The chloroplast twin arginine transport (Tat) component, Tha4, undergoes conformational changes leading to Tat protein transport

Journal of Biological Chemistry

Volumn 287, Issue 41, 2012, Pages 34752-34763

  Aldridge, Cassie ^a   Storm, Amanda ^b   Cline, Kenneth ^a   Dabney Smith, Carole ^b  

^a UNIVERSITY OF FLORIDA   (United States)

^b MIAMI UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMPHIPATHIC; BI-LAYER; CONFORMATIONAL CHANGE; ENERGY SOURCE; FOLDED PROTEINS; LABELING TECHNIQUES; MEMBRANE COMPONENTS; MEMBRANE INTERFACE; PROTECTION ASSAY; PROTEIN TRANSPORT; PROTON-MOTIVE FORCES; RESTING STATE; SIGNAL PEPTIDE; SUBSTRATE PROTEINS; TAT PROTEIN; THYLAKOIDS; TRANSLOCASES; TRANSMEMBRANES; TWIN ARGININE TRANSPORT (TAT);

ARGININE; CHLOROPHYLL; TOPOLOGY;

PROTEINS;

CARRIER PROTEIN; CYSTEINE; MEMBRANE PROTEIN; PROTEIN THA4; PROTEINASE; REAGENT; TWIN ARGININE TRANSPORT PROTEIN; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL LABELING; CHEMICAL MODIFICATION; CHLOROPLAST; CONFORMATIONAL TRANSITION; CONTROLLED STUDY; ENZYME ASSAY; MEMBRANE; NONHUMAN; PEA; PRIORITY JOURNAL; PROTEIN CLEAVAGE; PROTEIN TRANSPORT; SEEDLING;

CHLOROPLAST PROTEINS; CHLOROPLASTS; INTRACELLULAR MEMBRANES; MEMBRANE PROTEINS; PEAS; PLANT PROTEINS; PROTEIN STRUCTURE, SECONDARY; PROTEIN STRUCTURE, TERTIARY; PROTEIN TRANSPORT;

EID: 84867244934     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M112.385666     Document Type: Article

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