155 related articles for article (PubMed ID: 16934032)
1. 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]
2. 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]
3. 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]
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. Small peptides derived from the Lys active fragment of the mung bean trypsin inhibitor are fully active against trypsin.
Qi RF; Liu ZX; Xu SQ; Zhang L; Shao XX; Chi CW
FEBS J; 2010 Jan; 277(1):224-32. PubMed ID: 19954491
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Engineering a Constrained Peptidic Scaffold towards Potent and Selective Furin Inhibitors.
Fittler H; Depp A; Avrutina O; Dahms SO; Than ME; Empting M; Kolmar H
Chembiochem; 2015 Nov; 16(17):2441-4. PubMed ID: 26426719
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. Studies on an artificial trypsin inhibitor peptide derived from the mung bean trypsin inhibitor: chemical synthesis, refolding, and crystallographic analysis of its complex with trypsin.
Li Y; Huang Q; Zhang S; Liu S; Chi C; Tang Y
J Biochem; 1994 Jul; 116(1):18-25. PubMed ID: 7798176
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. 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]
14. Mapping the binding site of tissue kallikrein: preparation and testing of all possible substrate analog inhibitors homologous with the sequence of kininogen between Ser386 and Gln392.
Deshpande MS; Burton J
J Med Chem; 1992 Aug; 35(17):3094-102. PubMed ID: 1507198
[TBL] [Abstract][Full Text] [Related]
15. Two engineered eglin c mutants potently and selectively inhibiting kexin or furin.
Liu ZX; Fei H; Chi CW
FEBS Lett; 2004 Jan; 556(1-3):116-20. PubMed ID: 14706837
[TBL] [Abstract][Full Text] [Related]
16. Chemical replacement of P1' arginine residue at the first reactive site of peanut protease inhibitor B-III.
Kurokawa T; Hara S; Norioka S; Teshima T; Ikenaka T
J Biochem; 1987 Mar; 101(3):723-8. PubMed ID: 3597350
[TBL] [Abstract][Full Text] [Related]
17. Complete amino acid sequence of mung bean trypsin inhibitor.
Zhang Y; Luo S; Tan F; Qi Z; Xu L; Zhang A
Sci Sin B; 1982 Mar; 25(3):268-77. PubMed ID: 6125033
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. [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]
20. Effects of amino acid replacements around the reactive site of chicken ovomucoid domain 3 on the inhibitory activity toward chymotrypsin and trypsin.
Kojima S; Takagi N; Minagawa T; Fushimi N; Miura KI
Protein Eng; 1999 Oct; 12(10):857-62. PubMed ID: 10556246
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]