Reaction Details |
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Target | Thymidine kinase, cytosolic |
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Ligand | BDBM50131907 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_208213 (CHEMBL815478) |
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Ki | 280000±n/a nM |
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Citation | Vanheusden, V; Munier-Lehmann, H; Froeyen, M; Dugué, L; Heyerick, A; De Keukeleire, D; Pochet, S; Busson, R; Herdewijn, P; Van Calenbergh, S 3'-C-branched-chain-substituted nucleosides and nucleotides as potent inhibitors of Mycobacterium tuberculosis thymidine monophosphate kinase. J Med Chem46:3811-21 (2003) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Thymidine kinase, cytosolic |
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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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BDBM50131907 |
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n/a |
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Name | BDBM50131907 |
Synonyms: | Phosphoric acid mono-[3-aminomethyl-4-hydroxy-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-2-ylmethyl] ester |
Type | Small organic molecule |
Emp. Form. | C11H16N3O8P |
Mol. Mass. | 349.2349 |
SMILES | Cc1cn([C@@H]2O[C@H](COP([O-])([O-])=O)[C@@H](CN)[C@H]2O)c(=O)[nH]c1=O |
Structure |
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