133 related articles for article (PubMed ID: 34560176)
1. Semysinthetic biflavonoid Morelloflavone-7,4',7″,3‴,4‴-penta-O-butanoyl is a more potent inhibitor of Proprotein Convertases Subtilisin/Kexin PC1/3 than Kex2 and Furin.
de Souza AA; de Andrade DM; Siqueira FDS; Di Iorio JF; Veloso MP; Coelho CM; Viegas Junior C; Gontijo VS; Dos Santos MH; Meneghetti MCZ; Nader HB; Tersariol ILDS; Juliano L; Juliano MA; Judice WAS
Biochim Biophys Acta Gen Subj; 2021 Dec; 1865(12):130016. PubMed ID: 34560176
[TBL] [Abstract][Full Text] [Related]
2. Structure and function of eukaryotic proprotein processing enzymes of the subtilisin family of serine proteases.
Van de Ven WJ; Roebroek AJ; Van Duijnhoven HL
Crit Rev Oncog; 1993; 4(2):115-36. PubMed ID: 8420571
[TBL] [Abstract][Full Text] [Related]
3. The Role of Proprotein Convertases in the Regulation of the Function of Immune Cells in the Oncoimmune Response.
Rose M; Duhamel M; Rodet F; Salzet M
Front Immunol; 2021; 12():667850. PubMed ID: 33995401
[TBL] [Abstract][Full Text] [Related]
4. Engineered eglin c variants inhibit yeast and human proprotein processing proteases, Kex2 and furin.
Komiyama T; Fuller RS
Biochemistry; 2000 Dec; 39(49):15156-65. PubMed ID: 11106495
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. Comparative study of the binding pockets of mammalian proprotein convertases and its implications for the design of specific small molecule inhibitors.
Tian S; Jianhua W
Int J Biol Sci; 2010 Feb; 6(1):89-95. PubMed ID: 20151049
[TBL] [Abstract][Full Text] [Related]
8. Prohormone-converting enzymes: regulation and evaluation of function using antisense RNA.
Bloomquist BT; Eipper BA; Mains RE
Mol Endocrinol; 1991 Dec; 5(12):2014-24. PubMed ID: 1791845
[TBL] [Abstract][Full Text] [Related]
9. Kainic acid increases the expression of the prohormone convertases furin and PC1 in the mouse hippocampus.
Meyer A; Chrétien P; Massicotte G; Sargent C; Chrétien M; Marcinkiewicz M
Brain Res; 1996 Sep; 732(1-2):121-32. PubMed ID: 8891276
[TBL] [Abstract][Full Text] [Related]
10. Propeptides are sufficient to regulate organelle-specific pH-dependent activation of furin and proprotein convertase 1/3.
Dillon SL; Williamson DM; Elferich J; Radler D; Joshi R; Thomas G; Shinde U
J Mol Biol; 2012 Oct; 423(1):47-62. PubMed ID: 22743102
[TBL] [Abstract][Full Text] [Related]
11. Proprotein convertase PC1/3-related peptides are potent slow tight-binding inhibitors of murine PC1/3 and Hfurin.
Boudreault A; Gauthier D; Lazure C
J Biol Chem; 1998 Nov; 273(47):31574-80. PubMed ID: 9813073
[TBL] [Abstract][Full Text] [Related]
12. Chromogranin A processing and secretion: specific role of endogenous and exogenous prohormone convertases in the regulated secretory pathway.
Eskeland NL; Zhou A; Dinh TQ; Wu H; Parmer RJ; Mains RE; O'Connor DT
J Clin Invest; 1996 Jul; 98(1):148-56. PubMed ID: 8690787
[TBL] [Abstract][Full Text] [Related]
13. Purification and characterization of the prohormone convertase PC1(PC3).
Zhou Y; Lindberg I
J Biol Chem; 1993 Mar; 268(8):5615-23. PubMed ID: 8449925
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. The family of subtilisin/kexin like pro-protein and pro-hormone convertases: divergent or shared functions.
Seidah NG; Chrétien M; Day R
Biochimie; 1994; 76(3-4):197-209. PubMed ID: 7819324
[TBL] [Abstract][Full Text] [Related]
16. Leishmanicidal, antiproteolytic and antioxidant evaluation of natural biflavonoids isolated from Garcinia brasiliensis and their semisynthetic derivatives.
Gontijo VS; Judice WA; Codonho B; Pereira IO; Assis DM; Januário JP; Caroselli EE; Juliano MA; de Carvalho Dosatti A; Marques MJ; Viegas Junior C; Henrique dos Santos M
Eur J Med Chem; 2012 Dec; 58():613-23. PubMed ID: 23178961
[TBL] [Abstract][Full Text] [Related]
17. Cloning and primary sequence of a mouse candidate prohormone convertase PC1 homologous to PC2, Furin, and Kex2: distinct chromosomal localization and messenger RNA distribution in brain and pituitary compared to PC2.
Seidah NG; Marcinkiewicz M; Benjannet S; Gaspar L; Beaubien G; Mattei MG; Lazure C; Mbikay M; Chrétien M
Mol Endocrinol; 1991 Jan; 5(1):111-22. PubMed ID: 2017186
[TBL] [Abstract][Full Text] [Related]
18. Proprotein convertase models based on the crystal structures of furin and kexin: explanation of their specificity.
Henrich S; Lindberg I; Bode W; Than ME
J Mol Biol; 2005 Jan; 345(2):211-27. PubMed ID: 15571716
[TBL] [Abstract][Full Text] [Related]
19. How Do Enveloped Viruses Exploit the Secretory Proprotein Convertases to Regulate Infectivity and Spread?
Seidah NG; Pasquato A; Andréo U
Viruses; 2021 Jun; 13(7):. PubMed ID: 34202098
[TBL] [Abstract][Full Text] [Related]
20. Interplay between S1 and S4 subsites in Kex2 protease: Kex2 exhibits dual specificity for the P4 side chain.
Rockwell NC; Fuller RS
Biochemistry; 1998 Mar; 37(10):3386-91. PubMed ID: 9521659
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
