Pages that link to "Q33948566"

The following pages link to HOPS initiates vacuole docking by tethering membranes before trans-SNARE complex assembly (Q33948566):

Displaying 50 items.

• Mammalian CORVET is required for fusion and conversion of distinct early endosome subpopulations (Q24304619) (← links)
• Coat/Tether Interactions-Exception or Rule? (Q26744484) (← links)
• The Secret Life of Tethers: The Role of Tethering Factors in SNARE Complex Regulation (Q26744489) (← links)
• TRAPP Complexes in Secretion and Autophagy (Q26749341) (← links)
• Charcot-Marie-Tooth disease and intracellular traffic (Q26824841) (← links)
• DangER: protein ovERload. Targeting protein degradation to treat myeloma (Q26825417) (← links)
• Membrane trafficking and phagosome maturation during the clearance of apoptotic cells (Q26999431) (← links)
• Function and regulation of the endosomal fusion and fission machineries (Q27015677) (← links)
• The V-ATPase proteolipid cylinder promotes the lipid-mixing stage of SNARE-dependent fusion of yeast vacuoles. (Q27931031) (← links)
• HOPS prevents the disassembly of trans-SNARE complexes by Sec17p/Sec18p during membrane fusion (Q27932357) (← links)
• The HOPS/Class C Vps Complex Tethers High-Curvature Membranes via a Direct Protein-Membrane Interaction (Q27937119) (← links)
• Bioanalysis of eukaryotic organelles (Q28384122) (← links)
• Differential Effects of Munc18s on Multiple Degranulation-Relevant Trans-SNARE Complexes (Q28548276) (← links)
• The HOPS/class C Vps complex tethers membranes by binding to one Rab GTPase in each apposed membrane (Q30299905) (← links)
• Membranes linked by trans-SNARE complexes require lipids prone to non-bilayer structure for progression to fusion (Q30414376) (← links)
• The yeast vacuolar Rab GTPase Ypt7p has an activity beyond membrane recruitment of the homotypic fusion and protein sorting-Class C Vps complex (Q30415875) (← links)
• Phosphorylation of the effector complex HOPS by the vacuolar kinase Yck3p confers Rab nucleotide specificity for vacuole docking and fusion (Q30423896) (← links)
• Molecular architecture of the multisubunit homotypic fusion and vacuole protein sorting (HOPS) tethering complex (Q30505172) (← links)
• How and why intralumenal membrane fragments form during vacuolar lysosome fusion (Q30834820) (← links)
• Dynamic association of the PI3P-interacting Mon1-Ccz1 GEF with vacuoles is controlled through its phosphorylation by the type 1 casein kinase Yck3. (Q33604383) (← links)
• SM proteins Sly1 and Vps33 co-assemble with Sec17 and SNARE complexes to oppose SNARE disassembly by Sec18. (Q33764725) (← links)
• An update on transport vesicle tethering (Q34044145) (← links)
• Sequential analysis of trans-SNARE formation in intracellular membrane fusion (Q34137208) (← links)
• Tracking of the dynamic localization of the Rab-specific HOPS subunits reveal their distinct interaction with Ypt7 and vacuoles (Q34142922) (← links)
• A lipid-anchored SNARE supports membrane fusion (Q34223018) (← links)
• A distinct tethering step is vital for vacuole membrane fusion (Q34356679) (← links)
• Phosphoinositides Function Asymmetrically for Membrane Fusion, Promoting Tethering and 3Q-SNARE Subcomplex Assembly (Q34386086) (← links)
• The N-terminal domains of Vps3 and Vps8 are critical for localization and function of the CORVET tethering complex on endosomes (Q34807013) (← links)
• Yeast vacuolar HOPS, regulated by its kinase, exploits affinities for acidic lipids and Rab:GTP for membrane binding and to catalyze tethering and fusion. (Q34960727) (← links)
• Membrane fusion catalyzed by a Rab, SNAREs, and SNARE chaperones is accompanied by enhanced permeability to small molecules and by lysis (Q35579819) (← links)
• Sec17 can trigger fusion of trans-SNARE paired membranes without Sec18. (Q35590241) (← links)
• Vacuolar SNARE protein transmembrane domains serve as nonspecific membrane anchors with unequal roles in lipid mixing (Q35608147) (← links)
• Intrinsic tethering activity of endosomal Rab proteins (Q35656173) (← links)
• The phosphoinositide-associated protein Rush hour regulates endosomal trafficking in Drosophila (Q35712161) (← links)
• N-terminal domain of vacuolar SNARE Vam7p promotes trans-SNARE complex assembly (Q36397778) (← links)
• Sec1/Munc18 protein Vps33 binds to SNARE domains and the quaternary SNARE complex (Q36433806) (← links)
• Munc18-1 controls SNARE protein complex assembly during human sperm acrosomal exocytosis (Q36481882) (← links)
• The CORVET complex promotes tethering and fusion of Rab5/Vps21-positive membranes (Q36673162) (← links)
• Fusion proteins and select lipids cooperate as membrane receptors for the soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) Vam7p (Q37213774) (← links)
• The tethering complex HOPS catalyzes assembly of the soluble SNARE Vam7 into fusogenic trans-SNARE complexes (Q37348768) (← links)
• Caenorhabditis elegans HOPS and CCZ-1 mediate trafficking to lysosome-related organelles independently of RAB-7 and SAND-1. (Q37669229) (← links)
• HOPS catalyzes the interdependent assembly of each vacuolar SNARE into a SNARE complex. (Q37744204) (← links)
• New links between vesicle coats and Rab-mediated vesicle targeting (Q37774074) (← links)
• Secretive bacterial pathogens and the secretory pathway. (Q37849309) (← links)
• Pairing phosphoinositides with calcium ions in endolysosomal dynamics: phosphoinositides control the direction and specificity of membrane trafficking by regulating the activity of calcium channels in the endolysosomes (Q37871504) (← links)
• CAPS and Munc13: CATCHRs that SNARE Vesicles (Q38173360) (← links)
• Rab family of GTPases. (Q38388053) (← links)
• Chaperoning SNARE assembly and disassembly (Q38865222) (← links)
• Multivalent Rab interactions determine tether-mediated membrane fusion (Q39182367) (← links)
• The small GTPase Arl8b regulates assembly of the mammalian HOPS complex on lysosomes (Q40678357) (← links)