Evidence map›Paper›PMID 31718065›Full record

ArticleInternational journal of molecular sciences2019

Insights into the Effects of Cancer Associated Mutations at the UPF2 and ATP-Binding Sites of NMD Master Regulator: UPF1.

Umesh Kalathiya, Monikaben Padariya, Kamila Pawlicka, Chandra S Verma, Douglas Houston, Ted R Hupp, Javier Antonio Alfaro

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

11 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
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  6. DNA and RNA Binding Proteins: From Motifs to Roles in Cancer.International journal of molecular sciences · 2022
    Review
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  8. 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

7 authors at 4 institutions in 4 countries.

Umesh KalathiyaUniversity of Gdansk, International Centre for Cancer Vaccine Science, Wita Stwosza 63, 80-308 Gdansk, Poland.
Monikaben PadariyaUniversity of Gdansk, International Centre for Cancer Vaccine Science, Wita Stwosza 63, 80-308 Gdansk, Poland.
Kamila PawlickaUniversity of Edinburgh, Institute of Genetics and Molecular Medicine, Edinburgh, Scotland EH4 2XR, UK.
Chandra S VermaBioinformatics Institute, Agency for Science, Technology and Research (A*STAR), 30 Biopolis Street, 07-01 Matrix, Singapore 138671, Singapore.
Douglas HoustonUniversity of Edinburgh, Institute of Quantitative Biology, Biochemistry and Biotechnology, Edinburgh, Scotland EH9 3BF, UK.
Ted R HuppUniversity of Gdansk, International Centre for Cancer Vaccine Science, Wita Stwosza 63, 80-308 Gdansk, Poland.
Javier Antonio AlfaroUniversity of Gdansk, International Centre for Cancer Vaccine Science, Wita Stwosza 63, 80-308 Gdansk, Poland.
University of Gdańsk · PLAgency for Science, Technology and Research · SGInstitute of Genetics and Cancer · GBUniversity of Edinburgh · GB

Funding

International Research Agendas programme of the Foundation for Polish Science cofinanced by the European Union under the European Regional Development Fund
6 · The paper itself

Abstract

Nonsense-mediated mRNA decay (NMD) is a quality control mechanism that recognizes post-transcriptionally abnormal transcripts and mediates their degradation. The master regulator of NMD is UPF1, an enzyme with intrinsic ATPase and helicase activities. The cancer genomic sequencing data has identified frequently mutated residues in the CH-domain and ATP-binding site of UPF1. In silico screening of UPF1 stability change as a function over 41 cancer mutations has identified five variants with significant effects: K164R, R253W, T499M, E637K, and E833K. To explore the effects of these mutations on the associated energy landscape of UPF1, molecular dynamics simulations (MDS) were performed. MDS identified stable H-bonds between residues S152, S203, S205, Q230/R703, and UPF2/AMPPNP, and suggest that phosphorylation of Serine residues may control UPF1-UPF2 binding. Moreover, the alleles K164R and R253W in the CH-domain improved UPF1-UPF2 binding. In addition, E637K and E833K alleles exhibited improved UPF1-AMPPNP binding compared to the T499M variant; the lower binding is predicted from hindrance caused by the side-chain of T499M to the docking of the tri-phosphate moiety (AMPPNP) into the substrate site. The dynamics of wild-type/mutant systems highlights the flexible nature of the ATP-binding region in UPF1. These insights can facilitate the development of drug discovery strategies for manipulating NMD signaling in cell systems using chemical tools.

Indexed as

Molecular Dynamics SimulationMutation, MissenseAdenosine TriphosphateBinding SitesHumansProtein BindingRNA-Binding ProteinsRNA HelicasesTrans-ActivatorsAdenosine TriphosphateRNA-Binding ProteinsRNA HelicasesTrans-ActivatorsUPF1 protein, humanUPF2 protein, humanATP-binding sitecancer mutationsmolecular dynamics simulationsstructural stabilityUPF1UPF2

Identifiers

PMID31718065
PMCPMC6888360
OpenAlexW2985794778

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.