The C-terminal region of the γ subunit of the ATP synthase forms a "catch" with an anionic loop on one of the three β subunits within the catalytic αβ hexamer of the F1 segment. A series of single and multiple amino acid substitutions within this region of the chloroplast γ subunit were constructed utilizing site-directed mutagenesis. The mutations were reconstituted with α and β subunits into both hybrid and native enzymes. The kinetics analysis of the mutant enzymes suggests that the "catch" is not required for ATP hydrolysis but critical for proton coupling and ATP synthesis functions. Nucleotide binding and exchange studies using TNP-ADP showed that substituting three residues in the "catch" region simultaneously inhibited the nucleotid...
Driven by transmembrane electrochemical ion gradients, F-type ATP synthases are the primary source o...
AbstractThe vast majority of organisms produce ATP by a membrane-bound rotating protein complex, ter...
AbstractThe ability of subunit C of eukaryotic V-ATPases to bind ADP and ATP is demonstrated by phot...
The C-terminal region of the γ subunit of the ATP synthase forms a "catch" with an anionic loop on o...
AbstractH+-FOF1-ATP synthase couples proton flow through its membrane portion, FO, to the synthesis ...
AbstractElectron transport, the proton gradient and ATP synthesis were determined in thylakoids that...
AbstractGeneral structural features of the chloroplast ATP synthase are summarized highlighting diff...
AbstractATP synthase, CFoCF1, is both activated and driven by protonmotive force. Composed of more t...
AbstractChloroplast ATP synthase synthesizes ATP by utilizing a proton gradient as an energy supply,...
AbstractIn chloroplasts, synthesis of ATP is energetically coupled with the utilization of a proton ...
AbstractThe vast majority of organisms produce ATP by a membrane-bound rotating protein complex, ter...
AbstractMitochondrial F1FO ATP synthase (Complex V) catalyses ATP synthesis from ADP and inorganic p...
Adenosine triphosphate (ATP) contains energy-rich phosphoanhydride bonds that provide the energy nee...
Dissertation (Ph.D.)--University of Kansas, Molecular Biosciences, 2007.Strategically-placed dithiol...
Dissertation (Ph.D.)--University of Kansas, Molecular Biosciences, 2007.Strategically-placed dithiol...
Driven by transmembrane electrochemical ion gradients, F-type ATP synthases are the primary source o...
AbstractThe vast majority of organisms produce ATP by a membrane-bound rotating protein complex, ter...
AbstractThe ability of subunit C of eukaryotic V-ATPases to bind ADP and ATP is demonstrated by phot...
The C-terminal region of the γ subunit of the ATP synthase forms a "catch" with an anionic loop on o...
AbstractH+-FOF1-ATP synthase couples proton flow through its membrane portion, FO, to the synthesis ...
AbstractElectron transport, the proton gradient and ATP synthesis were determined in thylakoids that...
AbstractGeneral structural features of the chloroplast ATP synthase are summarized highlighting diff...
AbstractATP synthase, CFoCF1, is both activated and driven by protonmotive force. Composed of more t...
AbstractChloroplast ATP synthase synthesizes ATP by utilizing a proton gradient as an energy supply,...
AbstractIn chloroplasts, synthesis of ATP is energetically coupled with the utilization of a proton ...
AbstractThe vast majority of organisms produce ATP by a membrane-bound rotating protein complex, ter...
AbstractMitochondrial F1FO ATP synthase (Complex V) catalyses ATP synthesis from ADP and inorganic p...
Adenosine triphosphate (ATP) contains energy-rich phosphoanhydride bonds that provide the energy nee...
Dissertation (Ph.D.)--University of Kansas, Molecular Biosciences, 2007.Strategically-placed dithiol...
Dissertation (Ph.D.)--University of Kansas, Molecular Biosciences, 2007.Strategically-placed dithiol...
Driven by transmembrane electrochemical ion gradients, F-type ATP synthases are the primary source o...
AbstractThe vast majority of organisms produce ATP by a membrane-bound rotating protein complex, ter...
AbstractThe ability of subunit C of eukaryotic V-ATPases to bind ADP and ATP is demonstrated by phot...