Vacuole acidification is required for trans-SNARE pairing, LMA1 release, and homotypic fusion - Wikidata - awgldk - TriplyDB

Vacuole acidification is required for trans-SNARE pairing, LMA1 release, and homotypic fusion

Vacuole acidification is required for trans-SNARE pairing, LMA1 release, and homotypic fusion

http://www.wikidata.org/entity/Q35642673

about

GATE-16, a membrane transport modulator, interacts with NSF and the Golgi v-SNARE GOS-28 Localization to mature melanosomes by virtue of cytoplasmic dileucine motifs is required for human OCA2 function A role for glutamate transporters in the regulation of insulin secretion The Vtc proteins in vacuole fusion: coupling NSF activity to V(0) trans-complex formation.Cytosolic Hsp70s are involved in the transport of aminopeptidase 1 from the cytoplasm into the vacuole.Fusion of docked membranes requires the armadillo repeat protein Vac8p.Vam10p defines a Sec18p-independent step of priming that allows yeast vacuole tethering.Aut7p, a soluble autophagic factor, participates in multiple membrane trafficking processes.Ergosterol is required for the Sec18/ATP-dependent priming step of homotypic vacuole fusion Vac8p release from the SNARE complex and its palmitoylation are coupled and essential for vacuole fusion The V-ATPase membrane domain is a sensor of granular pH that controls the exocytotic machinery.Mechanisms of exocytosis in insulin-secreting B-cells and glucagon-secreting A-cells.Differential effects of TBC1D15 and mammalian Vps39 on Rab7 activation state, lysosomal morphology, and growth factor dependence.Genomic analysis of homotypic vacuole fusion Yeast vacuoles and membrane fusion pathways ATP-independent luminal oscillations and release of Ca2+ and H+ from mast cell secretory granules: implications for signal transduction.Mitofusins and the mitochondrial permeability transition: the potential downside of mitochondrial fusion The pH of the secretory pathway: measurement, determinants, and regulation.Vibrio effector protein VopQ inhibits fusion of V-ATPase-containing membranes.Acidic calcium stores of Saccharomyces cerevisiae.Amino acid transporters: roles in amino acid sensing and signalling in animal cells.Abscisic acid prevents the coalescence of protein storage vacuoles by upregulating expression of a tonoplast intrinsic protein gene in barley aleurone.Identification of domains within the V-ATPase accessory subunit Ac45 involved in V-ATPase transport and Ca2+-dependent exocytosis.Remodeling of organelle-bound actin is required for yeast vacuole fusion Proteins needed for vesicle budding from the Golgi complex are also required for the docking step of homotypic vacuole fusion.Target of rapamycin signaling mediates vacuolar fission caused by endoplasmic reticulum stress in Saccharomyces cerevisiae.SNARE function is not involved in early endosome docking SNAREs: cogs and coordinators in signaling and development.The vesicular ATPase: a missing link between acidification and exocytosis.A soluble SNARE drives rapid docking, bypassing ATP and Sec17/18p for vacuole fusion.Plant and yeast NHX antiporters: roles in membrane trafficking.Natamycin inhibits vacuole fusion at the priming phase via a specific interaction with ergosterol.The endosomal Na(+)/H(+) exchanger contributes to multivesicular body formation by regulating the recruitment of ESCRT-0 Vps27p to the endosomal membrane.Ablation of a small transmembrane protein of Trypanosoma brucei (TbVTC1) involved in the synthesis of polyphosphate alters acidocalcisome biogenesis and function, and leads to a cytokinesis defect.Both calmodulin and the unconventional myosin Myr4 regulate membrane trafficking along the recycling pathway of MDCK cells.The Coordinated Action of Calcineurin and Cathepsin D Protects Against α-Synuclein Toxicity.Vacuole membrane fusion: V0 functions after trans-SNARE pairing and is coupled to the Ca2+-releasing channel.Class C ABC transporters and Saccharomyces cerevisiae vacuole fusion Homotypic vacuole fusion in yeast requires organelle acidification and not the V-ATPase membrane domain.TPN-evoked dysfunction of islet lysosomal activity mediates impairment of glucose-stimulated insulin release.

P2860

Q22253422-8BB4B2AE-CE98-4EFB-8000-15203008724E Q24312002-3125A36B-6427-4B8D-822F-C145B5A1798F Q27329065-790949F2-ED39-4E3E-8E43-B8D52BA63068 Q27932292-E66D798A-F786-4FC1-8FC0-13A5B865FC6E Q27936886-C7C8E653-27F5-4D59-8B5D-7341567FE5E3 Q27937772-23CD706D-A7A4-4823-8556-546F4C17D91A Q27938299-0A4E319F-36DD-4C55-AFEB-F5B5169A3364 Q27939812-67F0EA94-D7C0-4E14-8C7F-69B3FBEE3B49 Q28345077-957771FC-9044-4288-B15B-C2C61FB348E9 Q28366806-9140CC08-E8ED-477F-931F-7A2FA11D390A Q30555694-3B485A47-0D4E-43DD-9882-1A5B04E27A2D Q31140262-DBC80FB9-EE7C-452A-80F2-641D00ED233C Q33883430-015EA3BE-89A2-4970-8DDF-6AEA8298280F Q34011710-46A8DC74-9E0F-4C61-9851-4F00F834C7E0 Q34086175-ED8044AA-B3FC-40D2-8AB6-F5D1630EAFFE Q34182292-EE0DD2F7-6500-43FE-A6F5-FB3FD88A56C8 Q34277591-DA24B047-5C84-48C2-8E15-95AF106B9C27 Q34340217-6C237119-EDB5-4AD7-96D5-97224C81B486 Q34926211-C7B548DA-756D-4C1A-B0B7-D5792ADAA083 Q35109222-AD3F250D-9EF2-4E27-9409-7906C7FB20C8 Q35184476-153F713A-D5BF-4D8B-BADC-C53D63EE55E6 Q35626651-B4D6C454-2C3D-4843-8923-5E7F0AC5EC42 Q36201966-B7D03CC7-D6AD-4D14-AA58-3F6340ADF053 Q36325643-AD0EC2A6-D65E-40DF-B759-711C5F63024C Q36326324-193EE1D3-7768-4DAA-8EA0-2A3669A7F7CC Q36368859-93A34A3B-D386-40C0-B7A4-57E13E0E232B Q36992967-DEC9A629-6EE5-40D5-8B66-4BA49380D2B6 Q37234785-0D5E0D71-90C6-488D-97F1-568CD4FD898F Q37267955-8C3971ED-67C1-4938-95BB-5541FABDF693 Q37491866-3B6CB05C-A660-4B4C-B18E-4212ED220E04 Q37973557-2FDA5ED2-58CF-4590-952C-34D716F0A26E Q38344916-4A8D1CD0-964F-4C82-8F8D-C06D8235BC5B Q38795805-E78573CE-18C9-4F1B-8782-CF50D5E6A9E6 Q38998824-D3406AA5-52F1-402D-8AB4-52A5C9096312 Q40826317-13876B0C-DA96-48D8-B5E5-1363CECBEC3D Q40998960-EFF14E44-5DAD-47C9-AB9A-B34C15F1A4BF Q41875865-95CBE6A0-FED0-48C8-851E-8DB62DDB4C5A Q42079678-768FDAFD-C7F5-4F4C-9246-45FB3F01A135 Q42105526-A7FF416E-729F-4CA1-A58D-0DF89476C1CA Q42505771-B173C7EB-1947-4124-B47F-571069CC2A84

P2860

Vacuole acidification is required for trans-SNARE pairing, LMA1 release, and homotypic fusion

http://www.wikidata.org/entity/Q35642673

description

1999 nî lūn-bûn

@nan

1999年の論文

@ja

1999年論文

@yue

1999年論文

@zh-hant

1999年論文

@zh-hk

1999年論文

@zh-mo

1999年論文

@zh-tw

1999年论文

@wuu

1999年论文

@zh

1999年论文

@zh-cn

name

Vacuole acidification is requi ...... release, and homotypic fusion

@ast

Vacuole acidification is requi ...... release, and homotypic fusion

@en

type

label

Vacuole acidification is requi ...... release, and homotypic fusion

@ast

Vacuole acidification is requi ...... release, and homotypic fusion

@en

prefLabel

Vacuole acidification is requi ...... release, and homotypic fusion

@ast

Vacuole acidification is requi ...... release, and homotypic fusion

@en

P1433

Q35642673-F5145581-8449-4AF9-A232-FAFFC83A6449

P1476

Q35642673-82ED889C-7395-4B80-9CD8-6AED4558066E

P2093

Q35642673-66F2E31B-21A4-4408-B7FE-C005A1D5B3FF

Q35642673-93AD49E8-AB1D-483A-9831-758932257BF5

Q35642673-CA40A717-192D-406C-ACF5-F3F384161554

P2860

Q35642673-084DACFA-C3EF-43AE-822E-C36A6077B0E9

Q35642673-0C9EBBD9-E6A2-4786-B180-85AC27525B3B

Q35642673-23F46B50-31F4-4CED-B9B0-D747A0CDDD31

Q35642673-366454F6-FEC8-485C-B02F-8E57BBDF45BF

Q35642673-3D577B9F-0F40-4CAB-A1CD-B8BF7C8AABA6

Q35642673-3FADE3FC-73AB-470D-972C-8AC5E34A3B88

Q35642673-58DB5AE5-1360-427B-8DA0-6737238F0555

Q35642673-6D649326-9D4F-4152-80FA-1FACD3ABDEE7

Q35642673-770EC386-4060-4E2B-A2D8-10E75F9E6073

Q35642673-7E9776FF-CD0F-4031-91DA-AF8D86BF6169

P304

Q35642673-7D3BAC15-72EC-4D46-93FD-40C0911E6226

P31

Q35642673-32585763-CD50-4FBB-9849-6F82736F4929

P356

Q35642673-6C45BEB9-430B-4C18-A5AF-D0431E837351

P407

Q35642673-7C4D12A2-0AFA-47D4-8DF7-3DA46972785E

P433

Q35642673-EDF143B0-4BA0-4C58-A685-86C47B95C626

P478

Q35642673-D4AE719E-D121-49F8-A1E7-6653A7A9568B

P577

Q35642673-490DCFCF-636D-4B0F-91CF-806D5A287B79

P5875

Q35642673-6A845D47-CB47-4DBD-9DC1-BEB505442714

P698

Q35642673-917D516D-2638-4D43-9BEE-AD1EC5261149

P932

Q35642673-AF361EB5-CF93-4BAE-82B9-C6D93F0FC722

P356

PNAS.96.20.11194

P1433

Proceedings of the National Academy of Sciences of the United States of America

P1476

Vacuole acidification is requi ...... release, and homotypic fusion

@en

P2093

C Ungermann

http://www.w3.org/2001/XMLSchema#string

W Wickner

http://www.w3.org/2001/XMLSchema#string

Z Xu

http://www.w3.org/2001/XMLSchema#string

P2860

The GTPase Ypt7p of Saccharomyces cerevisiae is required on both partner vacuoles for the homotypic fusion step of vacuole inheritance.

Calcineurin-dependent growth control in Saccharomyces cerevisiae mutants lacking PMC1, a homolog of plasma membrane Ca2+ ATPases

Three v-SNAREs and two t-SNAREs, present in a pentameric cis-SNARE complex on isolated vacuoles, are essential for homotypic fusion.

Endocytosis in yeast: evidence for the involvement of a small GTP-binding protein (Ypt7p).

Thioredoxin is required for vacuole inheritance in Saccharomyces cerevisiae

Vam7p, a vacuolar SNAP-25 homolog, is required for SNARE complex integrity and vacuole docking and fusion.

Docking of yeast vacuoles is catalyzed by the Ras-like GTPase Ypt7p after symmetric priming by Sec18p (NSF)

Homotypic vacuole fusion requires Sec17p (yeast alpha-SNAP) and Sec18p (yeast NSF)

Ca2+/calmodulin signals the completion of docking and triggers a late step of vacuole fusion.

Functional reconstitution of ypt7p GTPase and a purified vacuole SNARE complex.

P304

11194-11199

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1073/PNAS.96.20.11194

http://www.w3.org/2001/XMLSchema#string

P407

P433

20

http://www.w3.org/2001/XMLSchema#string

P478

96

http://www.w3.org/2001/XMLSchema#string

P577

1999-09-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

12800525

http://www.w3.org/2001/XMLSchema#string

P698

10500153

http://www.w3.org/2001/XMLSchema#string

P932

18010

http://www.w3.org/2001/XMLSchema#string