2J87
Structure of vaccinia virus thymidine kinase in complex with dTTP: insights for drug design
Summary for 2J87
Entry DOI | 10.2210/pdb2j87/pdb |
Descriptor | THYMIDINE KINASE, THYMIDINE-5'-TRIPHOSPHATE, ZINC ION, ... (4 entities in total) |
Functional Keywords | type 2 thymidine kinase, dna synthesis, nucleotide-binding, dttp, kinase, transferase, atp-binding, vaccinia virus thymidine kinase |
Biological source | VACCINIA VIRUS |
Total number of polymer chains | 4 |
Total formula weight | 82552.37 |
Authors | El Omari, K.,Solaroli, N.,Karlsson, A.,Balzarini, J.,Stammers, D.K. (deposition date: 2006-10-23, release date: 2006-11-13, Last modification date: 2024-11-06) |
Primary citation | El Omari, K.,Solaroli, N.,Karlsson, A.,Balzarini, J.,Stammers, D.K. Structure of Vaccinia Virus Thymidine Kinase in Complex with Dttp: Insights for Drug Design. Bmc Struct.Biol., 6:22-, 2006 Cited by PubMed Abstract: Development of countermeasures to bioterrorist threats such as those posed by the smallpox virus (variola), include vaccination and drug development. Selective activation of nucleoside analogues by virus-encoded thymidine (dThd) kinases (TK) represents one of the most successful strategies for antiviral chemotherapy as demonstrated for anti-herpes drugs. Vaccinia virus TK is a close orthologue of variola TK but also shares a relatively high sequence identity to human type 2 TK (hTK), thus achieving drug selectivity relative to the host enzyme is challenging. PubMed: 17062140DOI: 10.1186/1472-6807-6-22 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (3.1 Å) |
Structure validation
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