Evidence map›Paper›PMID 27620381›Full record

ArticleComputational biology and chemistry2016

Assessing the similarity of ligand binding conformations with the Contact Mode Score.

Yun Ding, Ye Fang, Juana Moreno, J Ramanujam, Mark Jarrell, Michal Brylinski

Abstract read
In one paragraph

Article in Computational biology and chemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing 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

35 citing papers in PubMed.

  1. Article
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  6. Potential Antidiabetic Inhibitors and Antimicrobials from the FungusJournal of microbiology and biotechnology · 2025
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  12. Computer-Aided Discovery ofBiomedical engineering and computational biology · 2024
    Article
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  15. Novel Anti-Acetylcholinesterase Effect ofLife (Basel, Switzerland) · 2023
    Article
  16. Article
  17. Review
  18. Article
  19. Article
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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

6 authors.

Yun DingDepartment of Physics and Astronomy, Louisiana State University, Baton Rouge, LA 70803, USA. Electronic address: yding8@lsu.edu.
Ye FangSchool of Electrical Engineering and Computer Science, Louisiana State University, Baton Rouge, LA 70803, USA; Center for Computation & Technology, Louisiana State University, Baton Rouge, LA 70803, USA. Electronic address: yfang11@lsu.edu.
Juana MorenoDepartment of Physics and Astronomy, Louisiana State University, Baton Rouge, LA 70803, USA; Center for Computation & Technology, Louisiana State University, Baton Rouge, LA 70803, USA. Electronic address: moreno@phys.lsu.edu.
J RamanujamSchool of Electrical Engineering and Computer Science, Louisiana State University, Baton Rouge, LA 70803, USA; Center for Computation & Technology, Louisiana State University, Baton Rouge, LA 70803, USA. Electronic address: ram@cct.lsu.edu.
Mark JarrellDepartment of Physics and Astronomy, Louisiana State University, Baton Rouge, LA 70803, USA; Center for Computation & Technology, Louisiana State University, Baton Rouge, LA 70803, USA. Electronic address: jarrellphysics@gmail.com.
Michal BrylinskiDepartment of Biological Sciences, Louisiana State University, Baton Rouge, LA 70803, USA; Center for Computation & Technology, Louisiana State University, Baton Rouge, LA 70803, USA. Electronic address: michal@brylinski.org.

Funding

Combining structure-based network biology and heterogeneous computing for rational drug repositioning and polypharmacologyR35GM119524 · NIGMS · LOUISIANA STATE UNIV A&M COL BATON ROUGE · PI BRYLINSKI, MICHAL · 2016 to 2020
$962k
NIGMS NIH HHS R35 GM119524
6 · The paper itself

Abstract

Structural and computational biologists often need to measure the similarity of ligand binding conformations. The commonly used root-mean-square deviation (RMSD) is not only ligand-size dependent, but also may fail to capture biologically meaningful binding features. To address these issues, we developed the Contact Mode Score (CMS), a new metric to assess the conformational similarity based on intermolecular protein-ligand contacts. The CMS is less dependent on the ligand size and has the ability to include flexible receptors. In order to effectively compare binding poses of non-identical ligands bound to different proteins, we further developed the eXtended Contact Mode Score (XCMS). We believe that CMS and XCMS provide a meaningful assessment of the similarity of ligand binding conformations. CMS and XCMS are freely available at http://brylinski.cct.lsu.edu/content/contact-mode-score and http://geaux-computational-bio.github.io/contact-mode-score/.

Indexed as

Models, MolecularMolecular Docking SimulationBinding SitesHumansLigandsParticle SizeProtein BindingProtein Structure, TertiaryLigandsCMSContact Mode ScoreeXtended Contact Mode ScoreLigand binding conformationsMolecular dockingRMSDRoot-mean-square deviationXCMS

Identifiers

PMID27620381
PMCPMC5159245

What OpenQuestion holds

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Registered trials

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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.