Literature DB >> 11852046

Catalytic site occupancy during ATP synthase catalysis.

Paul D Boyer1.   

Abstract

An early proposal was that for rapid ATP synthesis by the rotational ATP synthase, a specific second site must bind ADP and P(i), and for rapid ATP hydrolysis a different second site must bind ATP. Such bi-site activation was considered to occur whether or not an ADP or ATP was at a third site. In contrast, a more recent proposal is that rapid ATP hydrolysis requires that all three sites have bound ADP or ATP present. However, discovery that one second site binds ADP better than ATP, together with other data and considerations support the earlier proposal. The retention or rebinding of ADP can explain why three sites fill during hydrolysis as ATP concentration is increased although bi-site activation still prevails.

Entities:  

Mesh:

Substances:

Year:  2002        PMID: 11852046     DOI: 10.1016/s0014-5793(02)02293-7

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  21 in total

1.  The ATP-waiting conformation of rotating F1-ATPase revealed by single-pair fluorescence resonance energy transfer.

Authors:  Ryohei Yasuda; Tomoko Masaike; Kengo Adachi; Hiroyuki Noji; Hiroyasu Itoh; Kazuhiko Kinosita
Journal:  Proc Natl Acad Sci U S A       Date:  2003-07-22       Impact factor: 11.205

2.  Chemo-mechanical coupling in F(1)-ATPase revealed by catalytic site occupancy during catalysis.

Authors:  Rieko Shimo-Kon; Eiro Muneyuki; Hiroshi Sakai; Kengo Adachi; Masasuke Yoshida; Kazuhiko Kinosita
Journal:  Biophys J       Date:  2010-04-07       Impact factor: 4.033

3.  One rotary mechanism for F1-ATPase over ATP concentrations from millimolar down to nanomolar.

Authors:  Naoyoshi Sakaki; Rieko Shimo-Kon; Kengo Adachi; Hiroyasu Itoh; Shou Furuike; Eiro Muneyuki; Masasuke Yoshida; Kazuhiko Kinosita
Journal:  Biophys J       Date:  2004-12-30       Impact factor: 4.033

4.  Rapid hydrolysis of ATP by mitochondrial F1-ATPase correlates with the filling of the second of three catalytic sites.

Authors:  Yakov M Milgrom; Richard L Cross
Journal:  Proc Natl Acad Sci U S A       Date:  2005-09-19       Impact factor: 11.205

5.  Two distinct modes of processive kinesin movement in mixtures of ATP and AMP-PNP.

Authors:  Radhika Subramanian; Jeff Gelles
Journal:  J Gen Physiol       Date:  2007-11       Impact factor: 4.086

6.  Functional halt positions of rotary FOF1-ATPase correlated with crystal structures.

Authors:  Hendrik Sielaff; Henning Rennekamp; Siegfried Engelbrecht; Wolfgang Junge
Journal:  Biophys J       Date:  2008-08-22       Impact factor: 4.033

7.  Anatomy of F1-ATPase powered rotation.

Authors:  James L Martin; Robert Ishmukhametov; Tassilo Hornung; Zulfiqar Ahmad; Wayne D Frasch
Journal:  Proc Natl Acad Sci U S A       Date:  2014-02-24       Impact factor: 11.205

Review 8.  Control of rotation of the F1FO-ATP synthase nanomotor by an inhibitory α-helix from unfolded ε or intrinsically disordered ζ and IF1 proteins.

Authors:  Francisco Mendoza-Hoffmann; Mariel Zarco-Zavala; Raquel Ortega; José J García-Trejo
Journal:  J Bioenerg Biomembr       Date:  2018-09-28       Impact factor: 2.945

Review 9.  Molecular and Supramolecular Structure of the Mitochondrial Oxidative Phosphorylation System: Implications for Pathology.

Authors:  Salvatore Nesci; Fabiana Trombetti; Alessandra Pagliarani; Vittoria Ventrella; Cristina Algieri; Gaia Tioli; Giorgio Lenaz
Journal:  Life (Basel)       Date:  2021-03-15

10.  The b (arg36) contributes to efficient coupling in F(1)F (O) ATP synthase in Escherichia coli.

Authors:  Amanda K Welch; Shane B Claggett; Brian D Cain
Journal:  J Bioenerg Biomembr       Date:  2008-01-19       Impact factor: 2.945

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.