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8RPJ

JanthE from Janthinobacterium sp. HH01

8RPJ の概要
エントリーDOI10.2210/pdb8rpj/pdb
分子名称Thiamine pyrophosphate-binding protein, THIAMINE DIPHOSPHATE, FLAVIN-ADENINE DINUCLEOTIDE, ... (10 entities in total)
機能のキーワードthdp, fad, transferase
由来する生物種Janthinobacterium sp. HH01
タンパク質・核酸の鎖数6
化学式量合計416803.57
構造登録者
Lanza, L.,Leogrande, C.,Rabe von Pappenheim, F.,Tittmann, K.,Mueller, M. (登録日: 2024-01-16, 公開日: 2024-06-12, 最終更新日: 2024-08-21)
主引用文献Lanza, L.,Rabe von Pappenheim, F.,Bjarnesen, D.,Leogrande, C.,Paul, A.,Krug, L.,Tittmann, K.,Muller, M.
Identification and Characterization of Thiamine Diphosphate-Dependent Lyases with an Unusual CDG Motif.
Angew.Chem.Int.Ed.Engl., 63:e202404045-e202404045, 2024
Cited by
PubMed Abstract: The thiamine diphosphate (ThDP)-binding motif, characterized by the canonical GDG(X)N sequence, is highly conserved among ThDP-dependent enzymes. We investigated a ThDP-dependent lyase (JanthE from Janthinobacterium sp. HH01) with an unusual cysteine (C458) replacing the first glycine of this motif. JanthE exhibits a high substrate promiscuity and accepts long aliphatic α-keto acids as donors. Sterically hindered aromatic aldehydes or non-activated ketones are acceptor substrates, giving access to a variety of secondary and tertiary alcohols as carboligation products. The crystal structure solved at a resolution of 1.9 Å reveals that C458 is not primarily involved in cofactor binding as previously thought for the canonical glycine. Instead, it coordinates methionine 406, thus ensuring the integrity of the active site and the enzyme activity. In addition, we have determined the long-sought genuine tetrahedral intermediates formed with pyruvate and 2-oxobutyrate in the pre-decarboxylation states and deciphered the atomic details for their stabilization in the active site. Collectively, we unravel an unexpected role for the first residue of the ThDP-binding motif and unlock a family of lyases that can perform valuable carboligation reactions.
PubMed: 38874074
DOI: 10.1002/anie.202404045
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.9 Å)
構造検証レポート
Validation report summary of 8rpj
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2024-10-30に公開中

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