PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
9038161-9	1997	A consensus element with homology to the URS sequence of the ENO1 promoter was found in the promoters of the GPD1, GPP2, GCY1, and DAK1 genes.	Peptichemio	41-44	phosphopyruvate hydratase ENO1	Saccharomyces cerevisiae S288C	61-65	
7502579-1	1995	The activity of an upstream repression sequence (URS element) that mediates a 20-fold repression of ENO1 expression in cells grown in a medium containing glucose was characterized.	Peptichemio	49-52	phosphopyruvate hydratase ENO1	Saccharomyces cerevisiae S288C	100-104	
7502579-2	1995	Sequences that are sufficient for orientation-dependent ENO1 URS element activity were mapped between positions -241 and -126 relative to the ENO1 transcriptional initiation site.	Peptichemio	61-64	phosphopyruvate hydratase ENO1	Saccharomyces cerevisiae S288C	56-60	
7502579-2	1995	Sequences that are sufficient for orientation-dependent ENO1 URS element activity were mapped between positions -241 and -126 relative to the ENO1 transcriptional initiation site.	Peptichemio	61-64	phosphopyruvate hydratase ENO1	Saccharomyces cerevisiae S288C	142-146	
7502579-3	1995	The ENO1 URS element repressed transcription of the yeast CYC1 gene when positioned between the CYC1 upstream activation sequences (UAS elements) and TATAAA boxes.	Peptichemio	9-12	phosphopyruvate hydratase ENO1	Saccharomyces cerevisiae S288C	4-8	
7502579-4	1995	The ENO1 URS element failed to repress transcription of the wild-type yeast enolase gene ENO2; however, expression of an ENO2 gene lacking one of the ENO2 UAS elements was efficiently repressed by the ENO1 URS element, suggesting that the URS element interferes with the transcriptional activation by some, but not all, UAS elements.	Peptichemio	9-12	phosphopyruvate hydratase ENO1	Saccharomyces cerevisiae S288C	4-8	
7502579-4	1995	The ENO1 URS element failed to repress transcription of the wild-type yeast enolase gene ENO2; however, expression of an ENO2 gene lacking one of the ENO2 UAS elements was efficiently repressed by the ENO1 URS element, suggesting that the URS element interferes with the transcriptional activation by some, but not all, UAS elements.	Peptichemio	206-209	phosphopyruvate hydratase ENO1	Saccharomyces cerevisiae S288C	4-8	
7502579-4	1995	The ENO1 URS element failed to repress transcription of the wild-type yeast enolase gene ENO2; however, expression of an ENO2 gene lacking one of the ENO2 UAS elements was efficiently repressed by the ENO1 URS element, suggesting that the URS element interferes with the transcriptional activation by some, but not all, UAS elements.	Peptichemio	206-209	phosphopyruvate hydratase ENO1	Saccharomyces cerevisiae S288C	201-205	
7502579-4	1995	The ENO1 URS element failed to repress transcription of the wild-type yeast enolase gene ENO2; however, expression of an ENO2 gene lacking one of the ENO2 UAS elements was efficiently repressed by the ENO1 URS element, suggesting that the URS element interferes with the transcriptional activation by some, but not all, UAS elements.	Peptichemio	206-209	phosphopyruvate hydratase ENO1	Saccharomyces cerevisiae S288C	4-8	
7502579-4	1995	The ENO1 URS element failed to repress transcription of the wild-type yeast enolase gene ENO2; however, expression of an ENO2 gene lacking one of the ENO2 UAS elements was efficiently repressed by the ENO1 URS element, suggesting that the URS element interferes with the transcriptional activation by some, but not all, UAS elements.	Peptichemio	206-209	phosphopyruvate hydratase ENO1	Saccharomyces cerevisiae S288C	201-205	
7502579-5	1995	In contrast to the ENO1 gene, the ENO1 URS element repressed CYC1 and ENO2 expression in cells grown on glucose or glycerol plus lactate.	Peptichemio	39-42	phosphopyruvate hydratase ENO1	Saccharomyces cerevisiae S288C	34-38	
7502579-6	1995	Evidence is presented that the ENO1 URS element also functions during stationary growth phase.	Peptichemio	36-39	phosphopyruvate hydratase ENO1	Saccharomyces cerevisiae S288C	31-35	
8144571-1	1994	Cis-acting sequences that modulate ENO1 URS (upstream repression site) element activity were identified by base pair substitution mutagenesis.	Peptichemio	40-43	phosphopyruvate hydratase ENO1	Saccharomyces cerevisiae S288C	35-39	
8144571-4	1994	A binding site for the yeast REB1 protein was identified near the 5" terminus of the ENO1 URS element.	Peptichemio	90-93	phosphopyruvate hydratase ENO1	Saccharomyces cerevisiae S288C	85-89	
8144571-8	1994	Base substitution mutations within a second region of the ENO1 URS element caused a 38% loss of URS activity in vivo.	Peptichemio	63-66	phosphopyruvate hydratase ENO1	Saccharomyces cerevisiae S288C	58-62	
8144571-8	1994	Base substitution mutations within a second region of the ENO1 URS element caused a 38% loss of URS activity in vivo.	Peptichemio	96-99	phosphopyruvate hydratase ENO1	Saccharomyces cerevisiae S288C	58-62	
8144571-10	1994	Base substitution mutations within a third region near the 3" terminus of the ENO1 URS element caused a 70% loss of URS activity in vivo.	Peptichemio	83-86	phosphopyruvate hydratase ENO1	Saccharomyces cerevisiae S288C	78-82	
8144571-10	1994	Base substitution mutations within a third region near the 3" terminus of the ENO1 URS element caused a 70% loss of URS activity in vivo.	Peptichemio	116-119	phosphopyruvate hydratase ENO1	Saccharomyces cerevisiae S288C	78-82	
8144571-12	1994	These results showed that ENO1 URS element activity was modulated by multiple cis-acting sequences that bound distinct trans-acting factors.	Peptichemio	31-34	phosphopyruvate hydratase ENO1	Saccharomyces cerevisiae S288C	26-30