Automated Author Profile

M Orville, Allen

Current S-Index

0.9

Sum of Dataset Indices for all datasets

Average Dataset Index per Dataset

0.5

Average Dataset Index per dataset

Total Datasets

2

Total datasets for this author

Average FAIR Score

90.4%

Average FAIR Score per dataset

Total Citations

0

Total citations to the author's datasets

Total Mentions

0

Total mentions of the author's datasets

S-Index Interpretation

S-Index Over Time

Cumulative Citations Over Time

Cumulative Mentions Over Time

Datasets

Supplementary information files for The adaptability of the ion binding site by the Ag(I)/Cu(I) periplasmic chaperone SilF.

Supplementary files for article The adaptability of the ion binding site by the Ag(I)/Cu(I) periplasmic chaperone SilF.The periplasmic chaperone SilF has been identified as part of an Ag(I) detoxification system in Gram negative bacteria. Sil proteins also bind Cu(I), but with reported weaker affinity, therefore leading to the designation of a specific detoxification system for Ag(I). Using isothermal titration calorimetry we show that binding of both ions is not only tighter than previously thought, but of very similar affinities. We investigated the structural origins of ion binding using molecular dynamics and QM/MM simulations underpinned by structural and biophysical experiments. The results of this analysis showed that the binding site adapts to accommodate either ion, with key interactions with the solvent in the case of Cu(I). The implications of this are that Gram negative bacteria do not appear to have evolved a specific Ag(I) efflux system but take advantage of the existing Cu(I) detoxification system. Therefore, there are consequences for how we define a particular metal resistance mechanism and understand its evolution in the environment.

Authors

  • M Lithgo, Ryan ;
  • Hanževački, Marko ;
  • Harris, Gemma ;
  • JAG Kamps, Jos ;
  • Holden, Ellie ;
  • Gianga, Tiberiu-Marius ;
  • LP Benesch, Justin ;
  • M Jäger, Christof ;
  • Croft, Anna ;
  • Hussain, Rohannah ;
  • L Hobman, Jon ;
  • M Orville, Allen ;
  • Quigley, Andrew ;
  • B Carr, Stephen ;
  • J Scott, David
0 Citations0 Mentions90% FAIR0.5 Dataset Index
10.17028/rd.lboro.244206222023

Supplementary information files for The adaptability of the ion binding site by the Ag(I)/Cu(I) periplasmic chaperone SilF.

Supplementary files for article The adaptability of the ion binding site by the Ag(I)/Cu(I) periplasmic chaperone SilF.The periplasmic chaperone SilF has been identified as part of an Ag(I) detoxification system in Gram negative bacteria. Sil proteins also bind Cu(I), but with reported weaker affinity, therefore leading to the designation of a specific detoxification system for Ag(I). Using isothermal titration calorimetry we show that binding of both ions is not only tighter than previously thought, but of very similar affinities. We investigated the structural origins of ion binding using molecular dynamics and QM/MM simulations underpinned by structural and biophysical experiments. The results of this analysis showed that the binding site adapts to accommodate either ion, with key interactions with the solvent in the case of Cu(I). The implications of this are that Gram negative bacteria do not appear to have evolved a specific Ag(I) efflux system but take advantage of the existing Cu(I) detoxification system. Therefore, there are consequences for how we define a particular metal resistance mechanism and understand its evolution in the environment.

Authors

  • M Lithgo, Ryan ;
  • Hanževački, Marko ;
  • Harris, Gemma ;
  • JAG Kamps, Jos ;
  • Holden, Ellie ;
  • Gianga, Tiberiu-Marius ;
  • LP Benesch, Justin ;
  • M Jäger, Christof ;
  • Croft, Anna ;
  • Hussain, Rohannah ;
  • L Hobman, Jon ;
  • M Orville, Allen ;
  • Quigley, Andrew ;
  • B Carr, Stephen ;
  • J Scott, David
0 Citations0 Mentions90% FAIR0.5 Dataset Index
10.17028/rd.lboro.24420622.v12023