Proton-Translocating ATPases
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Subject Areas on Research
- ATP-sensitive K+ channels in a plasma membrane H+-ATPase mutant of the yeast Saccharomyces cerevisiae.
- Adaptation of skeletal muscle to increased contractile activity. Expression nuclear genes encoding mitochondrial proteins.
- Amino acid permeases require COPII components and the ER resident membrane protein Shr3p for packaging into transport vesicles in vitro.
- Amino acid sequence of the nucleotide binding region of chloroplast coupling factor 1.
- An Inhibitor of the F1 subunit of ATP synthase (IF1) modulates the activity of angiostatin on the endothelial cell surface.
- Assessment of the number of nucleotide binding sites on chloroplast coupling factor 1 by the continuous variation method.
- Binding stoichiometry and structural mapping of the epsilon polypeptide of chloroplast coupling factor 1.
- Cell surface F1Fo ATP synthase: a new paradigm?
- Characterization of three-subunit chloroplast coupling factor.
- Chemical modification and fluorescence studies of chloroplast coupling factor.
- Chloroplast coupling factor 1: dependence of rotational correlation time on polypeptide composition.
- Cloning and expression of the yeast plasma membrane ATPase in Escherichia coli.
- Co-evolutionary analysis of domains in interacting proteins reveals insights into domain-domain interactions mediating protein-protein interactions.
- Effects of inhibition of mitochondrial protein synthesis in skeletal muscle.
- Endothelial cell surface F1-F0 ATP synthase is active in ATP synthesis and is inhibited by angiostatin.
- Function of tightly bound nucleotides on membrane-bound chloroplast coupling factor.
- Further characterization of nucleotide binding sites on chloroplast coupling factor one.
- Immunological detection of the mitochondrial F1-ATPase alpha subunit in the matrix of rat liver peroxisomes. A protein involved in organelle biogenesis?
- Interaction of nucleotides with chloroplast coupling factor 1.
- Interaction of photoreactive and fluorescent nucleotides with chloroplast coupling factor 1.
- Interactions between nucleotide binding sites on chloroplast coupling factor during ATP hydrolysis.
- Interactions between sustained contractile activity and beta-adrenergic receptors in regulation of gene expression in skeletal muscles.
- Localization and regulation of the ATP6V0A4 (a4) vacuolar H+-ATPase subunit defective in an inherited form of distal renal tubular acidosis.
- MOP2 (SLA2) affects the abundance of the plasma membrane H(+)-ATPase of Saccharomyces cerevisiae.
- Maintenance treatment of gastroesophageal reflux disease: an evaluation of continuous and on-demand therapy with rabeprazole 20 mg.
- Mechanism for catalysis and regulation of adenosine 5'-triphosphate hydrolysis by chloroplast coupling factor 1.
- Mechanism of adenosine accumulation in the hippocampal slice during energy deprivation.
- Membrane potential mediates H(+)-ATPase dependence of "degradative pathway" endosomal fusion.
- Membrane-protein structural mapping of chloroplast coupling factor in asolectin vesicles.
- Mitochondrial adaptations to obesity-related oxidant stress.
- Molecular cloning and characterization of Atp6n1b: a novel fourth murine vacuolar H+-ATPase a-subunit gene.
- Mutations in ATP13A2 (PARK9) are associated with an amyotrophic lateral sclerosis-like phenotype, implicating this locus in further phenotypic expansion.
- Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness.
- Nitric oxide enhances salt secretion and Na(+) sequestration in a mangrove plant, Avicennia marina, through increasing the expression of H(+)-ATPase and Na(+)/H(+) antiporter under high salinity.
- Notochord vacuoles are lysosome-related organelles that function in axis and spine morphogenesis.
- Permeability properties of the mammalian bladder apical membrane.
- Plasma membrane proton ATPase Pma1p requires raft association for surface delivery in yeast.
- Polyunsaturated fatty acids reverse the lysosomal storage and accumulation of subunit 9 of mitochondrial F1F0-ATP synthase in cultured lymphoblasts from patients with Batten disease.
- Rhodamine 123 as a probe of transmembrane potential in isolated rat-liver mitochondria: spectral and metabolic properties.
- Role of subunit-9 of mitochondrial ATP synthase in Batten disease.
- Rotation of nucleotide sites is not required for the enzymatic activity of chloroplast coupling factor 1.
- Rotational dynamics of chloroplast ATP synthase in phospholipid vesicles.
- Spatial relationships between specific sites on reconstituted chloroplast proton adenosinetriphosphatase and the phospholipid vesicle surface.
- Steady state kinetic studies of purified yeast plasma membrane proton-translocating ATPase.
- Steady state kinetics of ATP synthesis and hydrolysis catalyzed by reconstituted chloroplast coupling factor.
- Steady-state ATP synthesis by bacteriorhodopsin and chloroplast coupling factor co-reconstituted into asolectin vesicles.
- Structural investigation of reconstituted chloroplast ATPase with fluorescence measurements.
- Structural map of the dicyclohexylcarbodiimide site of chloroplast coupling factor determined by resonance energy transfer.
- Structural mapping of chloroplast coupling factor.
- Structural mapping of nucleotide binding sites on chloroplast coupling factor.
- Structural organization of chloroplast coupling factor.
- Structure of oxidative- and photo-phosphorylation coupling factor complexes.
- Studies of the phosphoenzyme intermediate of the yeast plasma membrane proton-translocating ATPase.
- Targeting cell surface F1F0 ATP synthase in cancer therapy.
- The ATP binding site of the yeast plasma membrane proton-translocating ATPase.
- The connecting tubule is the main site of the furosemide-induced urinary acidification by the vacuolar H+-ATPase.
- Thermodynamic limits to the ATP/site stoichiometries of oxidative phosphorylation by rat liver mitochondria.
- Topology of the yeast plasma membrane proton-translocating ATPase.
- Two distinct genes encode small isoproteolipids affecting plasma membrane H(+)-ATPase activity of Saccharomyces cerevisiae.
- Unique expression of a sporophytic character on the gametophytes of notholaenid ferns (Pteridaceae).
- [Effects of valsartan and captopril on expressions and activities of tissue factor and tissue factor pathway inhibitor].
- pH dependence of adenosine 5'-triphosphate synthesis and hydrolysis catalyzed by reconstituted chloroplast coupling factor.
- vph6 mutants of Saccharomyces cerevisiae require calcineurin for growth and are defective in vacuolar H(+)-ATPase assembly.