A zinc binding site in viral serine proteinases

Raffaele De Francesco, Andrea Urbani, Maria Chiara Nardi, Licia Tomei, Christian Steinkühler, Anna Tramontano

Research output: Contribution to journalArticle

Abstract

The NS3 protein of hepatitis C virus contains a chymotrypsin-like serine proteinase domain. We built a homology model of this domain which predicts the presence of a tetradentate metal binding site formed by three cysteines and one histidine. These residues are strictly conserved in all known hepatitis C viral genotypes as well as in other recently discovered related hepatitis viruses. We show that the hepatitis C virus enzyme does indeed contain a Zn2+ ion with S3N ligation and that the metal is required for structural integrity and activity of the enzyme. Strikingly, the residues forming the metal binding site are also conserved in the chymotrypsin-like 2A cysteine proteinases of picornaviruses. Remarkably, in these highly variable vital genomes the metal binding site is more conserved than the catalytic residues and thus allows us to define a novel class of zinc binding chymotrypsin-like proteinases and to identify a new attractive target for antiviral therapy.

Original languageEnglish
Pages (from-to)13282-13287
Number of pages6
JournalBiochemistry
Volume35
Issue number41
DOIs
Publication statusPublished - 1996

ASJC Scopus subject areas

  • Biochemistry

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    De Francesco, R., Urbani, A., Nardi, M. C., Tomei, L., Steinkühler, C., & Tramontano, A. (1996). A zinc binding site in viral serine proteinases. Biochemistry, 35(41), 13282-13287. https://doi.org/10.1021/bi9616458