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Insight into HIV of IFN-induced myxovirus resistance 2 (MX2) expressed by traditional Chinese medicine.
- Source :
-
BioMed research international [Biomed Res Int] 2014; Vol. 2014, pp. 871576. Date of Electronic Publication: 2014 Jun 18. - Publication Year :
- 2014
-
Abstract
- Recently, an important topic of the acquired immunodeficiency syndrome (AIDS) had been published in 2013. In this report, the expression of the IFN-induced myxovirus resistance 2 (MX2) had been defined the function to kill the human immunodeficiency virus (HIV). The screening from the Traditional Chinese Medicine (TCM) database by simulating molecular docking and molecular dynamics could select candidate compounds, which may express MX2 against HIV. Saussureamine C, Crotalaburnine, and Precatorine are selected based on the highest docking score and other TCM compounds. The data from molecular dynamics are helpful in the analysis and detection of protein-ligand interactions. According to the docking poses, hydrophobic interactions, and hydrogen bond with structure variations, this research could assess the interaction between protein and ligand interaction. In addition to the detection of TCM compound efficacy, we suggest that Saussureamine C is better than the others in protein-ligand interaction and the structural variation to express MX2.
- Subjects :
- Acquired Immunodeficiency Syndrome genetics
Acquired Immunodeficiency Syndrome virology
Asparagine analogs & derivatives
Asparagine chemistry
Asparagine therapeutic use
Drugs, Chinese Herbal therapeutic use
Gene Expression Regulation drug effects
HIV drug effects
HIV genetics
Humans
Ligands
Molecular Docking Simulation
Molecular Dynamics Simulation
Myxovirus Resistance Proteins antagonists & inhibitors
Pyrrolizidine Alkaloids chemistry
Pyrrolizidine Alkaloids therapeutic use
Tryptophan analogs & derivatives
Tryptophan chemistry
Tryptophan therapeutic use
Acquired Immunodeficiency Syndrome drug therapy
Drugs, Chinese Herbal chemistry
Medicine, Chinese Traditional
Myxovirus Resistance Proteins biosynthesis
Subjects
Details
- Language :
- English
- ISSN :
- 2314-6141
- Volume :
- 2014
- Database :
- MEDLINE
- Journal :
- BioMed research international
- Publication Type :
- Academic Journal
- Accession number :
- 25045710
- Full Text :
- https://doi.org/10.1155/2014/871576