Ξ±-chymotrypsin from Bos taurus (bovine)

Enzyme Description

Extremophile
No
EC Number

Sequence

Length: 245 amino acids
CGVPAIQPVLSGLSRIVNGEEAVPGSWPWQVSLQDKTGFHFCGGSLINENWVVTAAHCGVTTSDVVVAGEFDQGSSSEKIQKLKIAKVFKNSKYNSLTINNDITLLKLSTAASFSQTVSAVCLPSASDDFAAGTTCVTTGWGLTRYTNANTPDRLQQASLPLLSNTNCKKYWGTKIKDAMICAGASGVSSCMGDSGGPLVCKKNGAWTLVGIVSWGSSTCSTSTPGVYARVTALVNWVQQTLAAN
Vadim V. Mozhaev et al. (1989) β€” Catalytic activity and denaturation of enzymes in water/organic cosolvent mixtures
European Journal of Biochemistry  Β· doi:10.1111/j.1432-1033.1989.tb15055.x β†—  Β· Stability - C50
16 measurements
Database ID
UniProt: P00766 β†—
Sequence Annotation
Inferred - from protein name
Protein Source
Commercially purchased

Experimental Data (16 measurements)

16 measurements
Property Assay Solvent Solvent Volume Aqueous Reference Measured Value Units Solution pH Temperature Substrate(s) Product(s) Cofactor(s) Shaking Comments
Stability - C50 Volume of organic solvent (in %) at which 50% of initial activity is lost, as measured by absorbance spectrophotometry (p-nitroaniline absorbance measurement, 375 nm) in the presence of organic solvent Methanol β€” β€” 32 % (v/v) 50 mM phosphate buffer 6.5-7 25 Β°C 50-400 micoMolar BTPNA (Benzoyl-L-tyrosine p-nitroanilide) N-Benzoyl-L-tyrosine , p-Nitroaniline β€” β€” Not applicable control (in % (v/v))
Stability - C50 Volume of organic solvent (in %) at which 50% of initial activity is lost, as measured by absorbance spectrophotometry (p-nitroaniline absorbance measurement, 375 nm) in the presence of organic solvent Ethanol β€” β€” 36 % (v/v) 50 mM phosphate buffer 6.5-7 25 Β°C 50-400 micoMolar BTPNA (Benzoyl-L-tyrosine p-nitroanilide) N-Benzoyl-L-tyrosine , p-Nitroaniline β€” β€” Not applicable control (in % (v/v))
Stability - C50 Volume of organic solvent (in %) at which 50% of initial activity is lost, as measured by absorbance spectrophotometry (p-nitroaniline absorbance measurement, 375 nm) in the presence of organic solvent 1-Propanol β€” β€” 27 % (v/v) 50 mM phosphate buffer 6.5-7 25 Β°C 50-400 micoMolar BTPNA (Benzoyl-L-tyrosine p-nitroanilide) N-Benzoyl-L-tyrosine , p-Nitroaniline β€” β€” Not applicable control (in % (v/v))
Stability - C50 Volume of organic solvent (in %) at which 50% of initial activity is lost, as measured by absorbance spectrophotometry (p-nitroaniline absorbance measurement, 375 nm) in the presence of organic solvent Isopropanol β€” β€” 33 % (v/v) 50 mM phosphate buffer 6.5-7 25 Β°C 50-400 micoMolar BTPNA (Benzoyl-L-tyrosine p-nitroanilide) N-Benzoyl-L-tyrosine , p-Nitroaniline β€” β€” Not applicable control (in % (v/v))
Stability - C50 Volume of organic solvent (in %) at which 50% of initial activity is lost, as measured by absorbance spectrophotometry (p-nitroaniline absorbance measurement, 375 nm) in the presence of organic solvent Isobutanol β€” β€” 10 % (v/v) 50 mM phosphate buffer 6.5-7 25 Β°C 50-400 micoMolar BTPNA (Benzoyl-L-tyrosine p-nitroanilide) N-Benzoyl-L-tyrosine , p-Nitroaniline β€” β€” Not applicable control (in % (v/v))
Stability - C50 Volume of organic solvent (in %) at which 50% of initial activity is lost, as measured by absorbance spectrophotometry (p-nitroaniline absorbance measurement, 375 nm) in the presence of organic solvent Ethylene Glycol β€” β€” 72 % (v/v) 50 mM phosphate buffer 6.5-7 25 Β°C 50-400 micoMolar BTPNA (Benzoyl-L-tyrosine p-nitroanilide) N-Benzoyl-L-tyrosine , p-Nitroaniline β€” β€” Not applicable control (in % (v/v))
Stability - C50 Volume of organic solvent (in %) at which 50% of initial activity is lost, as measured by absorbance spectrophotometry (p-nitroaniline absorbance measurement, 375 nm) in the presence of organic solvent Propylene Glycol β€” β€” 60 % (v/v) 50 mM phosphate buffer 6.5-7 25 Β°C 50-400 micoMolar BTPNA (Benzoyl-L-tyrosine p-nitroanilide) N-Benzoyl-L-tyrosine , p-Nitroaniline β€” β€” Not applicable control (in % (v/v))
Stability - C50 Volume of organic solvent (in %) at which 50% of initial activity is lost, as measured by absorbance spectrophotometry (p-nitroaniline absorbance measurement, 375 nm) in the presence of organic solvent 1,4-Butanediol β€” β€” 65 % (v/v) 50 mM phosphate buffer 6.5-7 25 Β°C 50-400 micoMolar BTPNA (Benzoyl-L-tyrosine p-nitroanilide) N-Benzoyl-L-tyrosine , p-Nitroaniline β€” β€” Not applicable control (in % (v/v))
Stability - C50 Volume of organic solvent (in %) at which 50% of initial activity is lost, as measured by absorbance spectrophotometry (p-nitroaniline absorbance measurement, 375 nm) in the presence of organic solvent 1,3-Butanediol β€” β€” 56 % (v/v) 50 mM phosphate buffer 6.5-7 25 Β°C 50-400 micoMolar BTPNA (Benzoyl-L-tyrosine p-nitroanilide) N-Benzoyl-L-tyrosine , p-Nitroaniline β€” β€” Not applicable control (in % (v/v))
Stability - C50 Volume of organic solvent (in %) at which 50% of initial activity is lost, as measured by absorbance spectrophotometry (p-nitroaniline absorbance measurement, 375 nm) in the presence of organic solvent 2,3-Butanediol β€” β€” 39 % (v/v) 50 mM phosphate buffer 6.5-7 25 Β°C 50-400 micoMolar BTPNA (Benzoyl-L-tyrosine p-nitroanilide) N-Benzoyl-L-tyrosine , p-Nitroaniline β€” β€” Not applicable control (in % (v/v))
Stability - C50 Volume of organic solvent (in %) at which 50% of initial activity is lost, as measured by absorbance spectrophotometry (p-nitroaniline absorbance measurement, 375 nm) in the presence of organic solvent Hexylene Glycol β€” β€” 50 % (v/v) 50 mM phosphate buffer 6.5-7 25 Β°C 50-400 micoMolar BTPNA (Benzoyl-L-tyrosine p-nitroanilide) N-Benzoyl-L-tyrosine , p-Nitroaniline β€” β€” Not applicable control (in % (v/v))
Stability - C50 Volume of organic solvent (in %) at which 50% of initial activity is lost, as measured by absorbance spectrophotometry (p-nitroaniline absorbance measurement, 375 nm) in the presence of organic solvent Glycerol β€” β€” 73 % (v/v) 50 mM phosphate buffer 6.5-7 25 Β°C 50-400 micoMolar BTPNA (Benzoyl-L-tyrosine p-nitroanilide) N-Benzoyl-L-tyrosine , p-Nitroaniline β€” β€” Not applicable control (in % (v/v))
Stability - C50 Volume of organic solvent (in %) at which 50% of initial activity is lost, as measured by absorbance spectrophotometry (p-nitroaniline absorbance measurement, 375 nm) in the presence of organic solvent 1,2,6-Hexanetriol β€” β€” 68 % (v/v) 50 mM phosphate buffer 6.5-7 25 Β°C 50-400 micoMolar BTPNA (Benzoyl-L-tyrosine p-nitroanilide) N-Benzoyl-L-tyrosine , p-Nitroaniline β€” β€” Not applicable control (in % (v/v))
Stability - C50 Volume of organic solvent (in %) at which 50% of initial activity is lost, as measured by absorbance spectrophotometry (p-nitroaniline absorbance measurement, 375 nm) in the presence of organic solvent Formamide β€” β€” 23 % (v/v) 50 mM phosphate buffer 6.5-7 25 Β°C 50-400 micoMolar BTPNA (Benzoyl-L-tyrosine p-nitroanilide) N-Benzoyl-L-tyrosine , p-Nitroaniline β€” β€” Not applicable control (in % (v/v))
Stability - C50 Volume of organic solvent (in %) at which 50% of initial activity is lost, as measured by absorbance spectrophotometry (p-nitroaniline absorbance measurement, 375 nm) in the presence of organic solvent n-Methylformamide (NMF) β€” β€” 29 % (v/v) 50 mM phosphate buffer 6.5-7 25 Β°C 50-400 micoMolar BTPNA (Benzoyl-L-tyrosine p-nitroanilide) N-Benzoyl-L-tyrosine , p-Nitroaniline β€” β€” Not applicable control (in % (v/v))
Stability - C50 Volume of organic solvent (in %) at which 50% of initial activity is lost, as measured by absorbance spectrophotometry (p-nitroaniline absorbance measurement, 375 nm) in the presence of organic solvent Dimethylformamide (DMF) β€” β€” 26 % (v/v) 50 mM phosphate buffer 6.5-7 25 Β°C 50-400 micoMolar BTPNA (Benzoyl-L-tyrosine p-nitroanilide) N-Benzoyl-L-tyrosine , p-Nitroaniline β€” β€” Not applicable control (in % (v/v))

Visualization : Stability β€” C50

Vadim V. Mozhaev et al. (1989)

One bar per measurement. Colour = solvent, shade = temperature. Hover for details.

Rosa M. Blanco et al. (1992) β€” Effect of immiscible organic solvents on activity/stability of native chymotrypsin and immobilized-stabilized derivatives
Biotechnology and Bioengineering  Β· doi:10.1002/bit.260390112 β†—  Β· Stability - Incubation
27 measurements
Hiroyasu Ogino et al. (1999) β€” Purification and characterization of organic solvent-stable protease from organic solvent-tolerant Pseudomonas aeruginosa PST-01
Journal of Bioscience and Bioengineering  Β· doi:10.1016/s1389-1723(99)80009-7 β†—  Β· Stability - Half-life
16 measurements
Guillermo R. Castro et al. (1999) β€” Enzymatic activities of proteases dissolved in organic solvents
Enzyme and Microbial Technology  Β· doi:10.1016/S0141-0229(99)00099-X β†—  Β· Activity - Michaelis-Menten
3 measurements
L.M. Simon et al. (2001) β€” Structure and Activity of Ξ±-Chymotrypsin and Trypsin in Aqueous Organic Media.
Biochemical and Biophysical Research Communications  Β· doi:10.1006/bbrc.2001.4282 β†—  Β· Activity - Michaelis-Menten Stability - Incubation
53 measurements
E. A. Belyaeva et al. (2002) β€” On the Mechanism of Interaction of Organic Solvents with the Active Site of Ξ±-Chymotrypsin
Biochemistry (Moscow)  Β· doi:10.1023/a:1020530220774 β†—  Β· Activity - Michaelis-Menten
31 measurements
Linus Olofsson et al. (2006) β€” Influence of Water Miscible Organic Solvents on Ξ±-chymotrypsin in Solution and Immobilized on Eupergit CM
Biotechnology Letters  Β· doi:10.1007/s10529-006-9025-7 β†—  Β· Activity + Stability - Incubation
45 measurements
Hiroyasu Ogino et al. (2007) β€” Stabilities and Conformational Transitions of Various Proteases in the Presence of an Organic Solvent
Biotechnology Progress  Β· doi:10.1021/bp060252p β†—  Β· Stability - Half-life
1 measurement
Lena Ostermeier et al. (2020) β€” The multifaceted effects of DMSO and high hydrostatic pressure on the kinetic constants of hydrolysis reactions catalyzed by Ξ±-chymotrypsin
Physical Chemistry Chemical Physics  Β· doi:10.1039/d0cp03062g β†—  Β· Activity - Classical Activity - Michaelis-Menten
12 measurements

Structure

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