A model-structure of a periplasm-facing state of the NhaA antiporter suggests the molecular underpinnings of pH-induced conformational changes

Journal of Biological Chemistry

Volumn 287, Issue 22, 2012, Pages 18249-18261

  Schushan, Maya ^a   Rimon, Abraham ^b   Haliloglu, Turkan ^c   Forrest, Lucy R ^d   Padan, Etana ^b   Ben Tal, Nir ^a  

^a TEL AVIV UNIVERSITY   (Israel)

^b HEBREW UNIVERSITY OF JERUSALEM   (Israel)

^c BOGAZICI UNIVERSITY   (Turkey)

^d MAX PLANCK INSTITUTE OF BIOPHYSICS   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ALKALINITY; CELL PROLIFERATION; CYTOLOGY; ESCHERICHIA COLI; FACINGS;

COMPUTATIONAL APPROACH; CONFORMATIONAL CHANGE; FUNCTIONAL DIRECTION; PH-DEPENDENT; ROTATIONAL MOTION; STRUCTURAL ARCHITECTURE; SYMMETRY AXIS; TRANSMEMBRANE HELICES;

CRYSTAL STRUCTURE;

ANTIPORTER; PROTEIN NHAA; UNCLASSIFIED DRUG;

ALKALINITY; ARTICLE; CONFORMATIONAL TRANSITION; CONTROLLED STUDY; CRYSTAL STRUCTURE; CYTOPLASM; ESCHERICHIA COLI; MOLECULAR MODEL; NONHUMAN; PH; PREDICTION; PRIORITY JOURNAL; PROTEIN CONFORMATION; PROTEIN CROSS LINKING; PROTEIN STRUCTURE;

ESCHERICHIA COLI;

EID: 84861557277     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M111.336446     Document Type: Article

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