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• W2896495928 abstract "Chlamydia trachomatis (C.t) is a gram-negative obligate intracellular bacteria, which is a major causative of infectious blindness and sexually transmitted diseases. A surge in multidrug resistance among chlamydial species has posed a challenge to adopt alternative drug targeting strategies. Recently, in C.t, L,L-diaminopimelate aminotransferase (CtDAP-AT) is proven to be a potential drug target due its essential role in cell survival and host nonspecificity. Hence, in this study, a multilevel precision-based virtual screening of CtDAP-AT was performed to identify potential inhibitors, wherein, an integrative stringent scoring and filtration were performed by coupling, glide docking score, binding free energy, ADMET (absorption, distribution, metabolism, and excretion, toxicity) prediction, density functional theory (quantum mechanics), and molecular dynamics simulation (molecular mechanics). On cumulative analysis, NSC_5485 (1,3-bis((7-chloro-4-quinolinyl)amino)-2-propanol) was found to be the most potential lead, as it showed higher order significance in terms of binding affinity, bonded interactions, favorable ADMET, chemical reactivity, and greater stabilization during complex formation. This is the first report on prioritization of small molecules from National Cancer Institute (NCI) and Maybridge data sets (341 519 compounds) towards targeting CtDAP-AT. Thus, the proposed compound shall aid in effective combating of a broad spectrum of C.t infections as it surpassed all the levels of prioritization." @default.
• W2896495928 created "2018-10-26" @default.
• W2896495928 creator A5069194917 @default.
• W2896495928 creator A5077785645 @default.
• W2896495928 date "2018-10-10" @default.
• W2896495928 modified "2023-10-16" @default.
• W2896495928 title "Identification of potential drugs targeting L,L‐diaminopimelate aminotransferase of Chlamydia trachomatis : An integrative pharmacoinformatics approach" @default.
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• W2896495928 doi "https://doi.org/10.1002/jcb.27553" @default.
• W2896495928 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30302805" @default.
• W2896495928 hasPublicationYear "2018" @default.
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