Molecular dissection of phage endolysin : An interdomain interaction confers host specificity in lysin a of mycobacterium phage D29

Journal of Biological Chemistry

Volumn 289, Issue 17, 2014, Pages 12085-12095

  Pohane, Amol Arunrao ^a   Joshi, Himanshu ^a   Jain, Vikas ^a  

^a INDIAN INSTITUTE OF SCIENCE EDUCATION AND RESEARCH BHOPAL   (India)

Author keywords

[No Author keywords available]

Indexed keywords

ESCHERICHIA COLI;

E. COLI; HOST CELLS; HOST-SPECIFICITY; IN-DEPTH STUDY; INTER-DOMAIN INTERACTIONS; MOLECULAR DISSECTION;

BACTERIOPHAGES;

BACTERIAL ENZYME; LYSIN A; PEPTIDOGLYCAN; UNCLASSIFIED DRUG;

ARTICLE; BACTERIAL CELL; BACTERIAL GROWTH; BACTERIAL SURVIVAL; BINDING AFFINITY; CELL STRUCTURE; CELL WALL; CYTOLYSIS; CYTOPLASM; ENZYME ACTIVITY; ENZYME BINDING; ESCHERICHIA COLI; GROWTH INHIBITION; MYCOBACTERIOPHAGE; MYCOBACTERIUM SMEGMATIS; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN INTERACTION; PROTEIN LOCALIZATION;

BACTERIOPHAGE; MYCOBACTERIA; PEPTIDOGLYCAN; PERIPLASMIC EXPRESSION; PROTEIN-PROTEIN INTERACTIONS; SURFACE PLASMON RESONANCE (SPR); ZYMOGRAPHY;

BASE SEQUENCE; CATALYTIC DOMAIN; ENDOPEPTIDASES; ESCHERICHIA COLI; HOST-PATHOGEN INTERACTIONS; HYDROLYSIS; MYCOBACTERIOPHAGES; MYCOBACTERIUM TUBERCULOSIS; OLIGONUCLEOTIDES; OPEN READING FRAMES;

EID: 84899444408     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M113.529594     Document Type: Article

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