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Front Physiol. 2017 Apr 11;8:202. doi: 10.3389/fphys.2017.00202. eCollection 2017.

Improved Model of Proton Pump Crystal Structure Obtained by Interactive Molecular Dynamics Flexible Fitting Expands the Mechanistic Model for Proton Translocation in P-Type ATPases.

Frontiers in physiology

Dorota Focht, Tristan I Croll, Bjorn P Pedersen, Poul Nissen

Affiliations

  1. Department of Molecular Biology and Genetics, Aarhus UniversityAarhus, Denmark.
  2. DANDRITE, Nordic-EMBL Partnership for Molecular Medicine, Aarhus UniversityAarhus, Denmark.
  3. PUMPkin, Danish National Research Foundation, Aarhus UniversityAarhus, Denmark.
  4. Institute of Health Biomedical Innovation, Queensland University of TechnologyBrisbane, QLD, Australia.
  5. Aarhus Institute of Advanced Studies, Aarhus UniversityAarhus, Denmark.

PMID: 28443028 PMCID: PMC5387105 DOI: 10.3389/fphys.2017.00202

Abstract

The plasma membrane H

Keywords: Arabidopsis thaliana AHA2; P-type ATPases; crystallography; iMDFF; membrane transport; molecular dynamics; plasma membrane proton pump; proton gradient

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