Evidence map›Paper›PMID 34222334›Full record

ArticleFrontiers in molecular biosciences2021

Aggregation is a Context-Dependent Constraint on Protein Evolution.

Michele Monti, Alexandros Armaos, Marco Fantini, Annalisa Pastore, Gian Gaetano Tartaglia

Open access · goldAbstract read
In one paragraph

Article in Frontiers in molecular biosciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-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

6 citing papers in PubMed, 13 citations in OpenAlex.

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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

5 authors at 5 institutions in 4 countries.

Michele MontiCentre for Genomic Regulation (CRG), The Barcelona Institute for Science and Technology, Barcelona, Spain.
Alexandros ArmaosCentre for Genomic Regulation (CRG), The Barcelona Institute for Science and Technology, Barcelona, Spain.
Marco FantiniDepartment of Chemistry, Columbia University, New York, NY, United States.
Annalisa Pastore3UK-DRI Centre at the Maurice Wohl Institute, Department of Clinical and Basic Neuroscience, King's College London, London, United Kingdom.
Gian Gaetano TartagliaCentre for Genomic Regulation (CRG), The Barcelona Institute for Science and Technology, Barcelona, Spain.
Barcelona Institute for Science and Technology · ESColumbia University · USInstitució Catalana de Recerca i Estudis Avançats · ESItalian Institute of Technology · ITUK Dementia Research Institute · GB

Funding

Medical Research Council MC_PC_13054Medical Research Council MC_U117584256
6 · The paper itself

Abstract

Solubility is a requirement for many cellular processes. Loss of solubility and aggregation can lead to the partial or complete abrogation of protein function. Thus, understanding the relationship between protein evolution and aggregation is an important goal. Here, we analysed two deep mutational scanning experiments to investigate the role of protein aggregation in molecular evolution. In one data set, mutants of a protein involved in RNA biogenesis and processing, human TAR DNA binding protein 43 (TDP-43), were expressed in

Indexed as

cellular fitnesscomputational modeldeep scanningevolutionprotein aggregation

Identifiers

PMID34222334
PMCPMC8249573
OpenAlexW3173575970

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.