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Multiple SNARE interactions of an SM protein: Sed5p/Sly1p binding is dispensable for transport
by
Peng, Renwang
, Gallwitz, Dieter
in
Amino Acid Sequence
/ Amino Acid Substitution
/ beta-Fructofuranosidase - secretion
/ Biological Transport
/ Carrier Proteins - chemistry
/ Carrier Proteins - genetics
/ Carrier Proteins - metabolism
/ Cathepsin A - metabolism
/ Conserved Sequence
/ EMBO20
/ Fungal Proteins - metabolism
/ Glutathione Transferase - metabolism
/ Golgi Apparatus - metabolism
/ Hydrophobic and Hydrophilic Interactions
/ membrane fusion
/ Membrane Proteins - metabolism
/ Microscopy, Fluorescence
/ Models, Biological
/ Molecular Sequence Data
/ Munc18 Proteins
/ Mutants
/ Precipitin Tests
/ Protein Binding
/ Proteins
/ Qa-SNARE Proteins
/ Saccharomyces cerevisiae - cytology
/ Saccharomyces cerevisiae - metabolism
/ Saccharomyces cerevisiae Proteins - chemistry
/ Saccharomyces cerevisiae Proteins - genetics
/ Saccharomyces cerevisiae Proteins - metabolism
/ Sec1/Munc18 family
/ Sequence Homology, Amino Acid
/ Sly1p
/ SNARE assembly
/ SNARE Proteins
/ vesicular transport
/ Vesicular Transport Proteins - metabolism
/ Yeasts
2004
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Multiple SNARE interactions of an SM protein: Sed5p/Sly1p binding is dispensable for transport
by
Peng, Renwang
, Gallwitz, Dieter
in
Amino Acid Sequence
/ Amino Acid Substitution
/ beta-Fructofuranosidase - secretion
/ Biological Transport
/ Carrier Proteins - chemistry
/ Carrier Proteins - genetics
/ Carrier Proteins - metabolism
/ Cathepsin A - metabolism
/ Conserved Sequence
/ EMBO20
/ Fungal Proteins - metabolism
/ Glutathione Transferase - metabolism
/ Golgi Apparatus - metabolism
/ Hydrophobic and Hydrophilic Interactions
/ membrane fusion
/ Membrane Proteins - metabolism
/ Microscopy, Fluorescence
/ Models, Biological
/ Molecular Sequence Data
/ Munc18 Proteins
/ Mutants
/ Precipitin Tests
/ Protein Binding
/ Proteins
/ Qa-SNARE Proteins
/ Saccharomyces cerevisiae - cytology
/ Saccharomyces cerevisiae - metabolism
/ Saccharomyces cerevisiae Proteins - chemistry
/ Saccharomyces cerevisiae Proteins - genetics
/ Saccharomyces cerevisiae Proteins - metabolism
/ Sec1/Munc18 family
/ Sequence Homology, Amino Acid
/ Sly1p
/ SNARE assembly
/ SNARE Proteins
/ vesicular transport
/ Vesicular Transport Proteins - metabolism
/ Yeasts
2004
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Multiple SNARE interactions of an SM protein: Sed5p/Sly1p binding is dispensable for transport
by
Peng, Renwang
, Gallwitz, Dieter
in
Amino Acid Sequence
/ Amino Acid Substitution
/ beta-Fructofuranosidase - secretion
/ Biological Transport
/ Carrier Proteins - chemistry
/ Carrier Proteins - genetics
/ Carrier Proteins - metabolism
/ Cathepsin A - metabolism
/ Conserved Sequence
/ EMBO20
/ Fungal Proteins - metabolism
/ Glutathione Transferase - metabolism
/ Golgi Apparatus - metabolism
/ Hydrophobic and Hydrophilic Interactions
/ membrane fusion
/ Membrane Proteins - metabolism
/ Microscopy, Fluorescence
/ Models, Biological
/ Molecular Sequence Data
/ Munc18 Proteins
/ Mutants
/ Precipitin Tests
/ Protein Binding
/ Proteins
/ Qa-SNARE Proteins
/ Saccharomyces cerevisiae - cytology
/ Saccharomyces cerevisiae - metabolism
/ Saccharomyces cerevisiae Proteins - chemistry
/ Saccharomyces cerevisiae Proteins - genetics
/ Saccharomyces cerevisiae Proteins - metabolism
/ Sec1/Munc18 family
/ Sequence Homology, Amino Acid
/ Sly1p
/ SNARE assembly
/ SNARE Proteins
/ vesicular transport
/ Vesicular Transport Proteins - metabolism
/ Yeasts
2004
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Multiple SNARE interactions of an SM protein: Sed5p/Sly1p binding is dispensable for transport
Journal Article
Multiple SNARE interactions of an SM protein: Sed5p/Sly1p binding is dispensable for transport
2004
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Overview
Sec1/Munc18 (SM) proteins are central to intracellular transport and neurotransmitter release but their exact role is still elusive. Several SM proteins, like the neuronal N‐Sec1 and the yeast Sly1 protein, bind their cognate t‐SNAREs with high affinity. This has been thought to be critical for their function. Here, we show that various mutant forms of Sly1p and the Golgi‐localized syntaxin Sed5p, which abolish their high‐affinity interaction, are fully functional
in vivo
, indicating that the tight interaction of the two molecules
per se
is not relevant for proper function. Mutant Sly1p unable to bind Sed5p is excluded from core SNARE complexes, also demonstrating that Sly1p function is not directly coupled to assembled SNARE complexes thought to execute membrane fusion. We also find that wild‐type Sly1p and mutant Sly1p unable to bind Sed5p directly interact with selected ER‐to‐Golgi and intra‐Golgi nonsyntaxin SNAREs. The newly identified, direct interactions of the SM protein with nonsytaxin SNAREs might provide a molecular mechanism by which SNAREs can be activated to engage in pairing and assemble into fusogenic SNARE complexes.
Publisher
John Wiley & Sons, Ltd,Nature Publishing Group UK,Springer Nature B.V,Nature Publishing Group
Subject
/ beta-Fructofuranosidase - secretion
/ Carrier Proteins - chemistry
/ Carrier Proteins - metabolism
/ EMBO20
/ Fungal Proteins - metabolism
/ Glutathione Transferase - metabolism
/ Golgi Apparatus - metabolism
/ Hydrophobic and Hydrophilic Interactions
/ Membrane Proteins - metabolism
/ Mutants
/ Proteins
/ Saccharomyces cerevisiae - cytology
/ Saccharomyces cerevisiae - metabolism
/ Saccharomyces cerevisiae Proteins - chemistry
/ Saccharomyces cerevisiae Proteins - genetics
/ Saccharomyces cerevisiae Proteins - metabolism
/ Sequence Homology, Amino Acid
/ Sly1p
/ Vesicular Transport Proteins - metabolism
/ Yeasts
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