scholarly article | Q13442814 |
P2093 | author name string | Chun Wan | |
Yinghui Liu | |||
Qian Yin | |||
Michael H B Stowell | |||
Haijia Yu | |||
Jingshi Shen | |||
Shailendra S Rathore | |||
MyeongSeon Lee | |||
P2860 | cites work | Crystal structure of HIV-1 gp41 including both fusion peptide and membrane proximal external regions | Q21090508 |
Membrane fusion: grappling with SNARE and SM proteins | Q24633113 | ||
Complexin controls the force transfer from SNARE complexes to membranes in fusion | Q26269883 | ||
Mapping of functional elements in the stem-anchor region of tick-borne encephalitis virus envelope protein E | Q27469713 | ||
Structural basis of viral invasion: lessons from paramyxovirus F | Q27481675 | ||
Viral membrane fusion | Q27486639 | ||
Helical extension of the neuronal SNARE complex into the membrane | Q27646399 | ||
Dynamic structure of lipid-bound synaptobrevin suggests a nucleation-propagation mechanism for trans-SNARE complex formation | Q27658206 | ||
Possible roles for Munc18-1 domain 3a and Syntaxin1 N-peptide and C-terminal anchor in SNARE complex formation | Q27666423 | ||
How synaptotagmin promotes membrane fusion. | Q27863355 | ||
The polybasic juxtamembrane region of Sso1p is required for SNARE function in vivo | Q27931683 | ||
SNAP receptors implicated in vesicle targeting and fusion | Q28131653 | ||
Molecular anatomy of a trafficking organelle | Q28274481 | ||
Synaptotagmin-mediated bending of the target membrane is a critical step in Ca(2+)-regulated fusion | Q28584744 | ||
Single vesicle millisecond fusion kinetics reveals number of SNARE complexes optimal for fast SNARE-mediated membrane fusion | Q30434163 | ||
The many mechanisms of viral membrane fusion proteins. | Q30435429 | ||
Liposome reconstitution of a minimal protein-mediated membrane fusion machine | Q30476143 | ||
Interaction of an amphipathic peptide with phosphatidycholine/phosphatidylethanolamine mixed membranes | Q31121981 | ||
Electrostatic attraction at the core of membrane fusion | Q33601109 | ||
Single-molecule studies of the neuronal SNARE fusion machinery | Q33789507 | ||
Role of the membrane-proximal domain in the initial stages of human immunodeficiency virus type 1 envelope glycoprotein-mediated membrane fusion. | Q33815984 | ||
How could SNARE proteins open a fusion pore? | Q33918609 | ||
SNARE bundle and syntaxin N-peptide constitute a minimal complement for Munc18-1 activation of membrane fusion. | Q34026722 | ||
Electrostatic properties of membranes containing acidic lipids and adsorbed basic peptides: theory and experiment | Q34171993 | ||
Bilayer conformation of fusion peptide of influenza virus hemagglutinin: a molecular dynamics simulation study | Q34186193 | ||
Membrane protein sequestering by ionic protein-lipid interactions | Q34226601 | ||
How SNARE molecules mediate membrane fusion: recent insights from molecular simulations | Q34256932 | ||
Protein-Lipid Interplay in Fusion and Fission of Biological Membranes | Q34267537 | ||
Role of the synaptobrevin C terminus in fusion pore formation | Q34276398 | ||
The membrane fusion enigma: SNAREs, Sec1/Munc18 proteins, and their accomplices--guilty as charged? | Q34305507 | ||
v-SNARE transmembrane domains function as catalysts for vesicle fusion | Q42382355 | ||
Juxtamembrane tryptophans of synaptobrevin 2 control the process of membrane fusion | Q42428152 | ||
Selective activation of cognate SNAREpins by Sec1/Munc18 proteins | Q42506708 | ||
Evidence that electrostatic interactions between vesicle-associated membrane protein 2 and acidic phospholipids may modulate the fusion of transport vesicles with the plasma membrane | Q42684322 | ||
HOPS drives vacuole fusion by binding the vacuolar SNARE complex and the Vam7 PX domain via two distinct sites | Q42801354 | ||
Regulation of neuronal SNARE assembly by the membrane | Q44436595 | ||
The Dual Function of the Polybasic Juxtamembrane Region of Syntaxin 1A in Clamping Spontaneous Release and Stimulating Ca2+-Triggered Release in Neuroendocrine Cells. | Q47407123 | ||
Structural determinants of synaptobrevin 2 function in synaptic vesicle fusion. | Q48489850 | ||
Fast vesicle fusion in living cells requires at least three SNARE complexes. | Q50541149 | ||
The Munc18-1 domain 3a loop is essential for neuroexocytosis but not for syntaxin-1A transport to the plasma membrane. | Q50912466 | ||
Investigation of the juxtamembrane region of neuronal-Synaptobrevin in synaptic transmission at the Drosophila neuromuscular junction. | Q52774642 | ||
Synaptobrevin transmembrane domain determines the structure and dynamics of the SNARE motif and the linker region. | Q53270497 | ||
Membrane curvature in synaptic vesicle fusion and beyond. | Q55052659 | ||
Lipid-dependence of target membrane stability during influenza viral fusion | Q56306951 | ||
Functional Reconstitution of Intracellular Vesicle Fusion Using Purified SNAREs and Sec1/Munc18 (SM) Proteins | Q57454590 | ||
v-SNARE Actions during Ca2+-Triggered Exocytosis | Q58343442 | ||
Munc18 and Munc13 serve as a functional template to orchestrate neuronal SNARE complex assembly | Q60917520 | ||
Munc18-1 catalyzes neuronal SNARE assembly by templating SNARE association | Q60958060 | ||
pH-induced destabilization of lipid bilayers by a lipopeptide derived from influenza hemagglutinin | Q73202087 | ||
Membrane-proximal tryptophans of synaptobrevin II stabilize priming of secretory vesicles | Q85392206 | ||
SNARE zippering requires activation by SNARE-like peptides in Sec1/Munc18 proteins | Q91047148 | ||
Syntaxin N-terminal peptide motif is an initiation factor for the assembly of the SNARE-Sec1/Munc18 membrane fusion complex | Q34450014 | ||
A structural role for the synaptobrevin 2 transmembrane domain in dense-core vesicle fusion pores | Q34470858 | ||
Conformation of the synaptobrevin transmembrane domain | Q34620674 | ||
SNARE-catalyzed fusion events are regulated by Syntaxin1A-lipid interactions | Q34713785 | ||
Mechanisms of membrane fusion: disparate players and common principles. | Q34780589 | ||
The Atlastin C-terminal tail is an amphipathic helix that perturbs the bilayer structure during endoplasmic reticulum homotypic fusion. | Q35103921 | ||
Reluctance to membrane binding enables accessibility of the synaptobrevin SNARE motif for SNARE complex formation | Q35149460 | ||
Fusion peptides and the mechanism of viral fusion | Q35182242 | ||
Vacuolar SNARE protein transmembrane domains serve as nonspecific membrane anchors with unequal roles in lipid mixing | Q35608147 | ||
Lipid interaction of the C terminus and association of the transmembrane segments facilitate atlastin-mediated homotypic endoplasmic reticulum fusion | Q36167580 | ||
Coarse-grain simulations reveal movement of the synaptobrevin C-terminus in response to piconewton forces. | Q36207983 | ||
Reconstituting Intracellular Vesicle Fusion Reactions: The Essential Role of Macromolecular Crowding | Q36263474 | ||
SNAREpins are functionally resistant to disruption by NSF and alphaSNAP. | Q36327510 | ||
The trans-SNARE-regulating function of Munc18-1 is essential to synaptic exocytosis | Q36344941 | ||
Structural and functional properties of an unusual internal fusion peptide in a nonenveloped virus membrane fusion protein | Q36510388 | ||
Protein-driven membrane stresses in fusion and fission | Q36566327 | ||
Exocytotic fusion pores are composed of both lipids and proteins | Q36589148 | ||
Importance of the membrane-perturbing properties of the membrane-proximal external region of human immunodeficiency virus type 1 gp41 to viral fusion | Q36673288 | ||
Mechanics of membrane fusion | Q36901510 | ||
Membrane fusion intermediates via directional and full assembly of the SNARE complex | Q36916260 | ||
The hemifusion structure induced by influenza virus haemagglutinin is determined by physical properties of the target membranes | Q36926306 | ||
Synip arrests soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE)-dependent membrane fusion as a selective target membrane SNARE-binding inhibitor. | Q36967305 | ||
Reconstitution of the vital functions of Munc18 and Munc13 in neurotransmitter release | Q37071048 | ||
Comparative studies of Munc18c and Munc18-1 reveal conserved and divergent mechanisms of Sec1/Munc18 proteins. | Q37143477 | ||
Capture and release of partially zipped trans-SNARE complexes on intact organelles | Q37237653 | ||
Membrane fusion: five lipids, four SNAREs, three chaperones, two nucleotides, and a Rab, all dancing in a ring on yeast vacuoles | Q37762546 | ||
Aromatic amino acids in the juxtamembrane domain of severe acute respiratory syndrome coronavirus spike glycoprotein are important for receptor-dependent virus entry and cell-cell fusion | Q38294473 | ||
Chaperoning SNARE assembly and disassembly | Q38865222 | ||
Binding of Munc18-1 to synaptobrevin and to the SNARE four-helix bundle | Q39482880 | ||
Reconstitution of Rab- and SNARE-dependent membrane fusion by synthetic endosomes. | Q39848704 | ||
The Membrane-Proximal Region of Vesicular Stomatitis Virus Glycoprotein G Ectodomain Is Critical for Fusion and Virus Infectivity | Q40173398 | ||
Membrane destabilizing properties of cell-penetrating peptides | Q40430708 | ||
Membrane destabilization by N-terminal peptides of viral envelope proteins | Q41085283 | ||
Synaptotagmin-1 utilizes membrane bending and SNARE binding to drive fusion pore expansion | Q41413294 | ||
SNARE proteins: one to fuse and three to keep the nascent fusion pore open | Q41920045 | ||
Phosphatidylserine-Dependent Catalysis of Stalk and Pore Formation by Synaptobrevin JMR-TMD Peptide. | Q42142889 | ||
Synaptobrevin N-terminally bound to syntaxin-SNAP-25 defines the primed vesicle state in regulated exocytosis | Q42176873 | ||
A direct role for the Sec1/Munc18-family protein Vps33 as a template for SNARE assembly | Q42288650 | ||
P433 | issue | 13 | |
P304 | page(s) | 4583-4592.e3 | |
P577 | publication date | 2019-12-01 | |
P1433 | published in | Cell Reports | Q5058165 |
P1476 | title | Intracellular Vesicle Fusion Requires a Membrane-Destabilizing Peptide Located at the Juxtamembrane Region of the v-SNARE | |
P478 | volume | 29 |
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