112 related articles for article (PubMed ID: 33474763)
1. Di-lysine motif-like sequences formed by deleting the C-terminal domain of aquaporin-4 prevent its trafficking to the plasma membrane.
Chau S; Fujii A; Wang Y; Vandebroek A; Goda W; Yasui M; Abe Y
Genes Cells; 2021 Mar; 26(3):152-164. PubMed ID: 33474763
[TBL] [Abstract][Full Text] [Related]
2. A C-terminal di-leucine motif controls plasma membrane expression of PMCA4b.
Antalffy G; Pászty K; Varga K; Hegedűs L; Enyedi Á; Padányi R
Biochim Biophys Acta; 2013 Dec; 1833(12):2561-2572. PubMed ID: 23830917
[TBL] [Abstract][Full Text] [Related]
3. NPA motifs play a key role in plasma membrane targeting of aquaporin-4.
Guan XG; Su WH; Yi F; Zhang D; Hao F; Zhang HG; Liu YJ; Feng XC; Ma TH
IUBMB Life; 2010 Mar; 62(3):222-6. PubMed ID: 20186918
[TBL] [Abstract][Full Text] [Related]
4. A role of the C-terminus of aquaporin 4 in its membrane expression in cultured astrocytes.
Nakahama K; Fujioka A; Nagano M; Satoh S; Furukawa K; Sasaki H; Shigeyoshi Y
Genes Cells; 2002 Jul; 7(7):731-41. PubMed ID: 12081649
[TBL] [Abstract][Full Text] [Related]
5. Topology and endoplasmic reticulum retention signals of the lysosomal storage disease-related membrane protein CLN6.
Heine C; Quitsch A; Storch S; Martin Y; Lonka L; Lehesjoki AE; Mole SE; Braulke T
Mol Membr Biol; 2007; 24(1):74-87. PubMed ID: 17453415
[TBL] [Abstract][Full Text] [Related]
6. Molecular determinants that mediate the sorting of human ATG9A from the endoplasmic reticulum.
Staudt C; Gilis F; Boonen M; Jadot M
Biochim Biophys Acta; 2016 Sep; 1863(9):2299-310. PubMed ID: 27316455
[TBL] [Abstract][Full Text] [Related]
7. C-Terminal Domain of Aquaporin-5 Is Required to Pass Its Protein Quality Control and Ensure Its Trafficking to Plasma Membrane.
Muroi SI; Isohama Y
Int J Mol Sci; 2021 Dec; 22(24):. PubMed ID: 34948259
[TBL] [Abstract][Full Text] [Related]
8. The Golgi-localization of yeast Emp47p depends on its di-lysine motif but is not affected by the ret1-1 mutation in alpha-COP.
Schröder S; Schimmöller F; Singer-Krüger B; Riezman H
J Cell Biol; 1995 Nov; 131(4):895-912. PubMed ID: 7490292
[TBL] [Abstract][Full Text] [Related]
9. A membrane-proximal basic domain and cysteine cluster in the C-terminal tail of CCR5 constitute a bipartite motif critical for cell surface expression.
Venkatesan S; Petrovic A; Locati M; Kim YO; Weissman D; Murphy PM
J Biol Chem; 2001 Oct; 276(43):40133-45. PubMed ID: 11514564
[TBL] [Abstract][Full Text] [Related]
10. The LxxxA motif in the third transmembrane helix of the maize aquaporin ZmPIP2;5 acts as an ER export signal.
Chevalier AS; Chaumont F
Plant Signal Behav; 2015; 10(3):e990845. PubMed ID: 25897469
[TBL] [Abstract][Full Text] [Related]
11. A C-terminal motif contributes to the plasma membrane localization of Arabidopsis STP transporters.
Yamada K; Osakabe Y; Yamaguchi-Shinozaki K
PLoS One; 2017; 12(10):e0186326. PubMed ID: 29028820
[TBL] [Abstract][Full Text] [Related]
12. Formation of aquaporin-4 arrays is inhibited by palmitoylation of N-terminal cysteine residues.
Suzuki H; Nishikawa K; Hiroaki Y; Fujiyoshi Y
Biochim Biophys Acta; 2008 Apr; 1778(4):1181-9. PubMed ID: 18179769
[TBL] [Abstract][Full Text] [Related]
13. The juxtamembrane sequence of cytochrome P-450 2C1 contains an endoplasmic reticulum retention signal.
Szczesna-Skorupa E; Kemper B
J Biol Chem; 2001 Nov; 276(48):45009-14. PubMed ID: 11557755
[TBL] [Abstract][Full Text] [Related]
14. AQP4 plasma membrane trafficking or channel gating is not significantly modulated by phosphorylation at COOH-terminal serine residues.
Assentoft M; Larsen BR; Olesen ET; Fenton RA; MacAulay N
Am J Physiol Cell Physiol; 2014 Nov; 307(10):C957-65. PubMed ID: 25231107
[TBL] [Abstract][Full Text] [Related]
15. Atrophic macular degeneration mutations in ELOVL4 result in the intracellular misrouting of the protein.
Ambasudhan R; Wang X; Jablonski MM; Thompson DA; Lagali PS; Wong PW; Sieving PA; Ayyagari R
Genomics; 2004 Apr; 83(4):615-25. PubMed ID: 15028284
[TBL] [Abstract][Full Text] [Related]
16. A specific endoplasmic reticulum export signal drives transport of stem cell factor (Kitl) to the cell surface.
Paulhe F; Imhof BA; Wehrle-Haller B
J Biol Chem; 2004 Dec; 279(53):55545-55. PubMed ID: 15475566
[TBL] [Abstract][Full Text] [Related]
17. Defining a minimal motif required to prevent connexin oligomerization in the endoplasmic reticulum.
Maza J; Das Sarma J; Koval M
J Biol Chem; 2005 Jun; 280(22):21115-21. PubMed ID: 15817491
[TBL] [Abstract][Full Text] [Related]
18. (Arg)3 within the N-terminal domain of glucosidase I contains ER targeting information but is not required absolutely for ER localization.
Hardt B; Kalz-Fuller B; Aparicio R; Volker C; Bause E
Glycobiology; 2003 Mar; 13(3):159-68. PubMed ID: 12626409
[TBL] [Abstract][Full Text] [Related]
19. Molecular mechanisms of subcellular localization of ABCG5 and ABCG8.
Hirata T; Okabe M; Kobayashi A; Ueda K; Matsuo M
Biosci Biotechnol Biochem; 2009 Mar; 73(3):619-26. PubMed ID: 19270375
[TBL] [Abstract][Full Text] [Related]
20. Routes to and from the plasma membrane: bulk flow versus signal mediated endocytosis.
Gershlick DC; Lousa Cde M; Farmer L; Denecke J
Plant Signal Behav; 2014; 9(10):e972813. PubMed ID: 25482763
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]