Published in J Bioenerg Biomembr on October 01, 1997
Pseudoxanthoma elasticum: mutations in the MRP6 gene encoding a transmembrane ATP-binding cassette (ABC) transporter. Proc Natl Acad Sci U S A (2000) 1.97
Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA. Science (1989) 40.22
Distantly related sequences in the alpha- and beta-subunits of ATP synthase, myosin, kinases and other ATP-requiring enzymes and a common nucleotide binding fold. EMBO J (1982) 38.14
ABC transporters: from microorganisms to man. Annu Rev Cell Biol (1992) 19.49
Structure at 2.8 A resolution of F1-ATPase from bovine heart mitochondria. Nature (1994) 15.84
Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis. Cell (1990) 9.21
Defensins. Natural peptide antibiotics of human neutrophils. J Clin Invest (1985) 8.63
Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitive. Nature (1992) 8.47
Bee and wasp venoms. Science (1972) 7.35
Cystic fibrosis airway epithelia fail to kill bacteria because of abnormal airway surface fluid. Cell (1996) 6.84
Structural model of ATP-binding proteins associated with cystic fibrosis, multidrug resistance and bacterial transport. Nature (1990) 6.41
Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis. Cell (1993) 6.25
Human beta-defensin-1 is a salt-sensitive antibiotic in lung that is inactivated in cystic fibrosis. Cell (1997) 5.99
ATP-binding site of adenylate kinase: mechanistic implications of its homology with ras-encoded p21, F1-ATPase, and other nucleotide-binding proteins. Proc Natl Acad Sci U S A (1986) 5.55
Defensins: antimicrobial and cytotoxic peptides of mammalian cells. Annu Rev Immunol (1993) 5.36
Structure of the recA protein-ADP complex. Nature (1992) 5.33
The relation between genotype and phenotype in cystic fibrosis--analysis of the most common mutation (delta F508). N Engl J Med (1990) 4.70
Expression of cystic fibrosis transmembrane conductance regulator corrects defective chloride channel regulation in cystic fibrosis airway epithelial cells. Nature (1990) 4.26
Tracheal antimicrobial peptide, a cysteine-rich peptide from mammalian tracheal mucosa: peptide isolation and cloning of a cDNA. Proc Natl Acad Sci U S A (1991) 3.98
Membrane pores induced by magainin. Biochemistry (1996) 3.97
Antimicrobial defensin peptides form voltage-dependent ion-permeable channels in planar lipid bilayer membranes. Proc Natl Acad Sci U S A (1990) 3.90
Phosphorylation of the R domain by cAMP-dependent protein kinase regulates the CFTR chloride channel. Cell (1991) 3.75
Cystic fibrosis: molecular biology and therapeutic implications. Science (1992) 3.72
Phosphorylation-regulated Cl- channel in CHO cells stably expressing the cystic fibrosis gene. Nature (1991) 3.61
CFTR regulates outwardly rectifying chloride channels through an autocrine mechanism involving ATP. Cell (1995) 3.46
Generation of cAMP-activated chloride currents by expression of CFTR. Science (1991) 3.45
Intracellular turnover of cystic fibrosis transmembrane conductance regulator. Inefficient processing and rapid degradation of wild-type and mutant proteins. J Biol Chem (1994) 3.43
Role of mutant CFTR in hypersusceptibility of cystic fibrosis patients to lung infections. Science (1996) 3.38
Antibacterial peptides: key components needed in immunity. Cell (1991) 3.22
Nucleoside triphosphates are required to open the CFTR chloride channel. Cell (1991) 3.21
Chloride conductance expressed by delta F508 and other mutant CFTRs in Xenopus oocytes. Science (1991) 3.12
Glycerol reverses the misfolding phenotype of the most common cystic fibrosis mutation. J Biol Chem (1996) 3.07
Primary structures of MCP-1 and MCP-2, natural peptide antibiotics of rabbit lung macrophages. J Biol Chem (1983) 3.00
Conformational maturation of CFTR but not its mutant counterpart (delta F508) occurs in the endoplasmic reticulum and requires ATP. EMBO J (1994) 2.93
The two nucleotide-binding domains of cystic fibrosis transmembrane conductance regulator (CFTR) have distinct functions in controlling channel activity. J Biol Chem (1995) 2.88
The spectrum of cystic fibrosis mutations. Trends Genet (1992) 2.88
Protein kinase A (PKA) still activates CFTR chloride channel after mutagenesis of all 10 PKA consensus phosphorylation sites. J Biol Chem (1993) 2.85
Peptides from frog skin. Annu Rev Biochem (1990) 2.67
The common variant of cystic fibrosis transmembrane conductance regulator is recognized by hsp70 and degraded in a pre-Golgi nonlysosomal compartment. Proc Natl Acad Sci U S A (1993) 2.48
Interaction of alytic polypeptide, melittin, with lipid membrane systems. J Biol Chem (1969) 2.31
Antimicrobial activity of synthetic magainin peptides and several analogues. Proc Natl Acad Sci U S A (1988) 2.24
Effects of pyrophosphate and nucleotide analogs suggest a role for ATP hydrolysis in cystic fibrosis transmembrane regulator channel gating. J Biol Chem (1994) 2.23
Control of CFTR chloride conductance by ATP levels through non-hydrolytic binding. Nature (1992) 2.19
Regulation by ATP and ADP of CFTR chloride channels that contain mutant nucleotide-binding domains. Science (1992) 2.18
Cystic fibrosis epithelial cells have a receptor for pathogenic bacteria on their apical surface. Proc Natl Acad Sci U S A (1995) 1.97
Neutrophils and host defense. Ann Intern Med (1988) 1.92
Structural model of the nucleotide-binding conserved component of periplasmic permeases. Proc Natl Acad Sci U S A (1991) 1.92
Three dimensional structure of adenyl kinase. Nature (1974) 1.88
The protein kinase A-regulated cardiac Cl- channel resembles the cystic fibrosis transmembrane conductance regulator. Nature (1992) 1.83
The cystic fibrosis mutation (delta F508) does not influence the chloride channel activity of CFTR. Nat Genet (1993) 1.72
Abnormal localization of cystic fibrosis transmembrane conductance regulator in primary cultures of cystic fibrosis airway epithelia. J Cell Biol (1992) 1.68
ATP-dependent transport systems in bacteria and humans: relevance to cystic fibrosis and multidrug resistance. Annu Rev Microbiol (1993) 1.65
Peptides with affinity for membranes. Annu Rev Biophys Biophys Chem (1987) 1.63
The chemistry of poisons in amphibian skin. Proc Natl Acad Sci U S A (1995) 1.62
Structure-function analysis of the histidine permease and comparison with cystic fibrosis mutations. J Biol Chem (1991) 1.62
Mapping of cystic fibrosis transmembrane conductance regulator membrane topology by glycosylation site insertion. J Biol Chem (1994) 1.42
Mutant (delta F508) cystic fibrosis transmembrane conductance regulator Cl- channel is functional when retained in endoplasmic reticulum of mammalian cells. J Biol Chem (1995) 1.41
Binding of Pseudomonas aeruginosa to respiratory epithelial cells from patients with various mutations in the cystic fibrosis transmembrane regulator. J Pediatr (1995) 1.40
Phosphorylation by cAMP-dependent protein kinase causes a conformational change in the R domain of the cystic fibrosis transmembrane conductance regulator. Biochemistry (1994) 1.32
Functional roles of the nucleotide-binding folds in the activation of the cystic fibrosis transmembrane conductance regulator. Proc Natl Acad Sci U S A (1993) 1.28
Regulation of CFTR channel gating. Trends Biochem Sci (1994) 1.24
The amino-terminal portion of CFTR forms a regulated Cl- channel. Cell (1994) 1.21
Cystic fibrosis transmembrane conductance regulator mutations that disrupt nucleotide binding. J Clin Invest (1994) 1.20
ATP synthases. Structure, reaction center, mechanism, and regulation of one of nature's most unique machines. J Biol Chem (1993) 1.20
Cystic fibrosis transmembrane conductance regulator: nucleotide binding to a synthetic peptide. Science (1991) 1.15
The ATP-binding component of a prokaryotic traffic ATPase is exposed to the periplasmic (external) surface. Proc Natl Acad Sci U S A (1993) 1.12
Cystic fibrosis: a disease of altered protein folding. J Bioenerg Biomembr (1997) 1.12
Intrinsic anion channel activity of the recombinant first nucleotide binding fold domain of the cystic fibrosis transmembrane regulator protein. Proc Natl Acad Sci U S A (1992) 1.12
The cystic fibrosis transmembrane conductance regulator. Effects of the most common cystic fibrosis-causing mutation on the secondary structure and stability of a synthetic peptide. J Biol Chem (1992) 1.11
Two conformations of crystalline adenylate kinase. J Mol Biol (1977) 1.11
Recombinant synthesis, purification, and nucleotide binding characteristics of the first nucleotide binding domain of the cystic fibrosis gene product. J Biol Chem (1992) 1.08
Sequence homologies between nucleotide binding regions of CFTR and G-proteins suggest structural and functional similarities. FEBS Lett (1995) 1.05
Structural and functional similarities between the nucleotide-binding domains of CFTR and GTP-binding proteins. Biophys J (1995) 1.04
Altered protein folding may be the molecular basis of most cases of cystic fibrosis. FEBS Lett (1992) 1.02
In vitro mutated beta subunits from the F1-ATPase of the thermophilic bacterium, PS3, containing glutamine in place of glutamic acid in positions 190 or 201 assembles with the alpha and gamma subunits to produce inactive complexes. Biochem Biophys Res Commun (1987) 1.02
Modeling of nucleotide binding domains of ABC transporter proteins based on a F1-ATPase/recA topology: structural model of the nucleotide binding domains of the cystic fibrosis transmembrane conductance regulator (CFTR). J Bioenerg Biomembr (1997) 0.99
Strategies for correcting the delta F508 CFTR protein-folding defect. J Bioenerg Biomembr (1997) 0.96
Mitochondrial ATP synthase. Quaternary structure of the F1 moiety at 3.6 A determined by x-ray diffraction analysis. J Biol Chem (1991) 0.90
Effects of the delta F508 mutation on the structure, function, and folding of the first nucleotide-binding domain of CFTR. J Bioenerg Biomembr (1993) 0.90
Regulation of CFTR Cl- conductance in secretion by cellular energy levels. Am J Physiol (1993) 0.90
Chemical ecology. Proc Natl Acad Sci U S A (1995) 0.89
The nucleotide binding folds of the cystic fibrosis transmembrane conductance regulator are extracellularly accessible. Biochemistry (1997) 0.86
Coupling of ATP hydrolysis with channel gating by purified, reconstituted CFTR. J Bioenerg Biomembr (1997) 0.86
Cystic fibrosis transmembrane conductance regulator: the first nucleotide binding fold targets the membrane with retention of its ATP binding function. Biochemistry (1997) 0.86
Spectrum of mutations in cystic fibrosis. J Bioenerg Biomembr (1993) 0.85
E. coli F1-ATPase: site-directed mutagenesis of the beta-subunit. FEBS Lett (1988) 0.85
Expression and functional properties of the second predicted nucleotide binding fold of the cystic fibrosis transmembrane conductance regulator fused to glutathione-S-transferase. FEBS Lett (1995) 0.83
Cystic fibrosis, lung infections, and a human tracheal antimicrobial peptide (hTAP). FEBS Lett (1997) 0.80
Rat liver ATP synthase. Relationship of the unique substructure of the F1 moiety to its nucleotide binding properties, enzymatic states, and crystalline form. J Biol Chem (1995) 0.80
Adenosine triphosphatase and nucleotide binding activity of isolated beta-subunit preparations from Escherichia coli F1F0-ATP synthase. J Biol Chem (1990) 0.79
The cystic fibrosis transmembrane conductance regulator. Nucleotide binding to a synthetic peptide segment from the second predicted nucleotide binding fold. J Biol Chem (1994) 0.78
NMR studies of the interactions of substrates with enzymes and their peptide fragments. FASEB J (1989) 0.75
Tumor mitochondria and the bioenergetics of cancer cells. Prog Exp Tumor Res (1978) 3.16
Hexokinase II: cancer's double-edged sword acting as both facilitator and gatekeeper of malignancy when bound to mitochondria. Oncogene (2006) 2.96
Preparation and characterization of mitochondria and submitochondrial particles of rat liver and liver-derived tissues. Methods Cell Biol (1978) 2.51
Defective protein folding as a basis of human disease. Trends Biochem Sci (1995) 2.22
High aerobic glycolysis of rat hepatoma cells in culture: role of mitochondrial hexokinase. Proc Natl Acad Sci U S A (1977) 2.20
Glucose catabolism in the rabbit VX2 tumor model for liver cancer: characterization and targeting hexokinase. Cancer Lett (2001) 2.11
Adenosine triphosphatase from rat liver mitochondria. I. Purification, homogeneity, and physical properties. J Biol Chem (1971) 2.04
The peripheral-type benzodiazepine receptor. Localization to the mitochondrial outer membrane. J Biol Chem (1986) 2.03
Functional significance of mitochondrial bound hexokinase in tumor cell metabolism. Evidence for preferential phosphorylation of glucose by intramitochondrially generated ATP. J Biol Chem (1988) 1.97
Glucose catabolism in cancer cells: identification and characterization of a marked activation response of the type II hexokinase gene to hypoxic conditions. J Biol Chem (2001) 1.84
Glucose catabolism in cancer cells. The type II hexokinase promoter contains functionally active response elements for the tumor suppressor p53. J Biol Chem (1997) 1.83
Determination of microgram quantities of protein in the presence of milligram levels of lipid with amido black 10B. Anal Biochem (1985) 1.75
Energy metabolism of tumor cells. Requirement for a form of hexokinase with a propensity for mitochondrial binding. J Biol Chem (1981) 1.63
Aberrant glycolytic metabolism of cancer cells: a remarkable coordination of genetic, transcriptional, post-translational, and mutational events that lead to a critical role for type II hexokinase. J Bioenerg Biomembr (1997) 1.57
Proton atpases: structure and mechanism. Annu Rev Biochem (1983) 1.52
Hexokinase receptor complex in hepatoma mitochondria: evidence from N,N'-dicyclohexylcarbodiimide-labeling studies for the involvement of the pore-forming protein VDAC. Biochemistry (1986) 1.49
The first nucleotide binding fold of the cystic fibrosis transmembrane conductance regulator can function as an active ATPase. J Biol Chem (1995) 1.48
Phosphate transport in rat liver mitochondria. Kinetics and energy requirements. J Biol Chem (1974) 1.35
A high-yield preparative method for isolation of rat liver mitochondria. Anal Biochem (1977) 1.32
Contributions of glycolysis and oxidative phosphorylation to adenosine 5'-triphosphate production in AS-30D hepatoma cells. Cancer Res (1984) 1.30
The 2.8-A structure of rat liver F1-ATPase: configuration of a critical intermediate in ATP synthesis/hydrolysis. Proc Natl Acad Sci U S A (1998) 1.30
Glucose catabolism in cancer cells: amplification of the gene encoding type II hexokinase. Cancer Res (1996) 1.29
Biochemical and ultrastructural properties of a mitochondrial inner membrane fraction deficient in outer membrane and matrix activities. J Cell Biol (1970) 1.26
Glucose catabolism in cancer cells. Isolation, sequence, and activity of the promoter for type II hexokinase. J Biol Chem (1995) 1.24
Glucose phosphorylation in tumor cells. Cloning, sequencing, and overexpression in active form of a full-length cDNA encoding a mitochondrial bindable form of hexokinase. J Biol Chem (1990) 1.20
Intracellular localization and properties of particulate hexokinase in the Novikoff ascites tumor. Evidence for an outer mitochondrial membrane location. J Biol Chem (1983) 1.20
Diethylstilbestrol. A novel F0-directed probe of the mitochondrial proton ATPase. J Biol Chem (1986) 1.19
Sensitive protein assay in presence of high levels of lipid. Methods Enzymol (1989) 1.19
Cystic fibrosis transmembrane conductance regulator: nucleotide binding to a synthetic peptide. Science (1991) 1.15
The kinetics and inhibition of the adenosine diphosphate-adenosine triphosphate exchange catalyzed by purified mitochondrial nucleoside diphosphokinase. J Biol Chem (1967) 1.11
The cystic fibrosis transmembrane conductance regulator. Effects of the most common cystic fibrosis-causing mutation on the secondary structure and stability of a synthetic peptide. J Biol Chem (1992) 1.11
Energy-linked anion transport. Cloning, sequencing, and characterization of a full length cDNA encoding the rat liver mitochondrial proton/phosphate symporter. J Biol Chem (1989) 1.11
Mitochondrial turnover in animal cells. Half-lives of mitochondria and mitochondrial subfractions of rat liver based on [14C]bicarbonate incorporation. J Biol Chem (1981) 1.11
Glucose phosphorylation. Site-directed mutations which impair the catalytic function of hexokinase. J Biol Chem (1991) 1.09
A translational study "case report" on the small molecule "energy blocker" 3-bromopyruvate (3BP) as a potent anticancer agent: from bench side to bedside. J Bioenerg Biomembr (2012) 1.09
Beta subunit of rat liver mitochondrial ATP synthase: cDNA cloning, amino acid sequence, expression in Escherichia coli, and structural relationship to adenylate kinase. Biochemistry (1988) 1.05
Glucose catabolism in African trypanosomes. Evidence that the terminal step is catalyzed by a pyruvate transporter capable of facilitating uptake of toxic analogs. J Biol Chem (1993) 1.04
Purification and characterization of a bindable form of mitochondrial bound hexokinase from the highly glycolytic AS-30D rat hepatoma cell line. Cancer Res (1988) 1.03
Isolation and reconstitution of the n-butylmalonate-sensitive dicarboxylate transporter from rat liver mitochondria. J Biol Chem (1985) 1.03
Altered protein folding may be the molecular basis of most cases of cystic fibrosis. FEBS Lett (1992) 1.02
Mechanism of action of human P-glycoprotein ATPase activity. Photochemical cleavage during a catalytic transition state using orthovanadate reveals cross-talk between the two ATP sites. J Biol Chem (1998) 1.02
Characterization of phosphate efflux pathways in rat liver mitochondria. Biochem J (1983) 1.01
Purification and characterization of the reconstitutively active phosphate transporter from rat liver mitochondria. J Biol Chem (1986) 1.01
A protein inhibitor of the mitochondrial adenosine triphosphatase complex of rat liver. Purification and characterization. J Biol Chem (1979) 0.99
Proton ATPase of rat liver mitochondria. Preparation and visualization of a functional complex using the novel zwitterionic detergent 3-[(3-cholamidopropyl)dimethylammonio]-1-propanesulfonate. J Biol Chem (1984) 0.99
Modeling of nucleotide binding domains of ABC transporter proteins based on a F1-ATPase/recA topology: structural model of the nucleotide binding domains of the cystic fibrosis transmembrane conductance regulator (CFTR). J Bioenerg Biomembr (1997) 0.99
ATP-dependent reactions catalyzed by inner membrane vesicles of rat liver mitochondria. Kinetics, substrate specificity, and bicarbonate sensitivity. J Biol Chem (1976) 0.99
Solubilization and reassembly of the mitochondrial benzodiazepine receptor. Biochemistry (1986) 0.98
Characteristics of phosphate uptake by Ehrlich ascites tumor cells. J Biol Chem (1982) 0.97
Regulation of the mitochondrial ATP synthase/ATPase complex. Arch Biochem Biophys (1986) 0.96
Mitochondrial hexokinase of rat hepatoma cells in culture: solubilization and kinetic properties. Biochemistry (1980) 0.95
Phosphate transport in rat liver mitochondria. Kinetics, inhibitor sensitivity, energy requirements, and labeled components. Mol Cell Biochem (1975) 0.95
Phosphate transport processes in eukaryotic cells. J Membr Biol (1989) 0.94
Cystic fibrosis transmembrane conductance regulator: the purified NBF1+R protein interacts with the purified NBF2 domain to form a stable NBF1+R/NBF2 complex while inducing a conformational change transmitted to the C-terminal region. Arch Biochem Biophys (2000) 0.94
Mitochondrial ATP synthase. Interaction of a synthetic 50-amino acid, beta-subunit peptide with ATP. J Biol Chem (1988) 0.93
Intracellular localization of rat kidney hexokinase. Evidence for an association with low density mitochondria. J Biol Chem (1984) 0.92
Variants in the dihydropyrimidine dehydrogenase, methylenetetrahydrofolate reductase and thymidylate synthase genes predict early toxicity of 5-fluorouracil in colorectal cancer patients. J Int Med Res (2010) 0.92
Hexokinase: the direct link between mitochondrial and glycolytic reactions in rapidly growing cancer cells. Adv Exp Med Biol (1978) 0.92
Phosphate transport in rat liver mitochondria. Energy-dependent accumulation of phosphate by inverted inner membrane vesicles. J Biol Chem (1978) 0.92
Overexpression of higher eukaryotic membrane proteins in bacteria. Novel insights obtained with the liver mitochondrial proton/phosphate symporter. J Biol Chem (1992) 0.91
Adenosine triphosphatase of rat liver mitochondria. Capacity of the homogeneous F1 component of the enzyme to restore ATP synthesis in urea-treated membranes. J Biol Chem (1978) 0.91
Glucose catabolism in brain. Intracellular localization of hexokinase. J Biol Chem (1990) 0.91
Adenosine triphosphatase from rat liver mitochondria. II. Interaction with adenosine diphosphate. J Biol Chem (1972) 0.90
Effects of the delta F508 mutation on the structure, function, and folding of the first nucleotide-binding domain of CFTR. J Bioenerg Biomembr (1993) 0.90
Mitochondrial ATP synthase. Quaternary structure of the F1 moiety at 3.6 A determined by x-ray diffraction analysis. J Biol Chem (1991) 0.90
Localization of oligomycin-sensitive ADP-ATP exchange activity in rat liver mitochondria. Biochem Biophys Res Commun (1968) 0.89
Chemical mechanism of ATP synthase. Magnesium plays a pivotal role in formation of the transition state where ATP is synthesized from ADP and inorganic phosphate. J Biol Chem (1999) 0.89
Mitochondrial ATP synthase. cDNA cloning, amino acid sequence, overexpression, and properties of the rat liver alpha subunit. J Biol Chem (1990) 0.88
Mitochondrial ATPase complex. A dispersed, cytochrome-deficient, oligomycin-sensitive preparation from rat liver containing molecules with a tripartite structural arrangement. J Biol Chem (1979) 0.88
Hexokinase receptors: preferential enzyme binding in normal cells to nonmitochondrial sites and in transformed cells to mitochondrial sites. J Bioenerg Biomembr (1992) 0.88
Novel insights into the chemical mechanism of ATP synthase. Evidence that in the transition state the gamma-phosphate of ATP is near the conserved alanine within the P-loop of the beta-subunit. J Biol Chem (1997) 0.88
Phosphate transport in rat liver mitochondria. Membrane components labeled by N-ethylmaleimide during inhibition of transport. J Biol Chem (1975) 0.88
F0 "proton channel" of rat liver mitochondria. Rapid purification of a functional complex and a study of its interaction with the unique probe diethylstilbestrol. J Biol Chem (1989) 0.87
Structure of the mitochondrial F1 ATPase at 9-A resolution. Proc Natl Acad Sci U S A (1982) 0.87
Cystic fibrosis: a brief look at some highlights of a decade of research focused on elucidating and correcting the molecular basis of the disease. J Bioenerg Biomembr (2001) 0.87
Proton--adenosinetriphosphatase complex of rat liver mitochondria: effect of energy state on its interaction with the adenosinetriphosphatase inhibitory peptide. Biochemistry (1981) 0.86
Adenosine triphosphatase from rat liver mitochondria: separate sites involved in ATP hydrolysis and in the reversible, high affinity binding of ADP. Biochem Biophys Res Commun (1975) 0.86
Cystic fibrosis transmembrane conductance regulator: the first nucleotide binding fold targets the membrane with retention of its ATP binding function. Biochemistry (1997) 0.86
The role of mitochondrial hexokinase binding in the abnormal energy metabolism of tumor cell lines. Ann N Y Acad Sci (1986) 0.86
Rat liver mitochondrial ATP synthase. Effects of mutations in the glycine-rich region of a beta subunit peptide on its interaction with adenine nucleotides. J Biol Chem (1990) 0.86
Protein inhibitor of mitochondrial ATP synthase: relationship of inhibitor structure to pH-dependent regulation. Arch Biochem Biophys (1996) 0.86
Adenosine triphosphatase from rat liver mitochondria. Crystallization and x-ray diffraction studies of the F1-component of the enzyme. J Biol Chem (1978) 0.86
Coupling of adenosine triphosphate formation in mitochondria to the formation of nucleoside triphosphates. Involvement of nucleoside diphosphokinase. J Biol Chem (1973) 0.86
Energy-dependent accumulation of calcium and phosphate by purified inner membrane vesicles of rat liver mitochondria. J Biol Chem (1972) 0.85
Enzymatic and spectral analysis of cytochrome oxidase in adult and fetal rat liver and Morris hepatoma 3924A. Cancer Res (1970) 0.85
Isolation and reconstitution of an N-ethylmaleimide-sensitive phosphate transport protein from rat liver mitochondria. Arch Biochem Biophys (1983) 0.85
ATP synthase. Conditions under which all catalytic sites of the F1 moiety are kinetically equivalent in hydrolyzing ATP. J Biol Chem (1996) 0.84
Adenosine triphosphatase from rat liver mitochondria. 3. Subunit composition. J Biol Chem (1973) 0.84
Isolation of mitochondria from Morris hepatomas. Methods Enzymol (1979) 0.84
Structure/function relationships in hexokinase. Site-directed mutational analyses and characterization of overexpressed fragments implicate different functions for the N- and C-terminal halves of the enzyme. J Biol Chem (1993) 0.84
The use of thin-layer chromatography on poly(ethyleneimine) cellulose to facilitate assays of ATP-ADP exchange, ATP-Pi exchange, adenylate kinase, and nucleoside diphosphokinase activity. Methods Enzymol (1979) 0.84
A comparison of some ultrastructural and biochemical properties of mitochondria from Morris hepatomas 9618A, 7800, and 3924A. Cancer Res (1970) 0.84
Correlation between thymidylate synthase gene variants, RNA and protein levels in primary colorectal adenocarcinomas. J Int Med Res (2010) 0.84
Regulation of the mitochondrial ATP synthase/ATPase complex: cDNA cloning, sequence, overexpression, and secondary structural characterization of a functional protein inhibitor. Arch Biochem Biophys (1993) 0.84
Mutational analysis of the consensus nucleotide binding sequences in the rat liver mitochondrial ATP synthase beta-subunit. J Biol Chem (1992) 0.83
The oligomycin-sensitive adenosine diphosphate-adenosine triphosphate exchange in an inner membrane matrix fraction of rat liver mitochondria. J Biol Chem (1969) 0.83
Adenosine triphosphatase from rat liver mitochondria - evidence for a mercurial-sensitive site for the activating anion bicarbonate. Biochem Biophys Res Commun (1976) 0.82
Proton adenosine triphosphatase complex of rat liver. The effect of trypsin on the F1 and F0 moieties of the enzyme. J Biol Chem (1981) 0.82
Effects of phosphotungstic acid and silicotungstic acid on respiration and integrity of rat liver mitochondria. Biochem Biophys Res Commun (1970) 0.82