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Items: 1 to 20 of 38

1.
Coupling High-Throughput and Targeted Screening for Identification of Nonobvious Metabolic Engineering Targets
Mahsa Babaei, Philip Tinggaard Thomsen, Marc Cernuda Pastor, Michael Krogh Jensen, Irina Borodina
ACS Synth Biol. 2024 Jan 19; 13(1): 168–182. Published online 2023 Dec 23. doi: 10.1021/acssynbio.3c00396
PMCID:
PMC10804409
AbstractArticlePDF–4.9M
2.
Differential regulation of the yeast isozymes of pyruvate carboxylase and the locus of action of acetyl CoA.
Sarawut Jitrapakdee, Abdussalam Adina-Zada, Paul G. Besant, Kathy H. Surinya, W. Wallace Cleland, John C. Wallace, Paul V. Attwood
Int J Biochem Cell Biol. Author manuscript; available in PMC 2008 Aug 22.
Published in final edited form as: Int J Biochem Cell Biol. 2007; 39(6): 1211–1223. Published online 2007 Mar 30. doi: 10.1016/j.biocel.2007.03.016
PMCID:
PMC2519008
AbstractArticlePDF–678K
3.
Yarrowia lipolytica Mutants Devoid of Pyruvate Carboxylase Activity Show an Unusual Growth Phenotype
Carmen-Lisset Flores, Carlos Gancedo
Eukaryot Cell. 2005 Feb; 4(2): 356–364. doi: 10.1128/EC.4.2.356-364.2005
PMCID:
PMC549329
AbstractArticlePDF–367K
4.
Polymorphism of the yeast pyruvate carboxylase 2 gene and protein: effects on protein biotinylation.
D L Val, A Chapman-Smith, M E Walker, J E Cronan, Jr, J C Wallace
Biochem J. 1995 Dec 15; 312(Pt 3): 817–825. doi: 10.1042/bj3120817
PMCID:
PMC1136188
SummaryPage BrowsePDF–2.0M
5.
Phosphoenolpyruvate Carboxykinase as the Sole Anaplerotic Enzyme in Saccharomyces cerevisiae
Rintze M. Zelle, Josh Trueheart, Jacob C. Harrison, Jack T. Pronk, Antonius J. A. van Maris
Appl Environ Microbiol. 2010 Aug; 76(16): 5383–5389. Published online 2010 Jun 25. doi: 10.1128/AEM.01077-10
PMCID:
PMC2918957
AbstractArticlePDF–447K
6.
Cardiolipin-deficient cells depend on anaplerotic pathways to ameliorate defective TCA cycle function
Vaishnavi Raja, Michael Salsaa, Amit S. Joshi, Yiran Li, Carlo W T van Roermund, Nadia Saadat, Pablo Lazcano, Michael Schmidtke, Maik Hüttemann, Smiti V. Gupta, Ronald J.A. Wanders, Miriam L. Greenberg
Biochim Biophys Acta Mol Cell Biol Lipids. Author manuscript; available in PMC 2020 May 1.
Published in final edited form as: Biochim Biophys Acta Mol Cell Biol Lipids. 2019 May; 1864(5): 654–661. Published online 2019 Feb 5. doi: 10.1016/j.bbalip.2019.02.001
Correction in:
Biochim Biophys Acta Mol Cell Biol Lipids. 2019 May 4
PMCID:
PMC6639082
AbstractArticlePDF–806K
7.
Reduced Ssy1-Ptr3-Ssy5 (SPS) Signaling Extends Replicative Life Span by Enhancing NAD+ Homeostasis in Saccharomyces cerevisiae
Felicia Tsang, Christol James, Michiko Kato, Victoria Myers, Irtqa Ilyas, Matthew Tsang, Su-Ju Lin
J Biol Chem. 2015 May 15; 290(20): 12753–12764. Published online 2015 Mar 30. doi: 10.1074/jbc.M115.644534
PMCID:
PMC4432292
AbstractArticlePDF–1.7M
8.
The ribosome‐associated chaperone Zuo1 controls translation upon TORC1 inhibition
Ailsa Black, Thomas D Williams, Flavie Soubigou, Ifeoluwapo M Joshua, Houjiang Zhou, Frederic Lamoliatte, Adrien Rousseau
EMBO J. 2023 Dec; 42(24): e113240. Published online 2023 Nov 20. doi: 10.15252/embj.2022113240
PMCID:
PMC10711665
AbstractArticlePDF–4.0M
9.
Acm1 contributes to nuclear positioning by inhibiting Cdh1-substrate interactions
Juan S Martinez, Hana Hall, Matthew D Bartolowits, Mark C Hall
Cell Cycle. 2012 Jan 15; 11(2): 384–394. Published online 2012 Jan 15. doi: 10.4161/cc.11.2.18944
PMCID:
PMC3293385
AbstractArticlePDF–7.6M
10.
Screening the yeast genome for energetic metabolism pathways involved in a phenotypic response to the anti-cancer agent 3-bromopyruvate
Paweł Lis, Paweł Jurkiewicz, Magdalena Cal-Bąkowska, Young H. Ko, Peter L. Pedersen, Andre Goffeau, Stanisław Ułaszewski
Oncotarget. 2016 Mar 1; 7(9): 10153–10173. Published online 2016 Feb 3. doi: 10.18632/oncotarget.7174
PMCID:
PMC4891110
AbstractArticlePDF–3.4M
11.
The elongation factor eEF3 (Yef3) interacts with mRNA in a translation independent manner
Nitzan Samra, Avigail Atir-Lande, Lilach Pnueli, Yoav Arava
BMC Mol Biol. 2015; 16: 17. Published online 2015 Sep 24. doi: 10.1186/s12867-015-0045-5
PMCID:
PMC4582935
AbstractArticlePDF–2.1M
12.
A yeast phenomic model for the gene interaction network modulating CFTR-ΔF508 protein biogenesis
Raymond J Louie, Jingyu Guo, John W Rodgers, Rick White, Najaf A Shah, Silvere Pagant, Peter Kim, Michael Livstone, Kara Dolinski, Brett A McKinney, Jeong Hong, Eric J Sorscher, Jennifer Bryan, Elizabeth A Miller, John L Hartman, IV
Genome Med. 2012; 4(12): 103. Published online 2012 Dec 27. doi: 10.1186/gm404
PMCID:
PMC3906889
AbstractArticlePDF–2.5M
13.
Comparative analysis of Saccharomyces cerevisiae WW domains and their interacting proteins
Jay R Hesselberth, John P Miller, Anna Golob, Jason E Stajich, Gregory A Michaud, Stanley Fields
Genome Biol. 2006; 7(4): R30. Published online 2006 Apr 10. doi: 10.1186/gb-2006-7-4-r30
PMCID:
PMC1557994
AbstractArticlePDF–778K
14.
Purified Smc5/6 Complex Exhibits DNA Substrate Recognition and Compaction
Pilar Gutierrez-Escribano, Silvia Hormeño, Julene Madariaga-Marcos, Roger Solé-Soler, Francis J. O’Reilly, Kyle Morris, Clara Aicart-Ramos, Ricardo Aramayo, Alex Montoya, Holger Kramer, Juri Rappsilber, Jordi Torres-Rosell, Fernando Moreno-Herrero, Luis Aragon
Mol Cell. 2020 Dec 17; 80(6): 1039–1054.e6. doi: 10.1016/j.molcel.2020.11.012
PMCID:
PMC7758880
AbstractArticle
15.
Global Functional Map of the p23 Molecular Chaperone Reveals an Extensive Cellular Network
Frank J. Echtenkamp, Elena Zelin, Ellinor Oxelmark, Joyce I. Woo, Brenda J. Andrews, Michael Garabedian, Brian C. Freeman
Mol Cell. Author manuscript; available in PMC 2012 Jul 22.
Published in final edited form as: Mol Cell. 2011 Jul 22; 43(2): 229–241. doi: 10.1016/j.molcel.2011.05.029
PMCID:
PMC3155841
AbstractArticlePDF–1.7M
16.
A global S. cerevisiae small ubiquitin-related modifier (SUMO) system interactome
Tharan Srikumar, Megan C Lewicki, Brian Raught
Mol Syst Biol. 2013; 9: 668. Published online 2013 May 28. doi: 10.1038/msb.2013.23
PMCID:
PMC4039371
AbstractArticlePDF–2.5M
17.
Identification of 14-3-3 Proteins, Polo kinase, and RNA-binding protein Pes4 as Key Regulators of Meiotic Commitment in Budding Yeast
Janardan N. Gavade, Chris M. Puccia, S. Grace Herod, Jonathan C. Trinidad, Luke E. Berchowitz, Soni Lacefield
Curr Biol. Author manuscript; available in PMC 2023 Apr 11.
Published in final edited form as: Curr Biol. 2022 Apr 11; 32(7): 1534–1547.e9. Published online 2022 Mar 2. doi: 10.1016/j.cub.2022.02.022
PMCID:
PMC9007917
AbstractArticlePDF–2.2M
18.
Clathrin light chain directs endocytosis by influencing the binding of the yeast Hip1R homologue, Sla2, to F-actin
Douglas R. Boettner, Helena Friesen, Brenda Andrews, Sandra K. Lemmon
Mol Biol Cell. 2011 Oct 1; 22(19): 3699–3714. doi: 10.1091/mbc.E11-07-0628
PMCID:
PMC3183023
AbstractArticlePDF–6.5M
19.
Xrn1 biochemically associates with eisosome proteins after the post diauxic shift in yeast
Baptiste Courtin, Abdelkader Namane, Maite Gomard, Laura Meyer, Alain Jacquier, Micheline Fromont-Racine
MicroPubl Biol. 2023; 2023: 10.17912/micropub.biology.000926. Published online 2023 Sep 7. doi: 10.17912/micropub.biology.000926
PMCID:
PMC10514700
AbstractArticlePDF–1.7M
20.
The Yeast Ess1 Prolyl Isomerase Controls Swi6 and Whi5 Nuclear Localization
David Atencio, Cassandra Barnes, Thomas M. Duncan, Ian M. Willis, Steven D. Hanes
G3 (Bethesda) 2014 Mar; 4(3): 523–537. Published online 2014 Jan 27. doi: 10.1534/g3.113.008763
PMCID:
PMC3962490
AbstractArticlePDF–2.3M

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