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Volumn 77, Issue 5, 2005, Pages 1222-1227
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Stoichiometric selection of tight-binding inhibitors by wild-type mutant forms of malarial (Plasmodium falciparum) dihydrofolate reductase
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Author keywords
[No Author keywords available]
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Indexed keywords
BINDING AFFINITY;
BOUND INHIBITORS;
CHEMICAL LIBRARIES;
STOICHIOMETRIC SELECTION;
BINDING ENERGY;
DISEASE CONTROL;
HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;
MASS SPECTROMETRY;
STOICHIOMETRY;
ULTRAFILTRATION;
ENZYME INHIBITION;
ANTIMALARIAL AGENT;
DIHYDROFOLATE REDUCTASE;
MUTANT PROTEIN;
PYRIMETHAMINE;
ARTICLE;
BINDING AFFINITY;
COMBINATORIAL CHEMISTRY;
DRUG PROTEIN BINDING;
DRUG SCREENING;
HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;
LIQUID CHROMATOGRAPHY;
MASS SPECTROMETRY;
PLASMODIUM FALCIPARUM;
STOICHIOMETRY;
WILD TYPE;
ALGORITHMS;
ANIMALS;
CHLOROGUANIDE;
CHROMATOGRAPHY, HIGH PRESSURE LIQUID;
COMBINATORIAL CHEMISTRY TECHNIQUES;
FOLIC ACID ANTAGONISTS;
HUMANS;
KINETICS;
MASS SPECTROMETRY;
MOLECULAR STRUCTURE;
MUTATION;
PLASMODIUM FALCIPARUM;
PROGUANIL;
PROTEIN BINDING;
PYRIMETHAMINE;
RECOMBINANT PROTEINS;
REPRODUCIBILITY OF RESULTS;
TETRAHYDROFOLATE DEHYDROGENASE;
TRIAZINES;
TRIMETHOPRIM;
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EID: 14744274646
PISSN: 00032700
EISSN: None
Source Type: Journal
DOI: 10.1021/ac0487597 Document Type: Article |
Times cited : (24)
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References (16)
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