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TargetThymidine kinase
LigandBDBM21876
Substrate/CompetitorBDBM21867
Meas. Tech.Thymidine Kinase Inhibition Assay
pH7.5±n/a
Temperature310.15±n/a K
IC50 1000±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:
BDBM21876
BDBM21867
NameBDBM21876
Synonyms:2,9-disubstituted 6-oxopurine, 10 | 4-[6-oxo-2-(phenylamino)-6,9-dihydro-3H-purin-9-yl]butanoic acid
TypeSmall organic molecule
Emp. Form.C15H15N5O3
Mol. Mass.313.3113
SMILESOC(=O)CCCn1cnc2c1nc(Nc1ccccc1)[nH]c2=O
Structure
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