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The selectivity of galardin and an azasugar-based hydroxamate compound for human matrix metalloproteases and bacterial metalloproteases
Inhibitors targeting bacterial enzymes should not interfere with enzymes of the host, and knowledge about structural determinants for selectivity is important for designing inhibitors with a therapeutic potential. We have determined the binding strengths of two hydroxamate compounds, galardin and co...
Autores principales: | Sylte, Ingebrigt, Dawadi, Rangita, Malla, Nabin, von Hofsten, Susannah, Nguyen, Tra-Mi, Solli, Ann Iren, Berg, Eli, Adekoya, Olayiwola A., Svineng, Gunbjørg, Winberg, Jan-Olof |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6075749/ https://www.ncbi.nlm.nih.gov/pubmed/30075004 http://dx.doi.org/10.1371/journal.pone.0200237 |
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