI10.2210/pdb9u01/pdb
関連するPDBエントリー9TZD
分子名称KempTIM1, 1,2-ETHANEDIOL (3 entities in total)
機能のキーワードkemp eliminase, de novo, tim barrel, de novo protein
由来する生物種synthetic construct
タンパク質・核酸の鎖数1
化学式量合計23903.06
構造登録者
Kriegel, M.,Beck, J.,Chica, R.A.,Hocker, B. (登録日: 2026-01-26, 公開日: 2026-06-24, 最終更新日: 2026-07-01)
主引用文献Beck, J.,Smith, B.J.,Kriegel, M.,Zarifi, N.,Freund, E.,Harsha, A.G.,Hartmann, J.,Chica, R.A.,Hocker, B.
Customizing the structure of minimal TIM barrels to craft efficient de novo enzymes.
Nat.Chem.Biol., 2026
Cited by
PubMed Abstract: The TIM barrel is the most prevalent fold in natural enzymes, supporting efficient catalysis of diverse reactions. While de novo TIM barrels have been designed, their minimalistic architecture lacks structural elements essential for substrate binding and catalysis. Here, we present CANVAS, a computational workflow that introduces a structural lid into a minimal de novo TIM barrel to anchor catalytic residues and form an active site. Starting from two scaffolds, we designed nine variants with tailored lids for the Kemp elimination. Four showed measurable activity, with the most active reaching a catalytic efficiency of 21,000 M s. A cocrystal structure with a transition-state analog confirmed the accuracy of the designed lid and active site. Using the structure of a lower-activity variant, we applied ensemble-based design, increasing catalytic efficiency >1,600-fold to 32,000 M s. These results demonstrate that de novo TIM barrels can be endowed with efficient catalytic function, establishing a platform for building enzymes from minimal protein scaffolds.
PubMed: 42297966
DOI: 10.1038/s41589-026-02250-w
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.25 Å)
構造検証レポート
Validation report summary of 9u01
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2026-07-08に公開中

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