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TargetThymidine kinase
LigandBDBM50206508
Substrate/Competitorn/a
Meas. Tech.ChEMBL_454748 (CHEMBL886771)
IC50 268000±n/a nM
Citation Ciliberti, NManfredini, SAngusti, ADurini, ESolaroli, NVertuani, SBuzzoni, LBonache, MCBen-Shalom, EKarlsson, ASaada, ABalzarini, J Novel selective human mitochondrial kinase inhibitors: design, synthesis and enzymatic activity. Bioorg Med Chem15:3065-81 (2007) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Thymidine kinase
Name:Thymidine kinase
Synonyms:KITH_VZVD | TK
Type:PROTEIN
Mol. Mass.:37819.99
Organism:Varicella-zoster virus (strain Dumas) (HHV-3) (Human herpesvirus 3)
Description:ChEMBL_444706
Residue:341
Sequence:
MSTDKTDVKMGVLRIYLDGAYGIGKTTAAEEFLHHFAITPNRILLIGEPLSYWRNLAGED
AICGIYGTQTRRLNGDVSPEDAQRLTAHFQSLFCSPHAIMHAKISALMDTSTSDLVQVNK
EPYKIMLSDRHPIASTICFPLSRYLVGDMSPAALPGLLFTLPAEPPGTNLVVCTVSLPSH
LSRVSKRARPGETVNLPFVMVLRNVYIMLINTIIFLKTNNWHAGWNTLSFCNDVFKQKLQ
KSECIKLREVPGIEDTLFAVLKLPELCGEFGNILPLWAWGMETLSNCSRSMSPFVLSLEQ
TPQHAAQELKTLLPQMTPANMSSGAWNILKELVNAVQDNTS
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50206508
n/a
NameBDBM50206508
Synonyms:1-(2'-O-phenylacetyl-beta-D-arabinofuranosyl)-5(E)-(2-bromovinyl)uracil | CHEMBL241407
TypeSmall organic molecule
Emp. Form.C19H19BrN2O7
Mol. Mass.467.267
SMILESOC[C@H]1O[C@H]([C@@H](OC(=O)Cc2ccccc2)[C@@H]1O)n1cc(C=CBr)c(=O)[nH]c1=O |w:22.24|
Structure
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