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Regulation Reference(s)

The Yeastract team, is actively curating each regulation evidence code, association type and environmental condition.
Transcription
Factor		 Target
ORF/Genes		 References Evidence
Code		 Evidence
Experiment		 Association
Type		 Strain Environmental
Condition
Cat8p YOL126C PubMed external link Haurie V et al., J Biol Chem, 2001 Jan 5;276(1):76-85Haurie V et al., J Biol Chem, 2001 Jan 5;276(1):76-85 Indirect Northern blot - wt vs TF mutant Positive S288c Diauxic shift; Cells cultivated in YNB growth medium and harvested after glucose exhaustion
PubMed external link Roth S et al., Yeast, 2001 Jan 30;18(2):151-62Roth S et al., Yeast, 2001 Jan 30;18(2):151-62 Direct EMSA N/A S288c N/A
PubMed external link Young ET et al., J Biol Chem, 2003 Jul 11;278(28):26146-58Young ET et al., J Biol Chem, 2003 Jul 11;278(28):26146-58 Indirect Microarray analysis - wt vs TF mutant Positive W303-1A Yeast cells were grown in rich (YP) medium, log-phase
PubMed external link Tachibana C et al., Mol Cell Biol, 2005 Mar;25(6):2138-46Tachibana C et al., Mol Cell Biol, 2005 Mar;25(6):2138-46 Direct ChIP N/A S288c Growth in glucose derepression conditions (0.05% glucose)
PubMed external link Tachibana C et al., J Biol Chem, 2007 Dec 28;282(52):37308-15Tachibana C et al., J Biol Chem, 2007 Dec 28;282(52):37308-15 Direct ChIP N/A S288c 0,05% glucose 6h
PubMed external link Biddick RK et al., PLoS One, 2008 Jan 16;3(1):e1436Biddick RK et al., PLoS One, 2008 Jan 16;3(1):e1436 Indirect RT-PCR - wt vs TF mutant Positive S288c Glucose starvation; Exponential cells cultivated in SM with 0.05% glucose
PubMed external link Reimand J et al., Nucleic Acids Res, 2010 Aug;38(14):4768-77Reimand J et al., Nucleic Acids Res, 2010 Aug;38(14):4768-77 Indirect Microarray analysis - wt vs TF mutant Negative S288c YPD medium; mid-log phase
PubMed external link Holland P et al., Nucleic Acids Res, 2019 Jun 4;47(10):4986-5000Holland P et al., Nucleic Acids Res, 2019 Jun 4;47(10):4986-5000 Direct ChIP-exo N/A CEN.PK 113-5D Cells were cultivated in chemostats in anaerobic glucose limited medium with a dilution rate of 0.1 h-1 at 30.C. Samples were collected after steady state was achieved for 48-60 h
Direct ChIP-exo N/A CEN.PK 113-5D Cells were cultivated in chemostats in ethanol limited medium with a dilution rate of 0.1 h-1 at 30.C. Samples were collected after steady state was achieved for 48-60 h
Direct ChIP-exo N/A CEN.PK 113-5D Cells were cultivated in chemostats in nitrogen limited medium with a dilution rate of 0.1 h-1 at 30.C. Samples were collected after steady state was achieved for 48-60 h
Direct ChIP-exo N/A CEN.PK 113-5D Cells were cultivated in chemostats in respiratory glucose limited medium with a dilution rate of 0.1 h-1 at 30.C. Samples were collected after steady state was achieved for 48-60 h
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