Evidence map›Paper›PMID 21071796›Full record

ArticleIEEE/ACM transactions on computational biology and bioinformatics

F2Dock: fast Fourier protein-protein docking.

Chandrajit Bajaj, Rezaul Chowdhury, Vinay Siddavanahalli

Abstract read
In one paragraph

Article in IEEE/ACM transactions on computational biology and bioinformatics. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. DOT2: Macromolecular docking with improved biophysical models.Journal of computational chemistry · 2013
    Article
  8. NONUNIFORM FOURIER TRANSFORMS FOR RIGID-BODY AND MULTI-DIMENSIONAL ROTATIONAL CORRELATIONS.SIAM journal on scientific computing : a publication of the Society for Industrial and Applied Mathematics · 2013
    Article
  9. Article
  10. Article
  11. Review
  12. AN EFFICIENT HIGHER-ORDER FAST MULTIPOLE BOUNDARY ELEMENT SOLUTION FOR POISSON-BOLTZMANN BASED MOLECULAR ELECTROSTATICS.SIAM journal on scientific computing : a publication of the Society for Industrial and Applied Mathematics · 2011
    Article
  13. 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

3 authors.

Chandrajit BajajComputational Visualization Center, Department of Computer Sciences and the Institute of Computational Engineering and Sciences, University of Texas at Austin, 1 University Station C0500, Austin, Texas 78712, USA. bajaj@cs.utexas.edu
Rezaul Chowdhury
Vinay Siddavanahalli

Funding

A New Approach to Rapid Protein-Protein DockingR01GM073087 · NIGMS · UNIVERSITY OF TEXAS AT AUSTIN · PI BAJAJ, CHANDRAJIT L · 2006 to 2008
$1.3M
Software Maintenance for Biomolecular ComplexesR01EB004873 · NIBIB · UNIVERSITY OF TEXAS AT AUSTIN · PI BAJAJ, CHANDRAJIT L · 2007 to 2010
$1.2M
Hierarchical Methods for Large BioMolecular ComplexesR01GM074258 · NIGMS · UNIVERSITY OF TEXAS AUSTIN · PI BAJAJ, CHANDRAJIT L · 2005 to 2010
$778k
NIBIB NIH HHS R01 EB004873NIBIB NIH HHS R01-EB004873NIGMS NIH HHS R01 GM073087NIGMS NIH HHS R01-GM073087NIGMS NIH HHS R01 GM074258
6 · The paper itself

Abstract

The functions of proteins are often realized through their mutual interactions. Determining a relative transformation for a pair of proteins and their conformations which form a stable complex, reproducible in nature, is known as docking. It is an important step in drug design, structure determination, and understanding function and structure relationships. In this paper, we extend our nonuniform fast Fourier transform-based docking algorithm to include an adaptive search phase (both translational and rotational) and thereby speed up its execution. We have also implemented a multithreaded version of the adaptive docking algorithm for even faster execution on multicore machines. We call this protein-protein docking code F2Dock (F2 = Fast Fourier). We have calibrated F2Dock based on an extensive experimental study on a list of benchmark complexes and conclude that F2Dock works very well in practice. Though all docking results reported in this paper use shape complementarity and Coulombic-potential-based scores only, F2Dock is structured to incorporate Lennard-Jones potential and reranking docking solutions based on desolvation energy .

Indexed as

AlgorithmsFourier AnalysisAnimalsBacterial ProteinsBinding SitesCattleComputational BiologyHumansModels, MolecularModels, StatisticalProtein BindingProtein Interaction MappingProteinsSoftwareStatic ElectricityBacterial ProteinsProteins

Identifiers

PMID21071796
PMCPMC3058388

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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.