311 related articles for article (PubMed ID: 8007974)
1. 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]
2. Palmitoylation of either Cys-3 or Cys-5 is required for the biological activity of the Lck tyrosine protein kinase.
Yurchak LK; Sefton BM
Mol Cell Biol; 1995 Dec; 15(12):6914-22. PubMed ID: 8524258
[TBL] [Abstract][Full Text] [Related]
3. A polybasic domain or palmitoylation is required in addition to the CAAX motif to localize p21ras to the plasma membrane.
Hancock JF; Paterson H; Marshall CJ
Cell; 1990 Oct; 63(1):133-9. PubMed ID: 2208277
[TBL] [Abstract][Full Text] [Related]
4. Differential membrane localization of ERas and Rheb, two Ras-related proteins involved in the phosphatidylinositol 3-kinase/mTOR pathway.
Takahashi K; Nakagawa M; Young SG; Yamanaka S
J Biol Chem; 2005 Sep; 280(38):32768-74. PubMed ID: 16046393
[TBL] [Abstract][Full Text] [Related]
5. Membrane targeting of the nucleotide exchange factor Sos is sufficient for activating the Ras signaling pathway.
Aronheim A; Engelberg D; Li N; al-Alawi N; Schlessinger J; Karin M
Cell; 1994 Sep; 78(6):949-61. PubMed ID: 7923364
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. Amino-terminal palmitate or polybasic domain can provide required second signal to myristate for membrane binding of p56lck.
Kwong J; Lublin DM
Biochem Biophys Res Commun; 1995 Feb; 207(2):868-76. PubMed ID: 7864883
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Post-translational modification of H-Ras is required for activation of, but not for association with, B-Raf.
Okada T; Masuda T; Shinkai M; Kariya K; Kataoka T
J Biol Chem; 1996 Mar; 271(9):4671-8. PubMed ID: 8617731
[TBL] [Abstract][Full Text] [Related]
11. Prenylation of Ras proteins is required for efficient hSOS1-promoted guanine nucleotide exchange.
Porfiri E; Evans T; Chardin P; Hancock JF
J Biol Chem; 1994 Sep; 269(36):22672-7. PubMed ID: 8077219
[TBL] [Abstract][Full Text] [Related]
12. Myristoylation and differential palmitoylation of the HCK protein-tyrosine kinases govern their attachment to membranes and association with caveolae.
Robbins SM; Quintrell NA; Bishop JM
Mol Cell Biol; 1995 Jul; 15(7):3507-15. PubMed ID: 7791757
[TBL] [Abstract][Full Text] [Related]
13. H-ras but not K-ras traffics to the plasma membrane through the exocytic pathway.
Apolloni A; Prior IA; Lindsay M; Parton RG; Hancock JF
Mol Cell Biol; 2000 Apr; 20(7):2475-87. PubMed ID: 10713171
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. Targeting proteins to membranes using signal sequences for lipid modification.
Solski PA; Quilliam LA; Coats SG; Der CJ; Buss JE
Methods Enzymol; 1995; 250():435-54. PubMed ID: 7651170
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. A polybasic domain allows nonprenylated Ras proteins to function in Saccharomyces cerevisiae.
Mitchell DA; Farh L; Marshall TK; Deschenes RJ
J Biol Chem; 1994 Aug; 269(34):21540-6. PubMed ID: 8063791
[TBL] [Abstract][Full Text] [Related]
19. Post-translational processing of purified human K-ras in Xenopus oocytes.
Kaplan JB; Sass PM
Cancer Commun; 1991; 3(12):383-8. PubMed ID: 16296004
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]