scholarly article | Q13442814 |
P819 | ADS bibcode | 2006PNAS..103.2701B |
P356 | DOI | 10.1073/PNAS.0511138103 |
P932 | PMC publication ID | 1413832 |
P698 | PubMed publication ID | 16469845 |
P5875 | ResearchGate publication ID | 51372689 |
P50 | author | Reinhard Jahn | Q2140756 |
P2093 | author name string | Thorsten Lang | |
Silvio O Rizzoli | |||
Undine Lippert | |||
Daniel Zwilling | |||
Dorothea Brandhorst | |||
P2860 | cites work | The Rab5 effector EEA1 interacts directly with syntaxin-6 | Q22010591 |
SNAREs contribute to the specificity of membrane fusion | Q22254210 | ||
Rabenosyn-5, a novel Rab5 effector, is complexed with hVPS45 and recruited to endosomes through a FYVE finger domain | Q24290477 | ||
The synaptic vesicle cycle | Q24297813 | ||
Distinct SNARE complexes mediating membrane fusion in Golgi transport based on combinatorial specificity | Q24534126 | ||
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 | ||
Hrs regulates early endosome fusion by inhibiting formation of an endosomal SNARE complex | Q24675805 | ||
Stimulation of NSF ATPase activity by alpha-SNAP is required for SNARE complex disassembly and exocytosis | Q24678373 | ||
Synapsin I (protein I), a nerve terminal-specific phosphoprotein. III. Its association with synaptic vesicles studied in a highly purified synaptic vesicle preparation | Q24681205 | ||
Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 | Q25938983 | ||
A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding | Q25938984 | ||
Crystal structure of the endosomal SNARE complex reveals common structural principles of all SNAREs | Q27637268 | ||
Crystal structure of a SNARE complex involved in synaptic exocytosis at 2.4 A resolution | Q27765619 | ||
Rab proteins as membrane organizers | Q27860861 | ||
The specificity of SNARE-dependent fusion is encoded in the SNARE motif | Q27932181 | ||
Sly1 protein bound to Golgi syntaxin Sed5p allows assembly and contributes to specificity of SNARE fusion complexes | Q27932523 | ||
Analysis of Sec22p in endoplasmic reticulum/Golgi transport reveals cellular redundancy in SNARE protein function | Q27935411 | ||
Compartmental specificity of cellular membrane fusion encoded in SNARE proteins | Q27935841 | ||
A multispecificity syntaxin homologue, Vam3p, essential for autophagic and biosynthetic protein transport to the vacuole | Q27937915 | ||
SNAREpins: minimal machinery for membrane fusion | Q28131697 | ||
Oligomeric complexes link Rab5 effectors with NSF and drive membrane fusion via interactions between EEA1 and syntaxin 13 | Q28142791 | ||
Mixed and non-cognate SNARE complexes. Characterization of assembly and biophysical properties | Q28144385 | ||
Snares and Munc18 in synaptic vesicle fusion | Q28216761 | ||
A protein assembly-disassembly pathway in vitro that may correspond to sequential steps of synaptic vesicle docking, activation, and fusion | Q28255534 | ||
A new syntaxin family member implicated in targeting of intracellular transport vesicles | Q28282159 | ||
Structure and conformational changes in NSF and its membrane receptor complexes visualized by quick-freeze/deep-etch electron microscopy | Q28581498 | ||
The SNARE Vti1a-beta is localized to small synaptic vesicles and participates in a novel SNARE complex | Q28581773 | ||
Endocytic recycling | Q29547737 | ||
Electroblotting of multiple gels: a simple apparatus without buffer tank for rapid transfer of proteins from polyacrylamide to nitrocellulose | Q29617478 | ||
Membrane fusion | Q29618140 | ||
rab5 controls early endosome fusion in vitro | Q29618144 | ||
The Rab5 effector EEA1 is a core component of endosome docking | Q29620568 | ||
Signal-dependent membrane protein trafficking in the endocytic pathway | Q29622948 | ||
Phosphatidylinositol-3-OH kinases are Rab5 effectors. | Q30638959 | ||
Structural insights into the SNARE mechanism | Q33967718 | ||
The SNAREs vti1a and vti1b have distinct localization and SNARE complex partners | Q34133588 | ||
Use of resonance energy transfer to monitor membrane fusion | Q34283693 | ||
Characterization of the early endosome and putative endocytic carrier vesicles in vivo and with an assay of vesicle fusion in vitro | Q36220495 | ||
Determinants of liposome fusion mediated by synaptic SNARE proteins | Q36852539 | ||
A soluble SNARE drives rapid docking, bypassing ATP and Sec17/18p for vacuole fusion. | Q37491866 | ||
A 38,000-dalton membrane protein (p38) present in synaptic vesicles | Q37691886 | ||
Fusion of endosomes involved in synaptic vesicle recycling | Q38613358 | ||
Synaptobrevin binding to synaptophysin: a potential mechanism for controlling the exocytotic fusion machine. | Q40805470 | ||
Relationships between EEA1 binding partners and their role in endosome fusion. | Q40809294 | ||
Cleavage of cellubrevin by tetanus toxin does not affect fusion of early endosomes. | Q41528457 | ||
SNARE interactions are not selective. Implications for membrane fusion specificity | Q41608272 | ||
Reinvestigation of the role of snapin in neurotransmitter release | Q44844867 | ||
A genomic perspective on membrane compartment organization. | Q44883436 | ||
Inhibition of transmitter release correlates with the proteolytic activity of tetanus toxin and botulinus toxin A in individual cultured synapses of Hirudo medicinalis. | Q48052623 | ||
A marker of early amacrine cell development in rat retina | Q48483977 | ||
Differential Control of the Releasable Vesicle Pools by SNAP-25 Splice Variants and SNAP-23 | Q58361606 | ||
Vesicle fusion following receptor-mediated endocytosis requires a protein active in Golgi transport | Q59068145 | ||
Relationship between NGF-mediated volume increase and “priming effect” in fast and slow reacting clones of PC12 pheochromocytoma cells | Q67294336 | ||
The yeast endosomal t-SNARE, Pep12p, functions in the absence of its transmembrane domain | Q73511572 | ||
P433 | issue | 8 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 2701-2706 | |
P577 | publication date | 2006-02-09 | |
P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
P1476 | title | Homotypic fusion of early endosomes: SNAREs do not determine fusion specificity | |
P478 | volume | 103 |
Q62593505 | A VPS33A-binding motif on syntaxin 17 controls autophagy completion in mammalian cells |
Q34356679 | A distinct tethering step is vital for vacuole membrane fusion |
Q43030501 | A fluorescence-based in vitro assay for investigating early endosome dynamics |
Q51424917 | A hypothetical model of cargo-selective rab recruitment during organelle maturation. |
Q33663162 | A new probe for super-resolution imaging of membranes elucidates trafficking pathways |
Q24306541 | A syntaxin 10-SNARE complex distinguishes two distinct transport routes from endosomes to the trans-Golgi in human cells |
Q47871599 | An Overview of Protein Secretion in Yeast and Animal Cells |
Q39608385 | Aspirin regulates SNARE protein expression and phagocytosis in dendritic cells |
Q38173360 | CAPS and Munc13: CATCHRs that SNARE Vesicles |
Q36623748 | COPI-mediated transport. |
Q35771431 | Calcium release through P2X4 activates calmodulin to promote endolysosomal membrane fusion |
Q34375927 | Cell-free fusion of bacteria-containing phagosomes with endocytic compartments |
Q40178739 | Characterization of immunoisolated human gastric parietal cells tubulovesicles: identification of regulators of apical recycling |
Q52334471 | Coat protein complex I facilitates dengue virus production. |
Q26744484 | Coat/Tether Interactions-Exception or Rule? |
Q37531906 | Coiled-coil interactions are required for post-Golgi R-SNARE trafficking |
Q37161770 | Direct targeting of membrane fusion by SNARE mimicry: Convergent evolution of Legionella effectors |
Q41873044 | Dissecting functions of the conserved oligomeric Golgi tethering complex using a cell-free assay |
Q40810796 | Distinct contributions of vacuolar Qabc- and R-SNARE proteins to membrane fusion specificity |
Q92087431 | Dynamic Growth and Shrinkage of the Salmonella-Containing Vacuole Determines the Intracellular Pathogen Niche |
Q24323269 | EARP is a multisubunit tethering complex involved in endocytic recycling |
Q27640677 | Early endosomal SNAREs form a structurally conserved SNARE complex and fuse liposomes with multiple topologies |
Q36190069 | Effect of EGF-receptor tyrosine kinase inhibitor on Rab5 function during endocytosis. |
Q35545284 | Endobrevin/VAMP-8 is the primary v-SNARE for the platelet release reaction |
Q40109713 | Endobrevin/VAMP8 mediates exocytotic release of hexosaminidase from rat basophilic leukaemia cells |
Q34112710 | Endosomal sorting of VAMP3 is regulated by PI4K2A. |
Q28579652 | Evidence for early endosome-like fusion of recently endocytosed synaptic vesicles |
Q36601705 | Expression of exocytosis proteins in rat supraoptic nucleus neurones |
Q24316004 | Fusogenic pairings of vesicle-associated membrane proteins (VAMPs) and plasma membrane t-SNAREs--VAMP5 as the exception |
Q37392295 | HID-1 is required for homotypic fusion of immature secretory granules during maturation |
Q27646399 | Helical extension of the neuronal SNARE complex into the membrane |
Q48360817 | Heterotypic endosomal fusion as an initial trigger for insulin-induced glucose transporter 4 (GLUT4) translocation in skeletal muscle |
Q41245604 | Identification and characterization of a novel botulinum neurotoxin. |
Q93602774 | Inhibition of Rab5 Activation During Insulin Receptor-Mediated Endocytosis |
Q37783445 | Membrane trafficking in protozoa SNARE proteins, H+-ATPase, actin, and other key players in ciliates |
Q64911556 | Molecular mechanisms of contractile-ring constriction and membrane trafficking in cytokinesis. |
Q37690043 | Molecular mechanisms of protein and lipid targeting to ciliary membranes. |
Q41909157 | Multiple and distinct strategies of yeast SNAREs to confer the specificity of membrane fusion |
Q37616690 | Multiple roles of the vesicular-SNARE TI-VAMP in post-Golgi and endosomal trafficking. |
Q21092770 | Munc18-bound syntaxin readily forms SNARE complexes with synaptobrevin in native plasma membranes |
Q41830957 | PIST (GOPC) modulates the oncogenic voltage-gated potassium channel KV10.1. |
Q27480343 | Participation of Rab5, an Early Endosome Protein, in Hepatitis C Virus RNA Replication Machinery |
Q27931637 | Reconstituted membrane fusion requires regulatory lipids, SNAREs and synergistic SNARE chaperones |
Q39848704 | Reconstitution of Rab- and SNARE-dependent membrane fusion by synthetic endosomes. |
Q39206639 | Regulation of EGFR signal transduction by analogue-to-digital conversion in endosomes. |
Q36290839 | Regulation of integrin endocytic recycling and chemotactic cell migration by syntaxin 6 and VAMP3 interaction |
Q39121955 | Reversible, cooperative reactions of yeast vacuole docking |
Q42174304 | Role of Rabex-5 in the sorting of ubiquitinated cargo at an early stage in the endocytic pathway |
Q36992967 | SNARE function is not involved in early endosome docking |
Q33325919 | SNARE protein mimicry by an intracellular bacterium |
Q50336120 | SNARE status regulates tether recruitment and function in homotypic COPII vesicle fusion |
Q64067692 | SNAREs define targeting specificity of trafficking vesicles by combinatorial interaction with tethering factors |
Q29547230 | SNAREs--engines for membrane fusion |
Q58321342 | Salmonella SipA mimics a cognate SNARE for host Syntaxin8 to promote fusion with early endosomes |
Q34137208 | Sequential analysis of trans-SNARE formation in intracellular membrane fusion |
Q57476150 | SipA mimics a cognate SNARE for host Syntaxin8 to promote fusion with early endosomes |
Q38930726 | Soluble NSF attachment protein receptor molecular mimicry by a Legionella pneumophila Dot/Icm effector. |
Q30047766 | Sorting in early endosomes reveals connections to docking- and fusion-associated factors |
Q27863371 | Synaptotagmin activates membrane fusion through a Ca2+-dependent trans interaction with phospholipids |
Q36967305 | Synip arrests soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE)-dependent membrane fusion as a selective target membrane SNARE-binding inhibitor. |
Q27967650 | Syntaxin 3 and SNAP-25 pairing, regulated by omega-3 docosahexaenoic acid, controls the delivery of rhodopsin for the biogenesis of cilia-derived sensory organelles, the rod outer segments |
Q38076778 | Tethering complexes in the endocytic pathway: CORVET and HOPS. |
Q92702770 | The NAE Pathway: Autobahn to the Nucleus for Cell Surface Receptors |
Q42548237 | The SNARE protein vti1a functions in dense-core vesicle biogenesis |
Q33952243 | The TIP30 protein complex, arachidonic acid and coenzyme A are required for vesicle membrane fusion |
Q37635044 | The early endosome: a busy sorting station for proteins at the crossroads. |
Q41829974 | The role of non-canonical SNAREs in synaptic vesicle recycling |
Q28574636 | The specificity of SNARE pairing in biological membranes is mediated by both proof-reading and spatial segregation |
Q36758608 | The synaptic vesicle proteome |
Q52566035 | Therapeutic Approaches of Botulinum Toxin in Gynecology. |
Q37447814 | Transmembrane protein-free membranes fuse into xenopus nuclear envelope and promote assembly of functional pores |
Q98292736 | Vesicle transport through interaction with t-SNAREs 1a (Vti1a)'s roles in neurons |
Q58707587 | Vti1a/b regulate synaptic vesicle and dense core vesicle secretion via protein sorting at the Golgi |
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