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1.
Structure of glyoxysomal malate dehydrogenase (MDH3) from Saccharomyces cerevisiae
Shu Moriyama, Kazuya Nishio, Tsunehiro Mizushima
Acta Crystallogr F Struct Biol Commun. 2018 Oct 1; 74(Pt 10): 617–624. Published online 2018 Sep 19. doi: 10.1107/S2053230X18011895
PMCID:
PMC6168765
AbstractArticlePDF–1.9M
2.
Malic Acid Production by Saccharomyces cerevisiae: Engineering of Pyruvate Carboxylation, Oxaloacetate Reduction, and Malate Export
Rintze M. Zelle, Erik de Hulster, Wouter A. van Winden, Pieter de Waard, Cor Dijkema, Aaron A. Winkler, Jan-Maarten A. Geertman, Johannes P. van Dijken, Jack T. Pronk, Antonius J. A. van Maris
Appl Environ Microbiol. 2008 May; 74(9): 2766–2777. Published online 2008 Mar 14. doi: 10.1128/AEM.02591-07
PMCID:
PMC2394876
AbstractArticlePDF–854K
3.
The membrane of peroxisomes in Saccharomyces cerevisiae is impermeable to NAD(H) and acetyl-CoA under in vivo conditions.
C W van Roermund, Y Elgersma, N Singh, R J Wanders, H F Tabak
EMBO J. 1995 Jul 17; 14(14): 3480–3486. doi: 10.1002/j.1460-2075.1995.tb07354.x
PMCID:
PMC394415
SummaryPage BrowsePDF–1.6M
4.
Isolation, nucleotide sequence analysis, and disruption of the MDH2 gene from Saccharomyces cerevisiae: evidence for three isozymes of yeast malate dehydrogenase.
K I Minard, L McAlister-Henn
Mol Cell Biol. 1991 Jan; 11(1): 370–380. doi: 10.1128/mcb.11.1.370
PMCID:
PMC359635
SummaryPage BrowsePDF–2.1M
5.
A piggybacking mechanism enables peroxisomal localization of the glyoxylate cycle enzyme Mdh2 in yeast
Shiran Gabay-Maskit, Luis Daniel Cruz-Zaragoza, Nadav Shai, Miriam Eisenstein, Chen Bibi, Nir Cohen, Tobias Hansen, Eden Yifrach, Nofar Harpaz, Ruth Belostotsky, Wolfgang Schliebs, Maya Schuldiner, Ralf Erdmann, Einat Zalckvar
J Cell Sci. 2020 Dec 15; 133(24): jcs244376. Published online 2020 Dec 17. doi: 10.1242/jcs.244376
PMCID:
PMC7758625
AbstractArticle
6.
Mutations in MDH2, Encoding a Krebs Cycle Enzyme, Cause Early-Onset Severe Encephalopathy
Samira Ait-El-Mkadem, Manal Dayem-Quere, Mirjana Gusic, Annabelle Chaussenot, Sylvie Bannwarth, Bérengère François, Emmanuelle C. Genin, Konstantina Fragaki, Catharina L.M. Volker-Touw, Christelle Vasnier, Valérie Serre, Koen L.I. van Gassen, Françoise Lespinasse, Susan Richter, Graeme Eisenhofer, Cécile Rouzier, Fanny Mochel, Anne De Saint-Martin, Marie-Thérèse Abi Warde, Monique G.M. de Sain-van der Velde, Judith J.M. Jans, Jeanne Amiel, Ziga Avsec, Christian Mertes, Tobias B. Haack, Tim Strom, Thomas Meitinger, Penelope E. Bonnen, Robert W. Taylor, Julien Gagneur, Peter M. van Hasselt, Agnès Rötig, Agnès Delahodde, Holger Prokisch, Sabine A. Fuchs, Véronique Paquis-Flucklinger
Am J Hum Genet. 2017 Jan 5; 100(1): 151–159. Published online 2016 Dec 15. doi: 10.1016/j.ajhg.2016.11.014
PMCID:
PMC5223029
AbstractArticlePDF–1.1M
7.
Saccharomyces cerevisiae PTS1 Receptor Pex5p Interacts with the SH3 Domain of the Peroxisomal Membrane Protein Pex13p in an Unconventional, Non-PXXP–related Manner
Gina Bottger, Phil Barnett, André T. J. Klein, Astrid Kragt, Henk F. Tabak, Ben Distel
Mol Biol Cell. 2000 Nov; 11(11): 3963–3976. doi: 10.1091/mbc.11.11.3963
PMCID:
PMC15050
AbstractArticlePDF–468K
8.
Two NAD-linked redox shuttles maintain the peroxisomal redox balance in Saccharomyces cerevisiae
Nadal A. Al-Saryi, Murtakab Y Al-Hejjaj, Carlo W. T. van Roermund, Georgia E. Hulmes, Lakhan Ekal, Chantell Payton, Ronald J. A. Wanders, Ewald H. Hettema
Sci Rep. 2017; 7: 11868. Published online 2017 Sep 19. doi: 10.1038/s41598-017-11942-2
PMCID:
PMC5605654
AbstractArticlePDF–2.9M
9.
Quantitative mass spectrometry reveals a role for the GTPase Rho1p in actin organization on the peroxisome membrane
Marcello Marelli, Jennifer J. Smith, Sunhee Jung, Eugene Yi, Alexey I. Nesvizhskii, Rowan H. Christmas, Ramsey A. Saleem, Yuen Yi C. Tam, Andrei Fagarasanu, David R. Goodlett, Ruedi Aebersold, Richard A. Rachubinski, John D. Aitchison
J Cell Biol. 2004 Dec 20; 167(6): 1099–1112. doi: 10.1083/jcb.200404119
PMCID:
PMC2172632
AbstractArticlePDF–4.8M
10.
Genetic Analysis of Peroxisomal Genes Required for Longevity in a Yeast Model of Citrin Deficiency
Chalongchai Chalermwat, Thitipa Thosapornvichai, Laran T. Jensen, Duangrurdee Wattanasirichaigoon
Diseases. 2020 Mar; 8(1): 2. Published online 2020 Jan 9. doi: 10.3390/diseases8010002
PMCID:
PMC7151034
AbstractArticlePDF–5.7M
11.
A Screen for RNA-Binding Proteins in Yeast Indicates Dual Functions for Many Enzymes
Tanja Scherrer, Nitish Mittal, Sarath Chandra Janga, André P. Gerber
PLoS One. 2010; 5(11): e15499. Published online 2010 Nov 11. doi: 10.1371/journal.pone.0015499
PMCID:
PMC2988813
AbstractArticlePDF–453K
12.
Origin, conservation, and loss of alternative splicing events that diversify the proteome in Saccharomycotina budding yeasts
Jennifer E. Hurtig, Minseon Kim, Luisa J. Orlando-Coronel, Jellisa Ewan, Michelle Foreman, Lee-Ann Notice, Michelle A. Steiger, Ambro van Hoof
RNA. 2020 Oct; 26(10): 1464–1480. doi: 10.1261/rna.075655.120
PMCID:
PMC7491326
AbstractArticlePDF–1.6M
13.
Proteome-Wide Search Reveals Unexpected RNA-Binding Proteins in Saccharomyces cerevisiae
Nikoleta G. Tsvetanova, Daniel M. Klass, Julia Salzman, Patrick O. Brown
PLoS One. 2010; 5(9): e12671. Published online 2010 Sep 10. doi: 10.1371/journal.pone.0012671
PMCID:
PMC2937035
AbstractArticlePDF–811K
14.
Phosphorylation of mitochondrial matrix proteins regulates their selective mitophagic degradation
Panagiota Kolitsida, Jianwen Zhou, Michal Rackiewicz, Vladimir Nolic, Jörn Dengjel, Hagai Abeliovich
Proc Natl Acad Sci U S A. 2019 Oct 8; 116(41): 20517–20527. Published online 2019 Sep 23. doi: 10.1073/pnas.1901759116
Correction in:
Proc Natl Acad Sci U S A. 2019 Nov 26; 116(48): 24374.
PMCID:
PMC6789754
AbstractArticlePDF–1.4M
15.
Genome-wide SWAp-tag yeast libraries for proteome exploration
Uri Weill, Ido Yofe, Ehud Sass, Bram Stynen, Dan Davidi, Janani Natarajan, Reut Ben Menachem, Zohar Avihou, Omer Goldman, Nofar Harpaz, Silvia Chuartzman, Kiril Kniazev, Barbara Knoblach, Janina Laborenz, Felix Boos, Jacqueline Kowarzyk, Shifra Ben-Dor, Einat Zalckvar, Johannes M. Herrmann, Richard A. Rachubinski, Ophry Pines, Doron Rapaport, Stephen W. Michnick, Emmanuel D. Levy, Maya Schuldiner
Nat Methods. Author manuscript; available in PMC 2019 Jan 9.
Published in final edited form as: Nat Methods. 2018 Aug; 15(8): 617–622. Published online 2018 Jul 9. doi: 10.1038/s41592-018-0044-9
Correction in:
Nat Methods. 2019 Jan 2
PMCID:
PMC6076999
AbstractArticlePDF–1.7M
16.
Revising the Representation of Fatty Acid, Glycerolipid, and Glycerophospholipid Metabolism in the Consensus Model of Yeast Metabolism
Hnin W. Aung, Susan A. Henry, Larry P. Walker
Ind Biotechnol (New Rochelle N Y) 2013 Aug; 9(4): 215–228. doi: 10.1089/ind.2013.0013
PMCID:
PMC3963290
AbstractArticlePDF–906K
17.
Regulation of lipid droplet dynamics in Saccharomyces cerevisiae depends on the Rab7-like Ypt7p, HOPS complex and V1-ATPase
Isabelle Bouchez, Marie Pouteaux, Michel Canonge, Mélanie Genet, Thierry Chardot, Alain Guillot, Marine Froissard
Biol Open. 2015 Jul 15; 4(7): 764–775. Published online 2015 May 6. doi: 10.1242/bio.20148615
PMCID:
PMC4571102
AbstractArticlePDF–1.0M
18.
Essential histone chaperones collaborate to regulate transcription and chromatin integrity
Olga Viktorovskaya, James Chuang, Dhawal Jain, Natalia I. Reim, Francheska López-Rivera, Magdalena Murawska, Dan Spatt, L. Stirling Churchman, Peter J. Park, Fred Winston
Genes Dev. 2021 May 1; 35(9-10): 698–712. doi: 10.1101/gad.348431.121
PMCID:
PMC8091981
AbstractArticlePDF–6.4M
19.
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
AbstractArticlePDF–322K
20.
Subgenic Pol II interactomes identify region‐specific transcription elongation regulators
Kevin M Harlen, L Stirling Churchman
Mol Syst Biol. 2017 Jan; 13(1): 900. Published online 2017 Jan 2. doi: 10.15252/msb.20167279
PMCID:
PMC5293154
AbstractArticlePDF–2.3M

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