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  <title>In Silico Analysis of Antibacterial Activity of Fatty Acids in Swietenia humilis Zucc. Seed Extract Against Staphylococcus aureus sortase A enzyme</title>
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  <namePart>Anjar Purba Asmara; Hernawan Hernawan; Cut Nuzlia</namePart>
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  <publisher>Serial JKPK (Jurnal Kimia dan Pendidikan Kimia)&#13;
UNS</publisher>
  <dateIssued></dateIssued>
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  <languageTerm type="code">ind</languageTerm>
  <languageTerm type="text">Indonesia</languageTerm>
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  <extent>Sumber artikel:Jurnal. Halaman: 227-242</extent>
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 <note>Abstract  This study utilised molecular docking to predict the binding affinity of various fatty acids (FAs) found in Swietenia humilis to the sortase A (SrtA) protein target from Staphylococcus aureus. Binding energies  measured in kcal/mol  indicated the strength and stability of ligand-protein interactions  with lower values signifying stronger binding. The binding affinities of eight FAs as the active constituents in n-hexane extract of S. humilis and the positive control  gentamicin  were compared to assess their theoretical antibacterial activity. Palmitoleic acid exhibited the strongest binding affinity (-5.6 kcal/mol) among the FAs  suggesting the highest potential antibacterial activity  followed by linoleic  palmitic  linolenic  arachidic  tricosanoic  stearic  and oleic acids in decreasing order of affinity. Despite having weaker binding energies than gentamicin  a common gram-positive inhibitor from aminoglycoside derivative  FAs showed multiple hydrogen bonds and van der Waals interactions with key residues like ARG197  VAL168  VAL166  and ILE182  contributing to their binding stability. Palmitoleic acid formed multiple hydrogen bonds (ARG197 and GLY119) and significant van der Waals interactions  highlighting its strong theoretical binding. Stearic and oleic acids  although having higher binding energies  also formed critical hydrogen bonds  suggesting moderate potential activity. Gentamicin  s single hydrogen bond suggests a highly specific binding site  which may result in high antibacterial activity despite fewer interaction points. The study indicated that FAs like palmitoleic and oleic acid show substantial potential as supplementary antibacterial agents  especially in the context of combating antibiotic resistance. This finding can pave a path for drug design and development to address the S. aureus  s resistance.      Keywords  fatty acids  Staphylococcus aureus  antibacterial  molecular modelling  sortase A       </note>
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  <topic>1. ASAM LEMAK - PEMODELAN MOLEKULAR</topic>
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 <classification>540 JKP</classification>
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