218 related articles for article (PubMed ID: 8537176)
1. Peptidyl substrates containing unnatural amino acid at the P'1 position are potent inhibitors of prohormone convertases.
Basak A; Schmidt C; Ismail AA; Seidah NG; Chrétien M; Lazure C
Int J Pept Protein Res; 1995; 46(3-4):228-37. PubMed ID: 8537176
[TBL] [Abstract][Full Text] [Related]
2. Design and synthesis of novel inhibitors of prohormone convertases.
Basak A; Jean F; Seidah NG; Lazure C
Int J Pept Protein Res; 1994 Sep; 44(3):253-61. PubMed ID: 7822102
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Fluorescent peptidyl substrates as an aid in studying the substrate specificity of human prohormone convertase PC1 and human furin and designing a potent irreversible inhibitor.
Jean F; Boudreault A; Basak A; Seidah NG; Lazure C
J Biol Chem; 1995 Aug; 270(33):19225-31. PubMed ID: 7642593
[TBL] [Abstract][Full Text] [Related]
5. Identification of inhibitors of prohormone convertases 1 and 2 using a peptide combinatorial library.
Apletalina E; Appel J; Lamango NS; Houghten RA; Lindberg I
J Biol Chem; 1998 Oct; 273(41):26589-95. PubMed ID: 9756897
[TBL] [Abstract][Full Text] [Related]
6. The specificity of carboxypeptidase Y may be altered by changing the hydrophobicity of the S'1 binding pocket.
Sørensen SB; Breddam K
Protein Sci; 1997 Oct; 6(10):2227-32. PubMed ID: 9336845
[TBL] [Abstract][Full Text] [Related]
7. Enzymic characterization in vitro of recombinant proprotein convertase PC4.
Basak A; Touré BB; Lazure C; Mbikay M; Chrétien M; Seidah NG
Biochem J; 1999 Oct; 343 Pt 1(Pt 1):29-37. PubMed ID: 10493908
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. 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]
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. Purification and characteristics of the candidate prohormone processing proteases PC2 and PC1/3 from bovine adrenal medulla chromaffin granules.
Azaryan AV; Krieger TJ; Hook VY
J Biol Chem; 1995 Apr; 270(14):8201-8. PubMed ID: 7713926
[TBL] [Abstract][Full Text] [Related]
13. Specificity of the dynorphin-processing endoprotease: comparison with prohormone convertases.
Berman Y; Juliano L; Devi LA
J Neurochem; 1999 May; 72(5):2120-6. PubMed ID: 10217293
[TBL] [Abstract][Full Text] [Related]
14. In vitro cleavage of internally quenched fluorogenic human proparathyroid hormone and proparathyroid-related peptide substrates by furin. Generation of a potent inhibitor.
Lazure C; Gauthier D; Jean F; Boudreault A; Seidah NG; Bennett HP; Hendy GN
J Biol Chem; 1998 Apr; 273(15):8572-80. PubMed ID: 9535830
[TBL] [Abstract][Full Text] [Related]
15. The specificity of clostripain from Clostridium histolyticum. Mapping the S' subsites via acyl transfer to amino acid amides and peptides.
Ullmann D; Jakubke HD
Eur J Biochem; 1994 Aug; 223(3):865-72. PubMed ID: 8055964
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Role of amino acid sequences flanking dibasic cleavage sites in precursor proteolytic processing. The importance of the first residue C-terminal of the cleavage site.
Rholam M; Brakch N; Germain D; Thomas DY; Fahy C; Boussetta H; Boileau G; Cohen P
Eur J Biochem; 1995 Feb; 227(3):707-14. PubMed ID: 7867629
[TBL] [Abstract][Full Text] [Related]
18. Role of prohormone convertases in pro-neuropeptide Y processing: coexpression and in vitro kinetic investigations.
Brakch N; Rist B; Beck-Sickinger AG; Goenaga J; Wittek R; Bürger E; Brunner HR; Grouzmann E
Biochemistry; 1997 Dec; 36(51):16309-20. PubMed ID: 9405066
[TBL] [Abstract][Full Text] [Related]
19. Characterization of the substrate specificity of the major cysteine protease (cruzipain) from Trypanosoma cruzi using a portion-mixing combinatorial library and fluorogenic peptides.
Nery ED; Juliano MA; Meldal M; Svendsen I; Scharfstein J; Walmsley A; Juliano L
Biochem J; 1997 Apr; 323 ( Pt 2)(Pt 2):427-33. PubMed ID: 9163334
[TBL] [Abstract][Full Text] [Related]
20. Application of the multiple antigenic peptides (MAP) strategy to the production of prohormone convertases antibodies: synthesis, characterization and use of 8-branched immunogenic peptides.
Basak A; Boudreault A; Chen A; Chrétien M; Seidah NG; Lazure C
J Pept Sci; 1995; 1(6):385-95. PubMed ID: 9223018
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
