(Q24309411)

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Identification of dominant negative mutants of Rheb GTPase and their use to implicate the involvement of human Rheb in the activation of p70S6K

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Identification of dominant negative mutants of Rheb GTPase and their use to implicate the involvement of human Rheb in the activation of p70S6K (English)

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GOA release 2020-03-11

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GOA release 2020-03-11

David H. Gutmann

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David H Gutmann

5

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author name string

Angel P Tabancay

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Chia-Ling Gau

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Iara M P Machado

3

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Erik J Uhlmann

4

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Lea Guo

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Fuyuhiko Tamanoi

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publication date

10 October 2003

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Journal of Biological Chemistry

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278

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41

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39921-30

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The Saccharomyces cerevisiae Rheb G-protein is involved in regulating canavanine resistance and arginine uptake

1 reference

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Characterization of Rheb functions using yeast and mammalian systems

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The Ras branch of small GTPases: Ras family members don't fall far from the tree

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A novel approach for expression cloning of small GTPases: identification, tissue distribution and chromosome mapping of the human homolog of rheb

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Failure to farnesylate Rheb protein contributes to the enrichment of G0/G1 phase cells in the Schizosaccharomyces pombe farnesyltransferase mutant

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Expression of the Aspergillus fumigatus rheb homologue, rhbA, is induced by nitrogen starvation

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Deletion of the Aspergillus fumigatus gene encoding the Ras-related protein RhbA reduces virulence in a model of Invasive pulmonary aspergillosis

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Drosophila Rheb GTPase is required for cell cycle progression and cell growth

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Protein farnesylation is critical for maintaining normal cell morphology and canavanine resistance in Schizosaccharomyces pombe

1 reference

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The Ras-related protein Rheb is farnesylated and antagonizes Ras signaling and transformation.

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A mammalian protein targeted by G1-arresting rapamycin-receptor complex

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Rheb promotes cell growth as a component of the insulin/TOR signalling network

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Rheb is an essential regulator of S6K in controlling cell growth in Drosophila

1 reference

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Rheb is in a high activation state and inhibits B-Raf kinase in mammalian cells

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Rheb interacts with Raf-1 kinase and may function to integrate growth factor- and protein kinase A-dependent signals

1 reference

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Tools of the trade: use of dominant-inhibitory mutants of Ras-family GTPases

1 reference

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RhoA inactivation inhibits cell migration but does not mediate the effects of polyamine depletion

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Rac is activated by erythropoietin or interleukin-3 and is involved in activation of the Erk signaling pathway

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The role of fnx1, a fission yeast multidrug resistance protein, in the transition of cells to a quiescent G0 state

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Molecular genetic analysis of fission yeast Schizosaccharomyces pombe

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Improved method for high efficiency transformation of intact yeast cells

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Mutant farnesyltransferase beta subunit of Saccharomyces cerevisiae that can substitute for geranylgeranyltransferase type I beta subunit

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A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

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RERG is a novel ras-related, estrogen-regulated and growth-inhibitory gene in breast cancer

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IRA2, an upstream negative regulator of RAS in yeast, is a RAS GTPase-activating protein

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The GTPase superfamily: conserved structure and molecular mechanism

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The structural basis of the activation of Ras by Sos

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Structure-based mutagenesis reveals distinct functions for Ras switch 1 and switch 2 in Sos-catalyzed guanine nucleotide exchange

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TOR, a central controller of cell growth

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Growth signaling: TSC takes its place.

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Refined crystal structure of the triphosphate conformation of H-ras p21 at 1.35 A resolution: implications for the mechanism of GTP hydrolysis

1 reference

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TATA box mutations in the Schizosaccharomyces pombe nmt1 promoter affect transcription efficiency but not the transcription start point or thiamine repressibility

1 reference

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Studies on the mechanism of resistance to rapamycin in human cancer cells

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Identifiers

10.1074/JBC.M306553200

1 reference

Consolidated OpenCitations Corpus – April 2017

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OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

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PubMed publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

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