Pages that link to "Q27646570"
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The following pages link to A Structure-Based Mechanism for Vesicle Capture by the Multisubunit Tethering Complex Dsl1 (Q27646570):
Displaying 50 items.
- Assembly and architecture of biogenesis of lysosome-related organelles complex-1 (BLOC-1). (Q24300804) (← links)
- Structural analysis of the RZZ complex reveals common ancestry with multisubunit vesicle tethering machinery (Q24311974) (← links)
- PtdIns(3)P-bound UVRAG coordinates Golgi-ER retrograde and Atg9 transport by differential interactions with the ER tether and the beclin 1 complex (Q24337031) (← links)
- Tethering Complexes in the Arabidopsis Endomembrane System (Q26744479) (← 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)
- Exorcising the exocyst complex (Q26824772) (← links)
- Moonlighting functions of the NRZ (mammalian Dsl1) complex (Q26825961) (← links)
- Structures and mechanisms of vesicle coat components and multisubunit tethering complexes (Q27009146) (← links)
- Sec20p YDR498C (Q27548944) (← links)
- Dsl1p YNL258C (Q27548983) (← links)
- SNAP receptor USE1 YGL098W (Q27549569) (← links)
- Tip20p YGL145W (Q27551437) (← links)
- Sec39p YLR440C (Q27552855) (← links)
- The structure of the Myo4p globular tail and its function in ASH1 mRNA localization (Q27661292) (← links)
- Crystal structure of -COP in complex with -COP provides insight into the architecture of the COPI vesicular coat (Q27662140) (← links)
- Structural basis for the wobbler mouse neurodegenerative disorder caused by mutation in the Vps54 subunit of the GARP complex (Q27663283) (← links)
- Structure of a C-terminal fragment of its Vps53 subunit suggests similarity of Golgi-associated retrograde protein (GARP) complex to a family of tethering complexes (Q27663610) (← links)
- The Crystal Structure of a Munc13 C-terminal Module Exhibits a Remarkable Similarity to Vesicle Tethering Factors (Q27675057) (← links)
- Comparative genomic analysis of multi-subunit tethering complexes demonstrates an ancient pan-eukaryotic complement and sculpting in Apicomplexa (Q27974681) (← links)
- Munc13 mediates the transition from the closed syntaxin-Munc18 complex to the SNARE complex (Q28569612) (← links)
- Sugar-free frosting, a homolog of SAD kinase, drives neural-specific glycan expression in the Drosophila embryo (Q30497802) (← links)
- Molecular architecture of the multisubunit homotypic fusion and vacuole protein sorting (HOPS) tethering complex (Q30505172) (← links)
- ER Import Sites and Their Relationship to ER Exit Sites: A New Model for Bidirectional ER-Golgi Transport in Higher Plants (Q30523967) (← links)
- Distinct Roles for the N- and C-terminal Regions of M-Sec in Plasma Membrane Deformation during Tunneling Nanotube Formation. (Q30811435) (← links)
- Structure and mechanism in membrane trafficking (Q34020731) (← links)
- An update on transport vesicle tethering (Q34044145) (← links)
- Transport vesicle uncoating: it's later than you think (Q34058499) (← links)
- Organization of SNAREs within the Golgi stack (Q34201603) (← links)
- Membrane tethering (Q34201957) (← links)
- A three-stage model of Golgi structure and function (Q34359527) (← links)
- ER-associated retrograde SNAREs and the Dsl1 complex mediate an alternative, Sey1p-independent homotypic ER fusion pathway (Q34428690) (← links)
- Cog5-Cog7 crystal structure reveals interactions essential for the function of a multisubunit tethering complex (Q34480754) (← links)
- Protein flexibility is required for vesicle tethering at the Golgi. (Q34504670) (← links)
- COPI selectively drives maturation of the early Golgi (Q34506701) (← links)
- Importance of the N-terminal domain of the Qb-SNARE Vti1p for different membrane transport steps in the yeast endosomal system (Q34776538) (← links)
- Transport according to GARP: receiving retrograde cargo at the trans-Golgi network. (Q34777250) (← links)
- Molecular organization of the COG vesicle tethering complex (Q35040357) (← links)
- 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 (Q35107512) (← links)
- Myosin V transports secretory vesicles via a Rab GTPase cascade and interaction with the exocyst complex (Q35621765) (← links)
- SNAREs support atlastin-mediated homotypic ER fusion in Saccharomyces cerevisiae (Q35912600) (← links)
- Structural basis for the binding of tryptophan-based motifs by δ-COP. (Q36306048) (← links)
- Subunit connectivity, assembly determinants and architecture of the yeast exocyst complex. (Q36577860) (← links)
- Retrograde traffic from the Golgi to the endoplasmic reticulum (Q36865153) (← links)
- A new role for RINT-1 in SNARE complex assembly at the trans-Golgi network in coordination with the COG complex (Q37167924) (← links)
- HID-1 is required for homotypic fusion of immature secretory granules during maturation (Q37392295) (← links)
- Inheritance of the fittest mitochondria in yeast (Q37423474) (← links)
- Sec3 promotes the initial binary t-SNARE complex assembly and membrane fusion (Q37607936) (← links)
- New links between vesicle coats and Rab-mediated vesicle targeting (Q37774074) (← links)
- Physical aspects of COPI vesicle formation. (Q37808481) (← links)