6FWL

Structure of an E333Q variant of the GH99 endo-alpha-mannanase from Bacteroides xylanisolvens in complex alpha-Glc-1,3-(1,2-anhydro-carba-mannose)

6FWL の概要

• エントリーDOI: 10.2210/pdb6fwl/pdb
• 関連するPDBエントリー: 6FWG 6FWI 6FWJ 6FWM 6FWO 6FWP 6FWQ
• 分子名称: Glycosyl hydrolase family 71, ACETATE ION, (1~{S},2~{S},3~{R},4~{R},6~{R})-4-(hydroxymethyl)-7-oxabicyclo[4.1.0]heptane-2,3-diol, ... (5 entities in total)
• 機能のキーワード: hydrolase
• 由来する生物種: Bacteroides xylanisolvens XB1A
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 44391.02

構造登録者

Sobala, L.F.,Speciale, G.,Hakki, Z.,Fernandes, P.Z.,Raich, L.,Rojas-Cervellera, V.,Bennet, A.,Thompson, A.J.,Bernardo-Seisdedos, G.,Millet, O.,Zhu, S.,Lu, D.,Sollogoub, M.,Rovira, C.,Jimenez-Barbero, J.,Davies, G.J.,Williams, S.J. (登録日: 2018-03-06, 公開日: 2019-09-18, 最終更新日: 2024-01-17)

主引用文献

Sobala, L.F.,Speciale, G.,Zhu, S.,Raich, L.,Sannikova, N.,Thompson, A.J.,Hakki, Z.,Lu, D.,Shamsi Kazem Abadi, S.,Lewis, A.R.,Rojas-Cervellera, V.,Bernardo-Seisdedos, G.,Zhang, Y.,Millet, O.,Jimenez-Barbero, J.,Bennet, A.J.,Sollogoub, M.,Rovira, C.,Davies, G.J.,Williams, S.J.
An Epoxide Intermediate in Glycosidase Catalysis.
Acs Cent.Sci., 6:760-770, 2020

PubMed Abstract: Retaining glycoside hydrolases cleave their substrates through stereochemical retention at the anomeric position. Typically, this involves two-step mechanisms using either an enzymatic nucleophile via a covalent glycosyl enzyme intermediate or neighboring-group participation by a substrate-borne 2-acetamido neighboring group via an oxazoline intermediate; no enzymatic mechanism with participation of the sugar 2-hydroxyl has been reported. Here, we detail structural, computational, and kinetic evidence for neighboring-group participation by a mannose 2-hydroxyl in glycoside hydrolase family 99 -α-1,2-mannanases. We present a series of crystallographic snapshots of key species along the reaction coordinate: a Michaelis complex with a tetrasaccharide substrate; complexes with intermediate mimics, a sugar-shaped cyclitol β-1,2-aziridine and β-1,2-epoxide; and a product complex. The 1,2-epoxide intermediate mimic displayed hydrolytic and transfer reactivity analogous to that expected for the 1,2-anhydro sugar intermediate supporting its catalytic equivalence. Quantum mechanics/molecular mechanics modeling of the reaction coordinate predicted a reaction pathway through a 1,2-anhydro sugar via a transition state in an unusual flattened, envelope ( ) conformation. Kinetic isotope effects ( / ) for anomeric-H and anomeric-C support an oxocarbenium ion-like transition state, and that for C2-O (1.052 ± 0.006) directly implicates nucleophilic participation by the C2-hydroxyl. Collectively, these data substantiate this unprecedented and long-imagined enzymatic mechanism.

PubMed: 32490192
DOI: 10.1021/acscentsci.0c00111

実験手法

X-RAY DIFFRACTION (1.12 Å)