157 related articles for article (PubMed ID: 18850049)
1. Design of peptide inhibitors for furin based on the C-terminal fragment of histone H1.2.
Wang S; Han J; Wang Y; Lu W; Chi C
Acta Biochim Biophys Sin (Shanghai); 2008 Oct; 40(10):848-54. PubMed ID: 18850049
[TBL] [Abstract][Full Text] [Related]
2. Template-assisted rational design of peptide inhibitors of furin using the lysine fragment of the mung bean trypsin inhibitor.
Tao H; Zhang Z; Shi J; Shao XX; Cui D; Chi CW
FEBS J; 2006 Sep; 273(17):3907-14. PubMed ID: 16934032
[TBL] [Abstract][Full Text] [Related]
3. The potent inhibitory activity of histone H1.2 C-terminal fragments on furin.
Han J; Zhang L; Shao X; Shi J; Chi C
FEBS J; 2006 Oct; 273(19):4459-69. PubMed ID: 16956366
[TBL] [Abstract][Full Text] [Related]
4. Histidine-rich human salivary peptides are inhibitors of proprotein convertases furin and PC7 but act as substrates for PC1.
Basak A; Ernst B; Brewer D; Seidah NG; Munzer JS; Lazure C; Lajoie GA
J Pept Res; 1997 Jun; 49(6):596-603. PubMed ID: 9266488
[TBL] [Abstract][Full Text] [Related]
5. Highly potent inhibitors of proprotein convertase furin as potential drugs for treatment of infectious diseases.
Becker GL; Lu Y; Hardes K; Strehlow B; Levesque C; Lindberg I; Sandvig K; Bakowsky U; Day R; Garten W; Steinmetzer T
J Biol Chem; 2012 Jun; 287(26):21992-2003. PubMed ID: 22539349
[TBL] [Abstract][Full Text] [Related]
6. Synthetic peptides derived from the prosegments of proprotein convertase 1/3 and furin are potent inhibitors of both enzymes.
Basak A; Lazure C
Biochem J; 2003 Jul; 373(Pt 1):231-9. PubMed ID: 12662153
[TBL] [Abstract][Full Text] [Related]
7. [Structure and properties of proprotein convertase inhibitors].
Kibirev VK; Osadchuk TV
Ukr Biokhim Zh (1999); 2012; 84(2):5-29. PubMed ID: 22642118
[TBL] [Abstract][Full Text] [Related]
8. Polyphenols with indirect proprotein convertase inhibitory activity.
Zhu J; Van de Ven W; Vermorken A
Int J Oncol; 2013 Sep; 43(3):947-55. PubMed ID: 23835774
[TBL] [Abstract][Full Text] [Related]
9. Barley serine proteinase inhibitor 2-derived cyclic peptides as potent and selective inhibitors of convertases PC1/3 and furin.
Villemure M; Fournier A; Gauthier D; Rabah N; Wilkes BC; Lazure C
Biochemistry; 2003 Aug; 42(32):9659-68. PubMed ID: 12911307
[TBL] [Abstract][Full Text] [Related]
10. Design, Synthesis, and Characterization of Macrocyclic Inhibitors of the Proprotein Convertase Furin.
Van Lam van T; Ivanova T; Hardes K; Heindl MR; Morty RE; Böttcher-Friebertshäuser E; Lindberg I; Than ME; Dahms SO; Steinmetzer T
ChemMedChem; 2019 Mar; 14(6):673-685. PubMed ID: 30680958
[TBL] [Abstract][Full Text] [Related]
11. An internally quenched fluorogenic substrate of prohormone convertase 1 and furin leads to a potent prohormone convertase inhibitor.
Jean F; Basak A; DiMaio J; Seidah NG; Lazure C
Biochem J; 1995 May; 307 ( Pt 3)(Pt 3):689-95. PubMed ID: 7741698
[TBL] [Abstract][Full Text] [Related]
12. [Furin and its biological role].
Kibirev VK; Osadchuk TV; Radavskiĭ IuL
Ukr Biokhim Zh (1999); 2007; 79(6):5-18. PubMed ID: 18712106
[TBL] [Abstract][Full Text] [Related]
13. Polyarginines are potent furin inhibitors.
Cameron A; Appel J; Houghten RA; Lindberg I
J Biol Chem; 2000 Nov; 275(47):36741-9. PubMed ID: 10958789
[TBL] [Abstract][Full Text] [Related]
14. A novel enediynyl peptide inhibitor of furin that blocks processing of proPDGF-A, B and proVEGF-C.
Basak A; Khatib AM; Mohottalage D; Basak S; Kolajova M; Bag SS; Basak A
PLoS One; 2009 Nov; 4(11):e7700. PubMed ID: 19956642
[TBL] [Abstract][Full Text] [Related]
15. Potent inhibitors of furin and furin-like proprotein convertases containing decarboxylated P1 arginine mimetics.
Becker GL; Sielaff F; Than ME; Lindberg I; Routhier S; Day R; Lu Y; Garten W; Steinmetzer T
J Med Chem; 2010 Feb; 53(3):1067-75. PubMed ID: 20038105
[TBL] [Abstract][Full Text] [Related]
16. Regulation of prohepcidin processing and activity by the subtilisin-like proprotein convertases Furin, PC5, PACE4 and PC7.
Scamuffa N; Basak A; Lalou C; Wargnier A; Marcinkiewicz J; Siegfried G; Chrétien M; Calvo F; Seidah NG; Khatib AM
Gut; 2008 Nov; 57(11):1573-82. PubMed ID: 18664504
[TBL] [Abstract][Full Text] [Related]
17. The SAAS granin exhibits structural and functional homology to 7B2 and contains a highly potent hexapeptide inhibitor of PC1.
Cameron A; Fortenberry Y; Lindberg I
FEBS Lett; 2000 May; 473(2):135-8. PubMed ID: 10812060
[TBL] [Abstract][Full Text] [Related]
18. Furin: a mammalian subtilisin/Kex2p-like endoprotease involved in processing of a wide variety of precursor proteins.
Nakayama K
Biochem J; 1997 Nov; 327 ( Pt 3)(Pt 3):625-35. PubMed ID: 9599222
[TBL] [Abstract][Full Text] [Related]
19. Short polybasic peptide sequences are potent inhibitors of PC5/6 and PC7: Use of positional scanning-synthetic peptide combinatorial libraries as a tool for the optimization of inhibitory sequences.
Fugere M; Appel J; Houghten RA; Lindberg I; Day R
Mol Pharmacol; 2007 Jan; 71(1):323-32. PubMed ID: 17012622
[TBL] [Abstract][Full Text] [Related]
20. Possible role of histone H1 in the regulation of furin-dependent proprotein processing.
Han J; Gu J; Chi C
Acta Biochim Biophys Sin (Shanghai); 2007 Mar; 39(3):173-80. PubMed ID: 17342255
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
