T Zbyryt|J Otlewski - JoVE Visualize

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Biological Chemistry Hoppe-Seyler|January 1, 1991

Chemical synthesis of new trypsin, chymotrypsin and elastase inhibitors by amino-acid substitutions in a trypsin inhibitor from squash seeds (CMTI III)K Rolka, G Kupryszewski, U Ragnarsson, et al.

Biochimica Et Biophysica Acta|July 24, 1998

Specificity of human cathepsin GJ Polanowska, I Krokoszynska, H Czapinska, et al.

Biological Chemistry Hoppe-Seyler|May 1, 1989

Synthesis of an elastase inhibitor by monosubstitution of arginine-5 with valine at the reactive site in a trypsin inhibitor from squash seeds (CMTI III)K Rolka, G Kupryszewski, U Ragnarsson, et al.

Nature|October 29, 1992

Structure of hisactophilin is similar to interleukin-1 beta and fibroblast growth factorJ Habazettl, D Gondol, R Wiltscheck, et al.

Journal of Molecular Biology|May 26, 1999

Interscaffolding additivity: binding of P1 variants of bovine pancreatic trypsin inhibitor to four serine proteasesD Krowarsch, M Dadlez, O Buczek, et al.

Journal of Molecular Biology|August 5, 2000

Substitutions at the P(1) position in BPTI strongly affect the association energy with serine proteinasesA Grzesiak, R Helland, A O Smalås, et al.

Acta Biochimica Polonica|January 1, 1987

Protein inhibitors of trypsin from the seeds of Cucurbitaceae plantsA Polanowski, E Cieślar, J Otlewski, et al.

Biological Chemistry Hoppe-Seyler|September 1, 1993

Glycine-rich analogues of Cucurbita maxima trypsin inhibitor (CMTI-III) substituted by valine in position 27 display relatively low antitrypsin activityJ Rózycki, G Kupryszewski, K Rolka, et al.

Biochemistry|July 26, 1988

Tyrosine hydrogen-bonding and environmental effects in proteins probed by ultraviolet resonance Raman spectroscopyP G Hildebrandt, R A Copeland, T G Spiro, et al.

Hoppe-Seyler'S Zeitschrift Fur Physiologische Chemie|August 1, 1983

Structural differences between trypsin-inhibitors isolated from Cucurbitaceae family seeds: immunological, NMR and CD studiesA Szewczuk, E Kurowska, E Prusak, et al.

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Showing results (51-60 of 64) with videos related to

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Pageof 7

Biological Chemistry Hoppe-Seyler|January 1, 1991

Chemical synthesis of new trypsin, chymotrypsin and elastase inhibitors by amino-acid substitutions in a trypsin inhibitor from squash seeds (CMTI III)K Rolka, G Kupryszewski, U Ragnarsson, et al.

Biochimica Et Biophysica Acta|July 24, 1998

Specificity of human cathepsin GJ Polanowska, I Krokoszynska, H Czapinska, et al.

Biological Chemistry Hoppe-Seyler|May 1, 1989

Synthesis of an elastase inhibitor by monosubstitution of arginine-5 with valine at the reactive site in a trypsin inhibitor from squash seeds (CMTI III)K Rolka, G Kupryszewski, U Ragnarsson, et al.

Nature|October 29, 1992

Structure of hisactophilin is similar to interleukin-1 beta and fibroblast growth factorJ Habazettl, D Gondol, R Wiltscheck, et al.

Journal of Molecular Biology|May 26, 1999

Interscaffolding additivity: binding of P1 variants of bovine pancreatic trypsin inhibitor to four serine proteasesD Krowarsch, M Dadlez, O Buczek, et al.

Journal of Molecular Biology|August 5, 2000

Substitutions at the P(1) position in BPTI strongly affect the association energy with serine proteinasesA Grzesiak, R Helland, A O Smalås, et al.

Acta Biochimica Polonica|January 1, 1987

Protein inhibitors of trypsin from the seeds of Cucurbitaceae plantsA Polanowski, E Cieślar, J Otlewski, et al.

Biological Chemistry Hoppe-Seyler|September 1, 1993

Glycine-rich analogues of Cucurbita maxima trypsin inhibitor (CMTI-III) substituted by valine in position 27 display relatively low antitrypsin activityJ Rózycki, G Kupryszewski, K Rolka, et al.

Biochemistry|July 26, 1988

Tyrosine hydrogen-bonding and environmental effects in proteins probed by ultraviolet resonance Raman spectroscopyP G Hildebrandt, R A Copeland, T G Spiro, et al.

Hoppe-Seyler'S Zeitschrift Fur Physiologische Chemie|August 1, 1983

Structural differences between trypsin-inhibitors isolated from Cucurbitaceae family seeds: immunological, NMR and CD studiesA Szewczuk, E Kurowska, E Prusak, et al.

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