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Volumn 10, Issue 3, 2002, Pages 357-367
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Crystals of peptide deformylase from Plasmodium falciparum reveal critical characteristics of the active site for drug design
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Author keywords
Deformylation; Drug design; Malaria; Metalloenzyme; PDF; Plasmodium
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Indexed keywords
AMINO ACID;
COBALT;
PEPTIDE DEFORMYLASE;
ARTICLE;
BINDING AFFINITY;
CATALYSIS;
CONTROLLED STUDY;
CRYSTAL STRUCTURE;
DRUG DESIGN;
DRUG TARGETING;
ENZYME ACTIVE SITE;
ENZYME ANALYSIS;
ENZYME CONFORMATION;
ENZYME SPECIFICITY;
ENZYME SUBUNIT;
ESCHERICHIA COLI;
METAL BINDING;
NONHUMAN;
PLASMODIUM FALCIPARUM;
PRIORITY JOURNAL;
AMIDOHYDROLASES;
AMINO ACID SEQUENCE;
AMINOPEPTIDASES;
ANIMALS;
ANTIMALARIALS;
BINDING SITES;
CATALYSIS;
COBALT;
CRYSTALLIZATION;
CRYSTALLOGRAPHY, X-RAY;
DRUG DESIGN;
ESCHERICHIA COLI;
HUMANS;
METALLOPROTEINS;
MODELS, MOLECULAR;
MOLECULAR SEQUENCE DATA;
MOLECULAR STRUCTURE;
PLASMODIUM FALCIPARUM;
PROTEIN STRUCTURE, QUATERNARY;
PROTEIN STRUCTURE, SECONDARY;
PROTEIN STRUCTURE, TERTIARY;
PROTEIN SUBUNITS;
SEQUENCE ALIGNMENT;
BACTERIA (MICROORGANISMS);
ESCHERICHIA COLI;
PLASMODIUM FALCIPARUM;
PROTOZOA;
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EID: 0036124280
PISSN: 09692126
EISSN: None
Source Type: Journal
DOI: 10.1016/S0969-2126(02)00719-0 Document Type: Article |
Times cited : (51)
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References (38)
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