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TargetThymidine kinase
LigandBDBM21870
Substrate/CompetitorBDBM21867
Meas. Tech.Thymidine Kinase Inhibition Assay
pH7.5±n/a
Temperature310.15±n/a K
IC50 750±n/a nM
Km1000±n/a nM
Citation Manikowski, AVerri, ALossani, AGebhardt, BMGambino, JFocher, FSpadari, SWright, GE Inhibition of herpes simplex virus thymidine kinases by 2-phenylamino-6-oxopurines and related compounds: structure-activity relationships and antiherpetic activity in vivo. J Med Chem48:3919-29 (2005) [PubMed]  Article
More Info.:Get all data from this article,   Solution Info,  Assay Method
 
Thymidine kinase
Name:Thymidine kinase
Synonyms:TK
Type:Transferase
Mol. Mass.:40915.49
Organism:Human herpesvirus 1
Description:O72346
Residue:376
Sequence:
MASYPCHQHASAFDQAARSRGHSNRRTALRPRRQQEATEVRPEQKMPTLLRVYIDGPHGM
GKTTTTQLLVALGSRDDIVYVPEPMTYWRVLGASETIANIYTTQHRLDQGEISAGDAAVV
MTSAQITMGMPYAVTDAVLAPHIGGEAGSSHAPPPALTLIFDRHPIAALLCYPAARYLMG
SMTPQAVLAFVALIPPTLPGTNIVLGALPEDRHIDRLAKRQRPGERLDLAMLAAIRRVYG
LLANTVRYLQGGGSWREDWGQLSGTAVPPQGAEPQSNAGPRPHIGDTLFTLFRAPELLAP
NGDLYNVFAWALDVLAKRLRPMHVFILDYDQSPAGCRDALLQLTSGMVQTHVTTPGSIPT
ICDLARTFAREMGEAN
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  Blast E-value cutoff:
BDBM21870
BDBM21867
NameBDBM21870
Synonyms:2,9-disubstituted 6-oxopurine, 4 | 9-(4-hydroxybutyl)-2-phenoxy-6,9-dihydro-3H-purin-6-one
TypeSmall organic molecule
Emp. Form.C15H16N4O3
Mol. Mass.300.3125
SMILESOCCCCn1cnc2c1nc(Oc1ccccc1)[nH]c2=O
Structure
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