7UF2

RibB from Vibrio cholera bound with D-xylulose-5-phosphate (D-Xy5P) and manganese

7UF2 の概要

• エントリーDOI: 10.2210/pdb7uf2/pdb
• 分子名称: 3,4-dihydroxy-2-butanone 4-phosphate synthase, 5-O-phosphono-D-xylulose, MANGANESE (II) ION, ... (5 entities in total)
• 機能のキーワード: ribb, riboflavin, 3, 4-dihydroxy-2-butanone 4-phosphate synthase, lyase
• 由来する生物種: Vibrio cholerae
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 23999.14

構造登録者

Kenjic, N.,Meneely, K.M.,Lamb, A.L. (登録日: 2022-03-22, 公開日: 2022-07-20, 最終更新日: 2023-10-18)

主引用文献

Kenjic, N.,Meneely, K.M.,Wherritt, D.J.,Denler, M.C.,Jackson, T.A.,Moran, G.R.,Lamb, A.L.
Evidence for the Chemical Mechanism of RibB (3,4-Dihydroxy-2-butanone 4-phosphate Synthase) of Riboflavin Biosynthesis.
J.Am.Chem.Soc., 144:12769-12780, 2022

PubMed Abstract: RibB (3,4-dihydroxy-2-butanone 4-phosphate synthase) is a magnesium-dependent enzyme that excises the C4 of d-ribulose-5-phosphate (d-Ru5P) as formate. RibB generates the four-carbon substrate for lumazine synthase that is incorporated into the xylene moiety of lumazine and ultimately the riboflavin isoalloxazine. The reaction was first identified by Bacher and co-workers in the 1990s, and their chemical mechanism hypothesis became canonical despite minimal direct evidence. X-ray crystal structures of RibB typically show two metal ions when solved in the presence of non-native metals and/or liganding non-substrate analogues, and the consensus hypothetical mechanism has incorporated this cofactor set. We have used a variety of biochemical approaches to further characterize the chemistry catalyzed by RibB from (VcRibB). We show that full activity is achieved at metal ion concentrations equal to the enzyme concentration. This was confirmed by electron paramagnetic resonance of the enzyme reconstituted with manganese and crystal structures liganded with Mn and a variety of sugar phosphates. Two transient species prior to the formation of products were identified using acid quench of single turnover reactions in combination with NMR for singly and fully C-labeled d-Ru5P. These data indicate that dehydration of C1 forms the first transient species, which undergoes rearrangement by a 1,2 migration, fusing C5 to C3 and generating a hydrated C4 that is poised for elimination as formate. Structures determined from time-dependent Mn soaks of VcRibB-d-Ru5P crystals show accumulation in crystallo of the same intermediates. Collectively, these data reveal for the first time crucial transient chemical states in the mechanism of RibB.

PubMed: 35802469
DOI: 10.1021/jacs.2c03376

実験手法

X-RAY DIFFRACTION (2 Å)