Mutation detail:
Mutation site | W225R |
Virus | Varicella-Zoster virus |
Mutation level ![]() |
Amino acid level |
Gene/protein/region type | ORF36 |
Gene ID | 1487667 |
Country | - |
Mutation type ![]() |
nonsynonymous mutation |
Genotype/subtype/clade | - |
Sample ![]() |
cell line |
Variants | - |
Viral reference sequence | AB097933.1 |
Drug/antibody/vaccine | acyclovir-resistant |
Transmissibility ![]() |
- |
Transmission mechanism | - |
Pathogenicity ![]() |
- |
Pathogenicity mechanism | - |
Immune escape mutation | - |
Immune escape mechanism | - |
RT-PCR primers probes | - |
Protein detail:
Protein name | Thymidine Kinase |
Uniprot protein ID | P09250 |
Protein length | 341 amino acids |
Protein description | Thymidine kinase catalyzes the transfer of the gamma-phospho group of ATP to thymidine to generate dTMP in the salvage pathway of pyrimidine synthesis. The dTMP serves as a substrate for DNA polymerase during viral DNA replication. Allows the virus to be reactivated and to grow in non-proliferative cells lacking a high concentration of phosphorylated nucleic acid precursors. |
Literature information:
Pubmed ID | 25712361 |
Clinical information | No |
Disease | - |
Published year | 2015 |
Journal | Antimicrob Agents Chemother |
Title | Drug Resistance of Clinical Varicella-Zoster Virus Strains Confirmed by Recombinant Thymidine Kinase Expression and by Targeted Resistance Mutagenesis of a Cloned Wild-Type Isolate |
Author | Anne-Kathrin Brunnemann,Kathrin Bohn-Wippert,Roland Zell,Andreas Henke,Martin Walther |
Evidence | Further, a selection marker was amplified from the plasmid pEPkan-S and inserted according to the principle of an passant mutagenesis. Single mutations resulting in L73I, A163stop, W225R, T256M, Q303stop, and N334stop were generated using the GeneArt site |