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7OJ2

Bacillus subtilis IMPDH in complex with Ap4A

7OJ2 の概要
エントリーDOI10.2210/pdb7oj2/pdb
分子名称Inosine-5'-monophosphate dehydrogenase,Inosine-5'-monophosphate dehydrogenase, PHOSPHATE ION, GLYCEROL, ... (4 entities in total)
機能のキーワードimp dehydrogenase, delta cbs mutant, signaling protein
由来する生物種Bacillus subtilis (strain 168)
詳細
タンパク質・核酸の鎖数1
化学式量合計41479.03
構造登録者
Giammarinaro, P.I.,Bange, G. (登録日: 2021-05-13, 公開日: 2022-09-14, 最終更新日: 2024-01-31)
主引用文献Giammarinaro, P.I.,Young, M.K.M.,Steinchen, W.,Mais, C.N.,Hochberg, G.,Yang, J.,Stevenson, D.M.,Amador-Noguez, D.,Paulus, A.,Wang, J.D.,Bange, G.
Diadenosine tetraphosphate regulates biosynthesis of GTP in Bacillus subtilis.
Nat Microbiol, 7:1442-1452, 2022
Cited by
PubMed Abstract: Diadenosine tetraphosphate (Ap4A) is a putative second messenger molecule that is conserved from bacteria to humans. Nevertheless, its physiological role and the underlying molecular mechanisms are poorly characterized. We investigated the molecular mechanism by which Ap4A regulates inosine-5'-monophosphate dehydrogenase (IMPDH, a key branching point enzyme for the biosynthesis of adenosine or guanosine nucleotides) in Bacillus subtilis. We solved the crystal structure of BsIMPDH bound to Ap4A at a resolution of 2.45 Å to show that Ap4A binds to the interface between two IMPDH subunits, acting as the glue that switches active IMPDH tetramers into less active octamers. Guided by these insights, we engineered mutant strains of B. subtilis that bypass Ap4A-dependent IMPDH regulation without perturbing intracellular Ap4A pools themselves. We used metabolomics, which suggests that these mutants have a dysregulated purine, and in particular GTP, metabolome and phenotypic analysis, which shows increased sensitivity of B. subtilis IMPDH mutant strains to heat compared with wild-type strains. Our study identifies a central role for IMPDH in remodelling metabolism and heat resistance, and provides evidence that Ap4A can function as an alarmone.
PubMed: 35953658
DOI: 10.1038/s41564-022-01193-x
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.76 Å)
構造検証レポート
Validation report summary of 7oj2
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2026-02-11に公開中

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