Mutation of a single residue in the ba3 oxidase specifically impairs protonation of the pump site

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

Volumn 112, Issue 11, 2015, Pages 3397-3402

  Von Ballmoos, Christoph ^a,c   Gonska, Nathalie ^a   Lachmann, Peter ^a,d   Gennis, Robert B ^b   Ädelroth, Pia ^a   Brzezinski, Peter ^a  

^a STOCKHOLM UNIVERSITY   (Sweden)

^b UNIVERSITY OF ILLINOIS AT URBANA CHAMPAIGN   (United States)

^c UNIVERSITY OF BERN   (Switzerland)

^d Applied Photophysics ^*  (United Kingdom)

Author keywords

Cytochrome aa3; Cytochrome c oxidase; Electron transfer; Membrane protein; Respiration

Indexed keywords

CUPRIC ION; CYTOCHROME C OXIDASE; CYTOCHROME C OXIDASE BA 3; HEME; PROTON; PROTON PUMP; UNCLASSIFIED DRUG; ASPARTIC ACID; CYTOCHROME B; CYTOCHROME BA3;

ARTICLE; CONTROLLED STUDY; DISSOCIATION; ELECTRON TRANSPORT; GENE MUTATION; LIGAND BINDING; PH; PRIORITY JOURNAL; PROTON TRANSPORT; THERMUS THERMOPHILUS; CHEMISTRY; ENZYMOLOGY; GENETICS; KINETICS; MUTATION; TIME FACTOR;

THERMUS THERMOPHILUS;

ASPARTIC ACID; CYTOCHROME B GROUP; ELECTRON TRANSPORT COMPLEX IV; HYDROGEN-ION CONCENTRATION; KINETICS; MUTATION; PROTON PUMPS; PROTONS; THERMUS THERMOPHILUS; TIME FACTORS;

EID: 84925276426     PISSN: 00278424     EISSN: 10916490     Source Type: Journal    
DOI: 10.1073/pnas.1422434112     Document Type: Article

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