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2Q9N

4-Substituted Trinems as Broad Spectrum-Lactamase Inhibitors: Structure-based Design, Synthesis and Biological Activity

Summary for 2Q9N
Entry DOI10.2210/pdb2q9n/pdb
Related1XX2
DescriptorBeta-lactamase, (1S,4R,7AR)-4-BUTOXY-1-[(1R)-1-FORMYLPROPYL]-2,4,5,6,7,7A-HEXAHYDRO-1H-ISOINDOLE-3-CARBOXYLIC ACID (3 entities in total)
Functional Keywordsbeta-lactamase inhibitor, tricyclic carbapenem, hydrolase
Biological sourceEnterobacter cloacae
Cellular locationPeriplasm (By similarity): P05364
Total number of polymer chains1
Total formula weight39349.92
Authors
Primary citationPlantan, I.,Selic, L.,Mesar, T.,Anderluh, P.S.,Oblak, M.,Prezelj, A.,Hesse, L.,Andrejasic, M.,Vilar, M.,Turk, D.,Kocijan, A.,Prevec, T.,Vilfan, G.,Kocjan, D.,Copar, A.,Urleb, U.,Solmajer, T.
4-Substituted Trinems as Broad Spectrum beta-Lactamase Inhibitors: Structure-Based Design, Synthesis, and Biological Activity
J.Med.Chem., 50:4113-4121, 2007
Cited by
PubMed: 17665896
DOI: 10.1021/jm0703237
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.2 Å)
Structure validation

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