Zobrazeno 1 - 6
of 6
pro vyhledávání: '"339"'
Autor:
Rachita Salkar, Lei Zeng, An-Qiang Sun, Shuhua Xu, Ming-Ming Zhou, Frederick J. Suchy, Sachchidanand
Publikováno v:
The Journal of biological chemistry. 278(6)
The rat ileal sodium-dependent bile acid transporter (Asbt) is a polytopic membrane glycoprotein, which is specifically expressed on the apical domain of the ileal brush-border membrane. In the present study, an essential 14-amino acid (aa 335-348) s
Autor:
Brian Bothner, Ting Liu, Edward A. Dratz, Algirdas J. Jesaitis, Connie I. Lord, Gal Keren-Aviram, Walid S. Maaty, Jeannie M. Gripentrog, Marcia H. Riesselman
Publikováno v:
The Journal of biological chemistry. 288(38)
Accumulation, activation, and control of neutrophils at inflammation sites is partly driven by N-formyl peptide chemoattractant receptors (FPRs). Occupancy of these G-protein-coupled receptors by formyl peptides has been shown to induce regulatory ph
Publikováno v:
The Journal of biological chemistry. 276(2)
The p53 tumor suppressor protein functions as an activator and also as a repressor of gene transcription. Currently, the mechanism of transcriptional repression by p53 remains poorly understood. To help clarify this mechanism, we carried out studies
Autor:
Jacques U. Baenziger, Jeremy J. Keusch, Stephen M. Manzella, Kwame Nyame, Richard D. Cummings
Publikováno v:
The Journal of biological chemistry. 275(33)
The large array of different glycolipids described in mammalian tissues is a reflection, in part, of diverse glycosyltransferase expression. Herein, we describe the cloning of a UDP-galactose: beta-d-galactosyl-1,4-glucosylceramide alpha-1, 3-galacto
Autor:
Anne S. Stone, J. Edwin Blalock, Stacie M. Propst, Elisabeth M. H. Ban, Robert D. LeBoeuf, Marino M. Green, J. David Tauber
Publikováno v:
The Journal of biological chemistry. 273(1)
Suppressin (SPN) is an inhibitor of cell proliferation that was originally identified and purified to homogeneity from bovine pituitaries (LeBoeuf, R. D., Burns, J. N., Bost, K. L., and Blalock, J. E. (1990) J. Biol. Chem. 265, 158-165). In this repo
Publikováno v:
Europe PubMed Central
Treatment of Ca2(+)-ATPase from sarcoplasmic reticulum with V8 protease from Staphylococcus aureus produced appreciable amounts of a Ca2(+)-ATPase fragment (p85) in the presence of Ca2+ (E1 conformation of the enzyme), along with many other peptide f