7ODJ
Exo-mannosidase from Cellvibrio mixtus bound to N-alkyl mannocyclophellitol aziridine
This is a non-PDB format compatible entry.
Summary for 7ODJ
| Entry DOI | 10.2210/pdb7odj/pdb |
| Descriptor | Man5A, SULFATE ION, ACETATE ION, ... (5 entities in total) |
| Functional Keywords | mannosidase, covalent inhibitor, cyclophellitol, cellvibrio, hydrolase |
| Biological source | Cellvibrio mixtus |
| Total number of polymer chains | 1 |
| Total formula weight | 51004.44 |
| Authors | McGregor, N.G.S.,Davies, G.J. (deposition date: 2021-04-29, release date: 2022-02-16, Last modification date: 2024-10-09) |
| Primary citation | McGregor, N.G.S.,Kuo, C.L.,Beenakker, T.J.M.,Wong, C.S.,Offen, W.A.,Armstrong, Z.,Florea, B.I.,Codee, J.D.C.,Overkleeft, H.S.,Aerts, J.M.F.G.,Davies, G.J. Synthesis of broad-specificity activity-based probes for exo -beta-mannosidases. Org.Biomol.Chem., 20:877-886, 2022 Cited by PubMed Abstract: -β-mannosidases are a broad class of stereochemically retaining hydrolases that are essential for the breakdown of complex carbohydrate substrates found in all kingdoms of life. Yet the detection of -β-mannosidases in complex biological samples remains challenging, necessitating the development of new methodologies. Cyclophellitol and its analogues selectively label the catalytic nucleophiles of retaining glycoside hydrolases, making them valuable tool compounds. Furthermore, cyclophellitol can be readily redesigned to enable the incorporation of a detection tag, generating activity-based probes (ABPs) that can be used to detect and identify specific glycosidases in complex biological samples. Towards the development of ABPs for -β-mannosidases, we present a concise synthesis of β--configured cyclophellitol, cyclophellitol aziridine, and -alkyl cyclophellitol aziridines. We show that these probes covalently label -β-mannosidases from GH families 2, 5, and 164. Structural studies of the resulting complexes support a canonical mechanism-based mode of action in which the active site nucleophile attacks the pseudoanomeric centre to form a stable ester linkage, mimicking the glycosyl enzyme intermediate. Furthermore, we demonstrate activity-based protein profiling using an -alkyl aziridine derivative by specifically labelling MANBA in mouse kidney tissue. Together, these results show that synthetic -configured cyclophellitol analogues hold promise for detecting -β-mannosidases in biological and biomedical research. PubMed: 35015006DOI: 10.1039/d1ob02287c PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (1.3 Å) |
Structure validation
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