Reaction Details |
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Target | Dihydrofolate Reductase-Thymidylate Synthase (DHFR-TS) Mutant KICB1 |
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Ligand | BDBM50110759 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_216585 |
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Ki | 0.6±n/a nM |
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Citation | Kamchonwongpaisan S; Quarrell R; Charoensetakul N; Ponsinet R; Vilaivan T; Vanichtanankul J; Tarnchompoo B; Sirawaraporn W; Lowe G; Yuthavong Y Inhibitors of multiple mutants of Plasmodium falciparum dihydrofolate reductase and their antimalarial activities. J Med Chem 47:673-80 (2004) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Dihydrofolate Reductase-Thymidylate Synthase (DHFR-TS) Mutant KICB1 |
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Name: | Dihydrofolate reductase |
Synonyms: | DHFR-TS | Dihydrofolate reductase | PfDHFR-TS double mutant (C59R+S108N) |
Type: | Enzyme |
Mol. Mass.: | 71822.51 |
Organism: | Plasmodium falciparum (isolate K1 / Thailand) |
Description: | The mutant clone was prepared by cassette mutagenesis using wildtype pfDHFR as a template, and expressed in E. coli. |
Residue: | 608 |
Sequence: | MMEQVCDVFDIYAICACCKVESKNEGKKNEVFNNYTFRGLGNKGVLPWKCNSLDMKYFRA
VTTYVNESKYEKLKYKRCKYLNKETVDNVNDMPNSKKLQNVVVMGRTNWESIPKKFKPLS
NRINVILSRTLKKEDFDEDVYIINKVEDLIVLLGKLNYYKCFIIGGSVVYQEFLEKKLIK
KIYFTRINSTYECDVFFPEINENEYQIISVSDVYTSNNTTLDFIIYKKTNNKMLNEQNCI
KGEEKNNDMPLKNDDKDTCHMKKLTEFYKNVDKYKINYENDDDDEEEDDFVYFNFNKEKE
EKNKNSIHPNDFQIYNSLKYKYHPEYQYLNIIYDIMMNGNKQSDRTGVGVLSKFGYIMKF
DLSQYFPLLTTKKLFLRGIIEELLWFIRGETNGNTLLNKNVRIWEANGTREFLDNRKLFH
REVNDLGPIYGFQWRHFGAEYTNMYDNYENKGVDQLKNIINLIKNDPTSRRILLCAWNVK
DLDQMALPPCHILCQFYVFDGKLSCIMYQRSCDLGLGVPFNIASYSIFTHMIAQVCNLQP
AQFIHVLGNAHVYNNHIDSLKIQLNRIPYPFPTLKLNPDIKNIEDFTISDFTIQNYVHHE
KISMDMAA
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BDBM50110759 |
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n/a |
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Name | BDBM50110759 |
Synonyms: | 4-(2,6-Diamino-5-phenyl-pyrimidin-4-yl)-butyric acid methyl ester | CHEMBL21407 |
Type | Small organic molecule |
Emp. Form. | C15H18N4O2 |
Mol. Mass. | 286.329 |
SMILES | COC(=O)CCCc1nc(N)nc(N)c1-c1ccccc1 |
Structure |
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