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rdf:type |
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lifeskim:mentions |
umls-concept:C0054036,
umls-concept:C0184512,
umls-concept:C0205369,
umls-concept:C1180347,
umls-concept:C1314939,
umls-concept:C1418978,
umls-concept:C1514562,
umls-concept:C1551336,
umls-concept:C1579373,
umls-concept:C1709915,
umls-concept:C1880389,
umls-concept:C1883204,
umls-concept:C1883221
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pubmed:issue |
3
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pubmed:dateCreated |
1999-4-26
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pubmed:abstractText |
We demonstrate that the major in vivo targets of brefeldin A (BFA) in the secretory pathway of budding yeast are the three members of the Sec7 domain family of ARF exchange factors: Gea1p and Gea2p (functionally interchangeable) and Sec7p. Specific residues within the Sec7 domain are important for BFA inhibition of ARF exchange activity, since mutations in these residues of Gea1p (sensitive to BFA) and of ARNO (resistant to BFA) reverse the sensitivity of each to BFA in vivo and in vitro. We show that the target of BFA inhibition of ARF exchange activity is an ARF-GDP-Sec7 domain protein complex, and that BFA acts to stabilize this complex to a greater extent for a BFA-sensitive Sec7 domain than for a resistant one.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/ADP-Ribosylation Factors,
http://linkedlifedata.com/resource/pubmed/chemical/Antifungal Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Brefeldin A,
http://linkedlifedata.com/resource/pubmed/chemical/Fungal Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/GEA1 protein, S cerevisiae,
http://linkedlifedata.com/resource/pubmed/chemical/GTP-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/GTPase-Activating Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Guanine Nucleotide Exchange Factors,
http://linkedlifedata.com/resource/pubmed/chemical/Guanosine Diphosphate,
http://linkedlifedata.com/resource/pubmed/chemical/Guanosine Triphosphate,
http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Fusion Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Saccharomyces cerevisiae Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Sec7 guanine nucleotide exchange...,
http://linkedlifedata.com/resource/pubmed/chemical/cytohesin-2
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
1097-2765
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
3
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
275-85
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:10198630-ADP-Ribosylation Factors,
pubmed-meshheading:10198630-Amino Acid Sequence,
pubmed-meshheading:10198630-Amino Acid Substitution,
pubmed-meshheading:10198630-Antifungal Agents,
pubmed-meshheading:10198630-Brefeldin A,
pubmed-meshheading:10198630-Drug Resistance, Microbial,
pubmed-meshheading:10198630-Fungal Proteins,
pubmed-meshheading:10198630-GTP-Binding Proteins,
pubmed-meshheading:10198630-GTPase-Activating Proteins,
pubmed-meshheading:10198630-Gene Dosage,
pubmed-meshheading:10198630-Guanine Nucleotide Exchange Factors,
pubmed-meshheading:10198630-Guanosine Diphosphate,
pubmed-meshheading:10198630-Guanosine Triphosphate,
pubmed-meshheading:10198630-Kinetics,
pubmed-meshheading:10198630-Molecular Sequence Data,
pubmed-meshheading:10198630-Mutation,
pubmed-meshheading:10198630-Recombinant Fusion Proteins,
pubmed-meshheading:10198630-Saccharomyces cerevisiae,
pubmed-meshheading:10198630-Saccharomyces cerevisiae Proteins
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pubmed:year |
1999
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pubmed:articleTitle |
Brefeldin A acts to stabilize an abortive ARF-GDP-Sec7 domain protein complex: involvement of specific residues of the Sec7 domain.
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pubmed:affiliation |
Service de Biochimie et Génétique Moléculaire, CEA/Saclay, Gif-sur-Yvette, France.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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