3.4.21.66: Thermitase
This is an abbreviated version!
For detailed information about Thermitase, go to the full flat file.
Word Map on EC 3.4.21.66
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3.4.21.66
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subtilisins
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3.4.21.14
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carlsberg
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subtilisin-like
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subtilases
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subtilisin-type
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eglin-c
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biotechnology
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analysis
- 3.4.21.66
- subtilisins
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3.4.21.14
-
carlsberg
-
subtilisin-like
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subtilases
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subtilisin-type
- eglin-c
- biotechnology
- analysis
Reaction
Hydrolysis of proteins, including collagen =
Synonyms
Alkaline protease, EC 3.4.21.14, EC 3.4.4.16, PLLA-degrading enzyme, PrlA, Proteinase, Thermoactinomyces vulgaris serine, proteolysin, Thermoactinomyces vulgaris serine proteinase, Thermophilic Streptomyces serine proteinase, thermostable serine protease
ECTree
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Inhibitors
Inhibitors on EC 3.4.21.66 - Thermitase
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2,2,5,5-Tetramethylpyrrolin-1-oxyl-3-carbonyl-Ala2-Phe methyl ketone
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2,2,5,5-Tetramethylpyrrolin-1-oxyl-3-carbonyl-Ala3-Phe methyl ketone
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Benzyloxycarbonyl-(Ala)n-Phe methyl ketone
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reacts irreversibly in a 1:1 ratio with the enzyme
Benzyloxycarbonyl-Ala2-Phe chloromethyl ketone
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and the corresponding methyl ketone
Dansyl-(Ala)n-PheCH2Cl
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n: 1, 2 and 3, and homologous carboxybenzoyl-protected peptides, with a higher inhibitory effect
guanidinium hydrochloride
6 M guanidinium hydrochloride gives a 40% reduction of activity after 1 h of incubation at 40°C
Peptide diazomethyl ketones
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reacts irreversibly in a 1:1 ratio with the enzyme
Peptide methyl ketones
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kinetic studies on the binding of N-acetylated peptide ketones as substrate analogous
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the presence of detergents, the protease is quite stable and residual activity lays between 73% and 82%
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additional information
the enzyme shows good activity and stability in the presence of organic solvents, detergents, and dithiothreitol, and it remains active in 6 M guanidinium hydrochloride
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additional information
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the enzyme shows good activity and stability in the presence of organic solvents, detergents, and dithiothreitol, and it remains active in 6 M guanidinium hydrochloride
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additional information
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structure of the active centre studied by use of spin-labeled peptide methyl ketones
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additional information
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stereospecificity of the binding of peptide ligands, diastereomeric tetrapeptides of the peptide ketone, benzoyl-(L-Ala)3-L-PheCH3, a competitive inhibitor
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