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Journal Abstract Search
190 related items for PubMed ID: 2822391
1. A short amino-terminal segment of microsomal cytochrome P-450 functions both as an insertion signal and as a stop-transfer sequence. Sakaguchi M, Mihara K, Sato R. EMBO J; 1987 Aug; 6(8):2425-31. PubMed ID: 2822391 [Abstract] [Full Text] [Related]
2. Mitochondrial porin can be translocated across both endoplasmic reticulum and mitochondrial membranes. Sakaguchi M, Hachiya N, Mihara K, Omura T. J Biochem; 1992 Aug; 112(2):243-8. PubMed ID: 1328170 [Abstract] [Full Text] [Related]
3. Signal recognition particle is required for co-translational insertion of cytochrome P-450 into microsomal membranes. Sakaguchi M, Mihara K, Sato R. Proc Natl Acad Sci U S A; 1984 Jun; 81(11):3361-4. PubMed ID: 6587354 [Abstract] [Full Text] [Related]
4. The influenza hemagglutinin insertion signal is not cleaved and does not halt translocation when presented to the endoplasmic reticulum membrane as part of a translocating polypeptide. Finidori J, Rizzolo L, Gonzalez A, Kreibich G, Adesnik M, Sabatini DD. J Cell Biol; 1987 Jun; 104(6):1705-14. PubMed ID: 3294860 [Abstract] [Full Text] [Related]
5. The carboxy-terminal 10 amino acid residues of cytochrome b5 are necessary for its targeting to the endoplasmic reticulum. Mitoma J, Ito A. EMBO J; 1992 Nov; 11(11):4197-203. PubMed ID: 1396600 [Abstract] [Full Text] [Related]
6. Positive charges at the NH2 terminus convert the membrane-anchor signal peptide of cytochrome P-450 to a secretory signal peptide. Szczesna-Skorupa E, Browne N, Mead D, Kemper B. Proc Natl Acad Sci U S A; 1988 Feb; 85(3):738-42. PubMed ID: 3422456 [Abstract] [Full Text] [Related]
7. The membrane-interactive tail of cytochrome b(5) can function as a stop-transfer sequence in concert with a signal sequence to give inversion of protein topology in the endoplasmic reticulum. Kaderbhai MA, Morgan R, Kaderbhai NN. Arch Biochem Biophys; 2003 Apr 15; 412(2):259-66. PubMed ID: 12667490 [Abstract] [Full Text] [Related]
8. The amino-terminal structures that determine topological orientation of cytochrome P-450 in microsomal membrane. Sato T, Sakaguchi M, Mihara K, Omura T. EMBO J; 1990 Aug 15; 9(8):2391-7. PubMed ID: 2369895 [Abstract] [Full Text] [Related]
9. Cytochrome P-450 related to P-4504 from phenobarbital-treated rabbit liver: molecular cloning of cDNA and characterization of cytochrome P-450 obtained by its expression in yeast cells. Imai Y. J Biochem; 1987 May 15; 101(5):1129-39. PubMed ID: 2820951 [Abstract] [Full Text] [Related]
10. Signals for the incorporation and orientation of cytochrome P450 in the endoplasmic reticulum membrane. Monier S, Van Luc P, Kreibich G, Sabatini DD, Adesnik M. J Cell Biol; 1988 Aug 15; 107(2):457-70. PubMed ID: 3047140 [Abstract] [Full Text] [Related]
11. Truncations of a secretory protein define minimum lengths required for binding to signal recognition particle and translocation across the endoplasmic reticulum membrane. Okun MM, Eskridge EM, Shields D. J Biol Chem; 1990 May 05; 265(13):7478-84. PubMed ID: 2185250 [Abstract] [Full Text] [Related]
12. 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 05; 267(34):24568-74. PubMed ID: 1447202 [Abstract] [Full Text] [Related]
13. Reinitiation of protein translocation across the endoplasmic reticulum membrane for the topogenesis of multispanning membrane proteins. Kuroiwa T, Sakaguchi M, Omura T, Mihara K. J Biol Chem; 1996 Mar 15; 271(11):6423-8. PubMed ID: 8626442 [Abstract] [Full Text] [Related]
14. The cytoplasmic and N-terminal transmembrane domains of cytochrome P450 contain independent signals for retention in the endoplasmic reticulum. Szczesna-Skorupa E, Ahn K, Chen CD, Doray B, Kemper B. J Biol Chem; 1995 Oct 13; 270(41):24327-33. PubMed ID: 7592644 [Abstract] [Full Text] [Related]
15. Microheterogeneity in the major phenobarbital-inducible forms of rabbit liver microsomal cytochrome P-450 as revealed by nucleotide sequencing of cloned cDNAs. Komori M, Imai Y, Tsunasawa S, Sato R. Biochemistry; 1988 Jan 12; 27(1):73-80. PubMed ID: 2831964 [Abstract] [Full Text] [Related]
16. The carboxyl terminus of the membrane-binding domain of cytochrome b5 spans the bilayer of the endoplasmic reticulum. Vergères G, Ramsden J, Waskell L. J Biol Chem; 1995 Feb 17; 270(7):3414-22. PubMed ID: 7852428 [Abstract] [Full Text] [Related]
17. Isolation and sequence analysis of three cloned cDNAs for rabbit liver proteins that are related to rabbit cytochrome P-450 (form 2), the major phenobarbital-inducible form. Leighton JK, DeBrunner-Vossbrinck BA, Kemper B. Biochemistry; 1984 Jan 17; 23(2):204-10. PubMed ID: 6546520 [Abstract] [Full Text] [Related]
18. cDNA and derived amino acid sequence of ethanol-inducible rabbit liver cytochrome P-450 isozyme 3a (P-450ALC). Khani SC, Zaphiropoulos PG, Fujita VS, Porter TD, Koop DR, Coon MJ. Proc Natl Acad Sci U S A; 1987 Feb 17; 84(3):638-42. PubMed ID: 3027695 [Abstract] [Full Text] [Related]
19. The transmembrane region of microsomal cytochrome P450 identified as the endoplasmic reticulum retention signal. Murakami K, Mihara K, Omura T. J Biochem; 1994 Jul 17; 116(1):164-75. PubMed ID: 7798174 [Abstract] [Full Text] [Related]
20. NH2-terminal substitutions of basic amino acids induce translocation across the microsomal membrane and glycosylation of rabbit cytochrome P450IIC2. Szczesna-Skorupa E, Kemper B. J Cell Biol; 1989 Apr 17; 108(4):1237-43. PubMed ID: 2494191 [Abstract] [Full Text] [Related] Page: [Next] [New Search]