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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
Pip2p YNL202W PubMed external link Karpichev IV et al., Mol Cell Biol, 1998 Nov;18(11):6560-70Karpichev IV et al., Mol Cell Biol, 1998 Nov;18(11):6560-70 Indirect Northern blot - wt vs TF mutant Positive W3031A YP-Glycerol-Oleate
PubMed external link Gurvitz A et al., Mol Gen Genet, 1999 Oct;262(3):481-92Gurvitz A et al., Mol Gen Genet, 1999 Oct;262(3):481-92 Indirect lacZ - wt vs TF mutant Positive S288c oleic acid-containing medium
PubMed external link Gurvitz A et al., Mol Cell Biol Res Commun, 2000 Aug;4(2):81-9Gurvitz A et al., Mol Cell Biol Res Commun, 2000 Aug;4(2):81-9 Indirect lacZ - wt vs TF mutant Positive S288c growth in YP with 0,2% oleic acid and 0.02% Tween 80
PubMed external link Smith JJ et al., Mol Syst Biol, 2007;():Smith JJ et al., Mol Syst Biol, 2007;(): Indirect Microarray analysis - wt vs TF mutant Positive BY4742 or BY4739 5-h induction in oleate
PubMed external link Gurvitz A et al., FEMS Yeast Res, 2009 Sep;9(6):821-31Gurvitz A et al., FEMS Yeast Res, 2009 Sep;9(6):821-31 Indirect RT-PCR - wt vs TF mutant Positive yAG561 Liquid oleic acid medium (YPO)
PubMed external link Ratnakumar S et al., J Biol Chem, 2010 Apr 2;285(14):10703-14Ratnakumar S et al., J Biol Chem, 2010 Apr 2;285(14):10703-14 Indirect RT-PCR - wt vs TF mutant Positive S288c Glucose derepression; Exponential-phase cells cultivated for 1 h in synthetic growth medium containing 0.1% oleate + 3% glycerol
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 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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