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Items: 1 to 20 of 47

1.
The RNA recognition motif of yeast translation initiation factor Tif3/eIF4B is required but not sufficient for RNA strand-exchange and translational activity.
N Niederberger, H Trachsel, M Altmann
RNA. 1998 Oct; 4(10): 1259–1267. doi: 10.1017/s1355838298980487
PMCID:
PMC1369698
SummaryPDF–495K
2.
A Saccharomyces cerevisiae homologue of mammalian translation initiation factor 4B contributes to RNA helicase activity.
M Altmann, P P Müller, B Wittmer, F Ruchti, S Lanker, H Trachsel
EMBO J. 1993 Oct; 12(10): 3997–4003. doi: 10.1002/j.1460-2075.1993.tb06077.x
PMCID:
PMC413682
SummaryPage BrowsePDF–1.3M
3.
The Saccharomyces cerevisiae translation initiation factor Tif3 and its mammalian homologue, eIF-4B, have RNA annealing activity.
M Altmann, B Wittmer, N Méthot, N Sonenberg, H Trachsel
EMBO J. 1995 Aug 1; 14(15): 3820–3827. doi: 10.1002/j.1460-2075.1995.tb00051.x
PMCID:
PMC394456
SummaryPage BrowsePDF–1.9M
4.
Yeast eIF4B binds to the head of the 40S ribosomal subunit and promotes mRNA recruitment through its N-terminal and internal repeat domains
Sarah E. Walker, Fujun Zhou, Sarah F. Mitchell, Victoria S. Larson, Leos Valasek, Alan G. Hinnebusch, Jon R. Lorsch
RNA. 2013 Feb; 19(2): 191–207. doi: 10.1261/rna.035881.112
PMCID:
PMC3543093
AbstractArticlePDF–1.5M
5.
A new yeast translation initiation factor suppresses a mutation in the eIF-4A RNA helicase.
R Coppolecchia, P Buser, A Stotz, P Linder
EMBO J. 1993 Oct; 12(10): 4005–4011. doi: 10.1002/j.1460-2075.1993.tb06078.x
PMCID:
PMC413683
SummaryPage BrowsePDF–1.3M
6.
eIF4B stimulates eIF4A ATPase and unwinding activities by direct interaction through its 7-repeats region
Alexandra Zoi Andreou, Ulf Harms, Dagmar Klostermeier
RNA Biol. 2017; 14(1): 113–123. Published online 2016 Nov 18. doi: 10.1080/15476286.2016.1259782
PMCID:
PMC5270515
AbstractArticlePDF–1.3M
7.
Identification and Characterization of Functionally Critical, Conserved Motifs in the Internal Repeats and N-terminal Domain of Yeast Translation Initiation Factor 4B (yeIF4B)
Fujun Zhou, Sarah E. Walker, Sarah F. Mitchell, Jon R. Lorsch, Alan G. Hinnebusch
J Biol Chem. 2014 Jan 17; 289(3): 1704–1722. Published online 2013 Nov 27. doi: 10.1074/jbc.M113.529370
Correction in:
J Biol Chem. 2014 Apr 25; 289(17): 11860.
PMCID:
PMC3894348
AbstractArticlePDF–3.5M
8.
Yeast Eukaryotic Initiation Factor 4B (eIF4B) Enhances Complex Assembly between eIF4A and eIF4G in Vivo
Eun-Hee Park, Sarah E. Walker, Fujun Zhou, Joseph M. Lee, Vaishnavi Rajagopal, Jon R. Lorsch, Alan G. Hinnebusch
J Biol Chem. 2013 Jan 25; 288(4): 2340–2354. Published online 2012 Nov 26. doi: 10.1074/jbc.M112.398537
PMCID:
PMC3554905
AbstractArticlePDF–1.7M
9.
Stress-Induced Translation Inhibition through Rapid Displacement of Scanning Initiation Factors
Stefan Bresson, Vadim Shchepachev, Christos Spanos, Tomasz W. Turowski, Juri Rappsilber, David Tollervey
Mol Cell. 2020 Nov 5; 80(3): 470–484.e8. doi: 10.1016/j.molcel.2020.09.021
PMCID:
PMC7657445
AbstractArticle
10.
The p20 and Ded1 proteins have antagonistic roles in eIF4E-dependent translation in Saccharomyces cerevisiae
Jesús de la Cruz, Isabelle Iost, Dieter Kressler, Patrick Linder
Proc Natl Acad Sci U S A. 1997 May 13; 94(10): 5201–5206. doi: 10.1073/pnas.94.10.5201
PMCID:
PMC24656
AbstractArticlePDF–436K
11.
An in vivo control map for the eukaryotic mRNA translation machinery
Helena Firczuk, Shichina Kannambath, Jürgen Pahle, Amy Claydon, Robert Beynon, John Duncan, Hans Westerhoff, Pedro Mendes, John EG McCarthy
Mol Syst Biol. 2013; 9: 635. Published online 2013 Jan 22. doi: 10.1038/msb.2012.73
PMCID:
PMC3564266
AbstractArticlePDF–1.2M
12.
A Cytosolic Network Suppressing Mitochondria-Mediated Proteostatic Stress and Cell Death
Xiaowen Wang, Xin Jie Chen
Nature. Author manuscript; available in PMC 2016 Feb 27.
Published in final edited form as: Nature. 2015 Aug 27; 524(7566): 481–484. Published online 2015 Jul 20. doi: 10.1038/nature14859
PMCID:
PMC4582408
AbstractArticlePDF–2.3M
13.
A Multi-Perspective Proximity View on the Dynamic Head Region of the Ribosomal 40S Subunit
Kerstin Schmitt, Alina-Andrea Kraft, Oliver Valerius
Int J Mol Sci. 2021 Nov; 22(21): 11653. Published online 2021 Oct 28. doi: 10.3390/ijms222111653
PMCID:
PMC8583833
AbstractArticlePDF–4.2M
14.
Quantitative proteomic analysis of purified yeast kinetochores identifies a PP1 regulatory subunit
Bungo Akiyoshi, Christian R. Nelson, Jeffrey A. Ranish, Sue Biggins
Genes Dev. 2009 Dec 15; 23(24): 2887–2899. doi: 10.1101/gad.1865909
Correction in:
Genes Dev. 2016 Oct 15; 30(20): 2339.
PMCID:
PMC2800092
AbstractArticlePDF–996K
15.
Dual Roles for Spt5 in Pre-mRNA Processing and Transcription Elongation Revealed by Identification of Spt5-Associated Proteins
D. L. Lindstrom, S. L. Squazzo, N. Muster, T. A. Burckin, K. C. Wachter, C. A. Emigh, J. A. McCleery, J. R. Yates, III, G. A. Hartzog
Mol Cell Biol. 2003 Feb; 23(4): 1368–1378. doi: 10.1128/MCB.23.4.1368-1378.2003
PMCID:
PMC141151
AbstractArticlePDF–328K
16.
mChIP-KAT-MS, a method to map protein interactions and acetylation sites for lysine acetyltransferases
Leslie Mitchell, Sylvain Huard, Michael Cotrut, Roghayeh Pourhanifeh-Lemeri, Anne-Lise Steunou, Akil Hamza, Jean-Philippe Lambert, Hu Zhou, Zhibin Ning, Amrita Basu, Jacques Côté, Daniel A. Figeys, Kristin Baetz
Proc Natl Acad Sci U S A. 2013 Apr 23; 110(17): E1641–E1650. Published online 2013 Apr 9. doi: 10.1073/pnas.1218515110
Correction in:
Proc Natl Acad Sci U S A. 2014 Mar 18; 111(11): 4346.
PMCID:
PMC3637784
AbstractArticlePDF–1.2M
17.
A Protein–Protein Interaction Analysis Suggests a Wide Range of New Functions for the p21-Activated Kinase (PAK) Ste20
Ifeoluwapo Matthew Joshua, Meng Lin, Ariestia Mardjuki, Alessandra Mazzola, Thomas Höfken
Int J Mol Sci. 2023 Nov; 24(21): 15916. Published online 2023 Nov 2. doi: 10.3390/ijms242115916
PMCID:
PMC10647699
AbstractArticlePDF–5.4M
18.
Mapping the functional yeast ABC transporter interactome
Jamie Snider, Asad Hanif, Mid Eum Lee, Ke Jin, Analyn R. Yu, Chris Graham, Matthew Chuk, Dunja Damjanovic, Marta Wierzbicka, Priscilla Tang, Dina Balderes, Victoria Wong, Matthew Jessulat, Katelyn D. Darowski, Bryan-Joseph San Luis, Igor Shevelev, Stephen L Sturley, Charles Boone, Jack F. Greenblatt, Zhaolei Zhang, Christian M. Paumi, Mohan Babu, Hay-Oak Park, Susan Michaelis, Igor Stagljar
Nat Chem Biol. Author manuscript; available in PMC 2014 Mar 1.
Published in final edited form as: Nat Chem Biol. 2013 Sep; 9(9): 565–572. Published online 2013 Jul 7. doi: 10.1038/nchembio.1293
PMCID:
PMC3835492
AbstractArticlePDF–1.2M
19.
Srs2 overexpression reveals a helicase-independent role at replication forks that requires diverse cell functions
Ana María León Ortiz, Robert J. D. Reid, John C. Dittmar, Rodney Rothstein, Alain Nicolas
DNA Repair (Amst) Author manuscript; available in PMC 2012 May 5.
Published in final edited form as: DNA Repair (Amst). 2011 May 5; 10(5): 506–517. Published online 2011 Apr 1. doi: 10.1016/j.dnarep.2011.02.004
PMCID:
PMC3084345
AbstractArticlePDF–3.2M
20.
The yeast protein kinase Sch9 adjusts V-ATPase assembly/disassembly to control pH homeostasis and longevity in response to glucose availability
Tobias Wilms, Erwin Swinnen, Elja Eskes, Laura Dolz-Edo, Alice Uwineza, Ruben Van Essche, Joëlle Rosseels, Piotr Zabrocki, Elisabetta Cameroni, Vanessa Franssens, Claudio De Virgilio, Gertien J. Smits, Joris Winderickx
PLoS Genet. 2017 Jun; 13(6): e1006835. Published online 2017 Jun 12. doi: 10.1371/journal.pgen.1006835
PMCID:
PMC5484544
AbstractArticlePDF–14M

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