scholarly article | Q13442814 |
P2093 | author name string | R H Scheller | |
J C Hay | |||
H Hirling | |||
P2860 | cites work | The syntaxin family of vesicular transport receptors | Q24310598 |
β-COP, a 110 kd protein associated with non-clathrin-coated vesicles and the golgi complex, shows homology to β-adaptin | Q24319220 | ||
Synaptobrevin: an integral membrane protein of 18,000 daltons present in small synaptic vesicles of rat brain | Q24567532 | ||
Point mutations define a sequence flanking the AUG initiator codon that modulates translation by eukaryotic ribosomes | Q27860600 | ||
Isolation of monoclonal antibodies specific for human c-myc proto-oncogene product | Q27860841 | ||
Predicting coiled coils from protein sequences | Q27861097 | ||
The yeast SLY gene products, suppressors of defects in the essential GTP-binding Ypt1 protein, may act in endoplasmic reticulum-to-Golgi transport | Q27935252 | ||
SED5 encodes a 39-kD integral membrane protein required for vesicular transport between the ER and the Golgi complex | Q27938084 | ||
Bos1p, an integral membrane protein of the endoplasmic reticulum to Golgi transport vesicles, is required for their fusion competence | Q27939021 | ||
Identification and structure of four yeast genes (SLY) that are able to suppress the functional loss of YPT1, a member of the RAS superfamily | Q27939653 | ||
SNAP receptors implicated in vesicle targeting and fusion | Q28131653 | ||
Syntaxin: a synaptic protein implicated in docking of synaptic vesicles at presynaptic active zones | Q28211190 | ||
Protein-protein interactions contributing to the specificity of intracellular vesicular trafficking | Q28249692 | ||
A protein assembly-disassembly pathway in vitro that may correspond to sequential steps of synaptic vesicle docking, activation, and fusion | Q28255534 | ||
SNAPs, a family of NSF attachment proteins involved in intracellular membrane fusion in animals and yeast | Q28299506 | ||
Rapid redistribution of Golgi proteins into the ER in cells treated with brefeldin A: evidence for membrane cycling from Golgi to ER | Q29615171 | ||
Distinct sets of SEC genes govern transport vesicle formation and fusion early in the secretory pathway | Q29618501 | ||
Microtubule-dependent retrograde transport of proteins into the ER in the presence of brefeldin A suggests an ER recycling pathway | Q29620187 | ||
A rab protein is required for the assembly of SNARE complexes in the docking of transport vesicles | Q29620271 | ||
BET1, BOS1, and SEC22 are members of a group of interacting yeast genes required for transport from the endoplasmic reticulum to the Golgi complex | Q34020613 | ||
The molecular machinery for secretion is conserved from yeast to neurons | Q36184412 | ||
Lectin-binding sites as markers of Golgi subcompartments: proximal-to-distal maturation of oligosaccharides | Q36207946 | ||
The response of the Golgi complex to microtubule alterations: the roles of metabolic energy and membrane traffic in Golgi complex organization | Q36221805 | ||
Dissociation of a 110-kD peripheral membrane protein from the Golgi apparatus is an early event in brefeldin A action | Q36224297 | ||
Oligomerization of a membrane protein correlates with its retention in the Golgi complex | Q36233449 | ||
A peripheral protein associated with the cis-Golgi network redistributes in the intermediate compartment upon brefeldin A treatment | Q36234266 | ||
Retention of p63 in an ER-Golgi intermediate compartment depends on the presence of all three of its domains and on its ability to form oligomers | Q36234357 | ||
Quality control in the secretory pathway: retention of a misfolded viral membrane glycoprotein involves cycling between the ER, intermediate compartment, and Golgi apparatus | Q36234402 | ||
Characteristics of endoplasmic reticulum-derived transport vesicles | Q36234617 | ||
Brefeldin A's effects on endosomes, lysosomes, and the TGN suggest a general mechanism for regulating organelle structure and membrane traffic | Q41659144 | ||
Brefeldin A causes a microtubule-mediated fusion of the trans-Golgi network and early endosomes | Q41659646 | ||
Expression of individual forms of peptidylglycine alpha-amidating monooxygenase in AtT-20 cells: endoproteolytic processing and routing to secretory granules | Q41971961 | ||
Ypt1p implicated in v-SNARE activation | Q59095937 | ||
Semi-intact cells permeable to macromolecules: use in reconstitution of protein transport from the endoplasmic reticulum to the Golgi complex | Q70186379 | ||
Biosynthesis of hepatocyte endoplasmic reticulum proteins | Q71150777 | ||
P433 | issue | 10 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | endoplasmic reticulum | Q79927 |
Golgi apparatus | Q83181 | ||
transporter activity | Q14864384 | ||
SEC22 homolog A, vesicle trafficking protein | Q21110061 | ||
P304 | page(s) | 5671-9 | |
P577 | publication date | 1996-03-08 | |
P1433 | published in | Journal of Biological Chemistry | Q867727 |
P1476 | title | Mammalian vesicle trafficking proteins of the endoplasmic reticulum and Golgi apparatus | |
P478 | volume | 271 |
Q27934687 | A conserved domain is present in different families of vesicular fusion proteins: a new superfamily |
Q24323984 | A human homolog can functionally replace the yeast vesicle-associated SNARE Vti1p in two vesicle transport pathways |
Q28282159 | A new syntaxin family member implicated in targeting of intracellular transport vesicles |
Q27631238 | A novel snare N-terminal domain revealed by the crystal structure of Sec22b |
Q24310308 | A novel synaptobrevin/VAMP homologous protein (VAMP5) is increased during in vitro myogenesis and present in the plasma membrane |
Q24648894 | A splice-isoform of vesicle-associated membrane protein-1 (VAMP-1) contains a mitochondrial targeting signal |
Q40845661 | COPI in ER/Golgi and intra-Golgi transport: do yeast COPI mutants point the way? |
Q36254565 | COPI-independent anterograde transport: cargo-selective ER to Golgi protein transport in yeast COPI mutants |
Q41566685 | COPII and secretory cargo capture into transport vesicles |
Q37015047 | Characterization of SNAREs determines the absence of a typical Golgi apparatus in the ancient eukaryote Giardia lamblia |
Q27930083 | Characterization of a novel yeast SNARE protein implicated in Golgi retrograde traffic |
Q37701779 | Components of the SNARE-containing regulon are co-regulated in root cells undergoing defense |
Q35197965 | Control of eukaryotic membrane fusion by N-terminal domains of SNARE proteins. |
Q22010801 | Differential roles of syntaxin 7 and syntaxin 8 in endosomal trafficking |
Q33932515 | Differential use of endoplasmic reticulum membrane for phagocytosis in J774 macrophages |
Q37383966 | Distinct cellular locations of the syntaxin family of proteins in rat pancreatic acinar cells |
Q64939137 | Diverse Role of SNARE Protein Sec22 in Vesicle Trafficking, Membrane Fusion, and Autophagy. |
Q24680860 | ERS-24, a mammalian v-SNARE implicated in vesicle traffic between the ER and the Golgi |
Q57010700 | Extracting Sequence Motifs and the Phylogenetic Features of SNARE-Dependent Membrane Traffic |
Q28579141 | GS15, a 15-kilodalton Golgi soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) homologous to rbet1 |
Q24317233 | Hsec22c: a homolog of yeast Sec22p and mammalian rsec22a and msec22b/ERS-24 |
Q37153718 | Lipid Regulated Intramolecular Conformational Dynamics of SNARE-Protein Ykt6. |
Q24682651 | Localization, dynamics, and protein interactions reveal distinct roles for ER and Golgi SNAREs |
Q31159570 | Macroarray analysis of coelomocyte gene expression in response to LPS in the sea urchin. Identification of unexpected immune diversity in an invertebrate |
Q24291271 | Molecular characterization of mammalian homologues of class C Vps proteins that interact with syntaxin-7 |
Q24309498 | Molecular cloning and localization of human syntaxin 16, a member of the syntaxin family of SNARE proteins |
Q38609841 | Morphological and functional association of Sec22b/ERS-24 with the pre-Golgi intermediate compartment |
Q28116211 | Protein interactions regulating vesicle transport between the endoplasmic reticulum and Golgi apparatus in mammalian cells |
Q40549095 | RACK1 inhibits the serum- and anchorage-independent growth of v-Src transformed cells |
Q35663489 | RACK1 regulates G1/S progression by suppressing Src kinase activity |
Q42828255 | RACK1 regulates Src-mediated Sam68 and p190RhoGAP signaling |
Q40617837 | SLY1 and Syntaxin 18 specify a distinct pathway for procollagen VII export from the endoplasmic reticulum. |
Q40826309 | SNARE protein trafficking in polarized MDCK cells |
Q46487364 | SNAREing the basis of multicellularity: consequences of protein family expansion during evolution |
Q41566661 | SNAREs and NSF in targeted membrane fusion |
Q28280386 | SNAREs and membrane fusion in the Golgi apparatus |
Q42257801 | Selective control of SNARE recycling by Golgi retention |
Q24308782 | Seven novel mammalian SNARE proteins localize to distinct membrane compartments |
Q92257375 | Stx5-Mediated ER-Golgi Transport in Mammals and Yeast |
Q28141448 | Subunit structure of a mammalian ER/Golgi SNARE complex |
Q28140261 | Syntaxin 13 is a developmentally regulated SNARE involved in neurite outgrowth and endosomal trafficking |
Q24682732 | Syntaxin 13 mediates cycling of plasma membrane proteins via tubulovesicular recycling endosomes |
Q22254741 | Syntaxin 17 is abundant in steroidogenic cells and implicated in smooth endoplasmic reticulum membrane dynamics |
Q28572919 | Syntaxin 6 functions in trans-Golgi network vesicle trafficking |
Q24678419 | Targeting of Arf-1 to the early Golgi by membrin, an ER-Golgi SNARE |
Q24561799 | The Exocyst is a multiprotein complex required for exocytosis in Saccharomyces cerevisiae |
Q98197853 | The Function of SEC22B and its Role in Human Diseases |
Q28571014 | The SNARE motif contributes to rbet1 intracellular targeting and dynamics independently of SNARE interactions |
Q24647979 | The armadillo repeat-containing protein, ARMCX3, physically and functionally interacts with the developmental regulatory factor Sox10 |
Q36487336 | The genetic basis of a craniofacial disease provides insight into COPII coat assembly. |
Q24677983 | The mammalian protein (rbet1) homologous to yeast Bet1p is primarily associated with the pre-Golgi intermediate compartment and is involved in vesicular transport from the endoplasmic reticulum to the Golgi apparatus |
Q33600192 | The specificity of vesicle trafficking: coat proteins and SNAREs |
Q22008531 | Three novel proteins of the syntaxin/SNAP-25 family |
Q41611092 | Transport of Trembler-J mutant peripheral myelin protein 22 is blocked in the intermediate compartment and affects the transport of the wild-type protein by direct interaction |
Q36854983 | UNC-18 promotes both the anterograde trafficking and synaptic function of syntaxin |
Q22003820 | VAMP-7 mediates vesicular transport from endosomes to lysosomes |
Q24649038 | Vesicle-associated membrane protein 4 is implicated in trans-Golgi network vesicle trafficking |
Q24305479 | Vesicle-associated membrane protein 7 is expressed in intestinal ER |
Q28185724 | Ykt6 forms a SNARE complex with syntaxin 5, GS28, and Bet1 and participates in a late stage in endoplasmic reticulum-Golgi transport |