4.7 Article

Lytic Water Dynamics Reveal Evolutionarily Conserved Mechanisms of ATP Hydrolysis by TIP49 AAA+ ATPases

Journal

STRUCTURE
Volume 22, Issue 4, Pages 549-559

Publisher

CELL PRESS
DOI: 10.1016/j.str.2014.02.002

Keywords

-

Funding

  1. Russian Federation for PhD Students [5651.2013.4]
  2. Research Councils UK Academic Fellowship
  3. Federal Program of the Russian Ministry of Education and Science [11.519.11.2002]
  4. intramural LBME
  5. CNRS
  6. Wellcome Trust [079351/Z/06/Z]
  7. BBSRC [BB/E008232/1]
  8. Wellcome Trust [079351/Z/06/Z] Funding Source: Wellcome Trust
  9. BBSRC [BB/H019332/1, BB/E008232/1] Funding Source: UKRI
  10. Biotechnology and Biological Sciences Research Council [BB/H019332/1, BB/E008232/1] Funding Source: researchfish

Ask authors/readers for more resources

Eukaryotic TIP49a (Pontin) and TIP49b (Reptin) AAA+ ATPases play essential roles in key cellular processes. How their weak ATPase activity contributes to their important functions remains largely unknown and difficult to analyze because of the divergent properties of TIP49a and TIP49b proteins and of their homo-and hetero-oligomeric assemblies. To circumvent these complexities, we have analyzed the single ancient TIP49 ortholog found in the archaeon Methanopyrus kandleri (mkTIP49). All-atom homology modeling and molecular dynamics simulations validated by biochemical assays reveal highly conserved organizational principles and identify key residues for ATP hydrolysis. An unanticipated crosstalk between Walker B and Sensor I motifs impacts the dynamics of water molecules and highlights a critical role of trans-acting aspartates in the lytic water activation step that is essential for the associative mechanism of ATP hydrolysis.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available