Literature DB >> 8224152

Stoichiometry of a Cl(-)-translocating ATPase.

G A Gerencser1.   

Abstract

It has been determined that Mg2+ stimulates phosphorylation while Cl- stimulates dephosphorylation of the chloride pump during its reaction sequence. The stoichiometry of ATP hydrolyzed to Cl- transported during a single cycle of the reaction sequence was ascertained. Intracellular concentrations of ATP, ADP and inorganic phosphate were determined and, coupled with an estimate of the standard free energy of hydrolysis for ATP, the operant free energy for ATP hydrolysis was calculated. Because the operating free energy of the pump is approximately one-half the energy obtained from the total free energy of ATP hydrolysis, the only possible integral stoichiometries are one or, at the most, two net charges transported per cycle per ATP hydrolyzed.

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 8224152     DOI: 10.1016/0014-5793(93)80391-7

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


  1 in total

1.  Reconstituted Cl- pump protein: a novel ion(Cl-)-motive ATPase.

Authors:  G A Gerencser; K R Purushotham
Journal:  J Bioenerg Biomembr       Date:  1996-12       Impact factor: 2.945

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.