Evidence map›Paper›PMID 30114370›Full record

ArticleJournal of chemical information and modeling2018

Efficiency of Stratification for Ensemble Docking Using Reduced Ensembles.

Bing Xie, John D Clark, David D L Minh

Erratum issuedAbstract read
In one paragraph

Article in Journal of chemical information and modeling, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. On Inactivation of the Coronavirus Main Protease.Journal of chemical information and modeling · 2024
    Article
  3. Benchmarking ensemble docking methods in D3R Grand Challenge 4.Journal of computer-aided molecular design · 2022
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Bing XieDepartment of Chemistry , Illinois Institute of Technology , Chicago , Illinois 60616 , United States.ORCID 0000-0002-1692-7199
John D ClarkDepartment of Chemistry , Illinois Institute of Technology , Chicago , Illinois 60616 , United States.
David D L MinhDepartment of Chemistry , Illinois Institute of Technology , Chicago , Illinois 60616 , United States.ORCID 0000-0002-4802-2618

Funding

Sound-stage Virtual Screening Based on Implicit Ligand TheoryR15GM114781 · NIGMS · ILLINOIS INSTITUTE OF TECHNOLOGY · PI MINH, DAVID DO LE · 2015 to 2015
$337k
NIGMS NIH HHS R15 GM114781
6 · The paper itself

Abstract

Molecular docking can account for receptor flexibility by combining the docking score over multiple rigid receptor conformations, such as snapshots from a molecular dynamics simulation. Here, we evaluate a number of common snapshot selection strategies using a quality metric from stratified sampling, the efficiency of stratification, which compares the variance of a selection strategy to simple random sampling. We also extend the metric to estimators of exponential averages (which involve an exponential transformation, averaging, and inverse transformation) and minima. For docking sets of over 500 ligands to four different proteins of varying flexibility, we observe that, for estimating ensemble averages and exponential averages, many clustering algorithms have similar performance trends: for a few snapshots (less than 25), medoids are the most efficient, while, for a larger number, optimal (the allocation that minimizes the variance) and proportional (to the size of each cluster) allocation become more efficient. Proportional allocation appears to be the most consistently efficient for estimating minima.

Indexed as

Molecular Docking SimulationBinding SitesCluster AnalysisModels, MolecularProtein BindingProtein Conformation

Identifiers

PMID30114370
PMCPMC6338335

What OpenQuestion holds

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LicenceTDM
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.