ICL1/YER065C Literature Guide Help

Other names published for ICL1: isocitrate lyase 1, YER065C

ICL1 - Protein Processing/Modification/Regulation (14)

ReferenceOther Genes Addressed
Casatta N, et al.  (2013) Lack of Sir2 increases acetate consumption and decreases extracellular pro-aging factors. Biochim Biophys Acta 1833(3):593-601
Gamberi T, et al.  (2012) Evaluation of SCO1 deletion on Saccharomyces cerevisiae metabolism through a proteomic approach. Proteomics 12(11):1767-80
Giardina BJ, et al.  (2012) Comparative Proteomic Analysis of Transition of Saccharomyces cerevisiae from Glucose-Deficient Medium to Glucose-Rich Medium. Proteome Sci 10(1):40
Lesur A, et al.  (2012) Peptides quantification by liquid chromatography with matrix-assisted laser desorption/ionization and selected reaction monitoring detection. J Proteome Res 11(10):4972-82
Costenoble R, et al.  (2011) Comprehensive quantitative analysis of central carbon and amino-acid metabolism in Saccharomyces cerevisiae under multiple conditions by targeted proteomics. Mol Syst Biol 7():464
Brown CR, et al.  (2010) The TOR complex 1 is distributed in endosomes and in retrograde vesicles that form from the vacuole membrane and plays an important role in the vacuole import and degradation pathway. J Biol Chem 285(30):23359-70
Orlandi I, et al.  (2010) Sir2-dependent asymmetric segregation of damaged proteins in ubp10 null mutants is independent of genomic silencing. Biochim Biophys Acta 1803(5):630-638
Rintala E, et al.  (2009) Low oxygen levels as a trigger for enhancement of respiratory metabolism in Saccharomyces cerevisiae. BMC Genomics 10():461
Belinchon MM and Gancedo JM  (2007) Glucose controls multiple processes in Saccharomyces cerevisiae through diverse combinations of signaling pathways. FEMS Yeast Res 7(6):808-18
Kolkman A, et al.  (2005) Comparative proteome analysis of Saccharomyces cerevisiae grown in chemostat cultures limited for glucose or ethanol. Mol Cell Proteomics 4(1):1-11
Monribot-Espagne C and Boucherie H  (2002) Differential gel exposure, a new methodology for the two-dimensional comparison of protein samples. Proteomics 2(3):229-40
Hammerle M, et al.  (1998) Proteins of newly isolated mutants and the amino-terminal proline are essential for ubiquitin-proteasome-catalyzed catabolite degradation of fructose-1,6-bisphosphatase of Saccharomyces cerevisiae. J Biol Chem 273(39):25000-5
Fernandez E, et al.  (1992) The ICL1 gene from Saccharomyces cerevisiae. Eur J Biochem 204(3):983-90
Holzer H  (1989) Proteolytic catabolite inactivation in Saccharomyces cerevisiae. Revis Biol Celular 21:305-19