| scholarly article | Q13442814 |
| P356 | DOI | 10.1126/SCIENCE.276.5316.1255 |
| P698 | PubMed publication ID | 9157884 |
| P2093 | author name string | M G Waters | |
| V V Lupashin | |||
| P433 | issue | 5316 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Syntaxin-binding protein YDR189W | Q27549533 |
| Rab family GTPase YPT1 YFL038C | Q27550120 | ||
| T-SNARE syntaxin YLR026C | Q27550421 | ||
| SNAP receptor SEC22 YLR268W | Q27553116 | ||
| P304 | page(s) | 1255-8 | |
| P577 | publication date | 1997-05-23 | |
| P1433 | published in | Science | Q192864 |
| P1476 | title | t-SNARE activation through transient interaction with a rab-like guanosine triphosphatase | |
| P478 | volume | 276 |
| Q33900880 | A 56-kDa selenium-binding protein participates in intra-Golgi protein transport |
| Q36382085 | A cell-free assay allows reconstitution of Vps33p-dependent transport to the yeast vacuole/lysosome |
| Q33929508 | A direct inhibitory role for the Rab3-specific effector, Noc2, in Ca2+-regulated exocytosis in neuroendocrine cells |
| Q48038736 | A neuronal Sec1 homolog regulates neurotransmitter release at the squid giant synapse. |
| Q29620529 | A novel Rab5 GDP/GTP exchange factor complexed to Rabaptin-5 links nucleotide exchange to effector recruitment and function |
| Q50337405 | A novel role for Rab5-GDI in ligand sequestration into clathrin-coated pits |
| Q77804064 | A phorbol ester-binding protein is required downstream of Rab5 in endosome fusion |
| Q41034610 | A putative heterotrimeric G protein inhibits the fusion of COPI-coated vesicles. Segregation of heterotrimeric G proteins from COPI-coated vesicles |
| Q27930001 | A role for Tlg1p in the transport of proteins within the Golgi apparatus of Saccharomyces cerevisiae |
| Q24683329 | A role for giantin in docking COPI vesicles to Golgi membranes |
| Q27940079 | A vacuolar v-t-SNARE complex, the predominant form in vivo and on isolated vacuoles, is disassembled and activated for docking and fusion |
| Q24550107 | Accumulation of rab4GTP in the cytoplasm and association with the peptidyl-prolyl isomerase pin1 during mitosis |
| Q43699054 | Acute inactivation of the Aspergillus nidulans Golgi membrane fusion machinery: correlation of apical extension arrest and tip swelling with cisternal disorganization. |
| Q40401709 | Akt regulates the subcellular localization of the Rab27a-binding protein JFC1 by phosphorylation. |
| Q27932451 | Asymmetric requirements for a Rab GTPase and SNARE proteins in fusion of COPII vesicles with acceptor membranes |
| Q41630373 | Better late than never: a role for rabs late in exocytosis |
| Q34156726 | Biogenesis of the sorting endosome: the role of Rab5. |
| Q24650821 | Calcium-triggered acrosomal exocytosis in human spermatozoa requires the coordinated activation of Rab3A and N-ethylmaleimide-sensitive factor |
| Q42485892 | Cell-cycle and developmental regulation of TbRAB31 localisation, a GTP-locked Rab protein from Trypanosoma brucei. |
| Q27930083 | Characterization of a novel yeast SNARE protein implicated in Golgi retrograde traffic |
| Q35541229 | Characterization of secretory genes ypt1/yptA and nsf1/nsfA from two filamentous fungi: induction of secretory pathway genes of Trichoderma reesei under secretion stress conditions |
| Q43827106 | Characterization of the sec1-1 and sec1-11 mutations |
| Q38331186 | Complexity of trypanosomatid endocytosis pathways revealed by Rab4 and Rab5 isoforms in Trypanosoma brucei |
| Q36546123 | Content mixing and membrane integrity during membrane fusion driven by pairing of isolated v-SNAREs and t-SNAREs. |
| Q77355829 | Current views in intracellular transport: insights from studies in immunology |
| Q38308721 | Definition of a minimal munc18c domain that interacts with syntaxin 4 |
| Q28578117 | Direct interaction of Rab4 with syntaxin 4 |
| Q24291404 | Direct interaction of the Rab3 effector RIM with Ca2+ channels, SNAP-25, and synaptotagmin |
| Q40635210 | Distinct pathways for the trafficking of angiotensin II and adrenergic receptors from the endoplasmic reticulum to the cell surface: Rab1-independent transport of a G protein-coupled receptor |
| Q77159584 | Docking and fusion in neurosecretion |
| Q42645523 | Dsl1p, an essential protein required for membrane traffic at the endoplasmic reticulum/Golgi interface in yeast |
| Q36301570 | ERG30, a VAP-33-related protein, functions in protein transport mediated by COPI vesicles |
| Q47706655 | Expression of Rab3A GTPase and other synaptic proteins is induced in differentiated NT2N neurons |
| Q30770626 | Expression of rab11a N124I in gastric parietal cells inhibits stimulatory recruitment of the H+-K+-ATPase |
| Q22253422 | GATE-16, a membrane transport modulator, interacts with NSF and the Golgi v-SNARE GOS-28 |
| Q48886377 | GTP hydrolysis by Ran is required for nuclear envelope assembly. |
| Q33888260 | GTP-binding proteins and regulated exocytosis |
| Q33719343 | GTPases in protozoan parasites: tools for cell biology and chemotherapy. |
| Q77057718 | Golgi division and membrane traffic |
| Q27932312 | Golgi-to-endoplasmic reticulum (ER) retrograde traffic in yeast requires Dsl1p, a component of the ER target site that interacts with a COPI coat subunit |
| Q37318803 | How to get to the right place at the right time: Rab/Ypt small GTPases and vesicle transport. |
| Q33884548 | Human rabaptin-5 is selectively cleaved by caspase-3 during apoptosis. |
| Q24673477 | Identification of a putative effector protein for rab11 that participates in transferrin recycling |
| Q24317648 | Implication of ZW10 in membrane trafficking between the endoplasmic reticulum and Golgi |
| Q38610585 | Inhibition of endosome fusion by wortmannin persists in the presence of activated Rab5. |
| Q27930897 | Initial docking of ER-derived vesicles requires Uso1p and Ypt1p but is independent of SNARE proteins |
| Q36274550 | Interaction of the conserved oligomeric Golgi complex with t-SNARE Syntaxin5a/Sed5 enhances intra-Golgi SNARE complex stability |
| Q48124347 | Interactions of (-)-ilimaquinone with methylation enzymes: implications for vesicular-mediated secretion |
| Q40878320 | Live Salmonella modulate expression of Rab proteins to persist in a specialized compartment and escape transport to lysosomes |
| Q36316409 | Live Salmonella recruits N-ethylmaleimide-sensitive fusion protein on phagosomal membrane and promotes fusion with early endosome |
| Q33181402 | Localization of a syntaxin isoform, syntaxin 2, to the acrosomal region of rodent spermatozoa |
| Q57824686 | Low levels of Ypt protein prenylation cause vesicle polarization defects and thermosensitive growth that can be suppressed by genes involved in cell wall maintenance |
| Q29614426 | Membrane fusion and exocytosis |
| Q40801638 | Membrane targeting of a Rab GTPase that fails to associate with Rab escort protein (REP) or guanine nucleotide dissociation inhibitor (GDI). |
| Q34156712 | Membrane tethering and fusion in the secretory and endocytic pathways |
| Q33597232 | Membrane transport: Take your fusion partners |
| Q27940327 | Mitochondrial fusion in yeast requires the transmembrane GTPase Fzo1p |
| Q42992153 | Molecular aspects of the endocytic pathway |
| Q41670724 | Molecular mechanisms of endocytosis |
| Q34228641 | Molecular mechanisms of neurotransmitter release |
| Q92763162 | Multiple Roles of Rab GTPases at the Golgi |
| Q57363020 | Munc18-2/syntaxin3 complexes are spatially separated from syntaxin3-containing SNARE complexes |
| Q33961324 | Munc18c function is required for insulin-stimulated plasma membrane fusion of GLUT4 and insulin-responsive amino peptidase storage vesicles |
| Q34854424 | Munc18c phosphorylation by the insulin receptor links cell signaling directly to SNARE exocytosis |
| Q27939138 | Mutations in a highly conserved region of the Arf1p activator GEA2 block anterograde Golgi transport but not COPI recruitment to membranes |
| Q33597697 | Mycobacterium tuberculosis phagosome |
| Q28142791 | Oligomeric complexes link Rab5 effectors with NSF and drive membrane fusion via interactions between EEA1 and syntaxin 13 |
| Q27938033 | Organelle membrane fusion: a novel function for the syntaxin homolog Ufe1p in ER membrane fusion |
| Q33898882 | Pancreatic beta-cell protein granuphilin binds Rab3 and Munc-18 and controls exocytosis |
| Q34672806 | Predicting the distribution, conservation, and functions of SNAREs and related proteins in fungi |
| Q36953236 | Promiscuity in Rab-SNARE interactions |
| Q33843204 | Protein-protein interactions in neurotransmitter release |
| Q35540873 | Proteomics Opens Doors to the Mechanisms of Developmentally Regulated Secretion |
| Q77135972 | Rab proteins |
| Q39862510 | Rab1 GTPase and dimerization in the cell surface expression of angiotensin II type 2 receptor |
| Q38613714 | Rab5 induces Rac-independent lamellipodia formation and cell migration |
| Q28262945 | Regulation of Munc-18/syntaxin 1A interaction by cyclin-dependent kinase 5 in nerve endings |
| Q27931498 | Regulation of SNARE complex assembly by an N-terminal domain of the t-SNARE Sso1p. |
| Q33637955 | Regulation of endosome fusion. |
| Q40536187 | Regulation of the cell surface expression and function of angiotensin II type 1 receptor by Rab1-mediated endoplasmic reticulum-to-Golgi transport in cardiac myocytes. |
| Q35564739 | Regulation of vesicle traffic and neurotransmitter release in isolated nerve terminals |
| Q34083308 | Regulators of membrane trafficking and Mycobacterium tuberculosis phagosome maturation block |
| Q27931624 | Ric1p and the Ypt6p GTPase function in a common pathway required for localization of trans-Golgi network membrane proteins |
| Q37626903 | Role of vesicle tethering factors in the ER-Golgi membrane traffic. |
| Q41028549 | SNAP-23 requirement for transferrin recycling in Streptolysin-O-permeabilized Madin-Darby canine kidney cells |
| Q30336208 | SNARE Protein Structure and Function |
| Q28131697 | SNAREpins: minimal machinery for membrane fusion |
| Q28280386 | SNAREs and membrane fusion in the Golgi apparatus |
| Q28571757 | SNAREs in native plasma membranes are active and readily form core complexes with endogenous and exogenous SNAREs |
| Q27939711 | Sec1p binds to SNARE complexes and concentrates at sites of secretion |
| Q36264678 | Sec35p, a novel peripheral membrane protein, is required for ER to Golgi vesicle docking |
| Q38675048 | Selective formation of Sed5p-containing SNARE complexes is mediated by combinatorial binding interactions. |
| Q36324604 | Sequential SNARE disassembly and GATE-16-GOS-28 complex assembly mediated by distinct NSF activities drives Golgi membrane fusion |
| Q28579136 | Sly1 binds to Golgi and ER syntaxins via a conserved N-terminal peptide motif |
| Q27932523 | Sly1 protein bound to Golgi syntaxin Sed5p allows assembly and contributes to specificity of SNARE fusion complexes |
| Q27935723 | Specific binding to a novel and essential Golgi membrane protein (Yip1p) functionally links the transport GTPases Ypt1p and Ypt31p |
| Q33680888 | Synaptic vesicle docking and fusion |
| Q22254009 | Syntaxin 18, a SNAP receptor that functions in the endoplasmic reticulum, intermediate compartment, and cis-Golgi vesicle trafficking |
| Q24550710 | Syntaxin 7 is localized to late endosome compartments, associates with Vamp 8, and Is required for late endosome-lysosome fusion |
| Q24534888 | Syntaxin 7, syntaxin 8, Vti1 and VAMP7 (vesicle-associated membrane protein 7) form an active SNARE complex for early macropinocytic compartment fusion in Dictyostelium discoideum |
| Q42498057 | Syntaxin, VAMP, and Rab3 are selectively expressed during sea urchin embryogenesis |
| Q37318808 | Tethering molecules in membrane traffic |
| Q39722880 | The C-terminal silencing domain of Rap1p is essential for the repression of ribosomal protein genes in response to a defect in the secretory pathway |
| Q24324758 | The COOH terminus of GATE-16, an intra-Golgi transport modulator, is cleaved by the human cysteine protease HsApg4A |
| Q24598866 | The Rab3 GDP/GTP exchange factor homolog AEX-3 has a dual function in synaptic transmission |
| Q22010591 | The Rab5 effector EEA1 interacts directly with syntaxin-6 |
| Q29620568 | The Rab5 effector EEA1 is a core component of endosome docking |
| Q36381446 | The Sec1p/Munc18 (SM) protein, Vps45p, cycles on and off membranes during vesicle transport |
| Q27937701 | The Sec34/Sec35p complex, a Ypt1p effector required for retrograde intra-Golgi trafficking, interacts with Golgi SNAREs and COPI vesicle coat proteins |
| Q27625463 | The X-ray crystal structure of neuronal Sec1 from squid sheds new light on the role of this protein in exocytosis |
| Q34093203 | The biology of cortical granules. |
| Q29620216 | The diversity of Rab proteins in vesicle transport |
| Q34156722 | The making and breaking of the endoplasmic reticulum |
| Q24682925 | The membrane transport factor TAP/p115 cycles between the Golgi and earlier secretory compartments and contains distinct domains required for its localization and function. |
| Q77304417 | The molecular characterization of transport vesicles |
| Q36881642 | The phosphatidylinositol 3-phosphate binding protein Vac1p interacts with a Rab GTPase and a Sec1p homologue to facilitate vesicle-mediated vacuolar protein sorting |
| Q52172779 | The prespore vesicles of Dictyostelium discoideum. Purification, characterization, and developmental regulation. |
| Q24336158 | The rod cGMP phosphodiesterase delta subunit dissociates the small GTPase Rab13 from membranes |
| Q27936863 | The vesicle transport protein Vps33p is an ATP-binding protein that localizes to the cytosol in an energy-dependent manner |
| Q28140447 | Three-dimensional structure of the neuronal-Sec1-syntaxin 1a complex |
| Q77159576 | Transport from the endoplasmic reticulum to the Golgi |
| Q33772639 | Transport-vesicle targeting: tethers before SNAREs |
| Q33888571 | Two distinct effectors of the small GTPase Rab5 cooperate in endocytic membrane fusion |
| Q39575922 | Vam7p, a SNAP-25-like molecule, and Vam3p, a syntaxin homolog, function together in yeast vacuolar protein trafficking |
| Q27933694 | Vam7p, a vacuolar SNAP-25 homolog, is required for SNARE complex integrity and vacuole docking and fusion |
| Q35095566 | Vesicle trafficking: pleasure and pain from SM genes. |
| Q48028756 | Vesicle transport: more work for the Rabs? |
| Q57364514 | Vesicular transport and the golgi apparatus in yeast |
| Q27934224 | Vesicular transport: how many Ypt/Rab-GTPases make a eukaryotic cell? |
| Q35169800 | What is the role of SNARE proteins in membrane fusion? |
| Q27929829 | Yeast VSM1 encodes a v-SNARE binding protein that may act as a negative regulator of constitutive exocytosis |
| Q42994573 | nSec-1 (munc-18) interacts with both primed and unprimed syntaxin 1A and associates in a dimeric complex on adrenal chromaffin granules |
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