Evidence map›Paper›PMID 32927888›Full record

ArticleInternational journal of molecular sciences2020

Molecular Modeling of Pathogenic Mutations in the Keratin 1B Domain.

Alexander J Hinbest, Sherif A Eldirany, Minh Ho, Christopher G Bunick

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 38% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Keratin 1 as a cell-surface receptor in cancer.Biochimica et biophysica acta. Reviews on cancer · 2022
    Review
  3. Recent insight into intermediate filament structure.Current opinion in cell biology · 2021
    Review
  4. First Case ofInternational journal of molecular sciences · 2020
    Article
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

4 authors at 2 institutions in 1 country.

Alexander J HinbestDepartment of Molecular Biology and Biochemistry, Wesleyan University, Middletown, CT 06459, USA.
Sherif A EldiranyYale School of Medicine, Yale University, New Haven, CT 06520, USA.
Minh HoDepartment of Dermatology, Yale University, New Haven, CT 06520, USA.ORCID 0000-0001-7192-3919
Christopher G BunickDepartment of Dermatology, Yale University, New Haven, CT 06520, USA.ORCID 0000-0002-4011-8308
Yale University · USWesleyan University · US

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Determining Structure and Function of Human Skin Barrier Proteins Using X-ray CrystallographyK08AR070290 · NIAMS · YALE UNIVERSITY · PI BUNICK, CHRISTOPHER GERARD · 2016 to 2020
$754k
Electron microscopy analysis of novel knob-pocket mechanism critical for intermediate filament assemblyR03AR076484 · NIAMS · YALE UNIVERSITY · PI BUNICK, CHRISTOPHER GERARD · 2020 to 2021
$165k
NCATS NIH HHS UL1 TR001863NIAMS NIH HHS K08 AR070290NIAMS NIH HHS K08AR070290NIAMS NIH HHS R03 AR076484NIAMS NIH HHS R03AR076484
6 · The paper itself

Abstract

Keratin intermediate filaments constitute the primary cytoskeletal component of epithelial cells. Numerous human disease phenotypes related to keratin mutation remain mechanistically elusive. Our recent crystal structures of the helix 1B heterotetramer from keratin 1/10 enabled further investigation of the effect of pathologic 1B domain mutations on keratin structure. We used our highest resolution keratin 1B structure as a template for homology-modeling the 1B heterotetramers of keratin 5/14 (associated with blistering skin disorders), keratin 8/18 (associated with liver disease), and keratin 74/28 (associated with hair disorder). Each structure was examined for the molecular alterations caused by incorporating pathogenic 1B keratin mutations. Structural modeling indicated keratin 1B mutations can harm the heterodimer interface (R265P

Indexed as

Models, MolecularHumansKeratin-1Keratoderma, Palmoplantar, EpidermolyticLiver DiseasesMutation, MissenseProtein Structure, QuaternaryKeratin-1KRT77 protein, humancytoskeletonepidermolysis bullosaintermediate filamentkeratinliver diseasemodelingmutationskin diseasestructure

Identifiers

PMID32927888
PMCPMC7555247
OpenAlexW3084413724

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.