ATP hydrolysis by UPF1 is required for efficient translation termination at premature stop codons. - Wikidata - awgldk - TriplyDB

ATP hydrolysis by UPF1 is required for efficient translation termination at premature stop codons.

ATP hydrolysis by UPF1 is required for efficient translation termination at premature stop codons.

http://www.wikidata.org/entity/Q37541693

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Dual function of UPF3B in early and late translation termination.Upf proteins: highly conserved factors involved in nonsense mRNA mediated decay.HTLV-1 Tax plugs and freezes UPF1 helicase leading to nonsense-mediated mRNA decay inhibition.An RNA decay factor wears a new coat: UPF3B modulates translation termination.Nonsense-mediated mRNA decay factors cure most [PSI+] prion variants.Uncovering the Role of RNA-Binding Proteins in Gene Expression in the Immune System.New insights into the interplay between the translation machinery and nonsense-mediated mRNA decay factors.UPF1-like helicase grip on nucleic acids dictates processivity

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ATP hydrolysis by UPF1 is required for efficient translation termination at premature stop codons.

http://www.wikidata.org/entity/Q37541693

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 23 December 2016

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

ATP hydrolysis by UPF1 is requ ...... tion at premature stop codons.

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ATP hydrolysis by UPF1 is requ ...... tion at premature stop codons.

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type

label

ATP hydrolysis by UPF1 is requ ...... tion at premature stop codons.

@en

ATP hydrolysis by UPF1 is requ ...... tion at premature stop codons.

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prefLabel

ATP hydrolysis by UPF1 is requ ...... tion at premature stop codons.

@en

ATP hydrolysis by UPF1 is requ ...... tion at premature stop codons.

@nl

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Nature Communications

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ATP hydrolysis by UPF1 is requ ...... tion at premature stop codons.

@en

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DaJuan L Whiteside

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Molecular mechanisms for the RNA-dependent ATPase activity of Upf1 and its regulation by Upf2

Binding of a novel SMG-1-Upf1-eRF1-eRF3 complex (SURF) to the exon junction complex triggers Upf1 phosphorylation and nonsense-mediated mRNA decay

Interactions between UPF1, eRFs, PABP and the exon junction complex suggest an integrated model for mammalian NMD pathways

Upf1 ATPase-dependent mRNP disassembly is required for completion of nonsense- mediated mRNA decay

The surveillance complex interacts with the translation release factors to enhance termination and degrade aberrant mRNAs

Additional modules for versatile and economical PCR-based gene deletion and modification in Saccharomyces cerevisiae

Dom34:Hbs1 promotes subunit dissociation and peptidyl-tRNA drop-off to initiate no-go decay.

Exosome-mediated recognition and degradation of mRNAs lacking a termination codon.

Genetic and biochemical characterization of mutations in the ATPase and helicase regions of the Upf1 protein

Nonsense-Mediated mRNA Decay: Degradation of Defective Transcripts Is Only Part of the Story

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14021

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scholarly article

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10.1038/NCOMMS14021

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7

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Kristian E Baker

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2016-12-23T00:00:00Z

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1012293866

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28008922

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5196439

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