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Literature summary for 3.4.21.1 extracted from

  • Spink, E.; Cosgrove, S.; Rogers, L.; Hewage, C.; Malthouse, J.P.
    13C and 1H NMR studies of ionizations and hydrogen bonding in chymotrypsin-glyoxal inhibitor complexes (2007), J. Biol. Chem., 282, 7852-7861.
    View publication on PubMed

Inhibitors

Inhibitors Comment Organism Structure
benzyloxycarbonyl-Ala-Ala-Phe-glyoxal
-
Bos taurus
benzyloxycarbonyl-Ala-Pro-Phe-glyoxal
-
Bos taurus

Organism

Organism UniProt Comment Textmining
Bos taurus
-
-
-

Source Tissue

Source Tissue Comment Organism Textmining
pancreas
-
Bos taurus
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
N-succinyl-Ala-Ala-Pro-Phe-p-nitroanilide + H2O
-
Bos taurus N-succinyl-Ala-Ala-Pro-Phe + p-nitroaniline
-
?

Synonyms

Synonyms Comment Organism
alpha-chymotrypsin
-
Bos taurus

Ki Value [mM]

Ki Value [mM] Ki Value maximum [mM] Inhibitor Comment Organism Structure
0.019
-
benzyloxycarbonyl-Ala-Pro-Phe-glyoxal at pH 7.23 and 25°C Bos taurus
0.024
-
benzyloxycarbonyl-Ala-Pro-Phe-glyoxal at pH 7.17 and 25°C Bos taurus
0.344
-
benzyloxycarbonyl-Ala-Ala-Phe-glyoxal at 25°C Bos taurus