8A90

Crystal structure of FrsH

8A90 の概要

• エントリーDOI: 10.2210/pdb8a90/pdb
• 分子名称: Non-heme diiron monooxygenase, ACETATE ION, GLYCEROL, ... (6 entities in total)
• 機能のキーワード: nrps, oxidoreductase
• 由来する生物種: Chromobacterium vaccinii
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 121196.19

構造登録者

Schneberger, N.,Wirtz, D.A.,Cruesemann, M.,Hagelueken, G. (登録日: 2022-06-27, 公開日: 2023-07-12, 最終更新日: 2025-10-01)

主引用文献

Wirtz, D.A.,Schneberger, N.,Kloppel, S.,Richarz, R.,Geyer, M.,Konig, G.M.,Hagelueken, G.,Crusemann, M.
Adenylation Domain-Guided Recruitment of Trans- Acting Nonheme Monooxygenases in Nonribosomal Peptide Biosynthesis.
Acs Chem.Biol., 18:1748-1759, 2023

PubMed Abstract: Nonheme diiron monooxygenases (NHDMs) interact with nonribosomal peptide synthetase (NRPS) assembly lines to install β-hydroxylations at thiolation-domain-bound amino acids during nonribosomal peptide biosynthesis. The high potential of this enzyme family to diversify the products of engineered assembly lines is disproportionate to the currently small knowledge about their structures and mechanisms of substrate recognition. Here, we report the crystal structure of FrsH, the NHDM which catalyzes the β-hydroxylation of l-leucines during biosynthesis of the depsipeptide G protein inhibitor FR900359. Using biophysical approaches, we provide evidence that FrsH interacts with the cognate monomodular NRPS FrsA. By AlphaFold modeling and mutational studies, we detect and examine structural features within the assembly line crucial to recruit FrsH for leucine β-hydroxylation. These are, in contrast to cytochrome-dependent NRPS β-hydroxylases, not located on the thiolation domain, but on the adenylation domain. FrsH can be functionally substituted by homologous enzymes from biosyntheses of the cell-wall-targeting antibiotics lysobactin and hypeptin, indicating that these features are generally applicable to members of the family of acting NHDMs. These insights give important directions for the construction of artificial assembly lines to yield bioactive and chemically complex peptide products.

PubMed: 37366538
DOI: 10.1021/acschembio.3c00106

実験手法

X-RAY DIFFRACTION (2.574 Å)