Structure of a type II thymidine kinase with bound dTTP

Authors:
  • LSLeonardo Scapozza
    Leonardo Scapozza
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Abstract
The structure of human cytosolic thymidine kinase in complex with its feedback inhibitor 2′‐deoxythymidine‐5′‐triphosphate was determined. This structure is the first representative of the type II thymidine kinases found in several pathogens. The structure deviates strongly from the known structures of type I thymidine kinases such as the Herpes simplex enzyme. It contains a zinc‐binding domain with four cysteines complexing a structural zinc ion. Interestingly, the backbone atoms of the type II enzyme bind thymine via hydrogen‐bonds, in contrast to type I, where side chains are involved. This results in a specificity difference exploited for antiviral therapy. The presented structure will foster the development of new drugs and prodrugs for numerous therapeutic applications.

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