Sialidases: Structures, biological significance and therapeutic potential

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Abstract

The structure-based design of a potent inhibitor of the influenza-virus neuraminidase (sialidase) is one of the outstanding successes of rational drug design. Recent clinical trials of the drug have stimulated many companies to seek a share of the potentially huge flu market. Sialidases, however, are involved in the pathogenesis of a whole range of other diseases, so perhaps the knowledge and expertise gained from the influenza story can be used in the design of other drugs, given that they all share certain structural features.

Original languageEnglish
Pages (from-to)830-837
Number of pages8
JournalCurrent Opinion in Structural Biology
Volume6
Issue number6
Publication statusPublished - Dec 1996

Keywords

  • INFLUENZA-VIRUS NEURAMINIDASE
  • CRUZI TRANS-SIALIDASE
  • VIBRIO-CHOLERAE NEURAMINIDASE
  • HEMAGGLUTININ-NEURAMINIDASE
  • 4-GUANIDINO-2,4-DIDEOXY-2,3-DEHYDRO-N-ACETYLNEURAMINIC ACID
  • BACTERIAL SIALIDASE
  • CRYSTAL-STRUCTURE
  • INHIBITORS
  • CELL
  • SEQUENCES

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