7OR2
Crystal structure of UDP-N-acetylenolpyruvoylglucosamine reductase (MurB) from Pseudomonas aeruginosa in complex with FAD and a pyrazole derivative (fragment 4)
Summary for 7OR2
Entry DOI | 10.2210/pdb7or2/pdb |
Descriptor | UDP-N-acetylenolpyruvoylglucosamine reductase, FLAVIN-ADENINE DINUCLEOTIDE, 5-methyl-1-phenyl-pyrazole-4-carboxylic acid, ... (4 entities in total) |
Functional Keywords | peptidoglycan-biosynthesis fragment based drug discovery, oxidoreductase |
Biological source | Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1) |
Total number of polymer chains | 1 |
Total formula weight | 38753.70 |
Authors | Acebron-Garcia de Eulate, M.,Blundell, T.L.,Kim, S.Y.,Mendes, V.,Abell, C. (deposition date: 2021-06-04, release date: 2021-11-03, Last modification date: 2024-01-31) |
Primary citation | Acebron-Garcia-de-Eulate, M.,Mayol-Llinas, J.,Holland, M.T.O.,Kim, S.Y.,Brown, K.P.,Marchetti, C.,Hess, J.,Di Pietro, O.,Mendes, V.,Abell, C.,Floto, R.A.,Coyne, A.G.,Blundell, T.L. Discovery of Novel Inhibitors of Uridine Diphosphate- N -Acetylenolpyruvylglucosamine Reductase (MurB) from Pseudomonas aeruginosa , an Opportunistic Infectious Agent Causing Death in Cystic Fibrosis Patients. J.Med.Chem., 65:2149-2173, 2022 Cited by PubMed: 35080396DOI: 10.1021/acs.jmedchem.1c01684 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.35 Å) |
Structure validation
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