5NE5
Crystal structure of family 47 alpha-1,2-mannosidase from Caulobacter K31 strain in complex with kifunensine
Summary for 5NE5
Entry DOI | 10.2210/pdb5ne5/pdb |
Descriptor | Mannosyl-oligosaccharide 1,2-alpha-mannosidase, KIFUNENSINE, CALCIUM ION, ... (6 entities in total) |
Functional Keywords | mannosidase glycosidase hydrolysis inhibitor, hydrolase |
Biological source | Caulobacter sp. |
Total number of polymer chains | 1 |
Total formula weight | 51091.25 |
Authors | Males, A.,Davies, G.J. (deposition date: 2017-03-09, release date: 2017-03-29, Last modification date: 2024-05-08) |
Primary citation | Males, A.,Raich, L.,Williams, S.J.,Rovira, C.,Davies, G.J. Conformational Analysis of the Mannosidase Inhibitor Kifunensine: A Quantum Mechanical and Structural Approach. Chembiochem, 18:1496-1501, 2017 Cited by PubMed Abstract: The varied yet family-specific conformational pathways used by individual glycoside hydrolases (GHs) offer a tantalising prospect for the design of tightly binding and specific enzyme inhibitors. A cardinal example of a GH-family-specific inhibitor, and one that finds widespread practical use, is the natural product kifunensine, which is a low-nanomolar inhibitor that is selective for GH family 47 inverting α-mannosidases. Here we show, through quantum-mechanical approaches, that kifunensine is restrained to a "ring-flipped" C conformation with another accessible, but higher-energy, region around the B conformation. The conformations of kifunensine in complex with a range of GH47 enzymes-including an atomic-level resolution (1 Å) structure of kifunensine with Caulobacter sp. CkGH47 reported herein and with GH family 38 and 92 α-mannosidases-were mapped onto the kifunensine free-energy landscape. These studies revealed that kifunensine has the ability to mimic the product state of GH47 enzymes but cannot mimic any conformational states relevant to the reaction coordinate of mannosidases from other families. PubMed: 28493500DOI: 10.1002/cbic.201700166 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.05 Å) |
Structure validation
Download full validation report
