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TargetThymidine phosphorylase
LigandBDBM20048
Substrate/CompetitorBDBM1
Meas. Tech.Enzyme Inhibition Assay
IC50 5400±n/a nM
Citation Nencka, RVotruba, IHrebabecký, HTloust'ová, EHorská, KMasojídková, MHolý, A Design and synthesis of novel 5,6-disubstituted uracil derivatives as potent inhibitors of thymidine phosphorylase. Bioorg Med Chem Lett16:1335-7 (2006) [PubMed]  Article
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Thymidine phosphorylase
Name:Thymidine phosphorylase
Synonyms:TYPH_ECOLI | TdRPase | Thymidine Phosphorylase (TP) | deoA | tpp | ttg
Type:Enzyme
Mol. Mass.:47198.54
Organism:Escherichia coli
Description:n/a
Residue:440
Sequence:
MFLAQEIIRKKRDGHALSDEEIRFFINGIRDNTISEGQIAALAMTIFFHDMTMPERVSLT
MAMRDSGTVLDWKSLHLNGPIVDKHSTGGVGDVTSLMLGPMVAACGGYIPMISGRGLGHT
GGTLDKLESIPGFDIFPDDNRFREIIKDVGVAIIGQTSSLAPADKRFYATRDITATVDSI
PLITASILAKKLAEGLDALVMDVKVGSGAFMPTYELSEALAEAIVGVANGAGVRTTALLT
DMNQVLASSAGNAVEVREAVQFLTGEYRNPRLFDVTMALCVEMLISGKLAKDDAEARAKL
QAVLDNGKAAEVFGRMVAAQKGPTDFVENYAKYLPTAMLTKAVYADTEGFVSEMDTRALG
MAVVAMGGGRRQASDTIDYSVGFTDMARLGDQVDGQRPLAVIHAKDENNWQEAAKAVKAA
IKLADKAPESTPTVYRRISE
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  Blast E-value cutoff:
BDBM20048
BDBM1
NameBDBM20048
Synonyms:5-chloro-6-[3-(hydroxymethyl)piperidin-1-yl]-1,3-diazinane-2,4-dione | uracil, 18
TypeSmall organic molecule
Emp. Form.C10H14ClN3O3
Mol. Mass.259.689
SMILESOCC1CCCN(C1)c1[nH]c(=O)[nH]c(=O)c1Cl
Structure
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