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Items: 1 to 20 of 30

1.
Ykt6p Is a Multifunctional Yeast R-SNARE That Is Required for Multiple Membrane Transport Pathways to the Vacuole
Youngseok Kweon, Anca Rothe, Elizabeth Conibear, Tom H. Stevens
Mol Biol Cell. 2003 May; 14(5): 1868–1881. doi: 10.1091/mbc.E02-10-0687
PMCID:
PMC165083
ArticlePDF–512K
2.
Multiple SNARE interactions of an SM protein: Sed5p/Sly1p binding is dispensable for transport
Renwang Peng, Dieter Gallwitz
EMBO J. 2004 Oct 13; 23(20): 3939–3949. Published online 2004 Sep 16. doi: 10.1038/sj.emboj.7600410
PMCID:
PMC524344
ArticlePDF–501K
3.
Distinct SNARE complexes mediating membrane fusion in Golgi transport based on combinatorial specificity
Francesco Parlati, Oleg Varlamov, Keren Paz, James A. McNew, David Hurtado, Thomas H. Söllner, James E. Rothman
Proc Natl Acad Sci U S A. 2002 Apr 16; 99(8): 5424–5429. doi: 10.1073/pnas.082100899
PMCID:
PMC122785
ArticlePDF–278K
4.
Characterization of a Novel Yeast SNARE Protein Implicated in Golgi Retrograde Traffic
Vladimir V. Lupashin, Irina D. Pokrovskaya, James A. McNew, M. Gerard Waters
Mol Biol Cell. 1997 Dec; 8(12): 2659–2676. doi: 10.1091/mbc.8.12.2659
PMCID:
PMC25735
ArticlePDF–721K
5.
Phylogeny of the SNARE vesicle fusion machinery yields insights into the conservation of the secretory pathway in fungi
Nickias Kienle, Tobias H Kloepper, Dirk Fasshauer
BMC Evol Biol. 2009; 9: 19. Published online 2009 Jan 23. doi: 10.1186/1471-2148-9-19
PMCID:
PMC2639358
ArticlePDF–1.2M
6.
The Roles of the SNARE Protein Sed5 in Autophagy in Saccharomyces cerevisiae
Shenshen Zou, Dan Sun, Yongheng Liang
Mol Cells. 2017 Sep 30; 40(9): 643–654. Published online 2017 Sep 20. doi: 10.14348/molcells.2017.0030
PMCID:
PMC5638772
ArticlePDF–8.9M
7.
Two syntaxin homologues in the TGN/endosomal system of yeast.
J C Holthuis, B J Nichols, S Dhruvakumar, H R Pelham
EMBO J. 1998 Jan 2; 17(1): 113–126. doi: 10.1093/emboj/17.1.113
PMCID:
PMC1170363
SummaryPDF–811K
8.
Interaction of the conserved oligomeric Golgi complex with t-SNARE Syntaxin5a/Sed5 enhances intra-Golgi SNARE complex stability
Anna Shestakova, Elena Suvorova, Oleksandra Pavliv, Galimat Khaidakova, Vladimir Lupashin
J Cell Biol. 2007 Dec 17; 179(6): 1179–1192. doi: 10.1083/jcb.200705145
PMCID:
PMC2140037
ArticlePDF–5.8M
9.
The yeast Batten disease orthologue Btn1 controls endosome–Golgi retrograde transport via SNARE assembly
Rachel Kama, Vydehi Kanneganti, Christian Ungermann, Jeffrey E. Gerst
J Cell Biol. 2011 Oct 17; 195(2): 203–215. doi: 10.1083/jcb.201102115
PMCID:
PMC3198160
ArticlePDF–2.2M
10.
Selective Formation of Sed5p-containing SNARE Complexes Is Mediated by Combinatorial Binding Interactions
Marco M.K. Tsui, William C.S. Tai, David K. Banfield
Mol Biol Cell. 2001 Mar; 12(3): 521–538. doi: 10.1091/mbc.12.3.521
PMCID:
PMC30961
ArticlePDF–923K
11.
Multiple and distinct strategies of yeast SNAREs to confer the specificity of membrane fusion
Noriko Furukawa, Joji Mima
Sci Rep. 2014; 4: 4277. Published online 2014 Mar 4. doi: 10.1038/srep04277
PMCID:
PMC3940976
ArticlePDF–3.9M
12.
Reconstitution of autophagosome nucleation defines Atg9 vesicles as seeds for membrane formation
Justyna Sawa-Makarska, Verena Baumann, Nicolas Coudevylle, Sören von Bülow, Veronika Nogellova, Christine Abert, Martina Schuschnig, Martin Graef, Gerhard Hummer, Sascha Martens
Science. Author manuscript; available in PMC 2021 May 13.
Published in final edited form as: Science. 2020 Sep 4; 369(6508): eaaz7714. Published online 2020 Sep 4. doi: 10.1126/science.aaz7714
PMCID:
PMC7610778
ArticlePDF–1.9M
13.
Ubiquitination drives COPI priming and Golgi SNARE localization
Swapneeta S Date, Peng Xu, Nathaniel L Hepowit, Nicholas S Diab, Jordan Best, Boyang Xie, Jiale Du, Eric R Strieter, Lauren P Jackson, Jason A MacGurn, Todd R Graham
eLife. 2022; 11: e80911. Published online 2022 Jul 29. doi: 10.7554/eLife.80911
PMCID:
PMC9374436
ArticlePDF–4.3M
14.
A Two-Hybrid Screen of the Yeast Proteome for Hsp90 Interactors Uncovers a Novel Hsp90 Chaperone Requirement in the Activity of a Stress-Activated Mitogen-Activated Protein Kinase, Slt2p (Mpk1p)
Stefan H. Millson, Andrew W. Truman, Victoria King, Chrisostomos Prodromou, Laurence H. Pearl, Peter W. Piper
Eukaryot Cell. 2005 May; 4(5): 849–860. doi: 10.1128/EC.4.5.849-860.2005
PMCID:
PMC1140089
ArticlePDF–322K
15.
ER exit sites are physical and functional core autophagosome biogenesis components
Martin Graef, Jonathan R. Friedman, Christopher Graham, Mohan Babu, Jodi Nunnari
Mol Biol Cell. 2013 Sep 15; 24(18): 2918–2931. doi: 10.1091/mbc.E13-07-0381
PMCID:
PMC3771953
ArticlePDF–2.2M
16.
Ubiquitin‐Activated Interaction Traps (UBAITs) identify E3 ligase binding partners
Hazel F O'Connor, Nancy Lyon, Justin W Leung, Poonam Agarwal, Caleb D Swaim, Kyle M Miller, Jon M Huibregtse
EMBO Rep. 2015 Dec; 16(12): 1699–1712. Published online 2015 Oct 27. doi: 10.15252/embr.201540620
PMCID:
PMC4693525
ArticlePDF–693K
17.
Yeast Ssd1 is a non-enzymatic member of the RNase II family with an alternative RNA recognition site
Rosemary A Bayne, Uma Jayachandran, Aleksandra Kasprowicz, Stefan Bresson, David Tollervey, Edward W J Wallace, Atlanta G Cook
Nucleic Acids Res. 2022 Mar 21; 50(5): 2923–2937. Published online 2021 Jul 24. doi: 10.1093/nar/gkab615
PMCID:
PMC8934651
ArticlePDF–4.4M
18.
Selective defects in gene expression control genome instability in yeast splicing mutants
Annie S. Tam, Tianna S. Sihota, Karissa L. Milbury, Anni Zhang, Veena Mathew, Peter C. Stirling
Mol Biol Cell. 2019 Jan 15; 30(2): 191–200. doi: 10.1091/mbc.E18-07-0439
PMCID:
PMC6589566
ArticlePDF–5.1M
19.
Large-scale identification of yeast integral membrane protein interactions
John P. Miller, Russell S. Lo, Asa Ben-Hur, Cynthia Desmarais, Igor Stagljar, William Stafford Noble, Stanley Fields
Proc Natl Acad Sci U S A. 2005 Aug 23; 102(34): 12123–12128. Published online 2005 Aug 10. doi: 10.1073/pnas.0505482102
PMCID:
PMC1189342
ArticlePDF–653K
20.
An APEX2-based proximity-dependent biotinylation assay with temporal specificity to study protein interactions during autophagy in the yeast Saccharomyces cerevisiae
Yasmina Filali-Mouncef, Alexandre Leytens, Prado Vargas Duarte, Mattia Zampieri, Jörn Dengjel, Fulvio Reggiori
Autophagy. 2024; 20(10): 2323–2337. Published online 2024 Jul 3. doi: 10.1080/15548627.2024.2366749
PMCID:
PMC11423678
ArticlePDF–1.7M

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