Rate of hydrolysis in ATP synthase is fine-tuned by α-subunit motif controlling active site conformation

Proceedings of the National Academy of Sciences of the United States of America

Volumn 110, Issue 6, 2013, Pages 2117-2122

  Beke Somfai, Tamás ^a   Lincoln, Per ^a   Nordén, Bengt ^a  

^a CHALMERS UNIVERSITY OF TECHNOLOGY   (Sweden)

Author keywords

Enzyme catalysis; Molecular dynamics; Protein structure

Indexed keywords

PROTON TRANSPORTING ADENOSINE TRIPHOSPHATE SYNTHASE;

ARTICLE; BINDING SITE; CATALYSIS; CONFORMATIONAL TRANSITION; CRYSTAL STRUCTURE; DYNAMICS; HYDROLYSIS; MOLECULAR MECHANICS; PRIORITY JOURNAL; PROTEIN MOTIF; QUANTUM MECHANICS; SIMULATION;

ADENOSINE TRIPHOSPHATE; ANIMALS; BIOPHYSICAL PHENOMENA; CATALYTIC DOMAIN; CATTLE; HYDROLYSIS; KINETICS; MITOCHONDRIAL PROTON-TRANSLOCATING ATPASES; MODELS, MOLECULAR; MOLECULAR DYNAMICS SIMULATION; PROTEIN CONFORMATION; PROTEIN SUBUNITS; QUANTUM THEORY;

EID: 84873455521     PISSN: 00278424     EISSN: 10916490     Source Type: Journal    
DOI: 10.1073/pnas.1214741110     Document Type: Article

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