295 related articles for article (PubMed ID: 8484716)
1. A novel N-terminal motif for palmitoylation of G-protein alpha subunits.
Parenti M; Viganó MA; Newman CM; Milligan G; Magee AI
Biochem J; 1993 Apr; 291 ( Pt 2)(Pt 2):349-53. PubMed ID: 8484716
[TBL] [Abstract][Full Text] [Related]
2. N-terminal fatty acylation of the alpha-subunit of the G-protein Gi1: only the myristoylated protein is a substrate for palmitoylation.
Galbiati F; Guzzi F; Magee AI; Milligan G; Parenti M
Biochem J; 1994 Nov; 303 ( Pt 3)(Pt 3):697-700. PubMed ID: 7980434
[TBL] [Abstract][Full Text] [Related]
3. Lipid modifications of G proteins: alpha subunits are palmitoylated.
Linder ME; Middleton P; Hepler JR; Taussig R; Gilman AG; Mumby SM
Proc Natl Acad Sci U S A; 1993 Apr; 90(8):3675-9. PubMed ID: 8475115
[TBL] [Abstract][Full Text] [Related]
4. Receptor regulation of G-protein palmitoylation.
Mumby SM; Kleuss C; Gilman AG
Proc Natl Acad Sci U S A; 1994 Mar; 91(7):2800-4. PubMed ID: 8146194
[TBL] [Abstract][Full Text] [Related]
5. Mutagenesis of palmitoylation sites in endothelial nitric oxide synthase identifies a novel motif for dual acylation and subcellular targeting.
Robinson LJ; Michel T
Proc Natl Acad Sci U S A; 1995 Dec; 92(25):11776-80. PubMed ID: 8524847
[TBL] [Abstract][Full Text] [Related]
6. The alpha-subunits of G-proteins G12 and G13 are palmitoylated, but not amidically myristoylated.
Veit M; Nürnberg B; Spicher K; Harteneck C; Ponimaskin E; Schultz G; Schmidt MF
FEBS Lett; 1994 Feb; 339(1-2):160-4. PubMed ID: 8313967
[TBL] [Abstract][Full Text] [Related]
7. Met-Gly-Cys motif from G-protein alpha subunit cannot direct palmitoylation when fused to heterologous protein.
Utsumi T; Tou E; Takemura D; Ishisaka R; Yabuki M; Iwata H
Arch Biochem Biophys; 1998 Jan; 349(2):216-24. PubMed ID: 9448708
[TBL] [Abstract][Full Text] [Related]
8. Palmitoylation of multiple Src-family kinases at a homologous N-terminal motif.
Koegl M; Zlatkine P; Ley SC; Courtneidge SA; Magee AI
Biochem J; 1994 Nov; 303 ( Pt 3)(Pt 3):749-53. PubMed ID: 7980442
[TBL] [Abstract][Full Text] [Related]
9. Palmitoylation of a G protein alpha i subunit requires membrane localization not myristoylation.
Degtyarev MY; Spiegel AM; Jones TL
J Biol Chem; 1994 Dec; 269(49):30898-903. PubMed ID: 7983022
[TBL] [Abstract][Full Text] [Related]
10. The role of palmitoylation of the guanine nucleotide binding protein G11 alpha in defining interaction with the plasma membrane.
McCallum JF; Wise A; Grassie MA; Magee AI; Guzzi F; Parenti M; Milligan G
Biochem J; 1995 Sep; 310 ( Pt 3)(Pt 3):1021-7. PubMed ID: 7575398
[TBL] [Abstract][Full Text] [Related]
11. N-terminally myristoylated Ras proteins require palmitoylation or a polybasic domain for plasma membrane localization.
Cadwallader KA; Paterson H; Macdonald SG; Hancock JF
Mol Cell Biol; 1994 Jul; 14(7):4722-30. PubMed ID: 8007974
[TBL] [Abstract][Full Text] [Related]
12. Biosynthesis and palmitoylation of endothelial nitric oxide synthase: mutagenesis of palmitoylation sites, cysteines-15 and/or -26, argues against depalmitoylation-induced translocation of the enzyme.
Liu J; García-Cardeña G; Sessa WC
Biochemistry; 1995 Sep; 34(38):12333-40. PubMed ID: 7547976
[TBL] [Abstract][Full Text] [Related]
13. Chemical inhibition of myristoylation of the G-protein Gi1 alpha by 2-hydroxymyristate does not interfere with its palmitoylation or membrane association. Evidence that palmitoylation, but not myristoylation, regulates membrane attachment.
Galbiati F; Guzzi F; Magee AI; Milligan G; Parenti M
Biochem J; 1996 Feb; 313 ( Pt 3)(Pt 3):717-20. PubMed ID: 8611146
[TBL] [Abstract][Full Text] [Related]
14. Lack of N terminal palmitoylation of G protein alpha subunits reduces membrane association.
Grassie MA; McCallum JF; Parenti M; Magee AI; Milligan G
Biochem Soc Trans; 1993 Nov; 21(4):499S. PubMed ID: 8132066
[No Abstract] [Full Text] [Related]
15. Mutations of the alpha 2A-adrenergic receptor that eliminate detectable palmitoylation do not perturb receptor-G-protein coupling.
Kennedy ME; Limbird LE
J Biol Chem; 1993 Apr; 268(11):8003-11. PubMed ID: 8385131
[TBL] [Abstract][Full Text] [Related]
16. Interaction with Gbetagamma is required for membrane targeting and palmitoylation of Galpha(s) and Galpha(q).
Evanko DS; Thiyagarajan MM; Wedegaertner PB
J Biol Chem; 2000 Jan; 275(2):1327-36. PubMed ID: 10625681
[TBL] [Abstract][Full Text] [Related]
17. The G protein alpha s subunit incorporates [3H]palmitic acid and mutation of cysteine-3 prevents this modification.
Degtyarev MY; Spiegel AM; Jones TL
Biochemistry; 1993 Aug; 32(32):8057-61. PubMed ID: 8347607
[TBL] [Abstract][Full Text] [Related]
18. Palmitoylation of G-protein alpha subunits.
Linder ME; Kleuss C; Mumby SM
Methods Enzymol; 1995; 250():314-30. PubMed ID: 7651161
[No Abstract] [Full Text] [Related]
19. Rapid plasma membrane anchoring of newly synthesized p59fyn: selective requirement for NH2-terminal myristoylation and palmitoylation at cysteine-3.
van't Hof W; Resh MD
J Cell Biol; 1997 Mar; 136(5):1023-35. PubMed ID: 9060467
[TBL] [Abstract][Full Text] [Related]
20. Targeting of a G alpha subunit (Gi1 alpha) and c-Src tyrosine kinase to caveolae membranes: clarifying the role of N-myristoylation.
Song KS; Sargiacomo M; Galbiati F; Parenti M; Lisanti MP
Cell Mol Biol (Noisy-le-grand); 1997 May; 43(3):293-303. PubMed ID: 9193783
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]