Evidence map›Paper›PMID 33909605›Full record

ArticlePLoS biology2021

Pathogenic missense protein variants affect different functional pathways and proteomic features than healthy population variants.

Anna Laddach, Joseph Chi Fung Ng, Franca Fraternali

Open access · goldAbstract readValidation Study
In one paragraph

Article in PLoS biology, 2021. 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
3.3field-weighted citation impact, top 8% 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

15 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. An interpretable molecular framework for predicting cancer driver missense mutations.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  12. Estimating clinical risk in gene regions from population sequencing cohort data.medRxiv : the preprint server for health sciences · 2023
    Article
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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.

Anna LaddachRandall Centre for Cell and Molecular Biophysics, King's College London, London, United Kingdom.
Joseph Chi Fung NgRandall Centre for Cell and Molecular Biophysics, King's College London, London, United Kingdom.ORCID 0000-0002-3617-5211
Franca FraternaliRandall Centre for Cell and Molecular Biophysics, King's College London, London, United Kingdom.ORCID 0000-0002-3143-6574
King's College London · GB

Funding

Biotechnology and Biological Sciences Research Council BB/H018409/1Biotechnology and Biological Sciences Research Council BB/T002212/1British Heart Foundation NH/12/2/29427British Heart Foundation RE/13/2/30182Medical Research Council MR/L01257X/1
6 · The paper itself

Abstract

Missense variants are present amongst the healthy population, but some of them are causative of human diseases. A classification of variants associated with "healthy" or "diseased" states is therefore not always straightforward. A deeper understanding of the nature of missense variants in health and disease, the cellular processes they may affect, and the general molecular principles which underlie these differences is essential to offer mechanistic explanations of the true impact of pathogenic variants. Here, we have formalised a statistical framework which enables robust probabilistic quantification of variant enrichment across full-length proteins, their domains, and 3D structure-defined regions. Using this framework, we validate and extend previously reported trends of variant enrichment in different protein structural regions (surface/core/interface). By examining the association of variant enrichment with available functional pathways and transcriptomic and proteomic (protein half-life, thermal stability, abundance) data, we have mined a rich set of molecular features which distinguish between pathogenic and population variants: Pathogenic variants mainly affect proteins involved in cell proliferation and nucleotide processing and are enriched in more abundant proteins. Additionally, rare population variants display features closer to common than pathogenic variants. We validate the association between these molecular features and variant pathogenicity by comparing against existing in silico variant impact annotations. This study provides molecular details into how different proteins exhibit resilience and/or sensitivity towards missense variants and provides the rationale to prioritise variant-enriched proteins and protein domains for therapeutic targeting and development. The ZoomVar database, which we created for this study, is available at fraternalilab.kcl.ac.uk/ZoomVar. It allows users to programmatically annotate missense variants with protein structural information and to calculate variant enrichment in different protein structural regions.

Indexed as

ProteomeAmino Acid SequenceComputational BiologyDatabases, ProteinGenetic Diseases, InbornGenetic Predisposition to DiseaseGerm-Line MutationHealthHumansMutant ProteinsMutation, MissenseProtein ConformationProtein FoldingProtein Interaction Domains and MotifsProtein Processing, Post-TranslationalProteinsMutant ProteinsProteinsProteome

Identifiers

PMID33909605
PMCPMC8110273
OpenAlexW3157830400

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.