Differences in active-site microarchitecture explain the dissimilar behaviors of PBP5 and 6 in Escherichia coli

Journal of Molecular Graphics and Modelling

Volumn 29, Issue 5, 2011, Pages 650-656

  Chowdhury, Chiranjit ^a   Ghosh, Anindya S ^a  

^a INDIAN INSTITUTE OF TECHNOLOGY   (India)

Author keywords

AutoDock; DD carboxypeptidase; Escherichia coli; MODELLER; Penicillin binding proteins

Indexed keywords

ACTIVE SITE; AUTODOCK; CARBOXYPEPTIDASE; CATALYTIC ACTIVITY; CELL SHAPES; ENZYMATIC ANALYSIS; HYDROGEN BONDING INTERACTIONS; IN-SILICO; KINETIC ANALYSIS; MICRO ARCHITECTURES; MODELLER; PENICILLIN-BINDING PROTEINS; PEPTIDE SUBSTRATES; PHYSIOLOGICAL FUNCTIONS; SOLVED CRYSTAL STRUCTURES; SUBSTRATE SPECIFICITY; THREE-DIMENSIONAL STRUCTURE;

BIOMIMETICS; CATALYST ACTIVITY; ESCHERICHIA COLI; HYDROGEN BONDS; MAINTENANCE; MORPHOLOGY; PROTEINS; SUBSTRATES;

CRYSTAL STRUCTURE;

PENICILLIN BINDING PROTEIN; PENICILLIN BINDING PROTEIN 5; PENICILLIN BINDING PROTEIN 6; UNCLASSIFIED DRUG;

ARTICLE; ENZYME ACTIVE SITE; ENZYME ACTIVITY; ENZYME KINETICS; ENZYME SPECIFICITY; ESCHERICHIA COLI; MOLECULAR DOCKING; MOLECULAR MODEL; MORPHOLOGY; NONHUMAN; PRIORITY JOURNAL; PROTEIN STRUCTURE;

CATALYTIC DOMAIN; ESCHERICHIA COLI; ESCHERICHIA COLI PROTEINS; MODELS, MOLECULAR; PENICILLIN-BINDING PROTEINS; PEPTIDES; PROTEIN CONFORMATION; SUBSTRATE SPECIFICITY;

ESCHERICHIA COLI;

EID: 79751527202     PISSN: 10933263     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jmgm.2010.11.009     Document Type: Article

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