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11LH

OgOGA IN COMPLEX WITH LIGAND 7

This is a non-PDB format compatible entry.
Summary for 11LH
Entry DOI10.2210/pdb11lh/pdb
DescriptorProtein O-GlcNAcase, N~4~-butyl-N~2~-(2,6-dichlorophenyl)pyridine-2,4-diamine (3 entities in total)
Functional Keywordsglycoside hydrolase, inhibitor, hydrolase, hydrolase-inhibitor complex, hydrolase/inhibitor
Biological sourceOceanicola granulosus HTCC2516
Total number of polymer chains1
Total formula weight50552.94
Authors
Shaffer, P.L. (deposition date: 2026-03-03, release date: 2026-07-01)
Primary citationBouton, J.,Bretteville, A.,Tresadern, G.,Shaffer, P.,Austin, N.,Buijnsters, P.,Cedervall, E.P.,Darville, N.,Fonteyn, I.,Leenaerts, J.,Lamenca, C.M.,Mertens, L.,Peeters, D.,Velter, A.I.,Roosbroeck, Y.V.,Ebneth, A.,Bartolome, J.M.,Trabanco, A.A.,Oehlrich, D.
Discovery of 5‐Azaindole Inhibitors of O‐GlcNAcase for the Treatment of Alzheimer's Disease and Related Tauopathies.
Acs Med.Chem.Lett., 17:1096-1105, 2026
Cited by
PubMed Abstract: Alzheimer's disease (AD) is a neurodegenerative disorder characterized by extracellular amyloid-β plaque accumulation and intracellular tau neurofibrillary tangles, with tau pathology correlating more closely with cognitive decline. Modulation of tau phosphorylation through the regulation of O-GlcNAcylation, a post-translational modification controlled by O-GlcNAcase (OGA), represents a promising therapeutic strategy. In this study, we report the optimization of a pyrimidine hit identified by high-throughput screening, leading to the discovery and optimization of a novel series of 5-azaindole-based OGA inhibitors. From this series, compound was identified as an tool candidate that demonstrated a favorable pharmacokinetic profile and measurable brain exposure. Pharmacodynamic studies in murine models demonstrated that compound induced a significant and transient elevation of brain O-GlcNAcylation levels, confirming the target engagement. These findings underscore the potential of 5-azaindole-based OGA inhibitors as a novel validated chemotype for modulation of O-GlcNAcylation.
PubMed: 42157845
DOI: 10.1021/acsmedchemlett.6c00017
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.44 Å)
Structure validation

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PDB entries from 2026-07-01

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