| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S0005-2728(00)00077-3 |
| P8608 | Fatcat ID | release_xtiexsuq3ndwhb5dt4vjph4psa |
| P698 | PubMed publication ID | 10838041 |
| P5875 | ResearchGate publication ID | 12480327 |
| P2093 | author name string | P D Boyer | |
| P2860 | cites work | Molecular architecture of the rotary motor in ATP synthase | Q27620502 |
| Structure at 2.8 A resolution of F1-ATPase from bovine heart mitochondria | Q27730864 | ||
| The binding change mechanism for ATP synthase--some probabilities and possibilities | Q28265156 | ||
| Energy transduction in the F1 motor of ATP synthase | Q28290141 | ||
| Direct observation of the rotation of F1-ATPase | Q29615360 | ||
| The ATP synthase--a splendid molecular machine | Q29617444 | ||
| The Escherichia coli FOF1 gammaM23K uncoupling mutant has a higher K0.5 for Pi. Transition state analysis of this mutant and others reveals that synthesis and hydrolysis utilize the same kinetic pathway | Q30471135 | ||
| Subunit rotation in Escherichia coli FoF1-ATP synthase during oxidative phosphorylation. | Q36589192 | ||
| Nucleotide-dependent movement of the epsilon subunit between alpha and beta subunits in the Escherichia coli F1F0-type ATPase | Q38356781 | ||
| Medium ADP and not ADP already tightly bound to phylakoid membranes forms the initial ATP in chloroplast phosphorylation | Q39120799 | ||
| Active/inactive state transitions of mitochondrial ATPase molecules influenced by Mg2+ , anions and aurovertin | Q39740727 | ||
| The mechanism and regulation of ATP synthesis by F1-ATPases | Q40218839 | ||
| ATP synthase--past and future | Q40847651 | ||
| Occurrence of an uncoupler-resistant intermediate type of phosphate-water oxygen exchange reaction catalyzed by heart submitochondrial particles | Q41872103 | ||
| Bi-site activation occurs with the native and nucleotide-depleted mitochondrial F1-ATPase | Q42989806 | ||
| Metal binding sites of H(+)-ATPase from chloroplast and Bacillus PS3 studied by EPR and pulsed EPR spectroscopy of bound manganese(II). | Q43024003 | ||
| ATP synthesis by F0F1-ATP synthase independent of noncatalytic nucleotide binding sites and insensitive to azide inhibition | Q43025119 | ||
| The alpha 3(beta Y341W)3 gamma subcomplex of the F1-ATPase from the thermophilic Bacillus PS3 fails to dissociate ADP when MgATP is hydrolyzed at a single catalytic site and attains maximal velocity when three catalytic sites are saturated with MgAT | Q43026078 | ||
| Kinetics of oxidative phosphorylation in Paracoccus denitrificans. 1. Mechanism of ATP synthesis at the active site(s) of F0F1-ATPase | Q43524201 | ||
| MgADP and free Pi as the substrates and the Mg2+ requirement for photophosphorylation | Q44042394 | ||
| Adenine nucleotide binding at a noncatalytic site of mitochondrial F1-ATPase accelerates a Mg(2+)- and ADP-dependent inactivation during ATP hydrolysis | Q44429211 | ||
| Do ATP4- and Mg2+ bind stepwise to the F1-ATPase of Halobacterium saccharovorum? | Q46286316 | ||
| Catalytic site nucleotide binding and hydrolysis in F1F0-ATP synthase | Q47732557 | ||
| F1-ATPase is a highly efficient molecular motor that rotates with discrete 120 degree steps | Q47872642 | ||
| Yeast mitochondrial F1-ATPase--effects of metal ions. | Q52372647 | ||
| 2,4-Dinitrophenol causes a marked increase in the apparent Km of Pi and of ADP for oxidative phosphorylation | Q52840721 | ||
| Energetics of ATP dissociation from the mitochondrial ATPase during oxidative phosphorylation. | Q53725617 | ||
| The F1Fo-ATPase Complex from Bovine Heart Mitochondria: The Molar Ratio of the Subunits in the Stalk Region Linking the F1and FoDomains | Q57840354 | ||
| ATP synthesis catalyzed by the ATP synthase of Escherichia coli reconstituted into liposomes | Q72715664 | ||
| F1-ATPase, roles of three catalytic site residues | Q73025369 | ||
| Functional regions of the H(+)-ATPase inhibitory protein from ox heart mitochondria | Q73423699 | ||
| Three-stepped rotation of subunits gamma and epsilon in single molecules of F-ATPase as revealed by polarized, confocal fluorometry | Q74586417 | ||
| How fumarase recycles after the malate --> fumarate reaction. Insights into the reaction mechanism | Q77917248 | ||
| Effect of the epsilon-subunit on nucleotide binding to Escherichia coli F1-ATPase catalytic sites | Q77926922 | ||
| P433 | issue | 2-3 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 252-262 | |
| P577 | publication date | 2000-05-01 | |
| P1433 | published in | Biochimica et Biophysica Acta | Q864239 |
| P1476 | title | Catalytic site forms and controls in ATP synthase catalysis | |
| P478 | volume | 1458 |
| Q56904697 | A Complex of the Bacteriophage T7 Primase-Helicase and DNA Polymerase Directs Primer Utilization |
| Q36160788 | A model for the cooperative free energy transduction and kinetics of ATP hydrolysis by F 1 -ATPase |
| Q36995302 | ATP synthase and the actions of inhibitors utilized to study its roles in human health, disease, and other scientific areas |
| Q54372352 | ATP synthase: the right size base model for nanomotors in nanomedicine. |
| Q34270492 | ATP synthesis and storage |
| Q64092769 | ATP synthesis at physiological nucleotide concentrations |
| Q41824526 | An alternative reaction pathway of F1-ATPase suggested by rotation without 80 degrees/40 degrees substeps of a sluggish mutant at low ATP |
| Q43672989 | Bi-site catalysis in F1-ATPase: does it exist? |
| Q42686059 | Binding affinities and protein ligand complex geometries of nucleotides at the F(1) part of the mitochondrial ATP synthase obtained by ligand docking calculations |
| Q34384279 | Catalysis and rotation of F1 motor: cleavage of ATP at the catalytic site occurs in 1 ms before 40 degree substep rotation |
| Q33196928 | Chemomechanical coupling in F1-ATPase revealed by simultaneous observation of nucleotide kinetics and rotation |
| Q43014682 | Complete inhibition and partial Re-activation of single F1-ATPase molecules by tentoxin: new properties of the re-activated enzyme |
| Q30525764 | Continuous monitoring of enzymatic activity within native electrophoresis gels: application to mitochondrial oxidative phosphorylation complexes |
| Q44392098 | Cross-linking of the endogenous inhibitor protein (IF1) with rotor (gamma, epsilon) and stator (alpha) subunits of the mitochondrial ATP synthase. |
| Q44264715 | Does F1-ATPase subunit gamma turn in the wrong direction? |
| Q34721063 | Double-lock ratchet mechanism revealing the role of alphaSER-344 in FoF1 ATP synthase |
| Q83818344 | Ectoadenylate kinase and plasma membrane ATP synthase activities of human vascular endothelial cells |
| Q44727114 | Energy-dependent transformation of F0.F1-ATPase in Paracoccus denitrificans plasma membranes |
| Q34804967 | Evidence for rotation of V1-ATPase. |
| Q42021441 | Fluorescence resonance energy transfer between coumarin-derived mitochondrial F(1)-ATPase gamma subunit and pyrenylmaleimide-labelled fragments of IF(1) and c subunit |
| Q36276833 | Identification of the betaTP site in the x-ray structure of F1-ATPase as the high-affinity catalytic site |
| Q43846826 | Inhibition of steady-state mitochondrial ATP synthesis by bicarbonate, an activating anion of ATP hydrolysis |
| Q35836739 | Inhibitory Mg-ADP-fluoroaluminate complexes bound to catalytic sites of F(1)-ATPases: are they ground-state or transition-state analogs? |
| Q34184926 | Insights into the molecular mechanism of rotation in the Fo sector of ATP synthase |
| Q35590752 | Large scale simulation of protein mechanics and function |
| Q33957859 | Mechanism of the F(1)F(0)-type ATP synthase, a biological rotary motor |
| Q52004227 | Motion of a rotatory molecular motor and the chemical reaction rate. |
| Q33571588 | Novel role of ATPase subunit C targeting peptides beyond mitochondrial protein import |
| Q45065676 | Observation of calcium-dependent unidirectional rotational motion in recombinant photosynthetic F1-ATPase molecules |
| Q34183062 | On the Mechanism of ATP Hydrolysis in F1-ATPase |
| Q42012253 | Optimization of ATP synthase function in mitochondria and chloroplasts via the adenylate kinase equilibrium |
| Q27662948 | P. aeruginosa PilT Structures with and without Nucleotide Reveal a Dynamic Type IV Pilus Retraction Motor |
| Q33949924 | Pause and rotation of F(1)-ATPase during catalysis |
| Q34183682 | Proton pumps: mechanism of action and applications |
| Q30328057 | Purine but not pyrimidine nucleotides support rotation of F(1)-ATPase. |
| Q33942984 | Resolution of distinct rotational substeps by submillisecond kinetic analysis of F1-ATPase |
| Q73096775 | Single-molecule imaging of rotation of F1-ATPase |
| Q45077616 | Spontaneous rhythmic motion of a polymer chain in a continuous-wave laser field |
| Q38290024 | Stepping rotation of F(1)-ATPase with one, two, or three altered catalytic sites that bind ATP only slowly |
| Q34478502 | Structural changes during ATP hydrolysis activity of the ATP synthase from Escherichia coli as revealed by fluorescent probes. |
| Q27634146 | Structure of bovine mitochondrial F(1)-ATPase with nucleotide bound to all three catalytic sites: implications for the mechanism of rotary catalysis |
| Q33933881 | Structure of dimeric mitochondrial ATP synthase: novel F0 bridging features and the structural basis of mitochondrial cristae biogenesis. |
| Q35234486 | The ATP-waiting conformation of rotating F1-ATPase revealed by single-pair fluorescence resonance energy transfer |
| Q34522937 | The molecular mechanism of ATP synthesis by F1F0-ATP synthase |
| Q39991977 | The new unified theory of ATP synthesis/hydrolysis and muscle contraction, its manifold fundamental consequences and mechanistic implications and its applications in health and disease |
| Q42015128 | The nonlinear chemo-mechanic coupled dynamics of the F 1 -ATPase molecular motor |
| Q41322985 | The nuclear encoded subunits gamma, delta and epsilon from the shrimp mitochondrial F1-ATP synthase, and their transcriptional response during hypoxia |
| Q59721082 | The transmembrane domain provides nucleotide binding specificity to the bacterial conjugation protein TrwB |
| Q44779402 | Three-dimensional organization of the archaeal A1-ATPase from Methanosarcina mazei Gö1. |
| Q46356146 | Why is the mechanical efficiency of F(1)-ATPase so high? |
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