ATP hydrolysis in ATP synthases can be differently coupled to proton transport and modulated by ADP and phosphate: A structure based model of the mechanism

Biochimica et Biophysica Acta - Bioenergetics

Volumn 1797, Issue 6-7, 2010, Pages 755-762

  D'Alessandro, Manuela ^a   Melandri, B Andrea ^a  

^a UNIVERSITY OF BOLOGNA   (Italy)

Author keywords

ATP synthase; Escherichia coli; Model for uncoupled hydrolysis; Modulation by ADP and phosphate; Proton transport; Rhodobacter capsulatus

Indexed keywords

ADENOSINE DIPHOSPHATE; ADENOSINE DIPHOSPHATE MAGNESIUM; ADENOSINE TRIPHOSPHATASE; ADENOSINE TRIPHOSPHATE; PHOSPHATE;

BINDING AFFINITY; BINDING SITE; CATALYSIS; CONFORMATIONAL TRANSITION; ENZYME STRUCTURE; ENZYME SYNTHESIS; ESCHERICHIA COLI; HYDROLYSIS; LIGAND BINDING; NONHUMAN; PRIORITY JOURNAL; PROTEIN FUNCTION; PROTON TRANSPORT; QUANTITATIVE ANALYSIS; REVIEW;

ADENOSINE DIPHOSPHATE; ADENOSINE TRIPHOSPHATE; ANIMALS; CATALYTIC DOMAIN; CATTLE; HYDROLYSIS; LIPOSOMES; MODELS, BIOLOGICAL; PHOSPHATES; PROTON-TRANSLOCATING ATPASES; PROTONS;

BOVINAE; ESCHERICHIA COLI; RHODOBACTER CAPSULATUS;

EID: 77953807965     PISSN: 00052728     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bbabio.2010.03.007     Document Type: Review

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