Evidence map›Paper›PMID 36829241›Full record

ArticleGenome biology2023

DIMPLE: deep insertion, deletion, and missense mutation libraries for exploring protein variation in evolution, disease, and biology.

Christian B Macdonald, David Nedrud, Patrick Rockefeller Grimes, Donovan Trinidad, James S Fraser, Willow Coyote-Maestas

Open access · goldAbstract read
In one paragraph

Article in Genome biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
10.9field-weighted citation impact, top 1% 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

52 citing papers in PubMed, 71 citations in OpenAlex.

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  11. Functional and antigenic constraints on the Nipah virus fusion protein.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  12. Article
  13. Review
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  16. Functional and antigenic constraints on the Nipah virus fusion protein.bioRxiv : the preprint server for biology · 2026
    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

6 authors at 2 institutions in 1 country.

Christian B MacdonaldDepartment of Bioengineering and Therapeutic Sciences, University of California, San Francisco, USA.
David NedrudBio-Techne, Minneapolis, Minnesota, USA.
Patrick Rockefeller GrimesDepartment of Bioengineering and Therapeutic Sciences, University of California, San Francisco, USA.
Donovan TrinidadDepartment of Medicine, Division of Infectious Disease, University of California, San Francisco, USA.
James S FraserDepartment of Bioengineering and Therapeutic Sciences, University of California, San Francisco, USA.
Willow Coyote-MaestasDepartment of Bioengineering and Therapeutic Sciences, University of California, San Francisco, USA. willow.coyote-maestas@ucsf.edu.ORCID http://orcid.org/0000-0001-9614-5340
University of California, San Francisco · USR&D Systems (United States) · US

Funding

Microbial Pathogenesis and Host DefenseT32AI060537 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Joanne N. Engel · 2004 to 2026
$6.5M
Equipment for Discovering and Manipulating Macromolecular Conformational EnsemblesR35GM145238 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI James Solomon Fraser · 2022 to 2026
$3.1M
Illumina NovaSeq 6000 Sequencing SystemS10OD028511 · OD · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CHOW, ERIC D · 2020 to 2020
$583k
Understanding the mechanisms of ESX secretion systems in mycobacteriaF31AI157438 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI TRINIDAD, DONOVAN DAVID · 2021 to 2023
$127k
Howard Hughes Medical InstituteNIAID NIH HHS F31 AI157438NIAID NIH HHS T32 AI060537NIGMS NIH HHS R35 GM145238NIH HHS S10 OD028511
6 · The paper itself

Abstract

Insertions and deletions (indels) enable evolution and cause disease. Due to technical challenges, indels are left out of most mutational scans, limiting our understanding of them in disease, biology, and evolution. We develop a low cost and bias method, DIMPLE, for systematically generating deletions, insertions, and missense mutations in genes, which we test on a range of targets, including Kir2.1. We use DIMPLE to study how indels impact potassium channel structure, disease, and evolution. We find deletions are most disruptive overall, beta sheets are most sensitive to indels, and flexible loops are sensitive to deletions yet tolerate insertions.

Indexed as

Mutation, MissenseProteinsBiologyINDEL MutationMutationProteins

Identifiers

PMID36829241
PMCPMC9951526
OpenAlexW4321787460

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.