Reference - Detail
| RRC ID | 50864 |
|---|---|
| Author | Taira J, Ito T, Nakatani H, Umei T, Baba H, Kawashima S, Maruoka T, Komatsu H, Sakamoto H, Aoki S. |
| Title | In silico structure-based drug screening of novel antimycobacterial pharmacophores by DOCK-GOLD tandem screening. |
| Journal | Int J Mycobacteriol |
| Abstract |
BACKGROUND:Enzymes responsible for cell wall development in Mycobacterium tuberculosis are considered as potential targets of anti-tuberculosis (TB) agents. Mycobacterial cyclopropane mycolic acid synthase 1 (CmaA1) is essential for mycobacterial survival because of its critical role in synthesizing mycolic acids. MATERIALS AND METHODS:We screened compounds that were capable of interacting with the mycobacterial CmaA1 active site using a virtual compound library with an in silico structure-based drug screening (SBDS). Following the selection of such compounds, their antimycobacterial activity was examined. RESULTS:With the in silico SBDS, for which we also used DOCK-GOLD programs and screening methods that utilized the structural similarity between the selected active compounds, we identified two compounds with potent inhibitory effects on mycobacterial growth. The antimycobacterial effect of the compounds was comparable to that of isoniazid, which is used as a first-line anti-TB drug. CONCLUSION:The compounds identified through SBDS were expected to be a novel class of anti-TB pharmacophores. |
| Volume | 6(2) |
| Pages | 142-148 |
| Published | 2017-1-1 |
| DOI | 10.4103/ijmy.ijmy_24_17 |
| PII | IntJMycobacteriol_2017_6_2_142_206597 |
| PMID | 28559515 |
| MeSH | Antitubercular Agents / chemistry* Antitubercular Agents / pharmacology* Computer Simulation Drug Design Drug Evaluation, Preclinical / methods* Humans Mycobacterium tuberculosis / drug effects* Mycobacterium tuberculosis / enzymology Mycobacterium tuberculosis / genetics Mycobacterium tuberculosis / metabolism Mycolic Acids / metabolism Tuberculosis / microbiology |
| Times Cited | 5 |
| Resource | |
| General Microbes | JCM 20379 |