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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
Ino4p YCL004W PubMed external link Shen H et al., J Biol Chem, 1998 May 8;273(19):11638-42Shen H et al., J Biol Chem, 1998 May 8;273(19):11638-42 Indirect lacZ - wt vs TF mutant Positive S288c Inositol presence
PubMed external link Dzugasová V et al., Curr Genet, 1998 Oct;34(4):297-302Dzugasová V et al., Curr Genet, 1998 Oct;34(4):297-302 Indirect lacZ - wt vs TF mutant Positive S288c cells grown to mid log phase in synthetic medium lacking inositol / choline (derepressing conditions)
PubMed external link Workman CT et al., Science, 2006 May 19;312(5776):1054-9Workman CT et al., Science, 2006 May 19;312(5776):1054-9 Direct Chip-on-chip N/A S288c N/A
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 Positive S288c YPD medium; mid-log phase
PubMed external link Bergenholm D et al., mSystems, 2018 Jul-Aug;3(4):Bergenholm D et al., mSystems, 2018 Jul-Aug;3(4): Direct ChIP-exo N/A CEN.PK 113-5D Steady state aerobic chemostat cultivation at 30 .C in glucose-limited minimal medium containing vitamins and trace metals and maintained at pH 5.0
Direct ChIP-exo N/A CEN.PK 113-5D Steady state chemostat cultivation at 30 .C in oxygen- and glucose-limited minimal medium containing vitamins and trace metals and maintained at pH 5.0
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 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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