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TargetThymidine kinase, cytosolic
LigandBDBM21868
Substrate/Competitorn/a
Meas. Tech.ChEMBL_208011 (CHEMBL816091)
Ki 2060±n/a nM
Citation Xu, HMaga, GFocher, FSmith, ERSpadari, SGambino, JWright, GE Synthesis, properties, and pharmacokinetic studies of N2-phenylguanine derivatives as inhibitors of herpes simplex virus thymidine kinases. J Med Chem38:49-57 (1995) [PubMed]
More Info.:Get all data from this article,  Assay Method
 
Thymidine kinase, cytosolic
Name:Thymidine kinase, cytosolic
Synonyms:KITH_HUMAN | TK1
Type:PROTEIN
Mol. Mass.:25476.50
Organism:Homo sapiens (Human)
Description:ChEMBL_1333884
Residue:234
Sequence:
MSCINLPTVLPGSPSKTRGQIQVILGPMFSGKSTELMRRVRRFQIAQYKCLVIKYAKDTR
YSSSFCTHDRNTMEALPACLLRDVAQEALGVAVIGIDEGQFFPDIVEFCEAMANAGKTVI
VAALDGTFQRKPFGAILNLVPLAESVVKLTAVCMECFREAAYTKRLGTEKEVEVIGGADK
YHSVCRLCYFKKASGQPAGPDNKENCPVPGKPGEAVAARKLFAPQQILQCSPAN
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BDBM21868
n/a
NameBDBM21868
Synonyms:2-amino-9-(4-hydroxybutyl)-6,9-dihydro-3H-purin-6-one | 9-(4-hydroxybutyl)guanine | CHEMBL258513 | HBG
TypeSmall organic molecule
Emp. Form.C9H13N5O2
Mol. Mass.223.2318
SMILESNc1nc2n(CCCCO)cnc2c(=O)[nH]1
Structure
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