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February 2, 2026Journal of Biomolecular Structure and Dynamics0 citations

In silico screening of UM-C162 and UM-4E as potential inhibitors of  Staphylococcus aureus virulence factors

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LQLujin Al QuwatliPPPrateek PaulJCJ. Chong

Key Points

  • The aim is to assess the inhibitory potential of UM-C162 and UM-4E against Staphylococcus aureus virulence factors.
  • Applied molecular docking and molecular dynamics simulations.
  • Evaluated interactions with key virulence factors like alpha toxin and sortase A.
  • Conducted 100 ns molecular dynamics simulations for selected complexes.
  • UM-4E exhibited the lowest binding energy scores and stronger binding affinity.
  • Molecular dynamics simulations showed stable complex conformations for UM-4E and UM-C162.
  • Key residues critical for interactions were identified in the complexes.

Abstract

Staphylococcus aureus (S. aureus) is one of the main pathogens responsible for both hospital-acquired and community-acquired infections. The rising prevalence of antibiotic resistance has shifted research focus towards alternative therapeutic strategies particularly anti-virulence agents. Unlike conventional antibiotics, these compounds target bacterial virulence factors without exerting bactericidal pressure, thereby reducing the risk of resistance development. Small-molecule inhibitors such as UM-4E and UM-C162 have emerged as promising candidates for this approach. This study applied molecular docking and molecular dynamics (MD) simulations to evaluate the inhibitory potential of UM-4E and UM-C162 against key virulence factors of S. aureus, namely alpha toxin (Hla), sortase A (SrtA), accessory gene regulator A (AgrA), and V8 protease (SspA). Docking analysis revealed that UM-4E consistently achieved the lowest binding energy scores across all receptors, followed by UM-C162. Subsequently, 100 ns MD simulations were performed for UM-4E-Hla and UM-C162-Hla complexes, showing stable and compact conformations throughout. Residue decomposition analysis highlighted VAL149 and THR109 as major contributors in UM-4E-Hla interactions, while PRO151, ILE107, and VAL149 played key roles in UM-C162-Hla. Overall, UM-4E demonstrated stronger binding affinity, stability, and residue-level interactions, suggesting its potential as a preferential Hla inhibitor. These computational findings provide a strong computational basis but warrant further validation through in vitro assays.

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Cite This Study

Quwatli et al. (2026) studied this question.

synapsesocial.com/papers/6980fcd6c1c9540dea80e9a9https://doi.org/10.1080/07391102.2026.2619888
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