The Chlamydia type III secretion system C-ring engages a chaperone-effector protein complex

PLoS Pathogens

Volumn 5, Issue 9, 2009, Pages

  Spaeth, Kris E ^a   Chen, Yi Shan ^a   Valdivia, Raphael H ^a  

^a DUKE UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BACTERIAL PROTEIN; CHAPERONE; MEMBRANE PROTEIN; CAP1 PROTEIN, CHLAMYDIA TRACHOMATIS; MULTIPROTEIN COMPLEX;

ARTICLE; CARBOXY TERMINAL SEQUENCE; CELL VACUOLE; CHLAMYDIA TRACHOMATIS; CONTROLLED STUDY; HUMAN; HUMAN CELL; HYBRID CELL; HYDROPHOBICITY; MOLECULAR RECOGNITION; NONHUMAN; PROTEIN BINDING; PROTEIN LOCALIZATION; PROTEIN PROTEIN INTERACTION; PROTEIN SECRETION; PROTEIN STABILITY; PROTEIN STRUCTURE; TYPE III SECRETION SYSTEM; AMINO ACID SEQUENCE; BIOLOGICAL MODEL; CHEMISTRY; GENETICS; HELA CELL; INTRACELLULAR SPACE; METABOLISM; METHODOLOGY; MOLECULAR GENETICS; PATHOGENICITY; PROTEIN ANALYSIS; SECRETORY PATHWAY; TWO HYBRID SYSTEM;

BACTERIA (MICROORGANISMS); CHLAMYDIA; NEGIBACTERIA;

AMINO ACID SEQUENCE; BACTERIAL PROTEINS; CHLAMYDIA TRACHOMATIS; HELA CELLS; HUMANS; INTRACELLULAR SPACE; MEMBRANE PROTEINS; MODELS, BIOLOGICAL; MOLECULAR CHAPERONES; MOLECULAR SEQUENCE DATA; MULTIPROTEIN COMPLEXES; PROTEIN BINDING; PROTEIN INTERACTION MAPPING; SECRETORY PATHWAY; TWO-HYBRID SYSTEM TECHNIQUES;

EID: 70349672695     PISSN: 15537366     EISSN: 15537374     Source Type: Journal    
DOI: 10.1371/journal.ppat.1000579     Document Type: Article

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