7TWA

Crystal structure of apo BesC from Streptomyces cattleya

7TWA の概要

• エントリーDOI: 10.2210/pdb7twa/pdb
• 分子名称: 4-chloro-allylglycine synthase, GLYCEROL, ACETATE ION, ... (7 entities in total)
• 機能のキーワード: heme-oxygenase-like diiron oxidase, biosynthetic protein
• 由来する生物種: Streptomyces cattleya
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 119674.66

構造登録者

Neugebauer, M.E.,McBride, M.J.,Boal, A.K.,Chang, M.C.Y. (登録日: 2022-02-07, 公開日: 2022-04-13, 最終更新日: 2024-11-06)

主引用文献

McBride, M.J.,Nair, M.A.,Sil, D.,Slater, J.W.,Neugebauer, M.E.,Chang, M.C.Y.,Boal, A.K.,Krebs, C.,Bollinger Jr., J.M.
Substrate-Triggered mu-Peroxodiiron(III) Intermediate in the 4-Chloro-l-Lysine-Fragmenting Heme-Oxygenase-like Diiron Oxidase (HDO) BesC: Substrate Dissociation from, and C4 Targeting by, the Intermediate.
Biochemistry, 61:689-702, 2022

PubMed Abstract: The enzyme BesC from the -thynyl-l-erine biosynthetic pathway in fragments 4-chloro-l-lysine (produced from l-Lysine by BesD) to ammonia, formaldehyde, and 4-chloro-l-allylglycine and can analogously fragment l-Lys itself. BesC belongs to the emerging family of O-activating non-heme-diiron enzymes with the "heme-oxygenase-like" protein fold (HDOs). Here, we show that the binding of l-Lys or an analogue triggers capture of O by the protein's diiron(II) cofactor to form a blue μ-peroxodiiron(III) intermediate analogous to those previously characterized in two other HDOs, the olefin-installing fatty acid decarboxylase, UndA, and the guanidino--oxygenase domain of SznF. The ∼5- and ∼30-fold faster decay of the intermediate in reactions with 4-thia-l-Lys and (4)-chloro-dl-lysine than in the reaction with l-Lys itself and the primary deuterium kinetic isotope effects (D-KIEs) on decay of the intermediate and production of l-allylglycine in the reaction with 4,4,5,5-[H]-l-Lys suggest that the peroxide intermediate or a reversibly connected successor complex abstracts a hydrogen atom from C4 to enable olefin formation. Surprisingly, the sluggish substrate l-Lys can dissociate after triggering intermediate formation, thereby allowing one of the better substrates to bind and react. The structure of apo BesC and the demonstrated linkage between Fe(II) and substrate binding suggest that the triggering event involves an induced ordering of ligand-providing helix 3 (α3) of the conditionally stable HDO core. As previously suggested for SznF, the dynamic α3 also likely initiates the spontaneous degradation of the diiron(III) product cluster after decay of the peroxide intermediate, a trait emerging as characteristic of the nascent HDO family.

PubMed: 35380785
DOI: 10.1021/acs.biochem.1c00774

実験手法

X-RAY DIFFRACTION (1.7 Å)