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Items: 1 to 20 of 104

1.

Regulation of Ste7 ubiquitination by Ste11 phosphorylation and the Skp1-Cullin-F-box complex.

Wang Y, Ge Q, Houston D, Thorner J, Errede B, Dohlman HG.

J Biol Chem. 2003 Jun 20;278(25):22284-9. Epub 2003 Mar 31.

2.

Dynamic ubiquitination of the mitogen-activated protein kinase kinase (MAPKK) Ste7 determines mitogen-activated protein kinase (MAPK) specificity.

Hurst JH, Dohlman HG.

J Biol Chem. 2013 Jun 28;288(26):18660-71. doi: 10.1074/jbc.M113.475707. Epub 2013 May 3.

3.

Pheromone-dependent ubiquitination of the mitogen-activated protein kinase kinase Ste7.

Wang Y, Dohlman HG.

J Biol Chem. 2002 May 3;277(18):15766-72. Epub 2002 Feb 25.

4.

Pheromone-dependent destruction of the Tec1 transcription factor is required for MAP kinase signaling specificity in yeast.

Bao MZ, Schwartz MA, Cantin GT, Yates JR 3rd, Madhani HD.

Cell. 2004 Dec 29;119(7):991-1000.

5.

Cdc53 is a scaffold protein for multiple Cdc34/Skp1/F-box proteincomplexes that regulate cell division and methionine biosynthesis in yeast.

Patton EE, Willems AR, Sa D, Kuras L, Thomas D, Craig KL, Tyers M.

Genes Dev. 1998 Mar 1;12(5):692-705. Erratum in: Genes Dev 1998 Oct 1;12(19):3144.

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Persistent activation by constitutive Ste7 promotes Kss1-mediated invasive growth but fails to support Fus3-dependent mating in yeast.

Maleri S, Ge Q, Hackett EA, Wang Y, Dohlman HG, Errede B.

Mol Cell Biol. 2004 Oct;24(20):9221-38.

9.

Cdc53/cullin and the essential Hrt1 RING-H2 subunit of SCF define a ubiquitin ligase module that activates the E2 enzyme Cdc34.

Seol JH, Feldman RM, Zachariae W, Shevchenko A, Correll CC, Lyapina S, Chi Y, Galova M, Claypool J, Sandmeyer S, Nasmyth K, Deshaies RJ, Shevchenko A, Deshaies RJ.

Genes Dev. 1999 Jun 15;13(12):1614-26.

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11.

A refined two-hybrid system reveals that SCF(Cdc4)-dependent degradation of Swi5 contributes to the regulatory mechanism of S-phase entry.

Kishi T, Ikeda A, Koyama N, Fukada J, Nagao R.

Proc Natl Acad Sci U S A. 2008 Sep 23;105(38):14497-502. doi: 10.1073/pnas.0806253105. Epub 2008 Sep 11.

13.

Complexes between STE5 and components of the pheromone-responsive mitogen-activated protein kinase module.

Marcus S, Polverino A, Barr M, Wigler M.

Proc Natl Acad Sci U S A. 1994 Aug 2;91(16):7762-6.

14.

Cdc34 and the F-box protein Met30 are required for degradation of the Cdk-inhibitory kinase Swe1.

Kaiser P, Sia RA, Bardes EG, Lew DJ, Reed SI.

Genes Dev. 1998 Aug 15;12(16):2587-97.

17.

Nucleus-specific and cell cycle-regulated degradation of mitogen-activated protein kinase scaffold protein Ste5 contributes to the control of signaling competence.

Garrenton LS, Braunwarth A, Irniger S, Hurt E, K├╝nzler M, Thorner J.

Mol Cell Biol. 2009 Jan;29(2):582-601. doi: 10.1128/MCB.01019-08. Epub 2008 Nov 10.

18.

Reconstitution of G1 cyclin ubiquitination with complexes containing SCFGrr1 and Rbx1.

Skowyra D, Koepp DM, Kamura T, Conrad MN, Conaway RC, Conaway JW, Elledge SJ, Harper JW.

Science. 1999 Apr 23;284(5414):662-5.

19.

Functional binding between Gbeta and the LIM domain of Ste5 is required to activate the MEKK Ste11.

Feng Y, Song LY, Kincaid E, Mahanty SK, Elion EA.

Curr Biol. 1998 Feb 26;8(5):267-78.

20.

BTB/POZ domain proteins are putative substrate adaptors for cullin 3 ubiquitin ligases.

Geyer R, Wee S, Anderson S, Yates J, Wolf DA.

Mol Cell. 2003 Sep;12(3):783-90.

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