242 related articles for article (PubMed ID: 17015442)
1. Saccharomyces cerevisiae Sit4 phosphatase is active irrespective of the nitrogen source provided, and Gln3 phosphorylation levels become nitrogen source-responsive in a sit4-deleted strain.
Tate JJ; Feller A; Dubois E; Cooper TG
J Biol Chem; 2006 Dec; 281(49):37980-92. PubMed ID: 17015442
[TBL] [Abstract][Full Text] [Related]
2. Tor pathway control of the nitrogen-responsive DAL5 gene bifurcates at the level of Gln3 and Gat1 regulation in Saccharomyces cerevisiae.
Georis I; Tate JJ; Cooper TG; Dubois E
J Biol Chem; 2008 Apr; 283(14):8919-29. PubMed ID: 18245087
[TBL] [Abstract][Full Text] [Related]
3. Stress-responsive Gln3 localization in Saccharomyces cerevisiae is separable from and can overwhelm nitrogen source regulation.
Tate JJ; Cooper TG
J Biol Chem; 2007 Jun; 282(25):18467-18480. PubMed ID: 17439949
[TBL] [Abstract][Full Text] [Related]
4. Sit4 and PP2A Dephosphorylate Nitrogen Catabolite Repression-Sensitive Gln3 When TorC1 Is Up- as Well as Downregulated.
Tate JJ; Tolley EA; Cooper TG
Genetics; 2019 Aug; 212(4):1205-1225. PubMed ID: 31213504
[No Abstract] [Full Text] [Related]
5. Gln3 phosphorylation and intracellular localization in nutrient limitation and starvation differ from those generated by rapamycin inhibition of Tor1/2 in Saccharomyces cerevisiae.
Cox KH; Kulkarni A; Tate JJ; Cooper TG
J Biol Chem; 2004 Mar; 279(11):10270-8. PubMed ID: 14679193
[TBL] [Abstract][Full Text] [Related]
6. Rapamycin-induced Gln3 dephosphorylation is insufficient for nuclear localization: Sit4 and PP2A phosphatases are regulated and function differently.
Tate JJ; Georis I; Feller A; Dubois E; Cooper TG
J Biol Chem; 2009 Jan; 284(4):2522-34. PubMed ID: 19015262
[TBL] [Abstract][Full Text] [Related]
7. Ammonia-specific regulation of Gln3 localization in Saccharomyces cerevisiae by protein kinase Npr1.
Tate JJ; Rai R; Cooper TG
J Biol Chem; 2006 Sep; 281(38):28460-9. PubMed ID: 16864577
[TBL] [Abstract][Full Text] [Related]
8. Nitrogen starvation and TorC1 inhibition differentially affect nuclear localization of the Gln3 and Gat1 transcription factors through the rare glutamine tRNACUG in Saccharomyces cerevisiae.
Tate JJ; Rai R; Cooper TG
Genetics; 2015 Feb; 199(2):455-74. PubMed ID: 25527290
[TBL] [Abstract][Full Text] [Related]
9. Distinct phosphatase requirements and GATA factor responses to nitrogen catabolite repression and rapamycin treatment in Saccharomyces cerevisiae.
Tate JJ; Georis I; Dubois E; Cooper TG
J Biol Chem; 2010 Jun; 285(23):17880-95. PubMed ID: 20378536
[TBL] [Abstract][Full Text] [Related]
10. TIP41 interacts with TAP42 and negatively regulates the TOR signaling pathway.
Jacinto E; Guo B; Arndt KT; Schmelzle T; Hall MN
Mol Cell; 2001 Nov; 8(5):1017-26. PubMed ID: 11741537
[TBL] [Abstract][Full Text] [Related]
11. Nitrogen-responsive regulation of GATA protein family activators Gln3 and Gat1 occurs by two distinct pathways, one inhibited by rapamycin and the other by methionine sulfoximine.
Georis I; Tate JJ; Cooper TG; Dubois E
J Biol Chem; 2011 Dec; 286(52):44897-912. PubMed ID: 22039046
[TBL] [Abstract][Full Text] [Related]
12. Actin cytoskeleton is required for nuclear accumulation of Gln3 in response to nitrogen limitation but not rapamycin treatment in Saccharomyces cerevisiae.
Cox KH; Tate JJ; Cooper TG
J Biol Chem; 2004 Apr; 279(18):19294-301. PubMed ID: 14970238
[TBL] [Abstract][Full Text] [Related]
13. Methionine sulfoximine treatment and carbon starvation elicit Snf1-independent phosphorylation of the transcription activator Gln3 in Saccharomyces cerevisiae.
Tate JJ; Rai R; Cooper TG
J Biol Chem; 2005 Jul; 280(29):27195-204. PubMed ID: 15911613
[TBL] [Abstract][Full Text] [Related]
14. Transmitting the signal of excess nitrogen in Saccharomyces cerevisiae from the Tor proteins to the GATA factors: connecting the dots.
Cooper TG
FEMS Microbiol Rev; 2002 Aug; 26(3):223-38. PubMed ID: 12165425
[TBL] [Abstract][Full Text] [Related]
15. Differing responses of Gat1 and Gln3 phosphorylation and localization to rapamycin and methionine sulfoximine treatment in Saccharomyces cerevisiae.
Kulkarni A; Buford TD; Rai R; Cooper TG
FEMS Yeast Res; 2006 Mar; 6(2):218-29. PubMed ID: 16487345
[TBL] [Abstract][Full Text] [Related]
16. More than One Way in: Three Gln3 Sequences Required To Relieve Negative Ure2 Regulation and Support Nuclear Gln3 Import in
Tate JJ; Rai R; Cooper TG
Genetics; 2018 Jan; 208(1):207-227. PubMed ID: 29113979
[TBL] [Abstract][Full Text] [Related]
17. N- and C-terminal Gln3-Tor1 interaction sites: one acting negatively and the other positively to regulate nuclear Gln3 localization.
Tate JJ; Rai R; De Virgilio C; Cooper TG
Genetics; 2021 Apr; 217(4):. PubMed ID: 33857304
[TBL] [Abstract][Full Text] [Related]
18. Normal function of the yeast TOR pathway requires the type 2C protein phosphatase Ptc1.
González A; Ruiz A; Casamayor A; Ariño J
Mol Cell Biol; 2009 May; 29(10):2876-88. PubMed ID: 19273591
[TBL] [Abstract][Full Text] [Related]
19. Nuclear localization domains of GATA activator Gln3 are required for transcription of target genes through dephosphorylation in Saccharomyces cerevisiae.
Numamoto M; Tagami S; Ueda Y; Imabeppu Y; Sasano Y; Sugiyama M; Maekawa H; Harashima S
J Biosci Bioeng; 2015 Aug; 120(2):121-7. PubMed ID: 25641578
[TBL] [Abstract][Full Text] [Related]
20. The protein phosphatase Siw14 controls caffeine-induced nuclear localization and phosphorylation of Gln3 via the type 2A protein phosphatases Pph21 and Pph22 in Saccharomyces cerevisiae.
Numamoto M; Sasano Y; Hirasaki M; Sugiyama M; Maekawa H; Harashima S
J Biochem; 2015 Jan; 157(1):53-64. PubMed ID: 25313402
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
