Literature DB >> 11841238

Gastric H/K-ATPase liberates two moles of Pi from one mole of phosphoenzyme formed from a high-affinity ATP binding site and one mole of enzyme-bound ATP at the low-affinity site during cross-talk between catalytic subunits.

Kazuhiro Abe1, Shunji Kaya, Toshiaki Imagawa, Kazuya Taniguchi.   

Abstract

The maximum amount of acid-stable phosphoenzyme (E32P)/mol of alpha chain of pig gastric H/K-ATPase from [gamma-32P]ATP (K(1/2) = 0.5 microM) was found to be approximately 0.5, which was half of that formed from 32P(i) (K(1/2) = 0.22 mM). The maximum 32P binding for the enzyme during turnover in the presence of [gamma-32P]ATP or [alpha-32P]ATP was due to 0.5 mol of E32P + 0.5 mol of an acid-labile enzyme-bound [gamma-32P]ATP (EATP) or 0.5 mol of an acid-labile enzyme-bound [alpha-32P]ATP, respectively. The K(1/2) for EATP formation in both cases was 0.12 approximately 0.14 mM. The turnover number of the enzyme (i.e., the H+-ATPase activity/(EP + EATP)) was very close to the apparent rate constants for EP breakdown and P(i) liberation, both of which decreased with increasing concentrations of ATP. The ratio of the amount of P(i) liberated to that of EP that disappeared increased from 1 to approximately 2 with increasing concentrations of ATP (i.e., equal amounts of EP and EATP exist, both of which release phosphate in the presence of high concentrations of ATP). This represents the first direct evidence, for the case of a P-type ATPase, in which 2 mol of P(i) liberation occurs simultaneously from 1 mol of EP for half of the enzyme molecules and 1 mol of EATP for the other half during ATP hydrolysis. Each catalytic alpha chain is involved in cross-talk, thus maintaining half-site phosphorylation and half-site ATP binding which are induced by high- and low-affinity ATP binding, respectively, in the presence of Mg2+.

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Year:  2002        PMID: 11841238     DOI: 10.1021/bi015622r

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  5 in total

1.  Intermolecular interactions in the mechanism of skeletal muscle sarcoplasmic reticulum Ca(2+)-ATPase (SERCA1): evidence for a triprotomer.

Authors:  James E Mahaney; David D Thomas; Iain K Farrance; Jeffrey P Froehlich
Journal:  Biochemistry       Date:  2008-12-23       Impact factor: 3.162

Review 2.  Mechanism of allosteric effects of ATP on the kinetics of P-type ATPases.

Authors:  Ronald James Clarke
Journal:  Eur Biophys J       Date:  2009-02-19       Impact factor: 1.733

3.  Inter-subunit interaction of gastric H+,K+-ATPase prevents reverse reaction of the transport cycle.

Authors:  Kazuhiro Abe; Kazutoshi Tani; Tomohiro Nishizawa; Yoshinori Fujiyoshi
Journal:  EMBO J       Date:  2009-04-23       Impact factor: 11.598

4.  Active detergent-solubilized H+,K+-ATPase is a monomer.

Authors:  Ingrid Dach; Claus Olesen; Luca Signor; Poul Nissen; Marc le Maire; Jesper V Møller; Christine Ebel
Journal:  J Biol Chem       Date:  2012-10-10       Impact factor: 5.157

5.  Systematic comparison of molecular conformations of H+,K+-ATPase reveals an important contribution of the A-M2 linker for the luminal gating.

Authors:  Kazuhiro Abe; Kazutoshi Tani; Yoshinori Fujiyoshi
Journal:  J Biol Chem       Date:  2014-09-17       Impact factor: 5.157

  5 in total

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