Evidence map›Paper›PMID 37574757›Full record

ArticleProtein science : a publication of the Protein Society2023

ParSe 2.0: A web tool to identify drivers of protein phase separation at the proteome level.

Colorado Wilson, Karen A Lewis, Nicholas C Fitzkee, Loren E Hough, Steven T Whitten

Abstract read
In one paragraph

Article in Protein science : a publication of the Protein Society, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

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  14. ParSe 2.0: A web tool to identify drivers of protein phase separation at the proteome level.Protein science : a publication of the Protein Society · 2023
    Article
  15. 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

5 authors.

Colorado WilsonDepartment of Chemistry and Biochemistry, Texas State University, San Marcos, Texas, USA.
Karen A LewisDepartment of Chemistry and Biochemistry, Texas State University, San Marcos, Texas, USA.
Nicholas C FitzkeeDepartment of Chemistry, Mississippi State University, Mississippi State, Mississippi, USA.ORCID 0000-0002-8993-2140
Loren E HoughDepartment of Physics, University of Colorado Boulder, Boulder, Colorado, USA.ORCID 0000-0002-1104-0126
Steven T WhittenDepartment of Chemistry and Biochemistry, Texas State University, San Marcos, Texas, USA.ORCID 0000-0003-1364-3956

Funding

Molecular dissection of the C-terminal tails of tubulin and the effect of their polyglycylation on binding and microtubule assemblyR35GM119755 · NIGMS · UNIVERSITY OF COLORADO · PI HOUGH, LOREN E · 2016 to 2020
$1.8M
Structure, Orientation, and Competitive Interactions of S. Epidermidis Biofilm Proteins on SurfacesR01AI139479 · NIAID · MISSISSIPPI STATE UNIVERSITY · PI FITZKEE, NICHOLAS C · 2018 to 2022
$1.8M
Molecular Mechanisms of the Posttranscriptional Regulator LARP6R15GM119096 · NIGMS · TEXAS STATE UNIVERSITY · PI LEWIS, KAREN ADELL · 2016 to 2019
$891k
NIAID NIH HHS R01 AI139479NIGMS NIH HHS R15 GM119096NIGMS NIH HHS R35 GM119755
6 · The paper itself

Abstract

We have developed an algorithm, ParSe, which accurately identifies from the primary sequence those protein regions likely to exhibit physiological phase separation behavior. Originally, ParSe was designed to test the hypothesis that, for flexible proteins, phase separation potential is correlated to hydrodynamic size. While our results were consistent with that idea, we also found that many different descriptors could successfully differentiate between three classes of protein regions: folded, intrinsically disordered, and phase-separating intrinsically disordered. Consequently, numerous combinations of amino acid property scales can be used to make robust predictions of protein phase separation. Built from that finding, ParSe 2.0 uses an optimal set of property scales to predict domain-level organization and compute a sequence-based prediction of phase separation potential. The algorithm is fast enough to scan the whole of the human proteome in minutes on a single computer and is equally or more accurate than other published predictors in identifying proteins and regions within proteins that drive phase separation. Here, we describe a web application for ParSe 2.0 that may be accessed through a browser by visiting https://stevewhitten.github.io/Parse_v2_FASTA to quickly identify phase-separating proteins within large sequence sets, or by visiting https://stevewhitten.github.io/Parse_v2_web to evaluate individual protein sequences.

Indexed as

Phase TransitionProteinsSoftwareAlgorithmsProteomeProteinsProteomeintrinsically disordered proteinintrinsically disordered regionsprotein phase separationprotein self-assemblyprotein sequencesubcellular organelle

Identifiers

PMID37574757
PMCPMC10464302

What OpenQuestion holds

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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.