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Items: 1 to 20 of 68

1.

The highly conserved eukaryotic DRG factors are required for efficient translation in a manner redundant with the putative RNA helicase Slh1.

Daugeron MC, Prouteau M, Lacroute F, Séraphin B.

Nucleic Acids Res. 2011 Mar;39(6):2221-33. doi: 10.1093/nar/gkq898. Epub 2010 Nov 13.

2.

Asc1, Hel2, and Slh1 couple translation arrest to nascent chain degradation.

Sitron CS, Park JH, Brandman O.

RNA. 2017 May;23(5):798-810. doi: 10.1261/rna.060897.117. Epub 2017 Feb 21.

3.

Motif III in superfamily 2 "helicases" helps convert the binding energy of ATP into a high-affinity RNA binding site in the yeast DEAD-box protein Ded1.

Banroques J, Doère M, Dreyfus M, Linder P, Tanner NK.

J Mol Biol. 2010 Mar 5;396(4):949-66. doi: 10.1016/j.jmb.2009.12.025. Epub 2009 Dec 21.

PMID:
20026132
4.

A conserved phenylalanine of motif IV in superfamily 2 helicases is required for cooperative, ATP-dependent binding of RNA substrates in DEAD-box proteins.

Banroques J, Cordin O, Doère M, Linder P, Tanner NK.

Mol Cell Biol. 2008 May;28(10):3359-71. doi: 10.1128/MCB.01555-07. Epub 2008 Mar 10.

6.

An essential GTPase promotes assembly of preribosomal RNA processing complexes.

Karbstein K, Jonas S, Doudna JA.

Mol Cell. 2005 Nov 23;20(4):633-43.

7.

The NUG1 GTPase reveals and N-terminal RNA-binding domain that is essential for association with 60 S pre-ribosomal particles.

Bassler J, Kallas M, Hurt E.

J Biol Chem. 2006 Aug 25;281(34):24737-44. Epub 2006 Jun 27.

8.

High-throughput genetic identification of functionally important regions of the yeast DEAD-box protein Mss116p.

Mohr G, Del Campo M, Turner KG, Gilman B, Wolf RZ, Lambowitz AM.

J Mol Biol. 2011 Nov 11;413(5):952-72. doi: 10.1016/j.jmb.2011.09.015. Epub 2011 Sep 16.

9.
10.

Novel G-protein complex whose requirement is linked to the translational status of the cell.

Carr-Schmid A, Pfund C, Craig EA, Kinzy TG.

Mol Cell Biol. 2002 Apr;22(8):2564-74.

11.

Requirement of the DEAD-Box protein ded1p for messenger RNA translation.

Chuang RY, Weaver PL, Liu Z, Chang TH.

Science. 1997 Mar 7;275(5305):1468-71.

13.

Quantitative analysis of snoRNA association with pre-ribosomes and release of snR30 by Rok1 helicase.

Bohnsack MT, Kos M, Tollervey D.

EMBO Rep. 2008 Dec;9(12):1230-6. doi: 10.1038/embor.2008.184. Epub 2008 Oct 3.

14.

The dynamin-related protein Mgm1p assembles into oligomers and hydrolyzes GTP to function in mitochondrial membrane fusion.

Meglei G, McQuibban GA.

Biochemistry. 2009 Mar 3;48(8):1774-84. doi: 10.1021/bi801723d.

PMID:
19236101
15.

Interaction of Sla2p's ANTH domain with PtdIns(4,5)P2 is important for actin-dependent endocytic internalization.

Sun Y, Kaksonen M, Madden DT, Schekman R, Drubin DG.

Mol Biol Cell. 2005 Feb;16(2):717-30. Epub 2004 Dec 1.

16.

Saccharomyces cerevisiae Rbg1 protein and its binding partner Gir2 interact on Polyribosomes with Gcn1.

Wout PK, Sattlegger E, Sullivan SM, Maddock JR.

Eukaryot Cell. 2009 Jul;8(7):1061-71. doi: 10.1128/EC.00356-08. Epub 2009 May 15.

17.

The newly discovered Q motif of DEAD-box RNA helicases regulates RNA-binding and helicase activity.

Cordin O, Tanner NK, Doère M, Linder P, Banroques J.

EMBO J. 2004 Jul 7;23(13):2478-87. Epub 2004 Jun 17.

18.

Has1p, a member of the DEAD-box family, is required for 40S ribosomal subunit biogenesis in Saccharomyces cerevisiae.

Emery B, de la Cruz J, Rocak S, Deloche O, Linder P.

Mol Microbiol. 2004 Apr;52(1):141-58.

19.

Nsa2 is an unstable, conserved factor required for the maturation of 27 SB pre-rRNAs.

Lebreton A, Saveanu C, Decourty L, Jacquier A, Fromont-Racine M.

J Biol Chem. 2006 Sep 15;281(37):27099-108. Epub 2006 Jul 21.

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