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PMID: 8464499 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Specificity domains distinguish the Ras-related GTPases Ypt1 and Sec4.

Nature ·Vol. 362 ·No. 6420 ·1993-04-08 ·Pages 563-5

Dunn B, Stearns T, Botstein D

Abstract

The essential Ras-related GTPases Ypt1 and Sec4 act at distinct stages of the secretion pathway in the yeast Saccharomyces cerevisiae: Ypt1 is required for vesicular transport from the endoplasmic reticulum to the Golgi apparatus, whereas Sec4 is required for fusion of secretory vesicles to the plasma membrane. Here we use chimaeras of the two proteins to identify a 9-residue segment of Ypt1 that, when substituted for the analogous segment of Sec4, allows the chimaera to perform the minimal functions of both proteins in vivo. This segment corresponds to loop L7 of the p21ras crystal structure. Substitution of a 24-residue Ypt1 segment, including the residues just mentioned, together with 12 residues of Ypt1 corresponding to the 'effector region' of p21ras (loop L2; refs 7,8), transforms Sec4 into a fully functional Ypt1 protein without residual Sec4 function.

Related Genes
MeSH Terms
Amino Acid Sequence Crystallization Fungal Proteins/chemistry GTP-Binding Proteins/chemistry Glycoside Hydrolases/metabolism Glycosylation Molecular Sequence Data Proto-Oncogene Proteins p21(ras)/chemistry Recombinant Fusion Proteins/chemistry Saccharomyces cerevisiae/chemistry Saccharomyces cerevisiae Proteins Sequence Homology, Amino Acid beta-Fructofuranosidase rab GTP-Binding Proteins
Chemicals
Fungal Proteins Recombinant Fusion Proteins Saccharomyces cerevisiae Proteins Glycoside Hydrolases beta-Fructofuranosidase GTP-Binding Proteins YPT1 protein, S cerevisiae SEC4 protein, S cerevisiae Proto-Oncogene Proteins p21(ras) rab GTP-Binding Proteins
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Dunn B
Department of Genetics, Stanford University School of Medicine, California 94305.
Stearns T
Botstein D
Article Info
Journal
Nature
Abbr.
Nature
ISSN
0028-0836
Published
1993-04-08
Pages
563-5
Language
English
Region
England
NLM ID
0410462
Subset
IM
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