Ambarwati, Yuli and Martoprawiro, Muhamad A. and Mulyani, Irma and Onggo, Djulia (2017) Docking Interaction of Protein Tyrosine Phosphatase and Complex Chromium(III) Nicotinate Compounds. Jurnal Kimia Valensi, 3 (2). ISSN 2460-6065
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Abstract
Docking simulation is important in the process of drug design. This study aims to understand the interaction between Chromium(III) nicotinate [Cr(O-nic)2(OH-) (H2O)3] and [Cr(N-nic)2(OH-)(H2O)3] with the position of trans and cis as a substrate with receptors Protein Tyrosine Phosphatase (PTP). The chromium(III) nicotinic complexes an antidiabetic supplements that have been demonstrated in vitro, to determine the role of chromium(III) nicotinic as a supplement antidiabetic learned through the docking mechanism. The optimization of the complex structure of chromium(III) nicotinic using Gaussian 09, the docking process is performed using Autodock Vina. The docking results showed that trans[Cr(O-nic)2(OH-)(H2O)3] position interact with Leu(13), Gly(14), Cys(17), Arg(18), Trp(49) and Asn(50) with the interaction energy is -6.5 kcal/mol. As for the structure model cis[Cr(O-nic)2(OH-)(H2O)3] have -6.1 kcal/mol interaction energy and the amino acid Ile(16), Trp(49), Asn(50), Arg(53), Asp(56) and Tyr(131). The similary things at model of N-coordinated to Cr with trans[Cr(N-nic)2(OH-)(H2O)3] position interact with amino acids Leu(13), Ser(47), Trp(49), Asn(50) and Tyr(131) the interaction energy is -6.5 kcal/mol. The ONIOM calculation showed the bond between the complexes of chromium(III) nicotinic with PTP is hydrogen bonding. The best interactions with the receptor is structure models trans[Cr(O-nic)2(OH-)(H2O)3] with the lowest interaction energy interaction.
Item Type: | Article |
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Subjects: | Q Science > QD Chemistry |
Divisions: | Fakultas Matematika dan Ilmu Pengetahuan Alam (FMIPA) > Prodi Kimia |
Depositing User: | Dr YULI AMBARWATI |
Date Deposited: | 16 Nov 2017 02:25 |
Last Modified: | 16 Nov 2017 02:25 |
URI: | http://repository.lppm.unila.ac.id/id/eprint/4430 |
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