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Volumn 132, Issue 4, 2010, Pages 1230-1231
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The structural basis of Cryptosporidium-specific IMP dehydrogenase inhibitor selectivity
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Author keywords
[No Author keywords available]
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Indexed keywords
BIOWARFARES;
CRYPTOSPORIDIUM;
CRYPTOSPORIDIUM PARVUM;
GUANINE NUCLEOTIDES;
INHIBITOR SELECTIVITY;
INOSINE;
MONOPHOSPHATES;
NANOMOLAR INHIBITORS;
PARASITE-;
STRUCTURAL BASIS;
DRUG THERAPY;
ENZYMES;
ENZYME INHIBITION;
INOSINATE DEHYDROGENASE INHIBITOR;
ANTIPROTOZOAL AGENT;
ENZYME INHIBITOR;
INOSINATE DEHYDROGENASE;
ARTICLE;
CRYPTOSPORIDIOSIS;
CRYPTOSPORIDIUM;
CRYSTAL STRUCTURE;
CRYSTALLIZATION;
DRUG POTENCY;
DRUG SELECTIVITY;
ENZYME INHIBITION;
HYDROGEN BOND;
NONHUMAN;
STEREOSPECIFICITY;
ANTAGONISTS AND INHIBITORS;
CHEMICAL STRUCTURE;
CHEMISTRY;
CRYPTOSPORIDIUM PARVUM;
ENZYMOLOGY;
HUMAN;
METABOLISM;
SYNTHESIS;
X RAY CRYSTALLOGRAPHY;
ANTIPROTOZOAL AGENTS;
CRYPTOSPORIDIOSIS;
CRYPTOSPORIDIUM PARVUM;
CRYSTALLOGRAPHY, X-RAY;
ENZYME INHIBITORS;
HUMANS;
IMP DEHYDROGENASE;
MODELS, MOLECULAR;
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EID: 77950442655
PISSN: 00027863
EISSN: 15205126
Source Type: Journal
DOI: 10.1021/ja909947a Document Type: Article |
Times cited : (63)
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References (16)
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