145 related articles for article (PubMed ID: 8428944)
1. Transformation of the signal peptide/membrane anchor domain of a type II transmembrane protein into a cleavable signal peptide.
Roy P; Chatellard C; Lemay G; Crine P; Boileau G
J Biol Chem; 1993 Feb; 268(4):2699-704. PubMed ID: 8428944
[TBL] [Abstract][Full Text] [Related]
2. Insertion of hydrophilic amino acid residues in the signal peptide/membrane anchor domain of neprilysin (neutral endopeptidase-24.11) results in its cleavage: role of the position of insertion.
Yang XF; Chatellard C; Lazure C; Crine P; Boileau G
Arch Biochem Biophys; 1994 Dec; 315(2):382-6. PubMed ID: 7986081
[TBL] [Abstract][Full Text] [Related]
3. Translocation of neutral endopeptidase 24.11 mutants with deletions of the NH2-terminal cytosolic domain.
Lemire I; Roy P; Boileau G
Biochem Cell Biol; 1994; 72(5-6):182-7. PubMed ID: 7840937
[TBL] [Abstract][Full Text] [Related]
4. Secretion of a type II integral membrane protein induced by mutation of the transmembrane segment.
Lemire I; Lazure C; Crine P; Boileau G
Biochem J; 1997 Feb; 322 ( Pt 1)(Pt 1):335-42. PubMed ID: 9078281
[TBL] [Abstract][Full Text] [Related]
5. Fusion of a cleavable signal peptide to the ectodomain of neutral endopeptidase (EC 3.4.24.11) results in the secretion of an active enzyme in COS-1 cells.
Lemay G; Waksman G; Roques BP; Crine P; Boileau G
J Biol Chem; 1989 Sep; 264(26):15620-3. PubMed ID: 2670943
[TBL] [Abstract][Full Text] [Related]
6. A cleavable N-terminal signal peptide is not a prerequisite for the biosynthesis of glycosylphosphatidylinositol-anchored proteins.
Howell S; Lanctôt C; Boileau G; Crine P
J Biol Chem; 1994 Jun; 269(25):16993-6. PubMed ID: 7516327
[TBL] [Abstract][Full Text] [Related]
7. Signal and membrane anchor functions overlap in the type II membrane protein I gamma CAT.
Lipp J; Dobberstein B
J Cell Biol; 1988 Jun; 106(6):1813-20. PubMed ID: 3290220
[TBL] [Abstract][Full Text] [Related]
8. The v-sis protein retains biological activity as a type II membrane protein when anchored by various signal-anchor domains, including the hydrophobic domain of the bovine papilloma virus E5 oncoprotein.
Xu YF; Meyer AN; Webster MK; Lee BA; Donoghue DJ
J Cell Biol; 1993 Nov; 123(3):549-60. PubMed ID: 8227125
[TBL] [Abstract][Full Text] [Related]
9. Residues flanking the COOH-terminal C-region of a model eukaryotic signal peptide influence the site of its cleavage by signal peptidase and the extent of coupling of its co-translational translocation and proteolytic processing in vitro.
Nothwehr SF; Hoeltzli SD; Allen KL; Lively MO; Gordon JI
J Biol Chem; 1990 Dec; 265(35):21797-803. PubMed ID: 2123875
[TBL] [Abstract][Full Text] [Related]
10. The nature of topogenic sequences determines the transport competence of topological mutants of neutral endopeptidase-24.11.
Yang XF; Crine P; Boileau G
Biochem J; 1995 Nov; 312 ( Pt 1)(Pt 1):99-105. PubMed ID: 7492341
[TBL] [Abstract][Full Text] [Related]
11. An amphiphilic lipid-binding domain influences the topology of a signal-anchor sequence in the mitochondrial outer membrane.
Steenaart NA; Silvius JR; Shore GC
Biochemistry; 1996 Mar; 35(12):3764-71. PubMed ID: 8619997
[TBL] [Abstract][Full Text] [Related]
12. A part of the transmembrane domain of pro-TNF can function as a cleavable signal sequence that generates a biologically active secretory form of TNF.
Ishisaka R; Sato N; Tanaka K; Takeshige T; Iwata H; Klostergaard J; Utsumi T
J Biochem; 1999 Aug; 126(2):413-20. PubMed ID: 10423538
[TBL] [Abstract][Full Text] [Related]
13. A nonfunctional sequence converted to a signal for glycophosphatidylinositol membrane anchor attachment.
Moran P; Caras IW
J Cell Biol; 1991 Oct; 115(2):329-36. PubMed ID: 1717483
[TBL] [Abstract][Full Text] [Related]
14. The signal anchor and stem regions of the beta-galactoside alpha 2,6-sialyltransferase may each act to localize the enzyme to the Golgi apparatus.
Colley KJ; Lee EU; Paulson JC
J Biol Chem; 1992 Apr; 267(11):7784-93. PubMed ID: 1560012
[TBL] [Abstract][Full Text] [Related]
15. The signal peptide of the G protein-coupled human endothelin B receptor is necessary for translocation of the N-terminal tail across the endoplasmic reticulum membrane.
Köchl R; Alken M; Rutz C; Krause G; Oksche A; Rosenthal W; Schülein R
J Biol Chem; 2002 May; 277(18):16131-8. PubMed ID: 11854280
[TBL] [Abstract][Full Text] [Related]
16. Structural features in the NH2-terminal region of a model eukaryotic signal peptide influence the site of its cleavage by signal peptidase.
Nothwehr SF; Gordon JI
J Biol Chem; 1990 Oct; 265(28):17202-8. PubMed ID: 2120214
[TBL] [Abstract][Full Text] [Related]
17. Deletion mutation in the signal anchor domain activates cleavage of the influenza virus neuraminidase, a type II transmembrane protein.
Hogue BG; Nayak DP
J Gen Virol; 1994 May; 75 ( Pt 5)():1015-22. PubMed ID: 8176363
[TBL] [Abstract][Full Text] [Related]
18. A tripartite structure of the signals that determine protein insertion into the endoplasmic reticulum membrane.
Haeuptle MT; Flint N; Gough NM; Dobberstein B
J Cell Biol; 1989 Apr; 108(4):1227-36. PubMed ID: 2784443
[TBL] [Abstract][Full Text] [Related]
19. Functional expression of bovine 17 alpha-hydroxylase in COS 1 cells is dependent upon the presence of an amino-terminal signal anchor sequence.
Clark BJ; Waterman MR
J Biol Chem; 1992 Dec; 267(34):24568-74. PubMed ID: 1447202
[TBL] [Abstract][Full Text] [Related]
20. Eukaryotic signal peptide structure/function relationships. Identification of conformational features which influence the site and efficiency of co-translational proteolytic processing by site-directed mutagenesis of human pre(delta pro)apolipoprotein A-II.
Nothwehr SF; Gordon JI
J Biol Chem; 1989 Mar; 264(7):3979-87. PubMed ID: 2537299
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
