| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1053215200 |
| P356 | DOI | 10.1038/35025076 |
| P3181 | OpenCitations bibliographic resource ID | 1581390 |
| P698 | PubMed publication ID | 11001058 |
| P2093 | author name string | J E Rothman | |
| F Parlati | |||
| J A McNew | |||
| R Fukuda | |||
| R Miller | |||
| T H Söllner | |||
| P2860 | cites work | 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 |
| Bet1p activates the v-SNARE Bos1p | Q37386267 | ||
| Kex2-dependent invertase secretion as a tool to study the targeting of transmembrane proteins which are involved in ER-->Golgi transport in yeast | Q40792817 | ||
| SNARE interactions are not selective. Implications for membrane fusion specificity | Q41608272 | ||
| Homotypic vacuolar fusion mediated by t- and v-SNAREs | Q48049888 | ||
| Functional architecture of an intracellular membrane t-SNARE | Q59051650 | ||
| Ypt1p implicated in v-SNARE activation | Q59095937 | ||
| The length of the flexible SNAREpin juxtamembrane region is a critical determinant of SNARE-dependent fusion | Q73075597 | ||
| The synaptobrevin-related domains of Bos1p and Sec22p bind to the syntaxin-like region of Sed5p | Q73456353 | ||
| TRAPP stably associates with the Golgi and is required for vesicle docking | Q24600972 | ||
| N-ethylmaleimide-sensitive fusion protein: a trimeric ATPase whose hydrolysis of ATP is required for membrane fusion | Q24673247 | ||
| Crystal structure of a SNARE complex involved in synaptic exocytosis at 2.4 A resolution | Q27765619 | ||
| Identification of 23 complementation groups required for post-translational events in the yeast secretory pathway | Q27931724 | ||
| Asymmetric requirements for a Rab GTPase and SNARE proteins in fusion of COPII vesicles with acceptor membranes | Q27932451 | ||
| Characterization of new mutants in the early part of the yeast secretory pathway isolated by a [3H]mannose suicide selection | Q27933497 | ||
| Compartmental specificity of cellular membrane fusion encoded in SNARE proteins | Q27935841 | ||
| Gos1p, a Saccharomyces cerevisiae SNARE protein involved in Golgi transport. | Q27936489 | ||
| SED5 encodes a 39-kD integral membrane protein required for vesicular transport between the ER and the Golgi complex | Q27938084 | ||
| 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 | ||
| SNAREpins: minimal machinery for membrane fusion | Q28131697 | ||
| Mixed and non-cognate SNARE complexes. Characterization of assembly and biophysical properties | Q28144385 | ||
| A protein assembly-disassembly pathway in vitro that may correspond to sequential steps of synaptic vesicle docking, activation, and fusion | Q28255534 | ||
| A rab protein is required for the assembly of SNARE complexes in the docking of transport vesicles | Q29620271 | ||
| The road taken: past and future foundations of membrane traffic | Q33824729 | ||
| 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 | ||
| Characteristics of endoplasmic reticulum-derived transport vesicles | Q36234617 | ||
| Close is not enough: SNARE-dependent membrane fusion requires an active mechanism that transduces force to membrane anchors | Q36342484 | ||
| The BOS1 gene encodes an essential 27-kD putative membrane protein that is required for vesicular transport from the ER to the Golgi complex in yeast | Q36529463 | ||
| P433 | issue | 6801 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | T-SNARE syntaxin YLR026C | Q27550421 |
| Bos1p YLR078C | Q27551106 | ||
| Bet1p YIL004C | Q27552511 | ||
| SNAP receptor SEC22 YLR268W | Q27553116 | ||
| P304 | page(s) | 194-8 | |
| P577 | publication date | 2000-09-14 | |
| P1433 | published in | Nature | Q180445 |
| P1476 | title | Topological restriction of SNARE-dependent membrane fusion | |
| P478 | volume | 407 |
| Q27935589 | A SNARE required for retrograde transport to the endoplasmic reticulum |
| Q46990070 | A multigene family encoding R-SNAREs in the ciliate Paramecium tetraurelia. |
| Q33916463 | A role of complexin-lipid interactions in membrane fusion |
| Q27936546 | A t-SNARE of the endocytic pathway must be activated for fusion. |
| Q42215504 | A tethering complex dimer catalyzes trans-SNARE complex formation in intracellular membrane fusion |
| Q47871599 | An Overview of Protein Secretion in Yeast and Animal Cells |
| Q27935411 | Analysis of Sec22p in endoplasmic reticulum/Golgi transport reveals cellular redundancy in SNARE protein function |
| Q53242013 | Application of immobilized thrombin for production of S-thanatin expressed in Escherichia coli. |
| Q51792417 | AtVPS45 is a positive regulator of the SYP41/SYP61/VTI12 SNARE complex involved in trafficking of vacuolar cargo. |
| Q37010711 | Binding interactions control SNARE specificity in vivo |
| Q38173360 | CAPS and Munc13: CATCHRs that SNARE Vesicles |
| Q36677270 | COG complexes form spatial landmarks for distinct SNARE complexes. |
| Q36623748 | COPI-mediated transport. |
| Q42062226 | Calcium-independent stimulation of membrane fusion and SNAREpin formation by synaptotagmin I. |
| Q37594134 | Cholesterol, regulated exocytosis and the physiological fusion machine |
| Q26744484 | Coat/Tether Interactions-Exception or Rule? |
| Q58698577 | Comparative in depth RNA sequencing of P. tricornutum's morphotypes reveals specific features of the oval morphotype |
| Q27935841 | Compartmental specificity of cellular membrane fusion encoded in SNARE proteins |
| Q91898495 | Conserved juxtamembrane domains in the yeast golgin Coy1 drive assembly of a megadalton-sized complex and mediate binding to tethering and SNARE proteins |
| Q30830165 | Control systems for membrane fusion in the ancestral eukaryote; evolution of tethering complexes and SM proteins |
| Q37220226 | Countercurrent distribution of two distinct SNARE complexes mediating transport within the Golgi stack |
| Q46816663 | Cysteine-disulfide cross-linking to monitor SNARE complex assembly during endoplasmic reticulum-Golgi transport |
| Q36852539 | Determinants of liposome fusion mediated by synaptic SNARE proteins |
| Q33932515 | Differential use of endoplasmic reticulum membrane for phagocytosis in J774 macrophages |
| Q27939504 | Dissection of COPII subunit-cargo assembly and disassembly kinetics during Sar1p-GTP hydrolysis |
| Q24534126 | Distinct SNARE complexes mediating membrane fusion in Golgi transport based on combinatorial specificity |
| Q34159211 | Do SNARE proteins confer specificity for vesicle fusion? |
| Q36610369 | Drosophila p24 and Sec22 regulate Wingless trafficking in the early secretory pathway |
| Q42645523 | Dsl1p, an essential protein required for membrane traffic at the endoplasmic reticulum/Golgi interface in yeast |
| Q34078604 | Dynamic transport of SNARE proteins in the Golgi apparatus |
| Q51465546 | ER to Golgi-Dependent Protein Secretion: The Conventional Pathway. |
| Q30559352 | ER-associated SNAREs and Sey1p mediate nuclear fusion at two distinct steps during yeast mating |
| Q27640677 | Early endosomal SNAREs form a structurally conserved SNARE complex and fuse liposomes with multiple topologies |
| Q37863963 | Entry and exit mechanisms at the cis-face of the Golgi complex |
| Q35536215 | Examination of Sec22 Homodimer Formation and Role in SNARE-dependent Membrane Fusion |
| Q57010700 | Extracting Sequence Motifs and the Phylogenetic Features of SNARE-Dependent Membrane Traffic |
| Q47855834 | Functional assays for the assessment of the pathogenicity of variants of GOSR2, an ER-to-Golgi SNARE involved in progressive myoclonus epilepsies. |
| Q35083786 | Fusing a lasting relationship between ER tubules |
| Q37592808 | GTP/GDP exchange by Sec12p enables COPII vesicle bud formation on synthetic liposomes |
| Q36321097 | Generation of nonidentical compartments in vesicular transport systems |
| Q36972087 | Hepatocyte polarity |
| Q33240861 | Identification and characterization of syntaxin 1 antisense variants in Limulus polyphemus |
| Q42727146 | Identification of functionally interacting SNAREs by using complementary substitutions in the conserved '0' layer |
| Q50205701 | Indication for differential sorting of the rat v-SNARE splice isoforms VAMP-1a and -1b. |
| Q28581158 | Inositol 1, 4, 5-trisphosphate receptor interacts with the SNARE domain of syntaxin 1B |
| Q27930589 | Interaction of the Saccharomyces cerevisiae cortical actin patch protein Rvs167p with proteins involved in ER to Golgi vesicle trafficking |
| Q33948745 | Interactions between syntaxins identify at least five SNARE complexes within the Golgi/prevacuolar system of the Arabidopsis cell |
| Q35131675 | Intracellular sorting and transport of proteins |
| Q35197977 | Involvement of LMA1 and GATE-16 family members in intracellular membrane dynamics |
| Q34499998 | Lipid metabolism and vesicle trafficking: more than just greasing the transport machinery |
| Q79281029 | Liposome fusion assay to monitor intracellular membrane fusion machines |
| Q24626407 | Localization and activity of the SNARE Ykt6 determined by its regulatory domain and palmitoylation |
| Q90099934 | MT1-MMP recruits the ER-Golgi SNARE Bet1 for efficient MT1-MMP transport to the plasma membrane |
| Q37764586 | Manipulation of host membrane machinery by bacterial pathogens |
| Q73308738 | Membrane fusion in a nutshell |
| Q24633113 | Membrane fusion: grappling with SNARE and SM proteins |
| Q34078457 | Membrane transport: deciphering fusion. |
| Q37394517 | Minimal membrane docking requirements revealed by reconstitution of Rab GTPase-dependent membrane fusion from purified components |
| Q44977587 | Modulation of N-ethylmaleimide-sensitive factor activity upon amino acid deprivation. |
| Q43632102 | Molecular mass, stoichiometry, and assembly of 20 S particles |
| Q40988714 | Multiple ER-Golgi SNARE transmembrane domains are dispensable for trafficking but required for SNARE recycling |
| Q27934496 | Multiple SNARE interactions of an SM protein: Sed5p/Sly1p binding is dispensable for transport |
| Q41909157 | Multiple and distinct strategies of yeast SNAREs to confer the specificity of membrane fusion |
| Q37248709 | Munc18/SNARE proteins' regulation of exocytosis in guinea pig duodenal Brunner's gland acini |
| Q42616483 | Munc18c interaction with syntaxin 4 monomers and SNARE complex intermediates in GLUT4 vesicle trafficking |
| Q42377339 | Mutations in Membrin/GOSR2 Reveal Stringent Secretory Pathway Demands of Dendritic Growth and Synaptic Integrity |
| Q35568641 | Neurotransmission and the synaptic vesicle cycle |
| Q42112087 | New Ca(2+)-dependent regulators of autophagosome maturation |
| Q34201603 | Organization of SNAREs within the Golgi stack |
| Q33779916 | Organization of the ER-Golgi interface for membrane traffic control |
| Q36896315 | Overexpression of Sly41 suppresses COPII vesicle-tethering deficiencies by elevating intracellular calcium levels |
| Q38955098 | Overexpression of native Saccharomyces cerevisiae ER-to-Golgi SNARE genes increased heterologous cellulase secretion |
| Q24297647 | Participation of the syntaxin 5/Ykt6/GS28/GS15 SNARE complex in transport from the early/recycling endosome to the trans-Golgi network |
| Q36514286 | Presentation of phagocytosed antigens by MHC class I and II. |
| Q33999406 | Protein determinants of SNARE-mediated lipid mixing |
| Q34460932 | Protein trafficking mechanisms associated with neurite outgrowth and polarized sorting in neurons. |
| Q42168119 | Purification and functional properties of yeast Sec12 GEF. |
| Q27860861 | Rab proteins as membrane organizers |
| Q27931637 | Reconstituted membrane fusion requires regulatory lipids, SNAREs and synergistic SNARE chaperones |
| Q42168129 | Reconstitution of cargo-dependent COPII coat assembly on proteoliposomes |
| Q36323855 | Regulation of membrane fusion by the membrane-proximal coil of the t-SNARE during zippering of SNAREpins |
| Q27932804 | Retrograde transport of the mannosyltransferase Och1p to the early Golgi requires a component of the COG transport complex |
| Q37967350 | Retrograde vesicle transport in the Golgi. |
| Q35197969 | Revisiting the role of SNAREs in exocytosis and membrane fusion |
| Q30336208 | SNARE Protein Structure and Function |
| Q34133877 | SNARE complexes--is there sufficient complexity for vesicle targeting specificity? |
| Q74045978 | SNARE hypothesis 2000 |
| Q27641907 | SNARE selectivity of the COPII coat |
| Q29619234 | SNARE-mediated membrane fusion |
| Q34825518 | SNAREs and associated regulators in the control of exocytosis in the RBL-2H3 mast cell line |
| Q29547230 | SNAREs--engines for membrane fusion |
| Q36274711 | Sec18p and Vam7p remodel trans-SNARE complexes to permit a lipid-anchored R-SNARE to support yeast vacuole fusion |
| Q27931711 | Sec1p directly stimulates SNARE-mediated membrane fusion in vitro |
| Q47657471 | Sec22p export from the endoplasmic reticulum is independent of SNARE pairing |
| Q35759972 | Sec24p and Sec16p cooperate to regulate the GTP cycle of the COPII coat |
| Q30513976 | Secretory pathway-dependent localization of the Saccharomyces cerevisiae Rho GTPase-activating protein Rgd1p at growth sites |
| Q38080412 | Secretory protein biogenesis and traffic in the early secretory pathway |
| Q42257801 | Selective control of SNARE recycling by Golgi retention |
| Q38675048 | Selective formation of Sed5p-containing SNARE complexes is mediated by combinatorial binding interactions. |
| Q34137208 | Sequential analysis of trans-SNARE formation in intracellular membrane fusion |
| Q24673491 | Sequential tethering of Golgins and catalysis of SNAREpin assembly by the vesicle-tethering protein p115 |
| Q30476464 | Single molecule observation of liposome-bilayer fusion thermally induced by soluble N-ethyl maleimide sensitive-factor attachment protein receptors (SNAREs) |
| 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 |
| Q34180129 | Strategies for prokaryotic expression of eukaryotic membrane proteins |
| Q48489850 | Structural determinants of synaptobrevin 2 function in synaptic vesicle fusion. |
| Q33967718 | Structural insights into the SNARE mechanism |
| Q92257375 | Stx5-Mediated ER-Golgi Transport in Mammals and Yeast |
| Q28208262 | Syntaxin 7 complexes with mouse Vps10p tail interactor 1b, syntaxin 6, vesicle-associated membrane protein (VAMP)8, and VAMP7 in b16 melanoma cells |
| 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 |
| Q34707458 | Syntaxin 8 has two functionally distinct di-leucine-based motifs. |
| Q37220626 | Syntaxin-6 SNARE involvement in secretory and endocytic pathways of cultured pancreatic beta-cells. |
| Q73294979 | The Arabidopsis genome. An abundance of soluble N-ethylmaleimide-sensitive factor adaptor protein receptors |
| Q35107512 | The Dsl1 tethering complex actively participates in soluble NSF (N-ethylmaleimide-sensitive factor) attachment protein receptor (SNARE) complex assembly at the endoplasmic reticulum in Saccharomyces cerevisiae |
| Q37107161 | The Golgi puppet master: COG complex at center stage of membrane trafficking interactions. |
| Q38631626 | The Golgin protein Coy1 functions in intra-Golgi retrograde transport and interacts with the COG complex and Golgi SNAREs |
| Q36143062 | The SNARE Protein Syntaxin 3 Confers Specificity for Polarized Axonal Trafficking in Neurons |
| Q28571014 | The SNARE motif contributes to rbet1 intracellular targeting and dynamics independently of SNARE interactions |
| Q84714131 | The SNARE protein SYP71 expressed in vascular tissues is involved in symbiotic nitrogen fixation in Lotus japonicus nodules |
| Q27938432 | The Yip1p.Yif1p complex is required for the fusion competence of endoplasmic reticulum-derived vesicles |
| Q43909608 | The abscisic acid-related SNARE homolog NtSyr1 contributes to secretion and growth: evidence from competition with its cytosolic domain |
| Q36555183 | The highly conserved COPII coat complex sorts cargo from the endoplasmic reticulum and targets it to the golgi |
| Q37825844 | The late stage of autophagy: cellular events and molecular regulation |
| Q48069250 | The principle of membrane fusion in the cell (Nobel lecture). |
| Q27932181 | The specificity of SNARE-dependent fusion is encoded in the SNARE motif |
| Q59089855 | The specifics of membrane fusion |
| Q48933075 | The transmembrane domain of syntaxin 1A is critical for cytoplasmic domain protein-protein interactions |
| Q35102649 | Topological arrangement of the intracellular membrane fusion machinery |
| Q34392098 | Tubulin is the endogenous inhibitor of the glyceraldehyde 3-phosphate dehydrogenase isoform that catalyzes membrane fusion: Implications for the coordinated regulation of glycolysis and membrane fusion |
| Q34921177 | Two coiled-coil domains of Chlamydia trachomatis IncA affect membrane fusion events during infection |
| Q35608147 | Vacuolar SNARE protein transmembrane domains serve as nonspecific membrane anchors with unequal roles in lipid mixing |
| Q36642826 | Vesicle trafficking in plant immune responses |
| Q98292736 | Vesicle transport through interaction with t-SNAREs 1a (Vti1a)'s roles in neurons |
| Q57364514 | Vesicular transport and the golgi apparatus in yeast |
| Q35169800 | What is the role of SNARE proteins in membrane fusion? |
| Q36321752 | i-SNAREs: inhibitory SNAREs that fine-tune the specificity of membrane fusion |
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