scholarly article | Q13442814 |
P819 | ADS bibcode | 2011PNAS..10817325X |
P356 | DOI | 10.1073/PNAS.1113888108 |
P932 | PMC publication ID | 3198343 |
P698 | PubMed publication ID | 21987819 |
P5875 | ResearchGate publication ID | 51708200 |
P50 | author | Youngsoo Jun | Q56989085 |
Hao Xu | Q56989070 | ||
P2093 | author name string | William T Wickner | |
Michael Zick | |||
P2860 | cites work | Ykt6p, a Prenylated SNARE Essential for Endoplasmic Reticulum-Golgi Transport | Q24315775 |
Distinct SNARE complexes mediating membrane fusion in Golgi transport based on combinatorial specificity | Q24534126 | ||
Membrane fusion: grappling with SNARE and SM proteins | Q24633113 | ||
The length of the flexible SNAREpin juxtamembrane region is a critical determinant of SNARE-dependent fusion | Q73075597 | ||
The transmembrane domain of Vam3 affects the composition of cis- and trans-SNARE complexes to promote homotypic vacuole fusion | Q78504151 | ||
Conserved structural features of the synaptic fusion complex: SNARE proteins reclassified as Q- and R-SNAREs | Q24656954 | ||
Vam3p structure reveals conserved and divergent properties of syntaxins | Q27630141 | ||
Helical extension of the neuronal SNARE complex into the membrane | Q27646399 | ||
Reconstituted membrane fusion requires regulatory lipids, SNAREs and synergistic SNARE chaperones | Q27931637 | ||
HOPS prevents the disassembly of trans-SNARE complexes by Sec17p/Sec18p during membrane fusion | Q27932357 | ||
HOPS proofreads the trans-SNARE complex for yeast vacuole fusion | Q27934773 | ||
The SNARE Ykt6 is released from yeast vacuoles during an early stage of fusion | Q27934973 | ||
Purification of active HOPS complex reveals its affinities for phosphoinositides and the SNARE Vam7p | Q27935373 | ||
Compartmental specificity of cellular membrane fusion encoded in SNARE proteins | Q27935841 | ||
Self-interaction of a SNARE transmembrane domain promotes the hemifusion-to-fusion transition | Q27936090 | ||
A Ypt/Rab effector complex containing the Sec1 homolog Vps33p is required for homotypic vacuole fusion | Q27939110 | ||
Hemifusion in SNARE-mediated membrane fusion | Q27939669 | ||
SNAREpins: minimal machinery for membrane fusion | Q28131697 | ||
Structure and conformational changes in NSF and its membrane receptor complexes visualized by quick-freeze/deep-etch electron microscopy | Q28581498 | ||
SNAREs--engines for membrane fusion | Q29547230 | ||
Overcoming expression and purification problems of RhoGDI using a family of "parallel" expression vectors | Q29617999 | ||
Geranylgeranylated SNAREs are dominant inhibitors of membrane fusion | Q30442013 | ||
HOPS initiates vacuole docking by tethering membranes before trans-SNARE complex assembly | Q33948566 | ||
Yeast vacuoles and membrane fusion pathways | Q34086175 | ||
Use of resonance energy transfer to monitor membrane fusion | Q34283693 | ||
Phosphoinositides Function Asymmetrically for Membrane Fusion, Promoting Tethering and 3Q-SNARE Subcomplex Assembly | Q34386086 | ||
Membrane fusion catalyzed by a Rab, SNAREs, and SNARE chaperones is accompanied by enhanced permeability to small molecules and by lysis | Q35579819 | ||
Excess vacuolar SNAREs drive lysis and Rab bypass fusion | Q35962879 | ||
Sec18p and Vam7p remodel trans-SNARE complexes to permit a lipid-anchored R-SNARE to support yeast vacuole fusion | Q36274711 | ||
Interdependent assembly of specific regulatory lipids and membrane fusion proteins into the vertex ring domain of docked vacuoles | Q36322803 | ||
Close is not enough: SNARE-dependent membrane fusion requires an active mechanism that transduces force to membrane anchors | Q36342484 | ||
Unraveling the mechanisms of synaptotagmin and SNARE function in neurotransmitter release | Q36477678 | ||
Regulation of SNARE-mediated membrane fusion during exocytosis | Q37140912 | ||
Capture and release of partially zipped trans-SNARE complexes on intact organelles | Q37237653 | ||
Membrane fusion: SNAREs and regulation | Q37251858 | ||
A soluble SNARE drives rapid docking, bypassing ATP and Sec17/18p for vacuole fusion. | Q37491866 | ||
Membrane fusion: five lipids, four SNAREs, three chaperones, two nucleotides, and a Rab, all dancing in a ring on yeast vacuoles | Q37762546 | ||
Neuronal SNAREs do not trigger fusion between synthetic membranes but do promote PEG-mediated membrane fusion | Q42077784 | ||
HOPS drives vacuole fusion by binding the vacuolar SNARE complex and the Vam7 PX domain via two distinct sites | Q42801354 | ||
P433 | issue | 42 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 17325-17330 | |
P577 | publication date | 2011-10-10 | |
P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
P1476 | title | A lipid-anchored SNARE supports membrane fusion | |
P478 | volume | 108 |
Q41808432 | A Central Small Amino Acid in the VAMP2 Transmembrane Domain Regulates the Fusion Pore in Exocytosis. |
Q57973663 | A novel in vitro assay reveals SNARE topology and the role of Ykt6 in autophagosome fusion with vacuoles |
Q49911437 | Dynamic Cycling of t-SNARE Acylation Regulates Platelet Exocytosis |
Q37719014 | Familial hemophagocytic lymphohistiocytosis: when rare diseases shed light on immune system functioning |
Q57454590 | Functional Reconstitution of Intracellular Vesicle Fusion Using Purified SNAREs and Sec1/Munc18 (SM) Proteins |
Q39123295 | Fusion pores and their control of neurotransmitter and hormone release. |
Q37703099 | Hemifusion in Synaptic Vesicle Cycle. |
Q37023429 | Individual vesicle fusion events mediated by lipid-anchored DNA. |
Q28079024 | Invited review: Mechanisms of GTP hydrolysis and conformational transitions in the dynamin superfamily |
Q28384856 | Lipid Geometry and Bilayer Curvature Modulate LC3/GABARAP-Mediated Model Autophagosomal Elongation |
Q26269847 | Lipid-anchored SNAREs lacking transmembrane regions fully support membrane fusion during neurotransmitter release |
Q36548383 | Lipid-anchored Synaptobrevin Provides Little or No Support for Exocytosis or Liposome Fusion. |
Q57173506 | Mechanism of neurotransmitter release coming into focus |
Q30414376 | Membranes linked by trans-SNARE complexes require lipids prone to non-bilayer structure for progression to fusion |
Q34277591 | Mitofusins and the mitochondrial permeability transition: the potential downside of mitochondrial fusion |
Q35451364 | Munc18a does not alter fusion rates mediated by neuronal SNAREs, synaptotagmin, and complexin |
Q42142889 | Phosphatidylserine-Dependent Catalysis of Stalk and Pore Formation by Synaptobrevin JMR-TMD Peptide. |
Q35055470 | Rho GTPases and the downstream effectors actin-related protein 2/3 (Arp2/3) complex and myosin II induce membrane fusion at self-contacts. |
Q38926137 | SM protein Munc18-2 facilitates transition of Syntaxin 11-mediated lipid mixing to complete fusion for T-lymphocyte cytotoxicity |
Q41215060 | Sec17/Sec18 act twice, enhancing membrane fusion and then disassembling cis-SNARE complexes. |
Q40627999 | Synaptobrevin Transmembrane Domain Dimerization Studied by Multiscale Molecular Dynamics Simulations |
Q39121037 | The Multifaceted Role of SNARE Proteins in Membrane Fusion. |
Q57056881 | The N-peptide binding mode is critical to Munc18-1 function in synaptic exocytosis |
Q90253180 | The Transmembrane Domain of Synaptobrevin Influences Neurotransmitter Flux through Synaptic Fusion Pores |
Q36344941 | The trans-SNARE-regulating function of Munc18-1 is essential to synaptic exocytosis |
Q35608147 | Vacuolar SNARE protein transmembrane domains serve as nonspecific membrane anchors with unequal roles in lipid mixing |