LMA1 binds to vacuoles at Sec18p (NSF), transfers upon ATP hydrolysis to a t-SNARE (Vam3p) complex, and is released during fusion.
about
GATE-16, a membrane transport modulator, interacts with NSF and the Golgi v-SNARE GOS-28Yeast VSM1 encodes a v-SNARE binding protein that may act as a negative regulator of constitutive exocytosis.The Vtc proteins in vacuole fusion: coupling NSF activity to V(0) trans-complex formation.Three v-SNAREs and two t-SNAREs, present in a pentameric cis-SNARE complex on isolated vacuoles, are essential for homotypic fusion.Involvement of long chain fatty acid elongation in the trafficking of secretory vesicles in yeastFusion of docked membranes requires the armadillo repeat protein Vac8p.A Ypt/Rab effector complex containing the Sec1 homolog Vps33p is required for homotypic vacuole fusionAut7p, a soluble autophagic factor, participates in multiple membrane trafficking processes.Ergosterol is required for the Sec18/ATP-dependent priming step of homotypic vacuole fusionCdc42p functions at the docking stage of yeast vacuole membrane fusionTransport-vesicle targeting: tethers before SNAREs.Phenotypic switching in Candida glabrata accompanied by changes in expression of genes with deduced functions in copper detoxification and stressGenomic analysis of homotypic vacuole fusionYeast vacuoles and membrane fusion pathwaysA genetic screen for suppressors of Drosophila NSF2 neuromuscular junction overgrowth.Phosphatidylinositol 4,5-bisphosphate regulates two steps of homotypic vacuole fusionSynaptic vesicle mobility and presynaptic F-actin are disrupted in a N-ethylmaleimide-sensitive factor allele of Drosophila.Vacuole acidification is required for trans-SNARE pairing, LMA1 release, and homotypic fusionCellular functions of NSF: not just SNAPs and SNAREs.Sequential SNARE disassembly and GATE-16-GOS-28 complex assembly mediated by distinct NSF activities drives Golgi membrane fusion.Peroxisome division in the yeast Yarrowia lipolytica is regulated by a signal from inside the peroxisome.The docking stage of yeast vacuole fusion requires the transfer of proteins from a cis-SNARE complex to a Rab/Ypt proteinProteins needed for vesicle budding from the Golgi complex are also required for the docking step of homotypic vacuole fusion.Raft association of SNAP receptors acting in apical trafficking in Madin-Darby canine kidney cells.The phosphatidylinositol 3-phosphate binding protein Vac1p interacts with a Rab GTPase and a Sec1p homologue to facilitate vesicle-mediated vacuolar protein sorting.Homotypic fusion of immature secretory granules during maturation requires syntaxin 6A soluble SNARE drives rapid docking, bypassing ATP and Sec17/18p for vacuole fusion.The amino-terminal domain of the golgi protein giantin interacts directly with the vesicle-tethering protein p115.A screen for dominant negative mutants of SEC18 reveals a role for the AAA protein consensus sequence in ATP hydrolysis.A novel subtilase inhibitor in plants shows structural and functional similarities to protease propeptides.The N-terminal domain of the t-SNARE Vam3p coordinates priming and docking in yeast vacuole fusionA signal from inside the peroxisome initiates its division by promoting the remodeling of the peroxisomal membrane.Phosphorylation of the autoinhibitory domain of the Sso t-SNAREs promotes binding of the Vsm1 SNARE regulator in yeast.Interaction of SNAREs with ArfGAPs precedes recruitment of Sec18p/NSF.Vacuole membrane fusion: V0 functions after trans-SNARE pairing and is coupled to the Ca2+-releasing channel.Genome-wide analysis reveals inositol, not choline, as the major effector of Ino2p-Ino4p and unfolded protein response target gene expression in yeast.Fusion of small peroxisomal vesicles in vitro reconstructs an early step in the in vivo multistep peroxisome assembly pathway of Yarrowia lipolytica.Drainin required for membrane fusion of the contractile vacuole in Dictyostelium is the prototype of a protein family also represented in mannSec-1 (munc-18) interacts with both primed and unprimed syntaxin 1A and associates in a dimeric complex on adrenal chromaffin granules.An NSF function distinct from ATPase-dependent SNARE disassembly is essential for Golgi membrane fusion.
P2860
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P248
Q22253422-14681BBC-C88F-4F64-B4EC-DB7323BD4669Q27929829-16EEC9ED-E6AA-482E-950B-1DCF0C9A53D7Q27932292-7AFE724B-5231-419D-9358-DCE75C8DE471Q27932817-CAF9B5D3-A528-4DBC-9598-CBE2872DA4B0Q27933276-31F0E67E-6716-40DF-B32E-0A945B32F58FQ27937772-D1F9E0A9-252F-40EB-8778-6189623BF289Q27939110-AB36A6F8-074E-47A3-AF72-6A0B8901692FQ27939812-E78D48F0-EE8A-42EB-A9B3-10847B79E2DBQ28345077-9DAB5C8C-D205-4C7B-84EB-0AF942747824Q28361330-37928F8D-333E-4C20-8B42-537A0071E243Q33772639-C611844D-801C-4376-8F7D-E94BAF13B00DQ33995600-F6F43A96-89AD-4969-AF61-36E066E36F30Q34011710-F627634B-5DC0-4F59-93F0-702241396ECBQ34086175-DEEB3356-C84F-4278-A85E-5DBE35312207Q34575456-2C2F6CC0-6EFF-4DA0-B903-10E8B9112D4FQ34689234-9F5C8AE2-7AB0-41EF-8A88-015217933BA0Q35128328-7317A2FF-8DDF-461E-970C-FAF46025FD47Q35642673-0C9EBBD9-E6A2-4786-B180-85AC27525B3BQ35940245-290FA128-6A96-40FA-866A-2662260D9A50Q36324604-08FEF93B-612E-4B20-9910-205864C7D1B1Q36325482-4A23088F-7551-4DD0-AAE7-A46072C96B5AQ36326304-4CE0084F-C145-4911-9D8A-6ADF672BCADDQ36326324-F01EE96D-EBDF-4B03-B238-01D4F759EEF7Q36450084-8A917B36-B9EA-4A55-A8B8-74FBC369D338Q36881642-EEAD61CC-5CFE-4E11-805D-6F17438638ECQ37069977-E2408BEC-E75E-4069-9580-8716463DD614Q37491866-76EEA420-5F00-4199-8E0C-66972EC57DD0Q38316271-B2DDDAB5-19A5-4F11-8FBF-089D3E17CDDDQ38481396-6A6D729D-2865-40CD-A4EF-146B81A91E7EQ38949308-8F652B0A-D6DD-402E-8295-0CD53AA9D7C0Q39230984-39593694-C486-4EA5-B9D4-D20F41D91103Q39736389-0EA368DF-3B1C-4C5C-A76E-C66DB337C492Q39855133-B9E6F663-62B9-45FF-9EF9-1AFC80EFAE68Q41812787-5DCE306E-43C8-4D92-97C4-A23038BBA057Q41875865-36B9488A-D2FD-4704-810B-1CA21F73F13BQ42010811-EDA2092D-4480-4708-8E28-2AC2E64433E9Q42068615-C60AEBF2-9D74-479B-89C0-30204F4D2958Q42675658-BB929089-6D77-4828-8832-70D630EFACECQ42994573-7E88D47D-7E32-4D88-82E2-014C4709AD87Q50336121-B29CF7E8-32FF-4CB1-B0A0-C70AD1775144
P2860
LMA1 binds to vacuoles at Sec18p (NSF), transfers upon ATP hydrolysis to a t-SNARE (Vam3p) complex, and is released during fusion.
description
1998 nî lūn-bûn
@nan
1998 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի հունիսին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
LMA1 binds to vacuoles at Sec1 ...... and is released during fusion.
@ast
LMA1 binds to vacuoles at Sec1 ...... and is released during fusion.
@en
LMA1 binds to vacuoles at Sec1 ...... and is released during fusion.
@nl
type
label
LMA1 binds to vacuoles at Sec1 ...... and is released during fusion.
@ast
LMA1 binds to vacuoles at Sec1 ...... and is released during fusion.
@en
LMA1 binds to vacuoles at Sec1 ...... and is released during fusion.
@nl
prefLabel
LMA1 binds to vacuoles at Sec1 ...... and is released during fusion.
@ast
LMA1 binds to vacuoles at Sec1 ...... and is released during fusion.
@en
LMA1 binds to vacuoles at Sec1 ...... and is released during fusion.
@nl
P2093
P1433
P1476
LMA1 binds to vacuoles at Sec1 ...... and is released during fusion.
@en
P2093
P304
P356
10.1016/S0092-8674(00)81457-9
P407
P577
1998-06-26T00:00:00Z