Evidence map›Paper›PMID 25547242›Full record

ArticleBMC bioinformatics2014

WEBnm@ v2.0: Web server and services for comparing protein flexibility.

Sandhya P Tiwari, Edvin Fuglebakk, Siv M Hollup, Lars Skjærven, Tristan Cragnolini, Svenn H Grindhaug, Kidane M Tekle, Nathalie Reuter

Abstract read
In one paragraph

Article in BMC bioinformatics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

59 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Force-regulated chaperone activity of BiP/ERdj3 is opposite to their homologs DnaK/DnaJ.Protein science : a publication of the Protein Society · 2024
    Article
  7. Article
  8. Article
  9. Computational Study of AmyloidβInorganic chemistry · 2024
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Sandhya P TiwariDepartment of Molecular Biology, University of Bergen, Bergen, Norway. Sandhya.Tiwari@mbi.uib.no.
Edvin FuglebakkComputational Biology Unit, Department of Informatics, University of Bergen, Bergen, Norway. Edvin.Fuglebakk@mbi.uib.no.
Siv M HollupComputational Biology Unit, Department of Informatics, University of Bergen, Bergen, Norway. siv.hollup@gmail.com.
Lars SkjærvenDepartment of Biomedicine, University of Bergen, Bergen, Norway. Lars.Skjarven@biomed.uib.no.
Tristan CragnoliniDepartment of Molecular Biology, University of Bergen, Bergen, Norway. tristan.cragnolini@gmail.com.
Svenn H GrindhaugComputational Biology Unit, Department of Informatics, University of Bergen, Bergen, Norway. svennhg@gmail.com.
Kidane M TekleComputational Biology Unit, Department of Informatics, University of Bergen, Bergen, Norway. kidane.tekle@cbu.uib.no.
Nathalie ReuterDepartment of Molecular Biology, University of Bergen, Bergen, Norway. Nathalie.Reuter@mbi.uib.no.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNormal mode analysis (NMA) using elastic network models is a reliable and cost-effective computational method to characterise protein flexibility and by extension, their dynamics. Further insight into the dynamics-function relationship can be gained by comparing protein motions between protein homologs and functional classifications. This can be achieved by comparing normal modes obtained from sets of evolutionary related proteins.

resultsWe have developed an automated tool for comparative NMA of a set of pre-aligned protein structures. The user can submit a sequence alignment in the FASTA format and the corresponding coordinate files in the Protein Data Bank (PDB) format. The computed normalised squared atomic fluctuations and atomic deformation energies of the submitted structures can be easily compared on graphs provided by the web user interface. The web server provides pairwise comparison of the dynamics of all proteins included in the submitted set using two measures: the Root Mean Squared Inner Product and the Bhattacharyya Coefficient. The Comparative Analysis has been implemented on our web server for NMA, WEBnm@, which also provides recently upgraded functionality for NMA of single protein structures. This includes new visualisations of protein motion, visualisation of inter-residue correlations and the analysis of conformational change using the overlap analysis. In addition, programmatic access to WEBnm@ is now available through a SOAP-based web service. Webnm@ is available at http://apps.cbu.uib.no/webnma .

conclusionWEBnm@ v2.0 is an online tool offering unique capability for comparative NMA on multiple protein structures. Along with a convenient web interface, powerful computing resources, and several methods for mode analyses, WEBnm@ facilitates the assessment of protein flexibility within protein families and superfamilies. These analyses can give a good view of how the structures move and how the flexibility is conserved over the different structures.

Indexed as

Databases, ProteinInternetMetabolic Networks and PathwaysSoftwareAdenylate KinaseHumansMultigene FamilyProtein ConformationProtein FoldingProtein Interaction Domains and MotifsProteinsSequence AlignmentAdenylate KinaseProteins

Identifiers

PMID25547242
PMCPMC4339738

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.