AI Article Synopsis
- Staphylococcus aureus is a gram-positive bacterium that causes a range of infections, making it a significant health concern.
- FtsZ, a key protein involved in bacterial cell division, was identified as a promising target for developing new antibiotics, leading to a structure-based screening of chemical compounds.
- Four lead compounds (C ID 16284, 25916, 15894, 13403) were selected based on their docking scores and molecular dynamics simulations, providing a basis for further experimental studies on FtsZ-related drug development.
Article Abstract
The gram-positive bacterium Staphylococcus aureus, responsible for a wide variety of diseases in human involve all organ systems ranging from localized skin infections to life-threatening systemic infections. FtsZ, the key protein of bacterial cell division was selected as a potent anti bacterial target. In order to identify the new compounds structure based screening process was carried out. An enrichment study was performed to select a suitable scoring function and to retrieve potential candidates against FtsZ from a large chemical database. The docking score and docking energy values were compared and their atomic interaction was also evaluated. Furthermore molecular dynamics simulation were also been performed to check the stability and the amino acids interacted towards the FtsZ. Finally we selected C ID 16284, 25916, 15894, 13403 as better lead compounds. From these results, we conclude that our insilico results will provide a framework for the detailed in vitro and in vivo studies about the FtsZ protein activity in drug development process.
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