Evidence map›Paper›PMID 27172383›Full record

ArticleProteins2017

A benchmark testing ground for integrating homology modeling and protein docking.

Tanggis Bohnuud, Lingqi Luo, Shoshana J Wodak, Alexandre M J J Bonvin, Zhiping Weng, Sandor Vajda, Ora Schueler-Furman, Dima Kozakov

Abstract read
In one paragraph

Article in Proteins, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Conservation of binding properties in protein models.Computational and structural biotechnology journal · 2021
    Article
  6. Article
  7. Article
  8. Article
  9. Homology models of mouse and rat estrogen receptor-Computational toxicology (Amsterdam, Netherlands) · 2019
    Article
  10. Review
  11. Review
  12. Dockground: A comprehensive data resource for modeling of protein complexes.Protein science : a publication of the Protein Society · 2018
    Article
  13. Article
  14. Article
  15. Article
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.

Tanggis BohnuudDepartment of Biomedical Engineering, Boston University, Boston, Massachusetts, 02215.
Lingqi LuoDepartment of Biomedical Engineering, Boston University, Boston, Massachusetts, 02215.
Shoshana J WodakVIB Structural Biology Research Center, VUB Pleinlaan 2, Brussels, 1050, Belgium.
Alexandre M J J BonvinBijvoet Center for Biomolecular Research, Faculty of Science, Chemistry, Utrecht University, Utrecht, 3584CH, The Netherlands.ORCID 0000-0001-7369-1322
Zhiping WengProgram in Bioinformatics and Integrative Biology, Department of Biochemistry and Molecular Pharmacology University of Massachusetts Medical School, Worcester, Massachusetts.
Sandor VajdaDepartment of Biomedical Engineering, Boston University, Boston, Massachusetts, 02215.
Ora Schueler-FurmanDepartment of Microbiology and Molecular Genetics, Institute for Medical Research Israel-Canada, Hadassah Medical School Hebrew University, Jerusalem, Israel.
Dima KozakovDepartment of Biomedical Engineering, Boston University, Boston, Massachusetts, 02215.

Funding

Analysis and Prediction of Molecular InteractionsR35GM118078 · NIGMS · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI SANDOR VAJDA · 2016 to 2026
$6.5M
A MULTISTAGE APPROACH TO PROTEIN-PROTEIN DOCKINGR01GM061867 · NIGMS · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI VAJDA, SANDOR · 2000 to 2016
$4.0M
Refinement Methods for Protein Docking based on Exploring Multi-Dimensional EnergR01GM093147 · NIGMS · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI KOZAKOV, DMYTRO, PASCHALIDIS, IOANNIS · 2011 to 2014
$1.2M
Continual Development of Protein Docking AlgorithmsR01GM084884 · NIGMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI WENG, ZHIPING · 2009 to 2012
$1.2M
NIGMS NIH HHS R01 GM061867NIGMS NIH HHS R01 GM084884NIGMS NIH HHS R01 GM093147NIGMS NIH HHS R35 GM118078
6 · The paper itself

Abstract

Protein docking procedures carry out the task of predicting the structure of a protein-protein complex starting from the known structures of the individual protein components. More often than not, however, the structure of one or both components is not known, but can be derived by homology modeling on the basis of known structures of related proteins deposited in the Protein Data Bank (PDB). Thus, the problem is to develop methods that optimally integrate homology modeling and docking with the goal of predicting the structure of a complex directly from the amino acid sequences of its component proteins. One possibility is to use the best available homology modeling and docking methods. However, the models built for the individual subunits often differ to a significant degree from the bound conformation in the complex, often much more so than the differences observed between free and bound structures of the same protein, and therefore additional conformational adjustments, both at the backbone and side chain levels need to be modeled to achieve an accurate docking prediction. In particular, even homology models of overall good accuracy frequently include localized errors that unfavorably impact docking results. The predicted reliability of the different regions in the model can also serve as a useful input for the docking calculations. Here we present a benchmark dataset that should help to explore and solve combined modeling and docking problems. This dataset comprises a subset of the experimentally solved 'target' complexes from the widely used Docking Benchmark from the Weng Lab (excluding antibody-antigen complexes). This subset is extended to include the structures from the PDB related to those of the individual components of each complex, and hence represent potential templates for investigating and benchmarking integrated homology modeling and docking approaches. Template sets can be dynamically customized by specifying ranges in sequence similarity and in PDB release dates, or using other filtering options, such as excluding sets of specific structures from the template list. Multiple sequence alignments, as well as structural alignments of the templates to their corresponding subunits in the target are also provided. The resource is accessible online or can be downloaded at http://cluspro.org/benchmark, and is updated on a weekly basis in synchrony with new PDB releases. Proteins 2016; 85:10-16. © 2016 Wiley Periodicals, Inc.

Indexed as

BenchmarkingMolecular Docking SimulationSoftwareStructural Homology, ProteinAmino Acid SequenceBinding SitesCaspase 9Databases, ProteinHumansInternetLigandsProtein BindingProtein Interaction Domains and MotifsProtein MultimerizationProtein Structure, SecondaryProtein Structure, TertiaryCASP9 protein, humanCaspase 9LigandsXIAP protein, humanX-Linked Inhibitor of Apoptosis ProteinCAPRI docking experimentmethod developmentprotein-protein dockingprotein structure predictionuser community

Identifiers

PMID27172383
PMCPMC5817996

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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.