(Q32053902)

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Amino acid residues in Std1 protein required for induction of SUC2 transcription are also required for suppression of TBPDelta57 growth defect in Saccharomyces cerevisiae

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Europe PubMed Central

6 July 2017

Amino acid residues in Std1 protein required for induction of SUC2 transcription are also required for suppression of TBPDelta57 growth defect in Saccharomyces cerevisiae (English)

1 reference

Europe PubMed Central

6 July 2017

Saccharomyces cerevisiae

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author name string

X Zhang

1

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Europe PubMed Central

6 July 2017

W Shen

2

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6 July 2017

M C Schmidt

3

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6 July 2017

language of work or name

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publication date

1 July 1998

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6 July 2017

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6 July 2017

215

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6 July 2017

131-141

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6 July 2017

1

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6 July 2017

The two-hybrid system: a method to identify and clone genes for proteins that interact with a protein of interest

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A family of versatile centromeric vectors designed for use in the sectoring-shuffle mutagenesis assay in Saccharomyces cerevisiae

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Limitations in the use of SSCP analysis

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Isolation of STD1, a high-copy-number suppressor of a dominant negative mutation in the yeast TATA-binding protein

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76 β-d-Fructofuranoside fructohydrolase from yeast

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Yeast/E. coli shuttle vectors with multiple unique restriction sites

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Dosage-dependent modulation of glucose repression by MSN3 (STD1) in Saccharomyces cerevisiae.

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Glucose regulates protein interactions within the yeast SNF1 protein kinase complex

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The Snf1 protein kinase and its activating subunit, Snf4, interact with distinct domains of the Sip1/Sip2/Gal83 component in the kinase complex

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7 January 2021

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Identification and characterization of a TFIID-like multiprotein complex from Saccharomyces cerevisiae

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In vitro mutagenesis and plasmid shuffling: from cloned gene to mutant yeast

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https://api.crossref.org/works/10.1016%2FS0378-1119%2898%2900276-5

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based on heuristic

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STD1 (MSN3) interacts directly with the TATA-binding protein and modulates transcription of the SUC2 gene of Saccharomyces cerevisiae

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2898%2900276-5

7 January 2021

based on heuristic

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Identifiers

10.1016/S0378-1119(98)00276-5

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Europe PubMed Central

6 July 2017

1 reference

Europe PubMed Central

6 July 2017

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