C M Jung, O Matsushita, S Katayama, J Minami, J Sakurai, A Okabe. J Bacteriol 1999
Times Cited: 53
Times Cited: 53
Times Cited
Times Co-cited
Similarity
A study of the collagen-binding domain of a 116-kDa Clostridium histolyticum collagenase.
O Matsushita, C M Jung, J Minami, S Katayama, N Nishi, A Okabe. J Biol Chem 1998
O Matsushita, C M Jung, J Minami, S Katayama, N Nishi, A Okabe. J Biol Chem 1998
47
Characterization of the individual collagenases from Clostridium histolyticum.
M D Bond, H E Van Wart. Biochemistry 1984
M D Bond, H E Van Wart. Biochemistry 1984
43
Gene duplication and multiplicity of collagenases in Clostridium histolyticum.
O Matsushita, C M Jung, S Katayama, J Minami, Y Takahashi, A Okabe. J Bacteriol 1999
O Matsushita, C M Jung, S Katayama, J Minami, Y Takahashi, A Okabe. J Bacteriol 1999
43
Purification and separation of individual collagenases of Clostridium histolyticum using red dye ligand chromatography.
M D Bond, H E Van Wart. Biochemistry 1984
M D Bond, H E Van Wart. Biochemistry 1984
39
A continuous spectrophotometric assay for Clostridium histolyticum collagenase.
H E Van Wart, D R Steinbrink. Anal Biochem 1981
H E Van Wart, D R Steinbrink. Anal Biochem 1981
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Matrix metalloproteinase inhibitors in arthritis.
K M Bottomley, W H Johnson, D S Walter. J Enzyme Inhib 1998
K M Bottomley, W H Johnson, D S Walter. J Enzyme Inhib 1998
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24
Substrate recognition by the collagen-binding domain of Clostridium histolyticum class I collagenase.
O Matsushita, T Koide, R Kobayashi, K Nagata, A Okabe. J Biol Chem 2001
O Matsushita, T Koide, R Kobayashi, K Nagata, A Okabe. J Biol Chem 2001
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Molecular Recognition of Proteinminus signLigand Complexes: Applications to Drug Design.
Robert E. Babine, Steven L. Bender. Chem Rev 1997
Robert E. Babine, Steven L. Bender. Chem Rev 1997
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A bacterial collagen-binding domain with novel calcium-binding motif controls domain orientation.
Jeffrey J Wilson, Osamu Matsushita, Akinobu Okabe, Joshua Sakon. EMBO J 2003
Jeffrey J Wilson, Osamu Matsushita, Akinobu Okabe, Joshua Sakon. EMBO J 2003
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Sulfonamide-based hydroxamic acids as potent inhibitors of mouse macrophage metalloelastase.
A Y Jeng, M Chou, D T Parker. Bioorg Med Chem Lett 1998
A Y Jeng, M Chou, D T Parker. Bioorg Med Chem Lett 1998
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Cloning and nucleotide sequence analysis of the colH gene from Clostridium histolyticum encoding a collagenase and a gelatinase.
K Yoshihara, O Matsushita, J Minami, A Okabe. J Bacteriol 1994
K Yoshihara, O Matsushita, J Minami, A Okabe. J Bacteriol 1994
18
Purification and characterization of Clostridium perfringens 120-kilodalton collagenase and nucleotide sequence of the corresponding gene.
O Matsushita, K Yoshihara, S Katayama, J Minami, A Okabe. J Bacteriol 1994
O Matsushita, K Yoshihara, S Katayama, J Minami, A Okabe. J Bacteriol 1994
18
Structure determination and analysis of human neutrophil collagenase complexed with a hydroxamate inhibitor.
F Grams, M Crimmin, L Hinnes, P Huxley, M Pieper, H Tschesche, W Bode. Biochemistry 1995
F Grams, M Crimmin, L Hinnes, P Huxley, M Pieper, H Tschesche, W Bode. Biochemistry 1995
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X-ray structures of human neutrophil collagenase complexed with peptide hydroxamate and peptide thiol inhibitors. Implications for substrate binding and rational drug design.
F Grams, P Reinemer, J C Powers, T Kleine, M Pieper, H Tschesche, R Huber, W Bode. Eur J Biochem 1995
F Grams, P Reinemer, J C Powers, T Kleine, M Pieper, H Tschesche, R Huber, W Bode. Eur J Biochem 1995
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Design and therapeutic application of matrix metalloproteinase inhibitors.
M Whittaker, C D Floyd, P Brown, A J Gearing. Chem Rev 1999
M Whittaker, C D Floyd, P Brown, A J Gearing. Chem Rev 1999
16
Protease inhibitors. Part 8: synthesis of potent Clostridium histolyticum collagenase inhibitors incorporating sulfonylated L-alanine hydroxamate moieties.
A Scozzafava, C T Supuran. Bioorg Med Chem 2000
A Scozzafava, C T Supuran. Bioorg Med Chem 2000
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Protease inhibitors: synthesis of potent bacterial collagenase and matrix metalloproteinase inhibitors incorporating N-4-nitrobenzylsulfonylglycine hydroxamate moieties.
A Scozzafava, C T Supuran. J Med Chem 2000
A Scozzafava, C T Supuran. J Med Chem 2000
19
Clostridial hydrolytic enzymes degrading extracellular components.
O Matsushita, A Okabe. Toxicon 2001
O Matsushita, A Okabe. Toxicon 2001
16
Aldehyde and ketone substrate analogues inhibit the collagenase of Clostridium histolyticum.
D Grobelny, R E Galardy. Biochemistry 1985
D Grobelny, R E Galardy. Biochemistry 1985
53
Carbonic anhydrase inhibitors. Arylsulfonylureido- and arylureido-substituted aromatic and heterocyclic sulfonamides: towards selective inhibitors of carbonic anhydrase isozyme I.
A Scozzafava, C T Supuran. J Enzyme Inhib 1999
A Scozzafava, C T Supuran. J Enzyme Inhib 1999
15
Hydroxamate derivatives of substrate-analogous peptides containing aminomalonic acid are potent inhibitors of matrix metalloproteinases.
D Krumme, H Wenzel, H Tschesche. FEBS Lett 1998
D Krumme, H Wenzel, H Tschesche. FEBS Lett 1998
47
Protease inhibitors: synthesis of clostridium histolyticum collagenase inhibitors incorporating sulfonyl-L-alanine hydroxamate moieties.
A Scozzafava, C T Supuran. Bioorg Med Chem Lett 2000
A Scozzafava, C T Supuran. Bioorg Med Chem Lett 2000
36
Carbonic anhydrase inhibitors. Synthesis of water-soluble, topically effective, intraocular pressure-lowering aromatic/heterocyclic sulfonamides containing cationic or anionic moieties: is the tail more important than the ring?
A Scozzafava, L Menabuoni, F Mincione, F Briganti, G Mincione, C T Supuran. J Med Chem 1999
A Scozzafava, L Menabuoni, F Mincione, F Briganti, G Mincione, C T Supuran. J Med Chem 1999
13
Picking the S1, S1' and S2' pockets of matrix metalloproteinases. A niche for potent acyclic sulfonamide inhibitors.
S Hanessian, S Bouzbouz, A Boudon, G C Tucker, D Peyroulan. Bioorg Med Chem Lett 1999
S Hanessian, S Bouzbouz, A Boudon, G C Tucker, D Peyroulan. Bioorg Med Chem Lett 1999
20
Discovery of CGS 27023A, a non-peptidic, potent, and orally active stromelysin inhibitor that blocks cartilage degradation in rabbits.
L J MacPherson, E K Bayburt, M P Capparelli, B J Carroll, R Goldstein, M R Justice, L Zhu, S Hu, R A Melton, L Fryer,[...]. J Med Chem 1997
L J MacPherson, E K Bayburt, M P Capparelli, B J Carroll, R Goldstein, M R Justice, L Zhu, S Hu, R A Melton, L Fryer,[...]. J Med Chem 1997
13
Protease inhibitors. Part 7. Inhibition of Clostridium histolyticum collagenase with sulfonylated derivatives of L-valine hydroxamate.
C T Supuran, A Scozzafava. Eur J Pharm Sci 2000
C T Supuran, A Scozzafava. Eur J Pharm Sci 2000
35
Protease inhibitors - part 5. Alkyl/arylsulfonyl- and arylsulfonylureido-/arylureido- glycine hydroxamate inhibitors of Clostridium histolyticum collagenase.
A Scozzafava, C T Supuran. Eur J Med Chem 2000
A Scozzafava, C T Supuran. Eur J Med Chem 2000
33
Clostridium histolyticum collagenases: a new look at some old enzymes.
K A Mookhtiar, H E Van Wart. Matrix Suppl 1992
K A Mookhtiar, H E Van Wart. Matrix Suppl 1992
13
Collagen-binding domain of a Clostridium histolyticum collagenase exhibits a broad substrate spectrum both in vitro and in vivo.
T Toyoshima, O Matsushita, J Minami, N Nishi, A Okabe, T Itano. Connect Tissue Res 2001
T Toyoshima, O Matsushita, J Minami, N Nishi, A Okabe, T Itano. Connect Tissue Res 2001
14
Biochemical characterization of the catalytic domains of three different Clostridial collagenases.
Ulrich Eckhard, Esther Schönauer, Paulina Ducka, Peter Briza, Dorota Nüss, Hans Brandstetter. Biol Chem 2009
Ulrich Eckhard, Esther Schönauer, Paulina Ducka, Peter Briza, Dorota Nüss, Hans Brandstetter. Biol Chem 2009
26
Carbonic anhydrase inhibitors: synthesis of water-soluble, aminoacyl/dipeptidyl sulfonamides possessing long-lasting intraocular pressure-lowering properties via the topical route.
A Scozzafava, F Briganti, G Mincione, L Menabuoni, F Mincione, C T Supuran. J Med Chem 1999
A Scozzafava, F Briganti, G Mincione, L Menabuoni, F Mincione, C T Supuran. J Med Chem 1999
11
Inhibition of membrane-type 1 matrix metalloproteinase by hydroxamate inhibitors: an examination of the subsite pocket.
M Yamamoto, H Tsujishita, N Hori, Y Ohishi, S Inoue, S Ikeda, Y Okada. J Med Chem 1998
M Yamamoto, H Tsujishita, N Hori, Y Ohishi, S Inoue, S Ikeda, Y Okada. J Med Chem 1998
11
Carbonic anhydrase inhibitors. Part 71. Synthesis and ocular pharmacology of a new class of water-soluble, topically effective intraocular pressure lowering sulfonamides incorporating picolinoyl moieties.
C T Supuran, A Scozzafava, L Menabuoni, F Mincione, F Briganti, G Mincione. Eur J Pharm Sci 1999
C T Supuran, A Scozzafava, L Menabuoni, F Mincione, F Briganti, G Mincione. Eur J Pharm Sci 1999
14
Carbonic anhydrase inhibitors: synthesis of water-soluble, topically effective intraocular pressure lowering aromatic/heterocyclic sulfonamides containing 8-quinoline-sulfonyl moieties: is the tail more important than the ring?
J Borras, A Scozzafava, L Menabuoni, F Mincione, F Briganti, G Mincione, C T Supuran. Bioorg Med Chem 1999
J Borras, A Scozzafava, L Menabuoni, F Mincione, F Briganti, G Mincione, C T Supuran. Bioorg Med Chem 1999
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Protease inhibitors: Synthesis of L-alanine hydroxamate sulfonylated derivatives as inhibitors of clostridium histolyticum collagenase.
C T Supuran, F Briganti, G Mincione, A Scozzafava. J Enzyme Inhib 2000
C T Supuran, F Briganti, G Mincione, A Scozzafava. J Enzyme Inhib 2000
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Protease inhibitors: current status and future prospects.
D Leung, G Abbenante, D P Fairlie. J Med Chem 2000
D Leung, G Abbenante, D P Fairlie. J Med Chem 2000
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[ON THE QUANTITATIVE DETERMINATION OF COLLAGENASE].
E WUENSCH, H G HEIDRICH. Hoppe Seylers Z Physiol Chem 1963
E WUENSCH, H G HEIDRICH. Hoppe Seylers Z Physiol Chem 1963
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Zinc coordination, function, and structure of zinc enzymes and other proteins.
B L Vallee, D S Auld. Biochemistry 1990
B L Vallee, D S Auld. Biochemistry 1990
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Crystallization and preliminary X-ray characterization of the catalytic domain of collagenase G from Clostridium histolyticum.
Ulrich Eckhard, Dorota Nüss, Paulina Ducka, Esther Schönauer, Hans Brandstetter. Acta Crystallogr Sect F Struct Biol Cryst Commun 2008
Ulrich Eckhard, Dorota Nüss, Paulina Ducka, Esther Schönauer, Hans Brandstetter. Acta Crystallogr Sect F Struct Biol Cryst Commun 2008
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Inhibition of Clostridium histolyticum collagenases by phosphonamide peptide inhibitors.
V Dive, A Yiotakis, A Nicolaou, F Toma. Eur J Biochem 1990
V Dive, A Yiotakis, A Nicolaou, F Toma. Eur J Biochem 1990
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Clostridium histolyticum collagenase: development of new thio ester, fluorogenic, and depsipeptide substrates and new inhibitors.
C F Vencill, D Rasnick, K V Crumley, N Nishino, J C Powers. Biochemistry 1985
C F Vencill, D Rasnick, K V Crumley, N Nishino, J C Powers. Biochemistry 1985
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The collagen shield as a collagenase inhibitor and clinical indicator of collagenase activity on the ocular surface.
W M Schiff, M G Speaker, S A McCormick. CLAO J 1992
W M Schiff, M G Speaker, S A McCormick. CLAO J 1992
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Inhibition of collagenase from Clostridium histolyticum by phosphoric and phosphonic amides.
R E Galardy, D Grobelny. Biochemistry 1983
R E Galardy, D Grobelny. Biochemistry 1983
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The collagen shield. A new vehicle for delivery of cyclosporin A to the eye.
J J Reidy, B M Gebhardt, H E Kaufman. Cornea 1990
J J Reidy, B M Gebhardt, H E Kaufman. Cornea 1990
10
Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.