2W4I
Crystal structure of Helicobacter pylori glutamate racemase in complex with D-Glutamate and an inhibitor
Summary for 2W4I
Entry DOI | 10.2210/pdb2w4i/pdb |
Related | 2JFX 2JFY 2JFZ |
Descriptor | GLUTAMATE RACEMASE, D-GLUTAMIC ACID, 1-[(3S)-5-PHENYL-3-THIOPHEN-2-YL-3H-1,4-BENZODIAZEPIN-2-YL]AZETIDIN-3-OL, ... (4 entities in total) |
Functional Keywords | isomerase, cell shape, glutamate racemase, cell wall biogenesis/degradation, peptidoglycan synthesis, peptidoglycan biosynthesis |
Biological source | HELICOBACTER PYLORI |
Total number of polymer chains | 4 |
Total formula weight | 115464.23 |
Authors | Lundqvist, T. (deposition date: 2008-11-25, release date: 2008-12-09, Last modification date: 2023-12-13) |
Primary citation | Geng, B.,Basarab, G.,Comita-Prevoir, J.,Gowravaram, M.,Hill, P.,Kiely, A.,Loch, J.,MacPherson, L.,Morningstar, M.,Mullen, G.,Osimboni, E.,Satz, A.,Eyermann, C.,Lundqvist, T. Potent and selective inhibitors of Helicobacter pylori glutamate racemase (MurI): pyridodiazepine amines. Bioorg. Med. Chem. Lett., 19:930-936, 2009 Cited by PubMed: 19097892DOI: 10.1016/j.bmcl.2008.11.113 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.87 Å) |
Structure validation
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