Oligomeric states of the Shigella translocator protein IpaB provide structural insights into formation of the type III secretion translocon

Protein Science

Volumn 22, Issue 5, 2013, Pages 614-627

  Dickenson, Nicholas E ^a   Choudhari, Shyamal P ^a   Adam, Philip R ^a   Kramer, Ryan M ^b   Joshi, Sangeeta B ^b   Middaugh, C Russell ^b   Picking, Wendy L ^a   Picking, William D ^a  

^a OKLAHOMA STATE UNIVERSITY   (United States)

^b UNIVERSITY OF KANSAS   (United States)

Author keywords

IpaB; Shigella; Translocon; Type III secretion

Indexed keywords

BACTERIAL PROTEIN; CARRIER PROTEIN; CHAPERONE; LIPOSOME; OLIGOMER; TRANSLOCATOR PROTEIN IPAB; TRANSLOCON; UNCLASSIFIED DRUG;

ARTICLE; CELL MEMBRANE; CYTOPLASM; ENVIRONMENTAL EXPOSURE; HOST CELL; HUMAN; HUMAN CELL; HYDROPHOBICITY; INTESTINE CELL; KINETOSOME; MOLECULAR LIBRARY; NONHUMAN; PHOSPHOLIPID MEMBRANE; PRIORITY JOURNAL; PROTEIN STABILITY; SHIGELLA FLEXNERI; SHIGELLOSIS; STRUCTURE ANALYSIS; TYPE III SECRETION SYSTEM;

BACTERIAL PROTEINS; DYSENTERY, BACILLARY; HOST-PATHOGEN INTERACTIONS; HUMANS; LIPOSOMES; PHOSPHOLIPIDS; PROTEIN CONFORMATION; PROTEIN MULTIMERIZATION; PROTEIN STABILITY; PROTEIN TRANSPORT; SHIGELLA FLEXNERI;

BACTERIA (MICROORGANISMS); SHIGELLA; SHIGELLA FLEXNERI;

EID: 84878317031     PISSN: 09618368     EISSN: 1469896X     Source Type: Journal    
DOI: 10.1002/pro.2245     Document Type: Article

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