In Silico Docking of HNF-1a Receptor Ligands

Abstract EN

Background.

HNF-1a is a transcription factor that regulates glucose metabolism by expression in various tissues.

Aim.

To dock potential ligands of HNF-1a using docking software in silico.

Methods.

We performed in silico studies using HNF-1a protein 2GYP·pdb and the following softwares: ISIS/Draw 2.5SP4, ARGUSLAB 4.0.1, and HEX5.1.

Observations.

The docking distances (in angstrom units: 1 angstrom unit (Å) = 0.1 nanometer or 1 × 10−10 metres) with ligands in decreasing order are as follows: resveratrol (3.8 Å), aspirin (4.5 Å), stearic acid (4.9 Å), retinol (6.0 Å), nitrazepam (6.8 Å), ibuprofen (7.9 Å), azulfidine (9.0 Å), simvastatin (9.0 Å), elaidic acid (10.1 Å), and oleic acid (11.6 Å).

Conclusion.

HNF-1a domain interacted most closely with resveratrol and aspirin