Molecular Docking Senyawa Aktif Ekstrak Daun Melinjo (Gnetum gnemon) dalam Penghambatan Enzim Histidin Dekarboksilase

Nelspon Gazpersz, Rahma El, Muhammad Daswar Ardian Baharudin, Zulaika Izmatul Hawa Bastio, Agnisia Indasari Ipaenin, M. R. Sohilait
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Abstract

Histamine in fish is formed due to histidine decarboxylase which occurs due to decay by bacteria. In the Maluku community, melinjo leaves (Gnetum gnemon) are used as boiled water in processing rotten fish so that the decay process is inhibited. The compound content of melinjo leaves is tethered to the macromolecule decarboxylase PDB ID (4E1O). Test ligands, seven components of melinjo leaves were optimized using Gaussian. Ligands were bound to the receptor with AutoDock-Vina in grid box size and evaluated with Discovery Studio. The tethering results showed no ligand with affinity exceeding the standard ligand. However, three test ligands were close to the standard such as, dehydrovomifoliol affinity -6.7 kcal/mol, inhibition constant 1.2269 x 10-5. P-cumaric acid and gnetumal affinity -6.1 kcal/mol, inhibition constant 3.3778 x 10-5. Amino acid residue interactions showed hydrogen and hydrophobic bonding. The results of the binding affinity of the test ligand have not been able to be equivalent to the affinity of the standard ligand. However, the dehydrovomifoliol ligand is close to the affinity of the standard with a value of -6.7 kcal/mol and an RMSD of 2 Å. Thus, dehydrovomifoliol compounds from melinjo leaves show antihistamine effects as histidine decarboxylase inhibitors with promising potential.
抑制组氨酸脱羧酶的 Melinjo(Gnetum gnemon)叶提取物活性化合物的分子对接研究
鱼肉中的组胺是由组氨酸脱羧酶形成的,而组氨酸脱羧酶是由细菌腐烂引起的。在马鲁古社区,人们在处理腐烂的鱼类时,会使用美林茹叶(Gnetum gnemon)作为开水,以抑制腐烂过程。Melinjo 树叶的化合物含量与大分子脱羧酶 PDB ID (4E1O) 有关。使用高斯对配体进行了测试,优化了瓜子叶中的七种成分。配体用 AutoDock-Vina 以网格框大小与受体结合,并用 Discovery Studio 进行评估。系联结果显示,没有配体的亲和力超过标准配体。不过,三种测试配体的亲和力接近标准配体,如去氢伏马索亲和力-6.7 kcal/mol,抑制常数 1.2269 x 10-5。对-古马酸和 gnetumal 的亲和力为 -6.1 kcal/mol,抑制常数为 3.3778 x 10-5。氨基酸残基的相互作用表现为氢键和疏水键。测试配体的结合亲和力结果无法与标准配体的亲和力相等。因此,美林茹叶中的脱氢木香酚化合物作为组氨酸脱羧酶抑制剂显示出抗组胺作用,具有广阔的应用前景。
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