6PWL
ADC-7 in complex with boronic acid transition state inhibitor LP06
Summary for 6PWL
Entry DOI | 10.2210/pdb6pwl/pdb |
Descriptor | Beta-lactamase, (7Z)-7-(2-amino-1,3-thiazol-4-yl)-1,1,3-trihydroxy-10,10-dimethyl-1,6-dioxo-2,9-dioxa-5,8-diaza-1lambda~5~-phospha-3-boraundec-7-en-11-oic acid, GLYCINE, ... (4 entities in total) |
Functional Keywords | inhibitor, beta-lactamase, batsi, adc-7., hydrolase |
Biological source | Acinetobacter baumannii |
Total number of polymer chains | 4 |
Total formula weight | 164949.47 |
Authors | Curtis, B.C.,Powers, R.A.,Wallar, B.J. (deposition date: 2019-07-23, release date: 2020-10-21, Last modification date: 2023-10-11) |
Primary citation | Curtis, B.N.,Smolen, K.A.,Barlow, S.J.,Caselli, E.,Prati, F.,Taracila, M.A.,Bonomo, R.A.,Wallar, B.J.,Powers, R.A. Structural Insights into Inhibition of the Acinetobacter-Derived Cephalosporinase ADC-7 by Ceftazidime and Its Boronic Acid Transition State Analog. Antimicrob.Agents Chemother., 64:-, 2020 Cited by PubMed: 32988830DOI: 10.1128/AAC.01183-20 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.67 Å) |
Structure validation
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