Evidence map›Paper›PMID 29020017›Full record

ArticlePloS one2017

Normal mode-guided transition pathway generation in proteins.

Byung Ho Lee, Sangjae Seo, Min Hyeok Kim, Youngjin Kim, Soojin Jo, Moon-Ki Choi, Hoomin Lee, Jae Boong Choi, Moon Ki Kim

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 27% 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

5 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Coarse-Grained Protein Dynamics Studies Using Elastic Network Models.International journal of molecular sciences · 2018
    Review
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

9 authors at 3 institutions in 2 countries.

Byung Ho LeeSchool of Mechanical Engineering, Sungkyunkwan University, Suwon, Republic of Korea.
Sangjae SeoDepartment of Materials Chemistry, Nagoya University, Nagoya, Japan.
Min Hyeok KimSchool of Computational Sciences, Korea Institute for Advanced Study, Seoul, Republic of Korea.
Youngjin KimSchool of Mechanical Engineering, Sungkyunkwan University, Suwon, Republic of Korea.
Soojin JoSchool of Mechanical Engineering, Sungkyunkwan University, Suwon, Republic of Korea.
Moon-Ki ChoiSchool of Mechanical Engineering, Sungkyunkwan University, Suwon, Republic of Korea.
Hoomin LeeSchool of Mechanical Engineering, Sungkyunkwan University, Suwon, Republic of Korea.
Jae Boong ChoiSchool of Mechanical Engineering, Sungkyunkwan University, Suwon, Republic of Korea.
Moon Ki KimSchool of Mechanical Engineering, Sungkyunkwan University, Suwon, Republic of Korea.ORCID http://orcid.org/0000-0003-0819-5909
Sungkyunkwan University · KRKorea Institute for Advanced Study · KRNagoya University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The biological function of proteins is closely related to its structural motion. For instance, structurally misfolded proteins do not function properly. Although we are able to experimentally obtain structural information on proteins, it is still challenging to capture their dynamics, such as transition processes. Therefore, we need a simulation method to predict the transition pathways of a protein in order to understand and study large functional deformations. Here, we present a new simulation method called normal mode-guided elastic network interpolation (NGENI) that performs normal modes analysis iteratively to predict transition pathways of proteins. To be more specific, NGENI obtains displacement vectors that determine intermediate structures by interpolating the distance between two end-point conformations, similar to a morphing method called elastic network interpolation. However, the displacement vector is regarded as a linear combination of the normal mode vectors of each intermediate structure, in order to enhance the physical sense of the proposed pathways. As a result, we can generate more reasonable transition pathways geometrically and thermodynamically. By using not only all normal modes, but also in part using only the lowest normal modes, NGENI can still generate reasonable pathways for large deformations in proteins. This study shows that global protein transitions are dominated by collective motion, which means that a few lowest normal modes play an important role in this process. NGENI has considerable merit in terms of computational cost because it is possible to generate transition pathways by partial degrees of freedom, while conventional methods are not capable of this.

Indexed as

AlgorithmsComputer SimulationModels, MolecularProteinsReproducibility of ResultsProteins

Identifiers

PMID29020017
PMCPMC5636086
OpenAlexW2763934161

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.