DETAILED INSIGHT INTO THE STRUCTURE AND BIOACTIVITY OF THYMOCARTIN, AS A POTENTIAL ANTICANCER AND ANTIBACTERIAL AGENT, THROUGH CONFORMATIONAL AND VIBRATIONAL ANALYSIS, MOLECULAR DOCKING, AND MOLECULAR DYNAMICS STUDIES


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ER A., ÇELİK S., ÖZEL A., AKYÜZ S.

BULLETIN OF THE CHEMICAL SOCIETY OF ETHIOPIA, cilt.40, sa.2, ss.319-339, 2026 (SCI-Expanded, Scopus) identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 40 Sayı: 2
  • Basım Tarihi: 2026
  • Doi Numarası: 10.4314/bcse.v40i2.5
  • Dergi Adı: BULLETIN OF THE CHEMICAL SOCIETY OF ETHIOPIA
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Directory of Open Access Journals
  • Sayfa Sayıları: ss.319-339
  • İstanbul Üniversitesi Adresli: Evet

Özet

Thymocartin, also known as Thymopoietin II (32-35), is a tetrapeptide fragment (Arg-Lys-Asp-Val) of thymopoietin with immunomodulatory properties. In this study, thymocartin was thoroughly examined for its structural features and antibacterial, antiviral, and anticancer activities. Conformational analysis was performed to investigate its conformational preferences and better understand its biological activity. The most stable conformer identified was optimized using density functional theory (DFT) at the B3LYP/6-311++G(d,p) level. The vibrational wavenumbers of the optimized structure were calculated and compared with experimental data to evaluate the accuracy of the computational structure. The potential of thymocartin as an anticancer agent was explored through molecular docking simulations with E. coli DNA Gyrase B (PDB ID: 6F86) and the epidermal growth factor receptor (EGFR; PDB ID: 4HJO). Following molecular docking, 200 ns all-atom molecular dynamics (MD) simulations were conducted on the top-scoring ligand-receptor complexes involving 4HJO and 6F86, providing further insight into ligand-receptor interactions. Overall, thymocartin showed diverse biological activities, especially antibacterial and anticancer effects.