| review article | Q7318358 |
| scholarly article | Q13442814 |
| P2093 | author name string | Joseph G Duman | |
| John G Forte | |||
| P2860 | cites work | Syntaphilin: a syntaxin-1 clamp that controls SNARE assembly | Q22253305 |
| Direct interaction of the Rab3 effector RIM with Ca2+ channels, SNAP-25, and synaptotagmin | Q24291404 | ||
| Amisyn, a novel syntaxin-binding protein that may regulate SNARE complex assembly | Q24302367 | ||
| Identification of a human homologue of the vesicle-associated membrane protein (VAMP)-associated protein of 33 kDa (VAP-33): a broadly expressed protein that binds to VAMP | Q24313250 | ||
| A conformational switch in syntaxin during exocytosis: role of munc18. | Q24534308 | ||
| The membrane-tethering protein p115 interacts with GBF1, an ARF guanine-nucleotide-exchange factor | Q24534602 | ||
| CFTR chloride channels are regulated by a SNAP-23/syntaxin 1A complex | Q24535872 | ||
| A SNARE complex mediating fusion of late endosomes defines conserved properties of SNARE structure and function | Q24595623 | ||
| Conserved structural features of the synaptic fusion complex: SNARE proteins reclassified as Q- and R-SNAREs | Q24656954 | ||
| Crystal structure of the endosomal SNARE complex reveals common structural principles of all SNAREs | Q27637268 | ||
| High resolution structure, stability, and synaptotagmin binding of a truncated neuronal SNARE complex | Q27640208 | ||
| Structure of influenza haemagglutinin at the pH of membrane fusion | Q27730888 | ||
| Crystal structure of a SNARE complex involved in synaptic exocytosis at 2.4 A resolution | Q27765619 | ||
| Phosphorylation of Munc18 by protein kinase C regulates the kinetics of exocytosis | Q27863317 | ||
| Yeast VSM1 encodes a v-SNARE binding protein that may act as a negative regulator of constitutive exocytosis | Q27929829 | ||
| Characterization of a novel yeast SNARE protein implicated in Golgi retrograde traffic | Q27930083 | ||
| Influence of lipid composition on physical properties and peg-mediated fusion of curved and uncurved model membrane vesicles: "nature's own" fusogenic lipid bilayer. | Q43563695 | ||
| Syntaxin 3 is required for cAMP-induced acid secretion: streptolysin O-permeabilized gastric gland model | Q43829120 | ||
| SNARE assembly and disassembly exhibit a pronounced hysteresis | Q43851628 | ||
| Intracellular distribution and functional importance of vesicle-associated membrane protein 2 in gastric parietal cells. | Q44054040 | ||
| Localization and function of soluble N-ethylmaleimide-sensitive factor attachment protein-25 and vesicle-associated membrane protein-2 in functioning gastric parietal cells | Q44184075 | ||
| Coiled coils in both intracellular vesicle and viral membrane fusion | Q44268531 | ||
| Functional impact of syntaxin on gating of N-type and Q-type calcium channels | Q44695195 | ||
| The synaptic SNARE complex is a parallel four-stranded helical bundle | Q46079288 | ||
| Distinct domains of syntaxin are required for synaptic vesicle fusion complex formation and dissociation | Q46887153 | ||
| Homotypic vacuolar fusion mediated by t- and v-SNAREs | Q48049888 | ||
| Hrs-2 is an ATPase implicated in calcium-regulated secretion | Q48053660 | ||
| Divalent cation-induced lipid mixing between phosphatidylserine liposomes studied by stopped-flow fluorescence measurements: effects of temperature, comparison of barium and calcium, and perturbation by DPX. | Q48304343 | ||
| Mechanism of calcium-independent synaptotagmin binding to target SNAREs | Q48421153 | ||
| Syntaxin 1A regulates ENaC via domain-specific interactions. | Q48836093 | ||
| The pallid gene encodes a novel, syntaxin 13-interacting protein involved in platelet storage pool deficiency | Q55951827 | ||
| Synip | Q56700520 | ||
| The riddle of the Sec1/Munc-18 proteins – new twists added to their interactions with SNAREs | Q57978966 | ||
| Inhibition of SNARE Complex Assembly Differentially Affects Kinetic Components of Exocytosis | Q57978998 | ||
| Control of the Terminal Step of Intracellular Membrane Fusion by Protein Phosphatase 1 | Q58197789 | ||
| Trans-complex formation by proteolipid channels in the terminal phase of membrane fusion | Q59067778 | ||
| Defining the functions of trans-SNARE pairs | Q59079276 | ||
| Ypt1p implicated in v-SNARE activation | Q59095937 | ||
| Vac1p coordinates Rab and phosphatidylinositol 3-kinase signaling in Vps45p-dependent vesicle docking/fusion at the endosome | Q27931703 | ||
| The Vtc proteins in vacuole fusion: coupling NSF activity to V(0) trans-complex formation. | Q27932292 | ||
| 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 | Q27932312 | ||
| Sly1 protein bound to Golgi syntaxin Sed5p allows assembly and contributes to specificity of SNARE fusion complexes | Q27932523 | ||
| Topological restriction of SNARE-dependent membrane fusion | Q27934715 | ||
| The yeast SLY gene products, suppressors of defects in the essential GTP-binding Ypt1 protein, may act in endoplasmic reticulum-to-Golgi transport | Q27935252 | ||
| Ca2+/calmodulin signals the completion of docking and triggers a late step of vacuole fusion. | Q27935567 | ||
| Compartmental specificity of cellular membrane fusion encoded in SNARE proteins | Q27935841 | ||
| Vps51p links the VFT complex to the SNARE Tlg1p | Q27935910 | ||
| t-SNARE activation through transient interaction with a rab-like guanosine triphosphatase | Q27937533 | ||
| A multispecificity syntaxin homologue, Vam3p, essential for autophagic and biosynthetic protein transport to the vacuole | Q27937915 | ||
| Vacuole fusion at a ring of vertex docking sites leaves membrane fragments within the organelle | Q27938160 | ||
| The yeast v-SNARE Vti1p mediates two vesicle transport pathways through interactions with the t-SNAREs Sed5p and Pep12p | Q27938749 | ||
| Sec1p binds to SNARE complexes and concentrates at sites of secretion | Q27939711 | ||
| SNAP receptors implicated in vesicle targeting and fusion | Q28131653 | ||
| SNAREpins: minimal machinery for membrane fusion | Q28131697 | ||
| Mixed and non-cognate SNARE complexes. Characterization of assembly and biophysical properties | Q28144385 | ||
| SNARE function analyzed in synaptobrevin/VAMP knockout mice | Q28203549 | ||
| Ca2+-dependent synaptotagmin binding to SNAP-25 is essential for Ca2+-triggered exocytosis | Q28204182 | ||
| Taxilin; a novel syntaxin-binding protein that is involved in Ca2+-dependent exocytosis in neuroendocrine cells | Q28206148 | ||
| Syntaxin 7 complexes with mouse Vps10p tail interactor 1b, syntaxin 6, vesicle-associated membrane protein (VAMP)8, and VAMP7 in b16 melanoma cells | Q28208262 | ||
| Synaptotagmin: a Ca(2+) sensor that triggers exocytosis? | Q28208303 | ||
| Rapid and selective binding to the synaptic SNARE complex suggests a modulatory role of complexins in neuroexocytosis | Q28212791 | ||
| The N-terminal domains of syntaxin 7 and vti1b form three-helix bundles that differ in their ability to regulate SNARE complex assembly | Q28214428 | ||
| Spring, a novel RING finger protein that regulates synaptic vesicle exocytosis | Q28214515 | ||
| Snares and Munc18 in synaptic vesicle fusion | Q28216761 | ||
| Action of complexin on SNARE complex | Q28219311 | ||
| A post-docking role for synaptobrevin in synaptic vesicle fusion | Q28243803 | ||
| 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 | ||
| Protease resistance of syntaxin.SNAP-25.VAMP complexes. Implications for assembly and structure | Q28268641 | ||
| A VAMP-binding protein from Aplysia required for neurotransmitter release | Q28297054 | ||
| SNAREs are concentrated in cholesterol-dependent clusters that define docking and fusion sites for exocytosis | Q28364095 | ||
| Content mixing and membrane integrity during membrane fusion driven by pairing of isolated v-SNAREs and t-SNAREs. | Q36546123 | ||
| The Saccharomyces cerevisiae v-SNARE Vti1p is required for multiple membrane transport pathways to the vacuole | Q36875646 | ||
| Vesicle-associated membrane protein-2/synaptobrevin binding to synaptotagmin I promotes O-glycosylation of synaptotagmin I. | Q38288598 | ||
| SNARE complex formation is triggered by Ca2+ and drives membrane fusion | Q38325384 | ||
| Mimicry and mechanism in phospholipid models of membrane fusion | Q39733207 | ||
| Fluorescence-based evaluation of the partitioning of lipids and lipidated peptides into liquid-ordered lipid microdomains: a model for molecular partitioning into "lipid rafts". | Q40168616 | ||
| Exocytosis requires asymmetry in the central layer of the SNARE complex | Q40388114 | ||
| Molecular mechanisms of clostridial neurotoxins | Q40642444 | ||
| Ca2+-dependent interaction of the growth-associated protein GAP-43 with the synaptic core complex | Q41099490 | ||
| Enveloped viruses: a common mode of membrane fusion?. | Q41585925 | ||
| SNARE interactions are not selective. Implications for membrane fusion specificity | Q41608272 | ||
| nSec1 binds a closed conformation of syntaxin1A. | Q41716307 | ||
| Intracellular Ca requirements for stimulus-secretion coupling in parietal cell | Q42489820 | ||
| The neuronal t-SNARE complex is a parallel four-helix bundle. | Q43558118 | ||
| Reconstituted syntaxin1a/SNAP25 interacts with negatively charged lipids as measured by lateral diffusion in planar supported bilayers | Q28367662 | ||
| Calmodulin and lipid binding to synaptobrevin regulates calcium-dependent exocytosis | Q28509919 | ||
| Identification of a novel SNAP25 interacting protein (SIP30) | Q28580586 | ||
| Structure and conformational changes in NSF and its membrane receptor complexes visualized by quick-freeze/deep-etch electron microscopy | Q28581498 | ||
| Molecular determinants of regulated exocytosis | Q28609688 | ||
| Membrane fusion and exocytosis | Q29614426 | ||
| Structure and function of membrane fusion peptides | Q30310337 | ||
| Ocsyn, a novel syntaxin-interacting protein enriched in the subapical region of inner hair cells. | Q31091111 | ||
| Globular tail of myosin-V is bound to vamp/synaptobrevin | Q31856369 | ||
| Complexins regulate a late step in Ca2+-dependent neurotransmitter release | Q31859100 | ||
| Membrane fusion: structure snared at last | Q33533780 | ||
| High calcium concentrations shift the mode of exocytosis to the kiss-and-run mechanism | Q33880066 | ||
| Genetic and morphological analyses reveal a critical interaction between the C-termini of two SNARE proteins and a parallel four helical arrangement for the exocytic SNARE complex. | Q33889805 | ||
| "Kiss and run" exocytosis at hippocampal synapses | Q33922918 | ||
| The ionic layer is required for efficient dissociation of the SNARE complex by alpha-SNAP and NSF. | Q33951771 | ||
| Mechanisms of synaptic vesicle exocytosis | Q34059661 | ||
| Yeast vacuoles and membrane fusion pathways | Q34086175 | ||
| VAP-A binds promiscuously to both v- and tSNAREs | Q34087281 | ||
| Members of the synaptobrevin/vesicle-associated membrane protein (VAMP) family in Drosophila are functionally interchangeable in vivo for neurotransmitter release and cell viability | Q34161948 | ||
| Structure and composition of the fusion pore | Q34180520 | ||
| Viral fusion peptides: a tool set to disrupt and connect biological membranes | Q34293668 | ||
| Genetic and electrophysiological studies of Drosophila syntaxin-1A demonstrate its role in nonneuronal secretion and neurotransmission | Q34317092 | ||
| The molecular mechanism of targeted vesicle transport in cytokinesis | Q34593516 | ||
| Putative fusogenic activity of NSF is restricted to a lipid mixture whose coalescence is also triggered by other factors | Q34667916 | ||
| Testing the 3Q:1R "rule": mutational analysis of the ionic "zero" layer in the yeast exocytic SNARE complex reveals no requirement for arginine | Q34776890 | ||
| Molecular analysis of SNAP-25 function in exocytosis | Q35001438 | ||
| SNARE proteins contribute to calcium cooperativity of synaptic transmission | Q35582307 | ||
| The SNARE machinery is involved in apical plasma membrane trafficking in MDCK cells. | Q36256141 | ||
| The tandem C2 domains of synaptotagmin contain redundant Ca2+ binding sites that cooperate to engage t-SNAREs and trigger exocytosis. | Q36294041 | ||
| Regulation of membrane fusion by the membrane-proximal coil of the t-SNARE during zippering of SNAREpins | Q36323855 | ||
| A cycle of Vam7p release from and PtdIns 3-P-dependent rebinding to the yeast vacuole is required for homotypic vacuole fusion | Q36324115 | ||
| Biochemical and functional studies of cortical vesicle fusion: the SNARE complex and Ca2+ sensitivity | Q36328525 | ||
| Close is not enough: SNARE-dependent membrane fusion requires an active mechanism that transduces force to membrane anchors | Q36342484 | ||
| Rapid and efficient fusion of phospholipid vesicles by the alpha-helical core of a SNARE complex in the absence of an N-terminal regulatory domain | Q36545881 | ||
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | C237-49 | |
| P577 | publication date | 2003-08-01 | |
| P1433 | published in | American Journal of Physiology - Cell Physiology | Q2227080 |
| P1476 | title | What is the role of SNARE proteins in membrane fusion? | |
| P478 | volume | 285 |
| Q44879652 | A role for SNAP-25 but not VAMPs in store-mediated Ca2+ entry in human platelets. |
| Q33797927 | Accessory proteins stabilize the acceptor complex for synaptobrevin, the 1:1 syntaxin/SNAP-25 complex |
| Q38017490 | Acid-dependent viral entry. |
| Q28554805 | An Interactome-Centered Protein Discovery Approach Reveals Novel Components Involved in Mitosome Function and Homeostasis in Giardia lamblia |
| Q33529109 | An electrostatically preferred lateral orientation of SNARE complex suggests novel mechanisms for driving membrane fusion |
| Q36205197 | Annexin A7 and SNAP23 interactions in alveolar type II cells and in vitro: a role for Ca(2+) and PKC. |
| Q36765145 | Annexin A7 trafficking to alveolar type II cell surface: possible roles for protein insertion into membranes and lamellar body secretion |
| Q52023311 | Assembly of spermatid acrosome depends on microtubule organization during mammalian spermiogenesis. |
| Q28384122 | Bioanalysis of eukaryotic organelles |
| Q42476572 | Changes in signaling pathways regulating neuroplasticity induced by neurokinin 1 receptor knockout |
| Q57364590 | Chapter 10 SNARE-Induced Fusion of Vesicles to a Planar Bilayer |
| Q45050313 | Cleavage of SNAP-25 and VAMP-2 impairs store-operated Ca2+ entry in mouse pancreatic acinar cells |
| Q28072803 | Commandeering Channel Voltage Sensors for Secretion, Cell Turgor, and Volume Control |
| Q34190786 | Correlation between vesicle quantal size and fusion pore release in chromaffin cell exocytosis |
| Q33598847 | Detection of lower levels of SNAP25 using multiple microarray systems and its functional significance in medulloblastoma |
| Q42459197 | Differential expression of synaptic proteins in unilateral 6-OHDA lesioned rat model-A comparative proteomics approach |
| Q40186173 | Differential localization of aquaporin-2 and glucose transporter 4 in polarized MDCK cells. |
| Q42555978 | Effect of Resveratrol Supplementation on the SNARE Proteins Expression in Adipose Tissue of Stroptozotocin-Nicotinamide Induced Type 2 Diabetic Rats |
| Q90055421 | Effect of resveratrol on SNARE proteins expression and insulin resistance in skeletal muscle of diabetic rats |
| Q34448732 | Enhanced Energy Expenditure, Glucose Utilization, and Insulin Sensitivity in VAMP8 Null Mice |
| Q24306602 | Evidence that an isoform of calpain-10 is a regulator of exocytosis in pancreatic beta-cells |
| Q33911047 | Evidence that the SpoIIIE DNA translocase participates in membrane fusion during cytokinesis and engulfment. |
| Q44353738 | Expression and regulation of SNAP-25 and synaptotagmin VII in developing mouse ovarian follicles via the FSH receptor |
| Q42129615 | Expression, localization and interaction of SNARE proteins in Arabidopsis are selectively altered by the dark |
| Q55184606 | Extracellular Vesicle: An Emerging Mediator of Intercellular Crosstalk in Lung Inflammation and Injury. |
| Q55265175 | Fusion pore diameter regulation by cations modulating local membrane anisotropy. |
| Q48261345 | Fusion pore stability of peptidergic vesicles. |
| Q47425397 | Gene encoding vesicle-associated membrane protein-associated protein from Triticum aestivum (TaVAP) confers tolerance to drought stress |
| Q48042734 | Hydrodynamics govern the pre-fusion docking time of synaptic vesicles. |
| Q24337043 | Identification of novel ATP13A2 interactors and their role in α-synuclein misfolding and toxicity |
| Q92535993 | Identifying SNAREs by Incorporating Deep Learning Architecture and Amino Acid Embedding Representation |
| Q44995705 | Inhibition of SNAP-25 phosphorylation at Ser187 is involved in chronic morphine-induced down-regulation of SNARE complex formation |
| Q33489548 | Model of SNARE-mediated membrane adhesion kinetics |
| Q34352647 | Molecular identification and reconstitution of depolarization-induced exocytosis monitored by membrane capacitance |
| Q28565862 | Myosin-Va regulates exocytosis through the submicromolar Ca2+-dependent binding of syntaxin-1A. |
| Q35558445 | Neurotransmitter Release at Central Synapses |
| Q35903567 | Osmotic regulation of renal betaine transport: transcription and beyond |
| Q33519916 | Pulling force generated by interacting SNAREs facilitates membrane hemifusion. |
| Q50890638 | Redistribution of soluble N-ethylmaleimide-sensitive-factor attachment protein receptors in mouse sperm membranes prior to the acrosome reaction. |
| Q34065172 | Regulation of the epithelial sodium channel (ENaC) by membrane trafficking |
| Q37086103 | Regulation of the epithelial sodium channel by membrane trafficking |
| Q36336697 | Role of tethering factors in secretory membrane traffic. |
| Q39138574 | Secretagogues of lung surfactant increase annexin A7 localization with ABCA3 in alveolar type II cells |
| Q30476464 | Single molecule observation of liposome-bilayer fusion thermally induced by soluble N-ethyl maleimide sensitive-factor attachment protein receptors (SNAREs) |
| Q50062928 | Solanaceous exocyst subunits are involved in immunity to diverse plant pathogens |
| Q36119934 | Store-operated Ca2+ entry: vesicle fusion or reversible trafficking and de novo conformational coupling? |
| Q27646758 | Structure and dynamics of gamma-SNAP: insight into flexibility of proteins from the SNAP family |
| Q37954277 | Targeted secretion inhibitors-innovative protein therapeutics |
| Q64107725 | The Catalytic Subunit of PKA Affects Energy Balance and Catecholaminergic Activity |
| Q48276655 | The Membrane Transport System of the Guard Cell and Its Integration for Stomatal Dynamics. |
| Q33259649 | The SNARE protein family of Leishmania major |
| Q27932181 | The specificity of SNARE-dependent fusion is encoded in the SNARE motif |
| Q92172254 | The transcriptome of the rumen ciliate Entodinium caudatum reveals some of its metabolic features |
| Q38774298 | Tissue kallikrein stimulates Ca(2+) reabsorption via PKC-dependent plasma membrane accumulation of TRPV5. |
| Q36714764 | Transient receptor potential channels and intracellular signaling |
| Q36910168 | Two distinct modes of exocytotic fusion pore expansion in large astrocytic vesicles |
| Q87475690 | Unzipping of neuronal snare protein with steered molecular dynamics occurs in three steps |
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