Evidence map›Paper›PMID 29286658›Full record

ArticleJournal of chemical information and modeling2018

Predicting Displaceable Water Sites Using Mixed-Solvent Molecular Dynamics.

Sarah E Graham, Richard D Smith, Heather A Carlson

Open access · greenAbstract readValidation Study
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. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-weighted citation impact, top 20% of its field
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

11 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Watermelon: setup and validation of anJournal of enzyme inhibition and medicinal chemistry · 2024
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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

3 authors at 1 institution in 1 country.

Sarah E GrahamDepartment of Biophysics and ‡Department of Medicinal Chemistry, College of Pharmacy, University of Michigan , 428 Church Street, Ann Arbor, Michigan 48109-1065, United States.ORCID 0000-0003-1271-2489
Richard D SmithDepartment of Biophysics and ‡Department of Medicinal Chemistry, College of Pharmacy, University of Michigan , 428 Church Street, Ann Arbor, Michigan 48109-1065, United States.
Heather A CarlsonDepartment of Biophysics and ‡Department of Medicinal Chemistry, College of Pharmacy, University of Michigan , 428 Church Street, Ann Arbor, Michigan 48109-1065, United States.ORCID 0000-0002-7495-1699
University of Michigan · US

Funding

Multiple Protein Structures in Computational Drug DesignR01GM065372 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CARLSON, HEATHER A · 2002 to 2021
$3.4M
NIGMS NIH HHS R01 GM065372
6 · The paper itself

Abstract

Water molecules are an important factor in protein-ligand binding. Upon binding of a ligand with a protein's surface, waters can either be displaced by the ligand or may be conserved and possibly bridge interactions between the protein and ligand. Depending on the specific interactions made by the ligand, displacing waters can yield a gain in binding affinity. The extent to which binding affinity may increase is difficult to predict, as the favorable displacement of a water molecule is dependent on the site-specific interactions made by the water and the potential ligand. Several methods have been developed to predict the location of water sites on a protein's surface, but the majority of methods are not able to take into account both protein dynamics and the interactions made by specific functional groups. Mixed-solvent molecular dynamics (MixMD) is a cosolvent simulation technique that explicitly accounts for the interaction of both water and small molecule probes with a protein's surface, allowing for their direct competition. This method has previously been shown to identify both active and allosteric sites on a protein's surface. Using a test set of eight systems, we have developed a method using MixMD to identify conserved and displaceable water sites. Conserved sites can be determined by an occupancy-based metric to identify sites which are consistently occupied by water even in the presence of probe molecules. Conversely, displaceable water sites can be found by considering the sites which preferentially bind probe molecules. Furthermore, the inclusion of six probe types allows the MixMD method to predict which functional groups are capable of displacing which water sites. The MixMD method consistently identifies sites which are likely to be nondisplaceable and predicts the favorable displacement of water sites that are known to be displaced upon ligand binding.

Indexed as

Molecular Dynamics SimulationAllosteric SiteAmyloid Precursor Protein Secretasesbeta-LactamasesBromodomain Containing ProteinsCell Cycle ProteinsHSP90 Heat-Shock ProteinsHumansLigandsNeuraminidaseNuclear ProteinsPepsin AProtein BindingProteinsReproducibility of ResultsSolventsAmyloid Precursor Protein Secretasesbeta-LactamasesBRD4 protein, humanBromodomain Containing ProteinsCell Cycle ProteinsHSP90 Heat-Shock ProteinsLigandsNeuraminidaseNuclear ProteinsPepsin AProteinsSolventsTetrahydrofolate DehydrogenaseThrombinTranscription FactorsWater

Identifiers

PMID29286658
PMCPMC6190669
OpenAlexW2777363962

What OpenQuestion holds

Textmetadata
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.