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  • |title=Capaldi RA (1973) On the subunit structure of oligomycin sensitive ATPase. Biochem Biophys Res Commun 53:1331-7. |abstract=The subunit structure of oligomycin sensitive ATPase has been determined. In addition to the components of F1, and the so-called
    743 bytes (95 words) - 16:12, 25 November 2015
  • == [[SUITbrowser]] question: Unspecific ATPase activity == = List of publications: ATPase =
    1 KB (160 words) - 10:35, 8 June 2020
  • ...in-dependent respiration and the metabolic cost of proton pumping by the V-ATPase. Physiol Biochem Zool 80:422-32. ...associated with maintaining these diverse proton gradients requires that V-ATPase activity be downregulated under anoxia in order to attain the almost comple
    2 KB (283 words) - 09:35, 9 November 2016
  • ...conformational plasticity of the intact ''Thermus thermophilus'' V/A-type ATPase. Science 365:eaaw9144. https://doi.org/10.1126/science.aaw9144 ...ission, and proton translocation, which are relevant for the entire V-type ATPase family.
    1 KB (180 words) - 20:06, 6 November 2023
  • ...liarani A (2016) Preferential nitrite inhibition of the mitochondrial F1FO-ATPase activities when activated by Ca(2+) in replacement of the natural cofactor ...1FO-ATPase activity activated by Ca<sup>2+</sup>, henceforth defined as Ca-ATPase(s), or by the natural cofactor Mg<sup>2+</sup>, was investigated by evaluat
    2 KB (352 words) - 17:51, 13 April 2016
  • ...rified from bakers' yeast mitochondria. The enzyme resembled mitochondrial ATPase from beef heart with respect to substrate specificity, cold lability, and o ...idative phosphorylation in submitochondrial yeast particles. Mitochondrial ATPase from beef heart or from Neurospora crassa was not inhibited by the antiseru
    2 KB (318 words) - 10:57, 20 February 2015
  • ...ble protein component (Fc2) which was also required for the sensitivity of ATPase to dicyclohexylcarbodiimide. ...ability to bind ATPase (F1). Addition of Fc2 restored the ability to bind ATPase. It is therefore proposed that Fc2 is a component which links the mitochond
    2 KB (218 words) - 16:33, 25 November 2015
  • |description='''ATP synthase''' or F-ATPase (F<sub>1</sub>F<sub>O</sub>-ATPase; the use of Complex V is discouraged) catalyzes the [[endergonic]] phosphor
    748 bytes (102 words) - 14:48, 17 November 2022
  • |title=Cyclophilin D stabilizes FOF1-ATPase dimers and cristae shape to modulate permeability transition pore. ...wide spectrum of insults, such as cardiac or brain ischemia. Although FOF1-ATPase dimers have been recently proposed as a core constituent of PTP, its comple
    2 KB (256 words) - 16:10, 14 December 2016
  • ...ria during the hydrolysis of ATP to ADP and Pi by the oligomycin-sensitive ATPase show that almost 2H+ ions are translocated outwards through the M phase of ...translocation quotient (→H+/P) of 2, corresponding to that of the type II ATPase of the chemiosmotic hypothesis.
    2 KB (233 words) - 00:31, 18 February 2022
  • |title=Covi JA (2005) V-ATPase expression and function in the brine shrimp, ''Artemia franciscana'': Role ...quiescence in these embryos. Whole embryo respirometry demonstrates that V-ATPase activity and processes immediately dependent on that activity constitute ap
    3 KB (444 words) - 09:35, 9 November 2016
  • ...n levels of CeRhr-1 and CeRhr-2, V-ATPase and Na<sup>+</sup>/K<sup>+</sup>-ATPase also increased significantly in response to 1 mmol l<sup>-1</sup> NH4Cl. |keywords=Vesicular transport, Na<sup>+</sup>/K<sup>+</sup>-ATPase, V-ATPase, Carbonic anhydrase
    3 KB (389 words) - 14:10, 15 April 2016
  • ...and compensatory increase in the content of Complexes III and IV. The same ATPase deficiency without an increase in respiratory chain complexes was found in
    2 KB (368 words) - 15:39, 9 November 2016
  • ...caused by different kinetic properties of soluble F,-ATPase and actomyosin ATPase. Therefore, phosphate seems to be in skeletal muscle in vivo only a modest
    2 KB (278 words) - 10:43, 23 January 2019
  • ...uman muscle fibers by caffeine can be explained by a stimulation of myosin ATPase caused by Ca<sup>2+</sup> release from sarcoplasmic reticulum.
    1 KB (185 words) - 11:00, 27 March 2018
  • the mitochondrial F1F0-ATPase begins to hydrolyze ATP to avoid the F1F0-ATPase, namely (i) reduction of the proton conductance of
    2 KB (263 words) - 09:30, 9 November 2016
  • ...stae remodeling by Opa1 modulates mitochondrial bioenergetics by promoting ATPase dimerization and activity. ...al function upon CIII inhbition also prevented the generation of ROS in an ATPase dependent manner; accordingly, we observed lower cell death of Opa1<sup>tg<
    3 KB (390 words) - 15:46, 9 November 2016
  • |abstract=# The purification o f a soluble ATPase from beef heart mitochondria is described. The activity is depend ...ssed in relation to particulate mitochondrial ATPase and to myosin ATPase.
    2 KB (209 words) - 16:09, 25 November 2015
  • |abbr=ATPase (PM) |info='''A: Determination of ATPase activity in [[mitochondrial preparations]].
    3 KB (400 words) - 12:36, 25 November 2020
  • ...medium with different 3BrPA concentrations promoted an increase in 40% in ATPase activity and protects the inhibition promoted by 3BrPA in calcium uptake ac |keywords=Sarco/endoplasmic reticulum calcium (Ca<sup>2+</sup>) ATPase (SERCA) type 1, 3-Bromopyruvate (3BrPA), White muscles, Sarco/endoplasmic r
    2 KB (302 words) - 13:09, 26 February 2015

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