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The yeast SEC17 gene product is functionally equivalent to mammalian alpha-SNAP protein.

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Griff, I.C., Schekman, R, Rothman, J.E., Kaiser, C.A.·1992·Journal of Biological Chemistry

Abstract

The SEC17 gene of Saccharomyces cerevisiae is required for vesicular transport between the endoplasmic reticulum and the Golgi apparatus. Here we report that the product of the SEC17 gene has the exact biochemical properties expected for a yeast homologue of the mammalian transport factor, alpha-SNAP. The DNA sequence of SEC17 codes for a protein of predicted molecular mass of 33 kDa. Immunoblotting indicates that Sec17p fractionates as a peripheral membrane protein and is mostly soluble when overexpressed, suggesting the presence of a saturable membrane receptor for Sec17p. Sec17p was purified from yeast cytosol using a SNAP-dependent in vitro mammalian Golgi transport assay. Kinetic analysis using this assay shows Sec17p acts temporally close to the fusion of transport vesicles with the medial Golgi compartment. In yeast extracts, Sec17p binds to Sec18p with a 1:1 stoichiometry. The interaction between Sec17p and Sec18p requires an activity provided by yeast membranes, and this putative membrane receptor activity is not extracted by high salt treatment of membranes.

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Metadata

Authors
Griff, I. C., Schekman, R., Rothman, J. E., & Kaiser, C. A.
Venue
Journal of Biological Chemistry
Publisher
Elsevier BV
Published
1992-06
Volume
267
Issue
17
Pages
12106-12115
ISSN
0021-9258 (ISSN-L)
OpenAlex
W1541462376
Cited by
159
References
0
FWCI
6.48
Type
journal article
Language
en
Open access
hybrid

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CoChat. (2026). Citation check: The yeast SEC17 gene product is functionally equivalent to mammalian alpha-SNAP protein. https://app.cochat.ai/papers/10.1016/s0021-9258(19)49812-8
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Griff, I. C., Schekman, R., Rothman, J. E., & Kaiser, C. A. (1992). The yeast SEC17 gene product is functionally equivalent to mammalian alpha-SNAP protein. Journal of Biological Chemistry. https://doi.org/10.1016/s0021-9258(19)49812-8

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