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TargetThymidylate synthase
LigandBDBM50316412
Substrate/Competitorn/a
Meas. Tech.ChEMBL_628088 (CHEMBL1107316)
IC50 340±n/a nM
Citation Tangeda, SJGarlapati, A Synthesis of new pyrrolo[2,3-d]pyrimidine derivatives and evaluation of their activities against human colon cancer cell lines. Eur J Med Chem45:1453-8 (2010) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Thymidylate synthase
Name:Thymidylate synthase
Synonyms:TS | TSase | TYMS | TYSY_HUMAN | Thymidylate synthase (TS) | Thymidylate synthase/GAR transformylase/AICAR transformylase
Type:Enzyme
Mol. Mass.:35718.07
Organism:Homo sapiens (Human)
Description:n/a
Residue:313
Sequence:
MPVAGSELPRRPLPPAAQERDAEPRPPHGELQYLGQIQHILRCGVRKDDRTGTGTLSVFG
MQARYSLRDEFPLLTTKRVFWKGVLEELLWFIKGSTNAKELSSKGVKIWDANGSRDFLDS
LGFSTREEGDLGPVYGFQWRHFGAEYRDMESDYSGQGVDQLQRVIDTIKTNPDDRRIIMC
AWNPRDLPLMALPPCHALCQFYVVNSELSCQLYQRSGDMGLGVPFNIASYALLTYMIAHI
TGLKPGDFIHTLGDAHIYLNHIEPLKIQLQREPRPFPKLRILRKVEKIDDFKAEDFQIEG
YNPHPTIKMEMAV
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  Blast E-value cutoff:
BDBM50316412
n/a
NameBDBM50316412
Synonyms:2-amino-4-oxo-5-thiopyridyl-6-methyl pyrrolo(2,3-d)pyrimidine | CHEMBL1096259
TypeSmall organic molecule
Emp. Form.C13H12N4OS
Mol. Mass.272.326
SMILESCc1[nH]c2nc(C)[nH]c(=O)c2c1Sc1ccncc1
Structure
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