5M17

Structure of the GH99 endo-alpha-mannanase from Bacteroides xylanisolvens in complex with mannose-alpha-1,3-1,2-dideoxymannose

Summary for 5M17

• Entry DOI: 10.2210/pdb5m17/pdb
• Related: 4AD1 4AD2 4AD3 4AD4 4AD5 4UTF 4V27 4V28
• Descriptor: Glycosyl hydrolase family 71, alpha-D-mannopyranose-(1-3)-1,5-anhydro-2-deoxy-D-arabino-hexitol, 1,2-ETHANEDIOL, ... (5 entities in total)
• Functional Keywords: endomannanase, endomannosidase, gh99, n-glycosylation, glycosylation, inhibitor, inhibition, shape, charge, mannobiose, mannose, glycobiology, hydrolase
• Biological source: Bacteroides xylanisolvens XB1A
• Total number of polymer chains: 1
• Total formula weight: 44427.07

Authors

Petricevic, M.,Sobala, L.F.,Fernandes, P.Z.,Raich, L.,Thompson, A.J.,Bernardo-Seisdedos, G.,Millet, O.,Zhu, S.,Sollogoub, M.,Rovira, C.,Jimenez-Barbero, J.,Davies, G.J.,Williams, S.J. (deposition date: 2016-10-07, release date: 2017-01-11, Last modification date: 2024-01-17)

Primary citation

Petricevic, M.,Sobala, L.F.,Fernandes, P.Z.,Raich, L.,Thompson, A.J.,Bernardo-Seisdedos, G.,Millet, O.,Zhu, S.,Sollogoub, M.,Jimenez-Barbero, J.,Rovira, C.,Davies, G.J.,Williams, S.J.
Contribution of Shape and Charge to the Inhibition of a Family GH99 endo-alpha-1,2-Mannanase.
J. Am. Chem. Soc., 139:1089-1097, 2017

PubMed Abstract: Inhibitor design incorporating features of the reaction coordinate and transition-state structure has emerged as a powerful approach for the development of enzyme inhibitors. Such inhibitors find use as mechanistic probes, chemical biology tools, and therapeutics. Endo-α-1,2-mannosidases and endo-α-1,2-mannanases, members of glycoside hydrolase family 99 (GH99), are interesting targets for inhibitor development as they play key roles in N-glycan maturation and microbiotal yeast mannan degradation, respectively. These enzymes are proposed to act via a 1,2-anhydrosugar "epoxide" mechanism that proceeds through an unusual conformational itinerary. Here, we explore how shape and charge contribute to binding of diverse inhibitors of these enzymes. We report the synthesis of neutral dideoxy, glucal and cyclohexenyl disaccharide inhibitors, their binding to GH99 endo-α-1,2-mannanases, and their structural analysis by X-ray crystallography. Quantum mechanical calculations of the free energy landscapes reveal how the neutral inhibitors provide shape but not charge mimicry of the proposed intermediate and transition state structures. Building upon the knowledge of shape and charge contributions to inhibition of family GH99 enzymes, we design and synthesize α-Man-1,3-noeuromycin, which is revealed to be the most potent inhibitor (K 13 nM for Bacteroides xylanisolvens GH99 enzyme) of these enzymes yet reported. This work reveals how shape and charge mimicry of transition state features can enable the rational design of potent inhibitors.

PubMed: 27992199
DOI: 10.1021/jacs.6b10075

Experimental method

X-RAY DIFFRACTION (1.03 Å)