Search research articles
Contact Us
Filters
Showing results (181-190 of 239) with videos related to
Page
of 24
Sort By:
Proteins
|
July 9, 1999
Differences in the effects of TFE on the folding pathways of human stefins A and B
E Zerovnik, R Virden, R Jerala, et al.
Proteins
|
August 26, 1998
On the mechanism of human stefin B folding: II. Folding from GuHCl unfolded, TFE denatured, acid denatured, and acid intermediate states
E Zerovnik, R Jerala, R Virden, et al.
Journal of Cellular Biochemistry
|
January 1, 1986
Viral therapy: prospects for protease inhibitors
B D Korant, T Towatari, L Ivanoff, et al.
The Journal of Biological Chemistry
|
April 5, 1993
Bovine stefin C, a new member of the stefin family
B Turk, I Krizaj, B Kralj, et al.
Structure (London, England : 1993)
|
April 4, 2000
Crystal structure of cathepsin X: a flip-flop of the ring of His23 allows carboxy-monopeptidase and carboxy-dipeptidase activity of the protease
G Guncar, I Klemencic, B Turk, et al.
Biochemistry
|
May 1, 2001
Human recombinant pro-dipeptidyl peptidase I (cathepsin C) can be activated by cathepsins L and S but not by autocatalytic processing
S W Dahl, T Halkier, C Lauritzen, et al.
European Journal of Biochemistry
|
March 27, 1999
Acidic pH as a physiological regulator of human cathepsin L activity
B Turk, I Dolenc, B Lenarcic, et al.
FEBS Letters
|
August 14, 1995
Inhibition of cruzipain, the major cysteine proteinase of the protozoan parasite, Trypanosoma cruzi, by proteinase inhibitors of the cystatin superfamily
V Stoka, M Nycander, B Lenarcic, et al.
The EMBO Journal
|
June 1, 1990
The refined 2.4 A X-ray crystal structure of recombinant human stefin B in complex with the cysteine proteinase papain: a novel type of proteinase inhibitor interaction
M T Stubbs, B Laber, W Bode, et al.
European Journal of Biochemistry
|
November 1, 1994
Structural characterisation of human stefin A in solution and implications for binding to cysteine proteinases
J R Martin, R Jerala, L Kroon-Zitko, et al.
Page
of 24
Search research articles
Search
Showing results (181-190 of 239) with videos related to
Sort By:
Page
of 24
Proteins
|
July 9, 1999
Differences in the effects of TFE on the folding pathways of human stefins A and B
E Zerovnik, R Virden, R Jerala, et al.
Proteins
|
August 26, 1998
On the mechanism of human stefin B folding: II. Folding from GuHCl unfolded, TFE denatured, acid denatured, and acid intermediate states
E Zerovnik, R Jerala, R Virden, et al.
Journal of Cellular Biochemistry
|
January 1, 1986
Viral therapy: prospects for protease inhibitors
B D Korant, T Towatari, L Ivanoff, et al.
The Journal of Biological Chemistry
|
April 5, 1993
Bovine stefin C, a new member of the stefin family
B Turk, I Krizaj, B Kralj, et al.
Structure (London, England : 1993)
|
April 4, 2000
Crystal structure of cathepsin X: a flip-flop of the ring of His23 allows carboxy-monopeptidase and carboxy-dipeptidase activity of the protease
G Guncar, I Klemencic, B Turk, et al.
Biochemistry
|
May 1, 2001
Human recombinant pro-dipeptidyl peptidase I (cathepsin C) can be activated by cathepsins L and S but not by autocatalytic processing
S W Dahl, T Halkier, C Lauritzen, et al.
European Journal of Biochemistry
|
March 27, 1999
Acidic pH as a physiological regulator of human cathepsin L activity
B Turk, I Dolenc, B Lenarcic, et al.
FEBS Letters
|
August 14, 1995
Inhibition of cruzipain, the major cysteine proteinase of the protozoan parasite, Trypanosoma cruzi, by proteinase inhibitors of the cystatin superfamily
V Stoka, M Nycander, B Lenarcic, et al.
The EMBO Journal
|
June 1, 1990
The refined 2.4 A X-ray crystal structure of recombinant human stefin B in complex with the cysteine proteinase papain: a novel type of proteinase inhibitor interaction
M T Stubbs, B Laber, W Bode, et al.
European Journal of Biochemistry
|
November 1, 1994
Structural characterisation of human stefin A in solution and implications for binding to cysteine proteinases
J R Martin, R Jerala, L Kroon-Zitko, et al.
Page
of 24