Results 11 to 20 of about 10,061 (190)

DEAD-Box RNA Helicases and Genome Stability [PDF]

open access: yesGenes, 2021
DEAD-box RNA helicases are important regulators of RNA metabolism and have been implicated in the development of cancer. Interestingly, these helicases constitute a major recurring family of RNA-binding proteins important for protecting the genome. Current studies have provided insight into the connection between genomic stability and several DEAD-box ...
Rasika Venkataraman, Stanley Lee
exaly   +5 more sources

AMP Sensing by DEAD-Box RNA Helicases [PDF]

open access: yesJournal of Molecular Biology, 2013
In eukaryotes, cellular levels of adenosine monophosphate (AMP) signal the metabolic state of the cell. AMP concentrations increase significantly upon metabolic stress, such as glucose deprivation in yeast. Here, we show that several DEAD-box RNA helicases are sensitive to AMP, which is not produced during ATP hydrolysis by these enzymes.
Eckhard Jankowsky, Andrea A Putnam
exaly   +5 more sources

Selective pharmacological targeting of a DEAD box RNA helicase.

open access: yesPLoS ONE, 2008
RNA helicases represent a large family of proteins implicated in many biological processes including ribosome biogenesis, splicing, translation and mRNA degradation. However, these proteins have little substrate specificity, making inhibition of selected
Lisa Lindqvist   +11 more
doaj   +8 more sources

Role of DEAD/DEAH-box helicases in immunity, infection and cancers

open access: yesCell Communication and Signaling
DEAD/DEAH-box helicases (DDX) are integral RNA-binding proteins within the RNA helicase superfamily 2 (SF2), characterized by distinct DEAD (Asp-Glu-Ala-Asp) and DEAH (Asp-Glu-Ala-His) motifs.
Rex Devasahayam Arokia Balaya   +3 more
doaj   +2 more sources

The expanding functions of cellular helicases: the tombusvirus RNA replication enhancer co-opts the plant eIF4AIII-like AtRH2 and the DDX5-like AtRH5 DEAD-box RNA helicases to promote viral asymmetric RNA replication.

open access: yesPLoS Pathogens, 2014
Replication of plus-strand RNA viruses depends on recruited host factors that aid several critical steps during replication. Several of the co-opted host factors bind to the viral RNA, which plays multiple roles, including mRNA function, as an assembly ...
Nikolay Kovalev, Peter D Nagy
doaj   +2 more sources

Genera specific distribution of DEAD-box RNA helicases in cyanobacteria. [PDF]

open access: yesMicrob Genom, 2021
Although RNA helicases are essentially ubiquitous and perform roles in all stages of RNA metabolism, phylogenetic analysis of the DEAD (Asp-Glu-Ala-Asp)-box RNA helicase family in a single phylum has not been performed. Here, we performed a phylogenetic analysis on DEAD-box helicases from all currently available cyanobacterial genomes, comprising a ...
Whitford DS, Whitman BT, Owttrim GW.
europepmc   +3 more sources

The DDX5/Dbp2 subfamily of DEAD-box RNA helicases. [PDF]

open access: yesWiley Interdiscip Rev RNA, 2019
The mammalian DEAD‐box RNA helicase DDX5, its paralog DDX17, and their orthologs in Saccharomyces cerevisiae and Drosophila melanogaster, namely Dbp2 and Rm62, define a subfamily of DEAD‐box proteins. Members from this subfamily share highly conserved protein sequences and cellular functions.
Xing Z, Ma WK, Tran EJ.
europepmc   +4 more sources

The emerging role of DEAD/H-box helicases in hepatitis B virus infection

open access: yesFrontiers in Cellular and Infection Microbiology, 2022
DEAD/H-box helicases are an essential protein family with a conserved motif containing unique amino acid sequences (Asp-Glu-Ala-Asp/His). Current evidence indicates that DEAD/H-box helicases regulate RNA metabolism and innate immune responses.
Hongjuan You   +11 more
doaj   +1 more source

Synthetic lethal interactions of DEAD/H-box helicases as targets for cancer therapy

open access: yesFrontiers in Oncology, 2023
DEAD/H-box helicases are implicated in virtually every aspect of RNA metabolism, including transcription, pre-mRNA splicing, ribosomes biogenesis, nuclear export, translation initiation, RNA degradation, and mRNA editing.
Ananna Bhadra Arna   +7 more
doaj   +1 more source

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