Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2001-6-7
pubmed:abstractText
The mating-specific heterotrimeric G(alpha) protein of Saccharomyces cerevisiae, Gpa1, negatively regulates activation of the pheromone response pathway both by sequestering G(beta)gamma and by triggering an adaptive response through an as yet unknown mechanism. Previous genetic studies identified mutant alleles of GPA1 that downregulate the pheromone response independently of the pheromone receptor (GPA1E364K), or through a receptor-dependent mechanism (GPA1N388D). To further our understanding of the mechanism of action of these mutant alleles, their corresponding proteins were purified and subjected to biochemical analysis. The receptor-dependent activity of Gpa1N388D was further analyzed using yeast strains expressing constitutively active receptor (Ste2) mutants, and C-terminal truncation mutant forms of Gpa1. A combination of G(alpha) affinity chromatography, GTP binding/hydrolysis studies, and genetic analysis allowed us to assign a distinct mechanism of action to each of these mutant proteins.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Aluminum Compounds, http://linkedlifedata.com/resource/pubmed/chemical/Fluorides, http://linkedlifedata.com/resource/pubmed/chemical/GPA1 protein, S cerevisiae, http://linkedlifedata.com/resource/pubmed/chemical/GTP-Binding Protein alpha Subunits, http://linkedlifedata.com/resource/pubmed/chemical/GTP-Binding Protein alpha..., http://linkedlifedata.com/resource/pubmed/chemical/GTP-Binding Protein beta Subunits, http://linkedlifedata.com/resource/pubmed/chemical/GTP-Binding Protein gamma Subunits, http://linkedlifedata.com/resource/pubmed/chemical/Guanosine 5'-O-(3-Thiotriphosphate), http://linkedlifedata.com/resource/pubmed/chemical/Guanosine Triphosphate, http://linkedlifedata.com/resource/pubmed/chemical/Heterotrimeric GTP-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Histidine, http://linkedlifedata.com/resource/pubmed/chemical/Pheromones, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Mating Factor, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Peptide, http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Fusion Proteins, http://linkedlifedata.com/resource/pubmed/chemical/STE18 protein, S cerevisiae, http://linkedlifedata.com/resource/pubmed/chemical/Saccharomyces cerevisiae Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Ste4 protein, S cerevisiae, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors, http://linkedlifedata.com/resource/pubmed/chemical/aluminum fluoride
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0006-291X
pubmed:author
pubmed:copyrightInfo
Copyright 2001 Academic Press.
pubmed:issnType
Print
pubmed:day
8
pubmed:volume
284
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
247-54
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:11394869-Adaptation, Physiological, pubmed-meshheading:11394869-Alleles, pubmed-meshheading:11394869-Aluminum Compounds, pubmed-meshheading:11394869-Amino Acid Substitution, pubmed-meshheading:11394869-Binding Sites, pubmed-meshheading:11394869-Chromatography, Affinity, pubmed-meshheading:11394869-Down-Regulation, pubmed-meshheading:11394869-Fluorides, pubmed-meshheading:11394869-GTP-Binding Protein alpha Subunits, pubmed-meshheading:11394869-GTP-Binding Protein alpha Subunits, Gq-G11, pubmed-meshheading:11394869-GTP-Binding Protein beta Subunits, pubmed-meshheading:11394869-GTP-Binding Protein gamma Subunits, pubmed-meshheading:11394869-Guanosine 5'-O-(3-Thiotriphosphate), pubmed-meshheading:11394869-Guanosine Triphosphate, pubmed-meshheading:11394869-Heterotrimeric GTP-Binding Proteins, pubmed-meshheading:11394869-Histidine, pubmed-meshheading:11394869-Models, Molecular, pubmed-meshheading:11394869-Mutation, pubmed-meshheading:11394869-Pheromones, pubmed-meshheading:11394869-Protein Binding, pubmed-meshheading:11394869-Receptors, Mating Factor, pubmed-meshheading:11394869-Receptors, Peptide, pubmed-meshheading:11394869-Recombinant Fusion Proteins, pubmed-meshheading:11394869-Saccharomyces cerevisiae, pubmed-meshheading:11394869-Saccharomyces cerevisiae Proteins, pubmed-meshheading:11394869-Signal Transduction, pubmed-meshheading:11394869-Transcription Factors
pubmed:year
2001
pubmed:articleTitle
Biochemical analysis of yeast G(alpha) mutants that enhance adaptation to pheromone.
pubmed:affiliation
Laboratory for Molecular Biology, University of Illinois at Chicago, Chicago, Illinois 60607, USA.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't