scholarly article | Q13442814 |
P50 | author | Christoph Gerle | Q41612234 |
P2093 | author name string | Christoph Gerle | |
P2860 | cites work | Bovine F1Fo ATP synthase monomers bend the lipid bilayer in 2D membrane crystals | Q21973554 |
A new concept for energy coupling in oxidative phosphorylation based on a molecular explanation of the oxygen exchange reactions | Q24562919 | ||
Role of the c subunit of the FO ATP synthase in mitochondrial permeability transition | Q24606978 | ||
Structure of the mitochondrial ATP synthase by electron cryomicroscopy | Q24633936 | ||
Structure and function of mitochondrial membrane protein complexes | Q26777934 | ||
Structure and flexibility of the C-ring in the electromotor of rotary F(0)F(1)-ATPase of pea chloroplasts | Q27324050 | ||
Structure of the mycobacterial ATP synthase Fo rotor ring in complex with the anti-TB drug bedaquiline | Q27342142 | ||
Molecular architecture of the rotary motor in ATP synthase | Q27620502 | ||
Mechanism of aquaporin-4's fast and highly selective water conduction and proton exclusion | Q27655332 | ||
High-resolution structure of the rotor ring of a proton-dependent ATP synthase | Q27657584 | ||
The structure of the membrane extrinsic region of bovine ATP synthase | Q27658548 | ||
Crystal Structure of the Mg·ADP-inhibited State of the Yeast F 1 c 10 -ATP Synthase | Q27663260 | ||
Bioenergetic cost of making an adenosine triphosphate molecule in animal mitochondria | Q27664534 | ||
Structure of dimeric ATP synthase from mitochondria: an angular association of monomers induces the strong curvature of the inner membrane | Q47710969 | ||
A 0.1-700 Hz current through a voltage-clamped pore: candidate protein for initiator of neural oscillations | Q48635251 | ||
Relevance of divalent cations to ATP-driven proton pumping in beef heart mitochondrial F0F1-ATPase. | Q50756366 | ||
Biased Brownian stepping rotation of FoF1-ATP synthase driven by proton motive force. | Q54314527 | ||
Population of ATP synthase molecules in mitochondria is limited by available 6.8-kDa proteolipid protein (MLQ). | Q54452905 | ||
The Ca2+-induced membrane transition in mitochondria | Q57309821 | ||
Structural and energetic basis for H+ versus Na+ binding selectivity in ATP synthase Fo rotors | Q58876292 | ||
The equivalent pore radius of intact and damaged mitochondria and the mechanism of active shrinkage | Q69397085 | ||
Mutations in the beta-subunit Thr(159) and Glu(184) of the Rhodospirillum rubrum F(0)F(1) ATP synthase reveal differences in ligands for the coupled Mg(2+)- and decoupled Ca(2+)-dependent F(0)F(1) activities | Q73334352 | ||
The central plug in the reconstituted undecameric c cylinder of a bacterial ATP synthase consists of phospholipids | Q74567318 | ||
Structural organization of mitochondrial ATP synthase | Q81293706 | ||
Microscopic rotary mechanism of ion translocation in the F(o) complex of ATP synthases | Q27665340 | ||
Common architecture of the flagellar type III protein export apparatus and F- and V-type ATPases | Q27666617 | ||
Structure of the yeast F1Fo-ATP synthase dimer and its role in shaping the mitochondrial cristae | Q27671154 | ||
The c-ring stoichiometry of ATP synthase is adapted to cell physiological requirements of alkaliphilic Bacillus pseudofirmus OF4 | Q27677536 | ||
Structure of the c10 ring of the yeast mitochondrial ATP synthase in the open conformation | Q27678521 | ||
Structure at 2.8 A resolution of F1-ATPase from bovine heart mitochondria | Q27730864 | ||
The Ca2+-induced membrane transition in mitochondria. III. Transitional Ca2+ release | Q28211160 | ||
Cyclophilin D-dependent mitochondrial permeability transition regulates some necrotic but not apoptotic cell death | Q28242641 | ||
Loss of cyclophilin D reveals a critical role for mitochondrial permeability transition in cell death | Q28242653 | ||
An uncoupling channel within the c-subunit ring of the F1FO ATP synthase is the mitochondrial permeability transition pore | Q28243052 | ||
Dimers of mitochondrial ATP synthase form the permeability transition pore | Q28287824 | ||
The Ca2+-induced membrane transition in mitochondria. I. The protective mechanisms | Q28305411 | ||
Cyclophilin D modulates mitochondrial F0F1-ATP synthase by interacting with the lateral stalk of the complex | Q28507223 | ||
Common evolutionary origin for the rotor domain of rotary ATPases and flagellar protein export apparatus | Q28533330 | ||
Association of two proteolipids of unknown function with ATP synthase from bovine heart mitochondria | Q28566113 | ||
Direct observation of the rotation of F1-ATPase | Q29615360 | ||
Coupling of phosphorylation to electron and hydrogen transfer by a chemi-osmotic type of mechanism | Q29616055 | ||
The ATP synthase--a splendid molecular machine | Q29617444 | ||
Essentials for ATP synthesis by F1F0 ATP synthases | Q30268372 | ||
36 degrees step size of proton-driven c-ring rotation in FoF1-ATP synthase | Q30490478 | ||
Macromolecular organization of ATP synthase and complex I in whole mitochondria. | Q30503729 | ||
Age-dependent dissociation of ATP synthase dimers and loss of inner-membrane cristae in mitochondria | Q30546211 | ||
Phospholipids occupy the internal lumen of the c ring of the ATP synthase of Escherichia coli | Q33233160 | ||
Channel formation by yeast F-ATP synthase and the role of dimerization in the mitochondrial permeability transition | Q33718426 | ||
ATP formation caused by acid-base transition of spinach chloroplasts | Q33802630 | ||
Structure of dimeric mitochondrial ATP synthase: novel F0 bridging features and the structural basis of mitochondrial cristae biogenesis. | Q33933881 | ||
ATP synthase--a marvellous rotary engine of the cell. | Q33954372 | ||
Structure of the rotor of the V-Type Na+-ATPase from Enterococcus hirae | Q33986124 | ||
The ATP synthase is involved in generating mitochondrial cristae morphology | Q34085619 | ||
Mitochondrial permeability transition in the crustacean Artemia franciscana: absence of a calcium-regulated pore in the face of profound calcium storage | Q34395582 | ||
ATP synthase | Q34470136 | ||
Direct observation of stepped proteolipid ring rotation in E. coli F₀F₁-ATP synthase | Q34488395 | ||
Structure and conformational states of the bovine mitochondrial ATP synthase by cryo-EM. | Q34496933 | ||
ATP synthase: an electrochemical transducer with rotatory mechanics | Q34743829 | ||
Human F1F0 ATP synthase, mitochondrial ultrastructure and OXPHOS impairment: a (super-)complex matter? | Q35009110 | ||
Knockdown of DAPIT (diabetes-associated protein in insulin-sensitive tissue) results in loss of ATP synthase in mitochondria | Q35063443 | ||
F-ATPase of Drosophila melanogaster forms 53-picosiemen (53-pS) channels responsible for mitochondrial Ca2+-induced Ca2+ release | Q35103850 | ||
Structural mechanisms of cyclophilin D-dependent control of the mitochondrial permeability transition pore. | Q35602894 | ||
Engineering rotor ring stoichiometries in the ATP synthase | Q36056515 | ||
Arrangement of subunits in intact mammalian mitochondrial ATP synthase determined by cryo-EM. | Q36122751 | ||
The Mitochondrial Permeability Transition Pore: Channel Formation by F-ATP Synthase, Integration in Signal Transduction, and Role in Pathophysiology. | Q36146320 | ||
An investigation of mitochondrial inner membranes by rapid-freeze deep-etch techniques | Q36220864 | ||
Superoxide flashes in single mitochondria | Q36900957 | ||
Foundations of vectorial metabolism and osmochemistry | Q37072399 | ||
Torque generation and elastic power transmission in the rotary F(O)F(1)-ATPase. | Q37490835 | ||
What is the nature of the mitochondrial permeability transition pore and what is it not? | Q38076069 | ||
The ATP synthase: the understood, the uncertain and the unknown. | Q38077205 | ||
The mitochondrial permeability transition pore: a mystery solved? | Q38106976 | ||
Molecular mechanisms of cell death: central implication of ATP synthase in mitochondrial permeability transition | Q38204222 | ||
Rotary ATPases: A New Twist to an Ancient Machine | Q38670458 | ||
Induction of the permeability transition pore in cells depleted of mitochondrial DNA. | Q39383128 | ||
Transient and long-lasting openings of the mitochondrial permeability transition pore can be monitored directly in intact cells by changes in mitochondrial calcein fluorescence | Q40137371 | ||
The proton-driven rotor of ATP synthase: ohmic conductance (10 fS), and absence of voltage gating | Q40286222 | ||
On the structure of the stator of the mitochondrial ATP synthase | Q41446369 | ||
GraDeR: Membrane Protein Complex Preparation for Single-Particle Cryo-EM. | Q41604454 | ||
Ribosome dynamics and tRNA movement by time-resolved electron cryomicroscopy | Q41618424 | ||
The c13 ring from a thermoalkaliphilic ATP synthase reveals an extended diameter due to a special structural region. | Q41621301 | ||
Dimer ribbons of ATP synthase shape the inner mitochondrial membrane | Q41623192 | ||
A heart mitochondrial Ca2(+)-dependent pore of possible relevance to re-perfusion-induced injury. Evidence that ADP facilitates pore interconversion between the closed and open states | Q41782125 | ||
Mass spectrometry of intact V-type ATPases reveals bound lipids and the effects of nucleotide binding | Q41961293 | ||
Mitochondrial channel activity studied by patch-clamping mitoplasts | Q42014495 | ||
The C Ring of the F1Fo ATP Synthase Forms the Mitochondrial Permeability Transition Pore: A Critical Appraisal | Q42082300 | ||
Cyclophilin D links programmed cell death and organismal aging in Podospora anserina | Q42971802 | ||
The affinity purification and characterization of ATP synthase complexes from mitochondria. | Q43223605 | ||
The mitochondrial megachannel is the permeability transition pore | Q44175602 | ||
Proton-powered subunit rotation in single membrane-bound F0F1-ATP synthase. | Q44733437 | ||
The inner mitochondrial membrane contains ion-conducting channels similar to those found in bacteria. | Q44810762 | ||
Structure of the rotor ring of F-Type Na+-ATPase from Ilyobacter tartaricus | Q46463032 | ||
Lipid organization of the plasma membrane | Q46837671 | ||
Inventing the dynamo machine: the evolution of the F-type and V-type ATPases | Q47265660 | ||
Horizontal membrane-intrinsic α-helices in the stator a-subunit of an F-type ATP synthase. | Q47435178 | ||
P433 | issue | 8 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 1191-1196 | |
P577 | publication date | 2016-03-09 | |
P1433 | published in | Biochimica et Biophysica Acta | Q864239 |
P1476 | title | On the structural possibility of pore-forming mitochondrial FoF1 ATP synthase | |
P478 | volume | 1857 |
Q41526704 | Cell Death in the Developing Brain after Hypoxia-Ischemia |
Q99418944 | Cryo-EM structure of the entire mammalian F-type ATP synthase |
Q60954151 | Cyclophilin D, Somehow a Master Regulator of Mitochondrial Function |
Q92403742 | Essay on Biomembrane Structure |
Q90232741 | Metabolomics of Aurantio-Obtusin-Induced Hepatotoxicity in Rats for Discovery of Potential Biomarkers |
Q64885181 | Mitochondria and aging: A role for the mitochondrial transition pore? |
Q47980436 | Mitochondrial bioenergetics decay in aging: beneficial effect of melatonin |
Q48348421 | Mitochondrial permeability transition involves dissociation of F1FO ATP synthase dimers and C-ring conformation |
Q47843948 | Molecular mechanisms of cell death: recommendations of the Nomenclature Committee on Cell Death 2018. |
Q90287798 | Purified F-ATP synthase forms a Ca2+-dependent high-conductance channel matching the mitochondrial permeability transition pore |
Q99233690 | Structure of the dimeric ATP synthase from bovine mitochondria |
Q48393368 | Sulphoraphane Improves Neuronal Mitochondrial Function in Brain Tissue in Acute Carbon Monoxide Poisoning Rats |
Q38945146 | The Mitochondrial Permeability Transition Pore and ATP Synthase. |
Q57177821 | The still uncertain identity of the channel-forming unit(s) of the mitochondrial permeability transition pore |
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