| Q35168727 | A SNARE complex containing SGR3/AtVAM3 and ZIG/VTI11 in gravity-sensing cells is important for Arabidopsis shoot gravitropism. |
| Q46264457 | A SNARE complex unique to seed plants is required for protein storage vacuole biogenesis and seed development of Arabidopsis thaliana |
| Q42000735 | A coiled coil trigger site is essential for rapid binding of synaptobrevin to the SNARE acceptor complex |
| Q34283635 | A complete set of SNAREs in yeast |
| Q44846207 | A mutant impaired in SNARE complex dissociation identifies the plasma membrane as first target of synaptobrevin 2. |
| Q45267195 | A partially zipped SNARE complex stabilized by the membrane |
| Q33558197 | A role for VAMP8/endobrevin in surface deployment of the water channel aquaporin 2 |
| Q28571561 | A second SNARE role for exocytic SNAP25 in endosome fusion |
| Q44686474 | A transient N-terminal interaction of SNAP-25 and syntaxin nucleates SNARE assembly |
| Q36633399 | All-atom simulations and free-energy calculations of coiled-coil peptides with lipid bilayers: binding strength, structural transition, and effect on lipid dynamics |
| Q35949003 | An elaborate classification of SNARE proteins sheds light on the conservation of the eukaryotic endomembrane system |
| Q33529109 | An electrostatically preferred lateral orientation of SNARE complex suggests novel mechanisms for driving membrane fusion |
| Q34580358 | An α-helical core encodes the dual functions of the chlamydial protein IncA. |
| Q52582200 | Arrest of trans-SNARE zippering uncovers loosely and tightly docked intermediates in membrane fusion. |
| Q35075467 | Asymmetric phospholipid distribution drives in vitro reconstituted SNARE-dependent membrane fusion. |
| Q34092721 | Autoinhibition of SNARE complex assembly by a conformational switch represents a conserved feature of syntaxins. |
| Q46964949 | Benzoylurea oligomers: synthetic foldamers that mimic extended alpha helices |
| Q37237653 | Capture and release of partially zipped trans-SNARE complexes on intact organelles |
| Q35940245 | Cellular functions of NSF: not just SNAPs and SNAREs |
| Q46982775 | Coarse-grain simulations of the R-SNARE fusion protein in its membrane environment detect long-lived conformational sub-states. |
| Q45266007 | Coiled-coil driven membrane fusion: zipper-like vs. non-zipper-like peptide orientation |
| Q24292734 | Combinatorial SNARE complexes with VAMP7 or VAMP8 define different late endocytic fusion events. |
| Q37866611 | Conservation of the biochemical properties of IncA from Chlamydia trachomatis and Chlamydia caviae: oligomerization of IncA mediates interaction between facing membranes |
| Q37259787 | Constitutive versus regulated SNARE assembly: a structural basis |
| Q35197965 | Control of eukaryotic membrane fusion by N-terminal domains of SNARE proteins. |
| Q27325771 | Cryo-EM structure of SNAP-SNARE assembly in 20S particle. |
| Q41077876 | Cryo-EM structures of the ATP-bound Vps4E233Q hexamer and its complex with Vta1 at near-atomic resolution |
| Q46816663 | Cysteine-disulfide cross-linking to monitor SNARE complex assembly during endoplasmic reticulum-Golgi transport |
| Q31149681 | Deletion of the SNARE vti1b in mice results in the loss of a single SNARE partner, syntaxin 8. |
| Q36852539 | Determinants of liposome fusion mediated by synaptic SNARE proteins |
| Q24311584 | Differential palmitoylation of the endosomal SNAREs syntaxin 7 and syntaxin 8 |
| Q37161770 | Direct targeting of membrane fusion by SNARE mimicry: Convergent evolution of Legionella effectors |
| Q28565327 | Disassembly of all SNARE complexes by N-ethylmaleimide-sensitive factor (NSF) is initiated by a conserved 1:1 interaction between α-soluble NSF attachment protein (SNAP) and SNARE complex |
| Q42574699 | Distinct domains of complexin I differentially regulate neurotransmitter release |
| Q33519864 | Distinct subcellular localization of a group of synaptobrevin-like SNAREs in Paramecium tetraurelia and effects of silencing SNARE-specific chaperone NSF. |
| Q36783820 | Docking of liposomes to planar surfaces mediated by trans-SNARE complexes |
| Q27935403 | Dsl1p, Tip20p, and the novel Dsl3(Sec39) protein are required for the stability of the Q/t-SNARE complex at the endoplasmic reticulum in yeast |
| Q27658206 | Dynamic structure of lipid-bound synaptobrevin suggests a nucleation-propagation mechanism for trans-SNARE complex formation |
| Q27640677 | Early endosomal SNAREs form a structurally conserved SNARE complex and fuse liposomes with multiple topologies |
| Q35536215 | Examination of Sec22 Homodimer Formation and Role in SNARE-dependent Membrane Fusion |
| Q45870100 | Explaining general anesthesia: a two-step hypothesis linking sleep circuits and the synaptic release machinery |
| Q40173276 | Expression of the Longin domain of TI-VAMP impairs lysosomal secretion and epithelial cell migration |
| Q30459493 | Gene-class analysis of expression patterns induced by psychoactive pharmaceutical exposure in fathead minnow (Pimephales promelas) indicates induction of neuronal systems. |
| Q36989116 | Hippocampal protein expression is differentially affected by chronic paroxetine treatment in adolescent and adult rats: a possible mechanism of "paradoxical" antidepressant responses in young persons |
| Q27640397 | Homotetrameric structure of the SNAP-23 N-terminal coiled-coil domain |
| Q34479771 | Homotypic fusion of early endosomes: SNAREs do not determine fusion specificity |
| Q28590768 | Identification of SNAP-47, a novel Qbc-SNARE with ubiquitous expression |
| Q42727146 | Identification of functionally interacting SNAREs by using complementary substitutions in the conserved '0' layer |
| Q27931667 | Identification of the yeast R-SNARE Nyv1p as a novel longin domain-containing protein |
| Q36888387 | Ins (endocytosis) and outs (exocytosis) of GLUT4 trafficking |
| Q89846118 | Inside(sight) of tiny communicator: exosome biogenesis, secretion, and uptake |
| Q36538279 | Interactions between neuronal fusion proteins explored by molecular dynamics |
| Q35071674 | Involvement of syntaxin 18, an endoplasmic reticulum (ER)-localized SNARE protein, in ER-mediated phagocytosis. |
| Q39023197 | Involvement of vesicle-associated membrane protein 7 in human gastric epithelial cell vacuolation induced by Helicobacter pylori-produced VacA. |
| Q50574368 | Luminescence detection of SNARE-SNARE interaction in Arabidopsis protoplasts. |
| Q36885390 | Lysosomes: fusion and function |
| Q28579640 | Mammalian ykt6 is a neuronal SNARE targeted to a specialized compartment by its profilin-like amino terminal domain |
| Q34780589 | Mechanisms of membrane fusion: disparate players and common principles. |
| Q64061680 | Mechanistic insights into the SNARE complex disassembly |
| Q35058666 | Mechanistic insights into the recycling machine of the SNARE complex |
| Q29618140 | Membrane fusion |
| Q57978971 | Membrane fusion |
| Q30311181 | Membrane fusion: a structural perspective on the interplay of lipids and proteins |
| Q48245402 | MicroRNA Detection by DNA-Mediated Liposome Fusion. |
| Q38165074 | Milk secretion: The role of SNARE proteins. |
| Q34154703 | Model systems for membrane fusion. |
| Q21563602 | Modification of a hydrophobic layer by a point mutation in syntaxin 1A regulates the rate of synaptic vesicle fusion |
| Q42407202 | Molecular identification of a SNAP-25-like SNARE protein in Paramecium |
| Q27934496 | Multiple SNARE interactions of an SM protein: Sed5p/Sly1p binding is dispensable for transport |
| Q35532161 | Multiple conformations of a single SNAREpin between two nanodisc membranes reveal diverse pre-fusion states |
| Q30841847 | Munc13-4 functions as a Ca2+ sensor for homotypic secretory granule fusion to generate endosomal exocytic vacuoles |
| Q42007390 | Myocilin, a component of a membrane-associated protein complex driven by a homologous Q-SNARE domain |
| Q81504869 | Opinion: Cell entry machines: a common theme in nature? |
| Q28085042 | Organization and dynamics of SNARE proteins in the presynaptic membrane |
| Q27936601 | Phosphatidylinositol-4,5-bisphosphate and phospholipase D-generated phosphatidic acid specify SNARE-mediated vesicle fusion for prospore membrane formation |
| Q44557666 | Phosphorylation of SNAP-23 in activated human platelets |
| Q33402655 | Phylogeny of the SNARE vesicle fusion machinery yields insights into the conservation of the secretory pathway in fungi |
| Q28714165 | Proteomic characterization of phagosomal membrane microdomains during phagolysosome biogenesis and evolution |
| Q37892093 | Requirements for the catalytic cycle of the N-ethylmaleimide-Sensitive Factor (NSF). |
| Q40895232 | SNARE Molecules in Marchantia polymorpha: Unique and Conserved Features of the Membrane Fusion Machinery. |
| Q30336208 | SNARE Protein Structure and Function |
| Q44973194 | SNARE assembly and membrane fusion, a kinetic analysis |
| Q34500224 | SNARE complex zero layer residues are not critical for N-ethylmaleimide-sensitive factor-mediated disassembly |
| Q34906866 | SNARE interactions in membrane trafficking: a perspective from mammalian central synapses |
| Q34775549 | SNARE motif: a common motif used by pathogens to manipulate membrane fusion |
| Q38413709 | SNARE protein analog-mediated membrane fusion. |
| Q33325919 | SNARE protein mimicry by an intracellular bacterium |
| Q26751424 | SNARE zippering |
| Q34418818 | SNARE-mediated lipid mixing depends on the physical state of the vesicles |
| Q28571757 | SNAREs in native plasma membranes are active and readily form core complexes with endogenous and exogenous SNAREs |
| Q29547230 | SNAREs--engines for membrane fusion |
| Q30705191 | Sealed with a twist: complexin and the synaptic SNARE complex |
| Q47657471 | Sec22p export from the endoplasmic reticulum is independent of SNARE pairing |
| Q38192676 | Secrets of platelet exocytosis - what do we really know about platelet secretion mechanisms? |
| Q31031114 | Single-molecule studies of SNARE complex assembly reveal parallel and antiparallel configurations |
| Q33789507 | Single-molecule studies of the neuronal SNARE fusion machinery |
| Q27932523 | Sly1 protein bound to Golgi syntaxin Sed5p allows assembly and contributes to specificity of SNARE fusion complexes |
| Q37117850 | Snapin associates with late endocytic compartments and interacts with late endosomal SNAREs |
| Q28216761 | Snares and Munc18 in synaptic vesicle fusion |
| Q38930726 | Soluble NSF attachment protein receptor molecular mimicry by a Legionella pneumophila Dot/Icm effector. |
| Q28570360 | Structural basis for the inhibitory role of tomosyn in exocytosis |
| Q41791766 | Structural characterization of full-length NSF and 20S particles |
| Q24619681 | Structural insight into KCNQ (Kv7) channel assembly and channelopathy |
| Q33967718 | Structural insights into the SNARE mechanism |
| Q30369961 | Supramolecular SNARE assembly precedes hemifusion in SNARE-mediated membrane fusion. |
| Q42176873 | Synaptobrevin N-terminally bound to syntaxin-SNAP-25 defines the primed vesicle state in regulated exocytosis |
| Q39578932 | Syntaxin 11 binds Vti1b and regulates late endosome to lysosome fusion in macrophages. |
| 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 |
| Q43162293 | Syntaxin 8 regulates platelet dense granule secretion, aggregation, and thrombus stability |
| Q48247313 | Syntaxin specificity of cytokinesis in Arabidopsis |
| Q34552505 | The Gos28 SNARE protein mediates intra-Golgi transport of rhodopsin and is required for photoreceptor survival |
| Q28214428 | The N-terminal domains of syntaxin 7 and vti1b form three-helix bundles that differ in their ability to regulate SNARE complex assembly |
| Q57978963 | The R-SNARE Motif of Tomosyn Forms SNARE Core Complexes with Syntaxin 1 and SNAP-25 and Down-regulates Exocytosis |
| Q27934671 | The SNARE Ykt6 mediates protein palmitoylation during an early stage of homotypic vacuole fusion |
| Q37069857 | The SNARE complex from yeast is partially unstructured on the membrane |
| Q33259649 | The SNARE protein family of Leishmania major |
| Q42548237 | The SNARE protein vti1a functions in dense-core vesicle biogenesis |
| Q27674764 | The binding of Varp to VAMP7 traps VAMP7 in a closed, fusogenically inactive conformation |
| Q38223284 | The immediate protective response to microbial challenge. |
| Q37952138 | The impact of bacterial infection on mast cell degranulation |
| Q34305507 | The membrane fusion enigma: SNAREs, Sec1/Munc18 proteins, and their accomplices--guilty as charged? |
| Q24298394 | The molecular basis for the endocytosis of small R-SNAREs by the clathrin adaptor CALM |
| Q64083553 | The multi-functional SNARE protein Ykt6 in autophagosomal fusion processes |
| Q57978966 | The riddle of the Sec1/Munc-18 proteins – new twists added to their interactions with SNAREs |
| Q34718568 | The role of the N-D1 linker of the N-ethylmaleimide-sensitive factor in the SNARE disassembly |
| Q27932181 | The specificity of SNARE-dependent fusion is encoded in the SNARE motif |
| Q27648876 | The structure of the yeast plasma membrane SNARE complex reveals destabilizing water-filled cavities |
| Q24317706 | The tetramer structure of the Nervy homology two domain, NHR2, is critical for AML1/ETO's activity |
| Q78504151 | The transmembrane domain of Vam3 affects the composition of cis- and trans-SNARE complexes to promote homotypic vacuole fusion |
| Q35102649 | Topological arrangement of the intracellular membrane fusion machinery |
| Q34921177 | Two coiled-coil domains of Chlamydia trachomatis IncA affect membrane fusion events during infection |
| Q82968058 | Unique mechanism of plant endocytic/vacuolar transport pathways |
| Q27932856 | Use1p is a yeast SNARE protein required for retrograde traffic to the ER. |
| Q24292933 | VAMP4 is required to maintain the ribbon structure of the Golgi apparatus |
| Q33748110 | Vesicle-associated membrane protein (VAMP) cleavage by a new metalloprotease from the Brazilian scorpion Tityus serrulatus |
| Q35169800 | What is the role of SNARE proteins in membrane fusion? |
| Q47830717 | v-SNARE function in chromaffin cells. |