Article ID Journal Published Year Pages File Type
10962195 Tuberculosis 2015 6 Pages PDF
Abstract
Our results indicate that ubiA is involved in EMB resistance in M. tuberculosis and that ubiA mutations that caused elevated DPA levels may be responsible for EMB resistance. The essentiality of UbiA, its involvement in EMB resistance, and lack of human homologs make UbiA an attractive target for new drug development.
Related Topics
Life Sciences Immunology and Microbiology Applied Microbiology and Biotechnology
Authors
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