-
1
-
-
0036152532
-
Intraerythrocytic Plasmodium falciparum utilizes only a fraction of the amino acids derived from the digestion of host cell cytosol for the biosynthesis of its proteins
-
Krugliak M., Zhang J., Ginsburg H. Intraerythrocytic Plasmodium falciparum utilizes only a fraction of the amino acids derived from the digestion of host cell cytosol for the biosynthesis of its proteins. Mol Biochem Parasitol 2002, 119:249-256.
-
(2002)
Mol Biochem Parasitol
, vol.119
, pp. 249-256
-
-
Krugliak, M.1
Zhang, J.2
Ginsburg, H.3
-
2
-
-
0033560719
-
Inhibition of the peroxidative degradation of haem as the basis of action of chloroquine and other quinoline antimalarials
-
Loria P., Miller S., Foley M., Tilley L. Inhibition of the peroxidative degradation of haem as the basis of action of chloroquine and other quinoline antimalarials. Biochem J 1999, 339:363-370.
-
(1999)
Biochem J
, vol.339
, pp. 363-370
-
-
Loria, P.1
Miller, S.2
Foley, M.3
Tilley, L.4
-
4
-
-
0024208917
-
A malarial cysteine proteinase is necessary for hemoglobin degradation by Plasmodium falciparum
-
Rosenthal P.J., McKerrow J.H., Aikawa M., Nagasawa H., Leech J.H. A malarial cysteine proteinase is necessary for hemoglobin degradation by Plasmodium falciparum. J Clin Invest 1988, 82:1560-1566.
-
(1988)
J Clin Invest
, vol.82
, pp. 1560-1566
-
-
Rosenthal, P.J.1
McKerrow, J.H.2
Aikawa, M.3
Nagasawa, H.4
Leech, J.H.5
-
5
-
-
5644247394
-
A Plasmodium falciparum dipeptidyl aminopeptidase I participates in vacuolar hemoglobin degradation
-
Klemba M., Gluzman I., Goldberg D.E. A Plasmodium falciparum dipeptidyl aminopeptidase I participates in vacuolar hemoglobin degradation. J Biol Chem 2004, 279:43000-43007.
-
(2004)
J Biol Chem
, vol.279
, pp. 43000-43007
-
-
Klemba, M.1
Gluzman, I.2
Goldberg, D.E.3
-
6
-
-
37249008065
-
Roles for two aminopeptidases in vacuolar hemoglobin catabolism in Plasmodium falciparum
-
Dalal S., Klemba M. Roles for two aminopeptidases in vacuolar hemoglobin catabolism in Plasmodium falciparum. J Biol Chem 2007, 282:35978-35987.
-
(2007)
J Biol Chem
, vol.282
, pp. 35978-35987
-
-
Dalal, S.1
Klemba, M.2
-
7
-
-
39349098031
-
Chemically mapping protease pathways involved in the regulation of erythrocyte rupture by the human malaria parasite Plasmodium falciparum
-
Arastu-Kapur S., Ponder E.L., Fonovic U.P., et al. Chemically mapping protease pathways involved in the regulation of erythrocyte rupture by the human malaria parasite Plasmodium falciparum. Nat Chem Biol 2008, 4:203-213.
-
(2008)
Nat Chem Biol
, vol.4
, pp. 203-213
-
-
Arastu-Kapur, S.1
Ponder, E.L.2
Fonovic, U.P.3
-
8
-
-
0036168150
-
Dipeptidyl peptidase I activates neutrophil-derived serine proteases and regulates the development of acute experimental arthritis
-
Adkison A.M., Raptis S.Z., Kelley D.G., Pham C.T. Dipeptidyl peptidase I activates neutrophil-derived serine proteases and regulates the development of acute experimental arthritis. J Clin Invest 2002, 109:363-371.
-
(2002)
J Clin Invest
, vol.109
, pp. 363-371
-
-
Adkison, A.M.1
Raptis, S.Z.2
Kelley, D.G.3
Pham, C.T.4
-
9
-
-
0033587689
-
Dipeptidyl peptidase I is required for the processing and activation of granzymes A and B in vivo
-
Pham C.T., Ley T.J. Dipeptidyl peptidase I is required for the processing and activation of granzymes A and B in vivo. Proc Natl Acad Sci USA 1999, 96:8627-8632.
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, pp. 8627-8632
-
-
Pham, C.T.1
Ley, T.J.2
-
10
-
-
0035947568
-
Dipeptidyl peptidase I is essential for activation of mast cell chymases, but not tryptases, in mice
-
Wolters P.J., Pham C.T., Muilenburg D.J., Ley T.J., Caughey G.H. Dipeptidyl peptidase I is essential for activation of mast cell chymases, but not tryptases, in mice. J Biol Chem 2001, 276:18551-18556.
-
(2001)
J Biol Chem
, vol.276
, pp. 18551-18556
-
-
Wolters, P.J.1
Pham, C.T.2
Muilenburg, D.J.3
Ley, T.J.4
Caughey, G.H.5
-
11
-
-
33646829091
-
Dipeptidyl nitriles as human dipeptidyl peptidase I inhibitors
-
Bondebjerg J., Fuglsang H., Valeur K.R., Pedersen J., Naerum L. Dipeptidyl nitriles as human dipeptidyl peptidase I inhibitors. Bioorg Med Chem Lett 2006, 16:3614-3617.
-
(2006)
Bioorg Med Chem Lett
, vol.16
, pp. 3614-3617
-
-
Bondebjerg, J.1
Fuglsang, H.2
Valeur, K.R.3
Pedersen, J.4
Naerum, L.5
-
12
-
-
34547133013
-
Inhibition of the activation of multiple serine proteases with a cathepsin C inhibitor requires sustained exposure to prevent pro-enzyme processing
-
Methot N., Rubin J., Guay D., et al. Inhibition of the activation of multiple serine proteases with a cathepsin C inhibitor requires sustained exposure to prevent pro-enzyme processing. J Biol Chem 2007, 282:20836-20846.
-
(2007)
J Biol Chem
, vol.282
, pp. 20836-20846
-
-
Methot, N.1
Rubin, J.2
Guay, D.3
-
13
-
-
0035850917
-
Tetrameric dipeptidyl peptidase I directs substrate specificity by use of the residual pro-part domain
-
Olsen J.G., Kadziola A., Lauritzen C., Pedersen J., Larsen S., Dahl S.W. Tetrameric dipeptidyl peptidase I directs substrate specificity by use of the residual pro-part domain. FEBS Lett 2001, 506:201-206.
-
(2001)
FEBS Lett
, vol.506
, pp. 201-206
-
-
Olsen, J.G.1
Kadziola, A.2
Lauritzen, C.3
Pedersen, J.4
Larsen, S.5
Dahl, S.W.6
-
14
-
-
17944366493
-
Structure of human dipeptidyl peptidase I (cathepsin C): exclusion domain added to an endopeptidase framework creates the machine for activation of granular serine proteases
-
Turk D., Janjic V., Stern I., et al. Structure of human dipeptidyl peptidase I (cathepsin C): exclusion domain added to an endopeptidase framework creates the machine for activation of granular serine proteases. EMBO J 2001, 20:6570-6582.
-
(2001)
EMBO J
, vol.20
, pp. 6570-6582
-
-
Turk, D.1
Janjic, V.2
Stern, I.3
-
15
-
-
0014211618
-
On the size of the active site in proteases. I. Papain
-
Schechter I., Berger A. On the size of the active site in proteases. I. Papain. Biochem Biophys Res Commun 1967, 27:157-162.
-
(1967)
Biochem Biophys Res Commun
, vol.27
, pp. 157-162
-
-
Schechter, I.1
Berger, A.2
-
16
-
-
0037039894
-
Expedient solid-phase synthesis of fluorogenic protease substrates using the 7-amino-4-carbamoylmethylcoumarin (ACC) fluorophore
-
Maly D.J., Leonetti F., Backes B.J., et al. Expedient solid-phase synthesis of fluorogenic protease substrates using the 7-amino-4-carbamoylmethylcoumarin (ACC) fluorophore. J Org Chem 2002, 67:910-915.
-
(2002)
J Org Chem
, vol.67
, pp. 910-915
-
-
Maly, D.J.1
Leonetti, F.2
Backes, B.J.3
-
17
-
-
20444455128
-
Novel semicarbazide-derived inhibitors of human dipeptidyl peptidase I (hDPPI)
-
Bondebjerg J., Fuglsang H., Valeur K.R., et al. Novel semicarbazide-derived inhibitors of human dipeptidyl peptidase I (hDPPI). Bioorg Med Chem 2005, 13:4408-4424.
-
(2005)
Bioorg Med Chem
, vol.13
, pp. 4408-4424
-
-
Bondebjerg, J.1
Fuglsang, H.2
Valeur, K.R.3
-
18
-
-
0035711194
-
Tobacco etch virus protease: mechanism of autolysis and rational design of stable mutants with wild-type catalytic proficiency
-
Kapust R.B., Tozser J., Fox J.D., et al. Tobacco etch virus protease: mechanism of autolysis and rational design of stable mutants with wild-type catalytic proficiency. Protein Eng 2001, 14:993-1000.
-
(2001)
Protein Eng
, vol.14
, pp. 993-1000
-
-
Kapust, R.B.1
Tozser, J.2
Fox, J.D.3
-
19
-
-
0035852855
-
Human recombinant pro-dipeptidyl peptidase I (cathepsin C) can be activated by cathepsins L and S but not by autocatalytic processing
-
Dahl S.W., Halkier T., Lauritzen C., et al. Human recombinant pro-dipeptidyl peptidase I (cathepsin C) can be activated by cathepsins L and S but not by autocatalytic processing. Biochemistry 2001, 40:1671-1678.
-
(2001)
Biochemistry
, vol.40
, pp. 1671-1678
-
-
Dahl, S.W.1
Halkier, T.2
Lauritzen, C.3
-
20
-
-
0034608931
-
Rapid and general profiling of protease specificity by using combinatorial fluorogenic substrate libraries
-
Harris J.L., Backes B.J., Leonetti F., Mahrus S., Ellman J.A., Craik C.S. Rapid and general profiling of protease specificity by using combinatorial fluorogenic substrate libraries. Proc Natl Acad Sci USA 2000, 97:7754-7759.
-
(2000)
Proc Natl Acad Sci USA
, vol.97
, pp. 7754-7759
-
-
Harris, J.L.1
Backes, B.J.2
Leonetti, F.3
Mahrus, S.4
Ellman, J.A.5
Craik, C.S.6
-
21
-
-
77049143386
-
The determination of enzyme inhibitor constants
-
Dixon M. The determination of enzyme inhibitor constants. Biochem J 1953, 55:170-171.
-
(1953)
Biochem J
, vol.55
, pp. 170-171
-
-
Dixon, M.1
-
22
-
-
0020345697
-
Buffers of constant ionic strength for studying pH-dependent processes
-
Ellis K.J., Morrison J.F. Buffers of constant ionic strength for studying pH-dependent processes. Methods Enzymol 1982, 87:405-426.
-
(1982)
Methods Enzymol
, vol.87
, pp. 405-426
-
-
Ellis, K.J.1
Morrison, J.F.2
-
23
-
-
33846868622
-
The crystal structure of human dipeptidyl peptidase I (cathepsin C) in complex with the inhibitor Gly-Phe-CHN2
-
Molgaard A., Arnau J., Lauritzen C., Larsen S., Petersen G., Pedersen J. The crystal structure of human dipeptidyl peptidase I (cathepsin C) in complex with the inhibitor Gly-Phe-CHN2. Biochem J 2007, 401:645-650.
-
(2007)
Biochem J
, vol.401
, pp. 645-650
-
-
Molgaard, A.1
Arnau, J.2
Lauritzen, C.3
Larsen, S.4
Petersen, G.5
Pedersen, J.6
-
24
-
-
0347567036
-
Soluble expression of a functionally active Plasmodium falciparum falcipain-2 fused to maltose-binding protein in Escherichia coli
-
Goh L.L., Loke P., Singh M., Sim T.S. Soluble expression of a functionally active Plasmodium falciparum falcipain-2 fused to maltose-binding protein in Escherichia coli. Protein Expr Purif 2003, 32:194-201.
-
(2003)
Protein Expr Purif
, vol.32
, pp. 194-201
-
-
Goh, L.L.1
Loke, P.2
Singh, M.3
Sim, T.S.4
-
25
-
-
26944435574
-
Cysteine protease falcipain 1 in Plasmodium falciparum is biochemically distinct from its isozymes
-
Goh S.L., Goh L.L., Sim T.S. Cysteine protease falcipain 1 in Plasmodium falciparum is biochemically distinct from its isozymes. Parasitol Res 2005, 97:295-301.
-
(2005)
Parasitol Res
, vol.97
, pp. 295-301
-
-
Goh, S.L.1
Goh, L.L.2
Sim, T.S.3
-
26
-
-
0035983443
-
The P1' specificity of tobacco etch virus protease
-
Kapust R.B., Tozser J., Copeland T.D., Waugh D.S. The P1' specificity of tobacco etch virus protease. Biochem Biophys Res Commun 2002, 294:949-955.
-
(2002)
Biochem Biophys Res Commun
, vol.294
, pp. 949-955
-
-
Kapust, R.B.1
Tozser, J.2
Copeland, T.D.3
Waugh, D.S.4
-
27
-
-
0033598777
-
Efficient folding of proteins with multiple disulfide bonds in the Escherichia coli cytoplasm
-
Bessette P.H., Aslund F., Beckwith J., Georgiou G. Efficient folding of proteins with multiple disulfide bonds in the Escherichia coli cytoplasm. Proc Natl Acad Sci USA 1999, 96:13703-13708.
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, pp. 13703-13708
-
-
Bessette, P.H.1
Aslund, F.2
Beckwith, J.3
Georgiou, G.4
-
28
-
-
0032420423
-
Active recombinant rat dipeptidyl aminopeptidase I (cathepsin C) produced using the baculovirus expression system
-
Lauritzen C., Pedersen J., Madsen M.T., Justesen J., Martensen P.M., Dahl S.W. Active recombinant rat dipeptidyl aminopeptidase I (cathepsin C) produced using the baculovirus expression system. Protein Expr Purif 1998, 14:434-442.
-
(1998)
Protein Expr Purif
, vol.14
, pp. 434-442
-
-
Lauritzen, C.1
Pedersen, J.2
Madsen, M.T.3
Justesen, J.4
Martensen, P.M.5
Dahl, S.W.6
-
29
-
-
0014008946
-
Cathepsin C: a chloride-requiring enzyme
-
McDonald J.K., Reilly T.J., Zeitman B.B., Ellis S. Cathepsin C: a chloride-requiring enzyme. Biochem Biophys Res Commun 1966, 22:771-775.
-
(1966)
Biochem Biophys Res Commun
, vol.22
, pp. 771-775
-
-
McDonald, J.K.1
Reilly, T.J.2
Zeitman, B.B.3
Ellis, S.4
-
30
-
-
0014690532
-
New observations on the substrate specificity of cathepsin C (dipeptidyl aminopeptidase I). Including the degradation of beta-corticotropin and other peptide hormones
-
McDonald J.K., Zeitman B.B., Reilly T.J., Ellis S. New observations on the substrate specificity of cathepsin C (dipeptidyl aminopeptidase I). Including the degradation of beta-corticotropin and other peptide hormones. J Biol Chem 1969, 244:2693-2709.
-
(1969)
J Biol Chem
, vol.244
, pp. 2693-2709
-
-
McDonald, J.K.1
Zeitman, B.B.2
Reilly, T.J.3
Ellis, S.4
-
32
-
-
0029163155
-
Oligomeric structure and substrate induced inhibition of human cathepsin C
-
Dolenc I., Turk B., Pungercic G., Ritonja A., Turk V. Oligomeric structure and substrate induced inhibition of human cathepsin C. J Biol Chem 1995, 270:21626-21631.
-
(1995)
J Biol Chem
, vol.270
, pp. 21626-21631
-
-
Dolenc, I.1
Turk, B.2
Pungercic, G.3
Ritonja, A.4
Turk, V.5
-
33
-
-
18544391789
-
Interdependency of sequence and positional specificities for cysteine proteases of the papain family
-
Nagler D.K., Tam W., Storer A.C., Krupa J.C., Mort J.S., Menard R. Interdependency of sequence and positional specificities for cysteine proteases of the papain family. Biochemistry 1999, 38:4868-4874.
-
(1999)
Biochemistry
, vol.38
, pp. 4868-4874
-
-
Nagler, D.K.1
Tam, W.2
Storer, A.C.3
Krupa, J.C.4
Mort, J.S.5
Menard, R.6
-
34
-
-
49749085508
-
Chemical mechanism of a cysteine protease, cathepsin C, as revealed by integration of both steady-state and pre-steady-state solvent kinetic isotope effects
-
Schneck J.L., Villa J.P., McDevitt P., McQueney M.S., Thrall S.H., Meek T.D. Chemical mechanism of a cysteine protease, cathepsin C, as revealed by integration of both steady-state and pre-steady-state solvent kinetic isotope effects. Biochemistry 2008, 47:8697-8710.
-
(2008)
Biochemistry
, vol.47
, pp. 8697-8710
-
-
Schneck, J.L.1
Villa, J.P.2
McDevitt, P.3
McQueney, M.S.4
Thrall, S.H.5
Meek, T.D.6
-
35
-
-
0345528107
-
Drug resistance-associated pfCRT mutations confer decreased Plasmodium falciparum digestive vacuolar pH
-
Bennett T.N., Kosar A.D., Ursos L.M., et al. Drug resistance-associated pfCRT mutations confer decreased Plasmodium falciparum digestive vacuolar pH. Mol Biochem Parasitol 2004, 133:99-114.
-
(2004)
Mol Biochem Parasitol
, vol.133
, pp. 99-114
-
-
Bennett, T.N.1
Kosar, A.D.2
Ursos, L.M.3
-
36
-
-
35748956775
-
Evaluation of pH during cytostomal endocytosis and vacuolar catabolism of hemoglobin in Plasmodium falciparum
-
Klonis N., Tan O., Jackson K., Goldberg D., Klemba M., Tilley L. Evaluation of pH during cytostomal endocytosis and vacuolar catabolism of hemoglobin in Plasmodium falciparum. Biochem J 2007, 407:343-354.
-
(2007)
Biochem J
, vol.407
, pp. 343-354
-
-
Klonis, N.1
Tan, O.2
Jackson, K.3
Goldberg, D.4
Klemba, M.5
Tilley, L.6
-
37
-
-
0022347074
-
Antimalarials increase vesicle pH in Plasmodium falciparum
-
Krogstad D.J., Schlesinger P.H., Gluzman I.Y. Antimalarials increase vesicle pH in Plasmodium falciparum. J Cell Biol 1985, 101:2302-2309.
-
(1985)
J Cell Biol
, vol.101
, pp. 2302-2309
-
-
Krogstad, D.J.1
Schlesinger, P.H.2
Gluzman, I.Y.3
-
38
-
-
33947125517
-
Quantitative pH measurements in Plasmodium falciparum-infected erythrocytes using pHluorin
-
Kuhn Y., Rohrbach P., Lanzer M. Quantitative pH measurements in Plasmodium falciparum-infected erythrocytes using pHluorin. Cell Microbiol 2007, 9:1004-1013.
-
(2007)
Cell Microbiol
, vol.9
, pp. 1004-1013
-
-
Kuhn, Y.1
Rohrbach, P.2
Lanzer, M.3
-
39
-
-
0028674466
-
Catalytic mechanism in papain family of cysteine peptidases
-
Storer A.C., Menard R. Catalytic mechanism in papain family of cysteine peptidases. Methods Enzymol 1994, 244:486-500.
-
(1994)
Methods Enzymol
, vol.244
, pp. 486-500
-
-
Storer, A.C.1
Menard, R.2
-
41
-
-
0033568737
-
Location of the binding site for chloride ion activation of cathepsin C
-
Cigic B., Pain R.H. Location of the binding site for chloride ion activation of cathepsin C. Eur J Biochem 1999, 264:944-951.
-
(1999)
Eur J Biochem
, vol.264
, pp. 944-951
-
-
Cigic, B.1
Pain, R.H.2
-
43
-
-
0345310073
-
Revised definition of substrate binding sites of papain-like cysteine proteases
-
Turk D., Guncar G., Podobnik M., Turk B. Revised definition of substrate binding sites of papain-like cysteine proteases. Biol Chem 1998, 379:137-147.
-
(1998)
Biol Chem
, vol.379
, pp. 137-147
-
-
Turk, D.1
Guncar, G.2
Podobnik, M.3
Turk, B.4
-
44
-
-
77951137373
-
Positional scanning synthetic combinatorial libraries for substrate profiling
-
Schneider E.L., Craik C.S. Positional scanning synthetic combinatorial libraries for substrate profiling. Methods Mol Biol 2009, 539:59-78.
-
(2009)
Methods Mol Biol
, vol.539
, pp. 59-78
-
-
Schneider, E.L.1
Craik, C.S.2
-
45
-
-
0037964447
-
Catalytic properties and inhibition of proline-specific dipeptidyl peptidases II, IV and VII
-
Leiting B., Pryor K.D., Wu J.K., et al. Catalytic properties and inhibition of proline-specific dipeptidyl peptidases II, IV and VII. Biochem J 2003, 371:525-532.
-
(2003)
Biochem J
, vol.371
, pp. 525-532
-
-
Leiting, B.1
Pryor, K.D.2
Wu, J.K.3
-
46
-
-
0037099714
-
Dipeptidyl peptidase I: importance of progranzyme activation sequences, other dipeptide sequences, and the N-terminal amino group of synthetic substrates for enzyme activity
-
Tran T.V., Ellis K.A., Kam C.M., Hudig D., Powers J.C. Dipeptidyl peptidase I: importance of progranzyme activation sequences, other dipeptide sequences, and the N-terminal amino group of synthetic substrates for enzyme activity. Arch Biochem Biophys 2002, 403:160-170.
-
(2002)
Arch Biochem Biophys
, vol.403
, pp. 160-170
-
-
Tran, T.V.1
Ellis, K.A.2
Kam, C.M.3
Hudig, D.4
Powers, J.C.5
-
47
-
-
0026752536
-
Purification and characterization of dipeptidyl peptidase I from human spleen
-
McGuire M.J., Lipsky P.E., Thiele D.L. Purification and characterization of dipeptidyl peptidase I from human spleen. Arch Biochem Biophys 1992, 295:280-288.
-
(1992)
Arch Biochem Biophys
, vol.295
, pp. 280-288
-
-
McGuire, M.J.1
Lipsky, P.E.2
Thiele, D.L.3
-
48
-
-
0040043343
-
Stoichiometry and heterogeneity of the pro-region chain in tetrameric human cathepsin C
-
Cigic B., Krizaj I., Kralj B., Turk V., Pain R.H. Stoichiometry and heterogeneity of the pro-region chain in tetrameric human cathepsin C. Biochim Biophys Acta 1998, 1382:143-150.
-
(1998)
Biochim Biophys Acta
, vol.1382
, pp. 143-150
-
-
Cigic, B.1
Krizaj, I.2
Kralj, B.3
Turk, V.4
Pain, R.H.5
-
49
-
-
0034633884
-
The residual pro-part of cathepsin C fulfills the criteria required for an intramolecular chaperone in folding and stabilizing the human proenzyme
-
Cigic B., Dahl S.W., Pain R.H. The residual pro-part of cathepsin C fulfills the criteria required for an intramolecular chaperone in folding and stabilizing the human proenzyme. Biochemistry 2000, 39:12382-12390.
-
(2000)
Biochemistry
, vol.39
, pp. 12382-12390
-
-
Cigic, B.1
Dahl, S.W.2
Pain, R.H.3
-
50
-
-
33744961634
-
Substrate profiling of cysteine proteases using a combinatorial peptide library identifies functionally unique specificities
-
Choe Y., Leonetti F., Greenbaum D.C., et al. Substrate profiling of cysteine proteases using a combinatorial peptide library identifies functionally unique specificities. J Biol Chem 2006, 281:12824-12832.
-
(2006)
J Biol Chem
, vol.281
, pp. 12824-12832
-
-
Choe, Y.1
Leonetti, F.2
Greenbaum, D.C.3
-
51
-
-
65249125790
-
Hemoglobin cleavage site-specificity of the Plasmodium falciparum cysteine proteases falcipain-2 and falcipain-3
-
Subramanian S., Hardt M., Choe Y., et al. Hemoglobin cleavage site-specificity of the Plasmodium falciparum cysteine proteases falcipain-2 and falcipain-3. PLoS ONE 2009, 4:e5156.
-
(2009)
PLoS ONE
, vol.4
-
-
Subramanian, S.1
Hardt, M.2
Choe, Y.3
-
52
-
-
0028968184
-
Crystal structures of recombinant rat cathepsin B and a cathepsin B-inhibitor complex. Implications for structure-based inhibitor design
-
Jia Z., Hasnain S., Hirama T., et al. Crystal structures of recombinant rat cathepsin B and a cathepsin B-inhibitor complex. Implications for structure-based inhibitor design. J Biol Chem 1995, 270:5527-5533.
-
(1995)
J Biol Chem
, vol.270
, pp. 5527-5533
-
-
Jia, Z.1
Hasnain, S.2
Hirama, T.3
-
54
-
-
0033610853
-
The collagenolytic activity of cathepsin K is unique among mammalian proteinases
-
Garnero P., Borel O., Byrjalsen I., et al. The collagenolytic activity of cathepsin K is unique among mammalian proteinases. J Biol Chem 1998, 273:32347-32352.
-
(1998)
J Biol Chem
, vol.273
, pp. 32347-32352
-
-
Garnero, P.1
Borel, O.2
Byrjalsen, I.3
-
55
-
-
0037007965
-
Selective inhibition of the collagenolytic activity of human cathepsin K by altering its S2 subsite specificity
-
Lecaille F., Choe Y., Brandt W., Li Z., Craik C.S., Bromme D. Selective inhibition of the collagenolytic activity of human cathepsin K by altering its S2 subsite specificity. Biochemistry 2002, 41:8447-8454.
-
(2002)
Biochemistry
, vol.41
, pp. 8447-8454
-
-
Lecaille, F.1
Choe, Y.2
Brandt, W.3
Li, Z.4
Craik, C.S.5
Bromme, D.6
-
56
-
-
0028198939
-
Purification and characterisation of a second cathepsin L proteinase secreted by the parasitic trematode Fasciola hepatica
-
Dowd A.J., Smith A.M., McGonigle S., Dalton J.P. Purification and characterisation of a second cathepsin L proteinase secreted by the parasitic trematode Fasciola hepatica. Eur J Biochem 1994, 223:91-98.
-
(1994)
Eur J Biochem
, vol.223
, pp. 91-98
-
-
Dowd, A.J.1
Smith, A.M.2
McGonigle, S.3
Dalton, J.P.4
-
57
-
-
33947718470
-
The S2 subsites of cathepsins K and L and their contribution to collagen degradation
-
Lecaille F., Chowdhury S., Purisima E., Bromme D., Lalmanach G. The S2 subsites of cathepsins K and L and their contribution to collagen degradation. Protein Sci 2007, 16:662-670.
-
(2007)
Protein Sci
, vol.16
, pp. 662-670
-
-
Lecaille, F.1
Chowdhury, S.2
Purisima, E.3
Bromme, D.4
Lalmanach, G.5
-
58
-
-
77953301193
-
An acid-loading chloride transport pathway in the intraerythrocytic malaria parasite, Plasmodium falciparum
-
Henry R.I., Cobbold S.A., Allen R.J.W., et al. An acid-loading chloride transport pathway in the intraerythrocytic malaria parasite, Plasmodium falciparum. J Biol Chem 2010, 285:18615-18626.
-
(2010)
J Biol Chem
, vol.285
, pp. 18615-18626
-
-
Henry, R.I.1
Cobbold, S.A.2
Allen, R.J.W.3
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