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  1. Investigation of the mycobacterial enzyme HsaD as a potential novel target for anti-tubercular agents using a fragment-based drug design approach
  2. The role of apolipoprotein N-acyl transferase, Lnt, in the lipidation of factor H binding protein of Neisseria meningitidis strain MC58 and its potential as a drug target
  3. Azoreductases in drug metabolism
  4. Mechanism-based inhibition of HsaD: a C-C bond hydrolase essential for survival ofMycobacterium tuberculosisin macrophage