Evidence map›Paper›PMID 34516109›Full record

ArticleJournal of chemical theory and computation2021

Machine-Learned Molecular Surface and Its Application to Implicit Solvent Simulations.

Haixin Wei, Zekai Zhao, Ray Luo

Abstract read
In one paragraph

Article in Journal of chemical theory and computation, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. A Concise Review of Biomolecule Visualization.Current issues in molecular biology · 2024
    Review
  5. Article
  6. AmberTools.Journal of chemical information and modeling · 2023
    Article
  7. 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.

Haixin WeiDepartments of Materials Science and Engineering, Molecular Biology and Biochemistry, Chemical and Biomolecular Engineering, and Biomedical Engineering, Graduate Program in Chemical and Materials Physics, University of California, Irvine, California 92697, United States.ORCID https://orcid.org/0000-0002-0954-4560
Zekai ZhaoDepartments of Materials Science and Engineering, Molecular Biology and Biochemistry, Chemical and Biomolecular Engineering, and Biomedical Engineering, Graduate Program in Chemical and Materials Physics, University of California, Irvine, California 92697, United States.
Ray LuoDepartments of Materials Science and Engineering, Molecular Biology and Biochemistry, Chemical and Biomolecular Engineering, and Biomedical Engineering, Graduate Program in Chemical and Materials Physics, University of California, Irvine, California 92697, United States.ORCID https://orcid.org/0000-0002-6346-8271

Funding

Multi-scaled Modeling of Electrostatic and Polarization Effects in BiomoleculesR35GM130367 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI RAY LUO · 2019 to 2026
$3.0M
AMBER/PBSA: An Open-Source Computer Program for Accurate and Scalable Solvation Analysis ofBiomoleculesR01GM093040 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI LUO, RAY · 2010 to 2018
$2.2M
NIGMS NIH HHS R01 GM093040NIGMS NIH HHS R35 GM130367
6 · The paper itself

Abstract

Implicit solvent models, such as Poisson-Boltzmann models, play important roles in computational studies of biomolecules. A vital step in almost all implicit solvent models is to determine the solvent-solute interface, and the solvent excluded surface (SES) is the most widely used interface definition in these models. However, classical algorithms used for computing SES are geometry-based, so that they are neither suitable for parallel implementations nor convenient for obtaining surface derivatives. To address the limitations, we explored a machine learning strategy to obtain a level set formulation for the SES. The training process was conducted in three steps, eventually leading to a model with over 95% agreement with the classical SES. Visualization of tested molecular surfaces shows that the machine-learned SES overlaps with the classical SES in almost all situations. Further analyses show that the machine-learned SES is incredibly stable in terms of rotational variation of tested molecules. Our timing analysis shows that the machine-learned SES is roughly 2.5 times as efficient as the classical SES routine implemented in Amber/PBSA on a tested central processing unit (CPU) platform. We expect further performance gain on massively parallel platforms such as graphics processing units (GPUs) given the ease in converting the machine-learned SES to a parallel procedure. We also implemented the machine-learned SES into the Amber/PBSA program to study its performance on reaction field energy calculation. The analysis shows that the two sets of reaction field energies are highly consistent with a 1% deviation on average. Given its level set formulation, we expect the machine-learned SES to be applied in molecular simulations that require either surface derivatives or high efficiency on parallel computing platforms.

Identifiers

PMID34516109
PMCPMC9132718

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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.