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Volumn 286, Issue 36, 2011, Pages 31771-31780
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Increased structural flexibility at the active site of a fluorophore-conjugated β-lactamase distinctively impacts its binding toward diverse cephalosporin antibiotics
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Author keywords
[No Author keywords available]
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Indexed keywords
ACTIVE SITE;
BINDING KINETICS;
BIOSENSING SYSTEMS;
CEPHALOSPORIN ANTIBIOTICS;
CONFORMATIONAL CHANGE;
ENVIRONMENT-SENSITIVE;
EVOLUTIONARY STRATEGIES;
FLUORESCENCE SIGNALS;
HYDROLYTIC ACTIVITIES;
LACTAMASES;
MOLECULAR EVOLUTION;
SIGNIFICANT IMPACTS;
STERIC HINDRANCES;
STRUCTURAL CHANGE;
STRUCTURAL FLEXIBILITIES;
STRUCTURAL INFORMATION;
STRUCTURAL STUDIES;
SUBSTRATE PROFILE;
SUBSTRATE-BINDING SITES;
ANTIBIOTICS;
ENZYME KINETICS;
EVOLUTIONARY ALGORITHMS;
FLUORESCENCE;
FLUOROPHORES;
KINETICS;
MOLECULAR BIOLOGY;
SEWAGE TREATMENT PLANTS;
STRUCTURAL DYNAMICS;
SUBSTRATES;
BETA LACTAMASE;
CEFALORIDINE;
CEFALOTIN;
CEFOTAXIME;
CEFOXITIN;
CEFTAZIDIME;
CEFTRIAXONE;
CEFUROXIME;
CEPHALOSPORIN DERIVATIVE;
FLUORESCENT DYE;
PENICILLIN G;
ARTICLE;
BINDING KINETICS;
BINDING SITE;
CONFORMATIONAL TRANSITION;
DRUG DESIGN;
DRUG PROTEIN BINDING;
ELECTROSPRAY MASS SPECTROMETRY;
ENZYME ACTIVE SITE;
ENZYME BINDING;
ENZYME KINETICS;
ENZYME STABILITY;
ENZYME STRUCTURE;
ENZYME SUBSTRATE;
FLUORESCENCE ANALYSIS;
GENETIC ENGINEERING;
GENETIC PROCEDURES;
MUTATIONAL ANALYSIS;
PRIORITY JOURNAL;
BETA-LACTAMASES;
BINDING SITES;
CATALYTIC DOMAIN;
CEPHALOSPORINS;
FLUORESCENT DYES;
KINETICS;
MOLECULAR CONFORMATION;
MOLECULAR PROBES;
MUTAGENESIS, SITE-DIRECTED;
PLIABILITY;
PROTEIN ENGINEERING;
SUBSTRATE SPECIFICITY;
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EID: 80052398961
PISSN: 00219258
EISSN: 1083351X
Source Type: Journal
DOI: 10.1074/jbc.M110.198895 Document Type: Article |
Times cited : (18)
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References (23)
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