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- W2024269853 abstract "The terminal dipeptide, d-Ala-d-Ala, of the peptidoglycan precursor UDPMurNAc-pentapetide is a crucial building block involved in peptidoglycan cross-linking. It is synthesized in the bacterial cytoplasm by the enzyme d-alanine:d-alanine ligase (Ddl). Structure-based virtual screening of the NCI diversity set of almost 2000 compounds was performed with a DdlB isoform from Escherichia coli using the computational tool AutoDock 4.0. The 130 best-ranked compounds from this screen were tested in an in vitro assay for their inhibition of E. coli DdlB. Three compounds were identified that inhibit the enzyme with Ki values in micromolar range. Two of these also have promising antibacterial activities against Gram-positive and Gram-negative bacteria." @default.
- W2024269853 created "2016-06-24" @default.
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- W2024269853 date "2008-11-14" @default.
- W2024269853 modified "2023-09-27" @default.
- W2024269853 title "Discovery of New Inhibitors of <scp>d</scp>-Alanine:<scp>d</scp>-Alanine Ligase by Structure-Based Virtual Screening" @default.
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- W2024269853 doi "https://doi.org/10.1021/jm800726b" @default.
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