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Unique fold and active site in cytomegalovirus protease

Nature volume 383, pages 275279 (19 September 1996) | Download Citation

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Abstract

HUMAN herpesviruses are responsible for a variety of diseases. They are divided into three subfamilies: alpha includes herpes simplex viruses (HSV-1 and HSV-2) and varicella-zoster virus (VZV); beta includes cytomegalovirus (CMV) and human herpes-virus-6 (HHV-6); and gamma includes Epstein–Barr virus (EBV).Each virus encodes a serine protease that is essential for its replication1–14 and is a potential target for therapeutic intervention. Human CMV is a ubiquitous opportunistic pathogen that can result in life-threatening infections in congenitally infected infants, immunocompromised individuals and immuno-suppressed cancer or transplant patients15. Here we report the crystal structure of human CMV protease at 2.5 Å resolution. The structure reveals a fold that has not been reported for any other serine protease, and an active site consisting of a novel catalytic triad in which the third member is a histidine instead of an aspartic acid, or possibly a catalytic tetrad consisting of a serine, two histidines and an aspartic acid. An unusual dimer interface that is important to the protease activity has also been identified.

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Author information

Affiliations

  1. Department of Macromolecular Sciences, SmithKline Beecham Pharmaceuticals, 709 Swedeland Road, King of Prussia, Pennsylvania 19406, USA

    • Xiayang Qiu
    • , Susan S. Hoog
    • , Ward W. Smith
    •  & Sherin S. Abdel-Meguid
  2. Department of Protein Biochemistry, SmithKline Beecham Pharmaceuticals, 709 Swedeland Road, King of Prussia, Pennsylvania 19406, USA

    • Jeffrey S. Culp
    • , Brian Hellmig
    •  & Cheryl A. Janson
  3. Department of Molecular Genetics, SmithKline Beecham Pharmaceuticals, 709 Swedeland Road, King of Prussia, Pennsylvania 19406, USA

    • Anthony G. DiLella

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https://doi.org/10.1038/383275a0

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