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TargetThymidine kinase
LigandBDBM50100410
Substrate/Competitorn/a
Meas. Tech.ChEBML_208206
IC50>1000000±n/a nM
Citation Manfredini, SBaraldi, PGDurini, EPorcu, LAngusti, AVertuani, SSolaroli, NDe Clercq, EKarlsson, ABalzarini, J Design, synthesis and enzymatic activity of highly selective human mitochondrial thymidine kinase inhibitors. Bioorg Med Chem Lett11:1329-32 (2001) [PubMed]
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:
BDBM50100410
n/a
NameBDBM50100410
Synonyms:BDBM50206503 | CHEMBL392346 | Pentanoic acid 4-hydroxy-5-hydroxymethyl-2-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl ester
TypeSmall organic molecule
Emp. Form.C15H22N2O7
Mol. Mass.342.3444
SMILESCCCCC(=O)O[C@H]1[C@H](O)[C@@H](CO)O[C@H]1n1cc(C)c(=O)[nH]c1=O
Structure
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