759 related articles for article (PubMed ID: 22940866)
21. Unwinding by local strand separation is critical for the function of DEAD-box proteins as RNA chaperones.
Del Campo M; Mohr S; Jiang Y; Jia H; Jankowsky E; Lambowitz AM
J Mol Biol; 2009 Jun; 389(4):674-93. PubMed ID: 19393667
[TBL] [Abstract][Full Text] [Related]
22. Fluorescence methods in the investigation of the DEAD-box helicase mechanism.
Andreou AZ; Klostermeier D
Exp Suppl; 2014; 105():161-92. PubMed ID: 25095995
[TBL] [Abstract][Full Text] [Related]
23. Exploring the molecular basis of dsRNA recognition by Mss116p using molecular dynamics simulations and free-energy calculations.
Xue Q; Zhang JL; Zheng QC; Cui YL; Chen L; Chu WT; Zhang HX
Langmuir; 2013 Sep; 29(35):11135-44. PubMed ID: 23895307
[TBL] [Abstract][Full Text] [Related]
24. The RNA helicase Mtr4p is a duplex-sensing translocase.
Patrick EM; Srinivasan S; Jankowsky E; Comstock MJ
Nat Chem Biol; 2017 Jan; 13(1):99-104. PubMed ID: 27870836
[TBL] [Abstract][Full Text] [Related]
25. Involvement of DEAD-box proteins in group I and group II intron splicing. Biochemical characterization of Mss116p, ATP hydrolysis-dependent and -independent mechanisms, and general RNA chaperone activity.
Halls C; Mohr S; Del Campo M; Yang Q; Jankowsky E; Lambowitz AM
J Mol Biol; 2007 Jan; 365(3):835-55. PubMed ID: 17081564
[TBL] [Abstract][Full Text] [Related]
26. Measurement of ATP utilization in RNA unwinding and RNA chaperone activities by DEAD-box helicase proteins.
Jarmoskaite I; Helmers AE; Russell R
Methods Enzymol; 2022; 673():53-76. PubMed ID: 35965018
[TBL] [Abstract][Full Text] [Related]
27. 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. PubMed ID: 18332124
[TBL] [Abstract][Full Text] [Related]
28. AMP sensing by DEAD-box RNA helicases.
Putnam AA; Jankowsky E
J Mol Biol; 2013 Oct; 425(20):3839-45. PubMed ID: 23702290
[TBL] [Abstract][Full Text] [Related]
29. The mechanism of RNA duplex recognition and unwinding by DEAD-box helicase DDX3X.
Song H; Ji X
Nat Commun; 2019 Jul; 10(1):3085. PubMed ID: 31300642
[TBL] [Abstract][Full Text] [Related]
30. The DEAH-box splicing factor Prp16 unwinds RNA duplexes in vitro.
Wang Y; Wagner JD; Guthrie C
Curr Biol; 1998 Apr; 8(8):441-51. PubMed ID: 9550699
[TBL] [Abstract][Full Text] [Related]
31. The conformational plasticity of eukaryotic RNA-dependent ATPases.
Ozgur S; Buchwald G; Falk S; Chakrabarti S; Prabu JR; Conti E
FEBS J; 2015 Mar; 282(5):850-63. PubMed ID: 25645110
[TBL] [Abstract][Full Text] [Related]
32. The DEAD-box helicase eIF4A: paradigm or the odd one out?
Andreou AZ; Klostermeier D
RNA Biol; 2013 Jan; 10(1):19-32. PubMed ID: 22995829
[TBL] [Abstract][Full Text] [Related]
33. Dynamics of the DEAD-box ATPase Prp5 RecA-like domains provide a conformational switch during spliceosome assembly.
Beier DH; Carrocci TJ; van der Feltz C; Tretbar US; Paulson JC; Grabowski N; Hoskins AA
Nucleic Acids Res; 2019 Nov; 47(20):10842-10851. PubMed ID: 31712821
[TBL] [Abstract][Full Text] [Related]
34. The DEAD-box protein DDX43 (HAGE) is a dual RNA-DNA helicase and has a K-homology domain required for full nucleic acid unwinding activity.
Talwar T; Vidhyasagar V; Qing J; Guo M; Kariem A; Lu Y; Singh RS; Lukong KE; Wu Y
J Biol Chem; 2017 Jun; 292(25):10429-10443. PubMed ID: 28468824
[TBL] [Abstract][Full Text] [Related]
35. DEAD-box helicases form nucleotide-dependent, long-lived complexes with RNA.
Liu F; Putnam AA; Jankowsky E
Biochemistry; 2014 Jan; 53(2):423-33. PubMed ID: 24367975
[TBL] [Abstract][Full Text] [Related]
36. Allosteric regulation of helicase core activities of the DEAD-box helicase YxiN by RNA binding to its RNA recognition motif.
Samatanga B; Andreou AZ; Klostermeier D
Nucleic Acids Res; 2017 Feb; 45(4):1994-2006. PubMed ID: 28115633
[TBL] [Abstract][Full Text] [Related]
37. Prp43p contains a processive helicase structural architecture with a specific regulatory domain.
Walbott H; Mouffok S; Capeyrou R; Lebaron S; Humbert O; van Tilbeurgh H; Henry Y; Leulliot N
EMBO J; 2010 Jul; 29(13):2194-204. PubMed ID: 20512115
[TBL] [Abstract][Full Text] [Related]
38. A conformational change in the helicase core is necessary but not sufficient for RNA unwinding by the DEAD box helicase YxiN.
Karow AR; Klostermeier D
Nucleic Acids Res; 2009 Jul; 37(13):4464-71. PubMed ID: 19474341
[TBL] [Abstract][Full Text] [Related]
39. Structural basis for RNA translocation by DEAH-box ATPases.
Hamann F; Enders M; Ficner R
Nucleic Acids Res; 2019 May; 47(8):4349-4362. PubMed ID: 30828714
[TBL] [Abstract][Full Text] [Related]
40. Purified human SUV3p exhibits multiple-substrate unwinding activity upon conformational change.
Shu Z; Vijayakumar S; Chen CF; Chen PL; Lee WH
Biochemistry; 2004 Apr; 43(16):4781-90. PubMed ID: 15096047
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
