4KQR
CRYSTAL STRUCTURE OF PENICILLIN-BINDING PROTEIN 3 FROM PSEUDOMONAS AERUGINOSA IN COMPLEX WITH (5S)-Penicilloic Acid
Summary for 4KQR
Entry DOI | 10.2210/pdb4kqr/pdb |
Related | 4KQO 4KQQ |
Descriptor | Penicillin-binding protein 3, (2S,4S)-2-[(R)-carboxy{[(2R)-2-{[(4-ethyl-2,3-dioxopiperazin-1-yl)carbonyl]amino}-2-phenylacetyl]amino}methyl]-5,5-dimethyl-1,3-thiazolidine-4-carboxylic acid, CHLORIDE ION, ... (6 entities in total) |
Functional Keywords | penicillin-binding proteins, piperacillin, (5s)-penicilloic acid, cell wall biosynthesis, transpeptidase, out periplasmic membrane, biosynthetic protein, biosynthetic protein-antibiotic complex, biosynthetic protein/antibiotic |
Biological source | Pseudomonas aeruginosa |
Total number of polymer chains | 2 |
Total formula weight | 124589.69 |
Authors | Nettleship, J.E.,Stuart, D.I.,Owens, R.J.,Ren, J. (deposition date: 2013-05-15, release date: 2013-11-06, Last modification date: 2023-09-20) |
Primary citation | van Berkel, S.S.,Nettleship, J.E.,Leung, I.K.,Brem, J.,Choi, H.,Stuart, D.I.,Claridge, T.D.,McDonough, M.A.,Owens, R.J.,Ren, J.,Schofield, C.J. Binding of (5S)-Penicilloic Acid to Penicillin Binding Protein 3. Acs Chem.Biol., 8:2112-2116, 2013 Cited by PubMed Abstract: β-Lactam antibiotics react with penicillin binding proteins (PBPs) to form relatively stable acyl-enzyme complexes. We describe structures derived from the reaction of piperacillin with PBP3 (Pseudomonas aeruginosa) including not only the anticipated acyl-enzyme complex but also an unprecedented complex with (5S)-penicilloic acid, which was formed by C-5 epimerization of the nascent (5R)-penicilloic acid product. Formation of the complex was confirmed by solution studies, including NMR. Together, these results will be useful in the design of new PBP inhibitors and raise the possibility that noncovalent PBP inhibition by penicilloic acids may be of clinical relevance. PubMed: 23899657DOI: 10.1021/cb400200h PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.01 Å) |
Structure validation
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