PDB ID: 6B1W
Hetero Atom Contents
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SO4 | Sulfate ion | PoSSuM | |||
CL | Chloride ion | PoSSuM | |||
C8V | (2s,5r)-1-formyl-N'-[(3r)-piperidine-3-carbonyl]-5-[(sulfooxy)amino]piperidine-2-carbohydrazide | PoSSuM |
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Download interaction data: 6B1W
Structure summary
Code : | 6B1W PDBj RCSB PDB PDBe | ||||||||||||
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Header : | HYDROLASE/HYDROLASE Inhibitor | ||||||||||||
Title : | Crystal structure KPC-2 beta-lactamase complexed with WCK 5107 by co-crystallization | ||||||||||||
Release Data : | 2018-08-01 | ||||||||||||
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Authors : | van den Akker, F., Nguyen, N.Q. | ||||||||||||
Keywords : | Inhibitor, complex, HYDROLASE, HYDROLASE-HYDROLASE Inhibitor complex | ||||||||||||
Exp. method : | X-RAY DIFFRACTION ( 1.7300 Å ) | ||||||||||||
Citation : |
Strategic Approaches to Overcome Resistance against Gram-Negative Pathogens Using beta-Lactamase Inhibitors and beta-Lactam Enhancers: Activity of Three Novel Diazabicyclooctanes WCK 5153, Zidebactam (WCK 5107), and WCK 4234.
Papp-Wallace, K.M.,Nguyen, N.Q.,Jacobs, M.R.
et al.
PubMed: 29627985 |
Reaction
Chain : | A, B | ||||||||
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UniProt : | Q9F663 (BLKPC_KLEPN) | ||||||||
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