Esterase (gene CrmE10) from Croceicoccus marinus E4A9T

Enzyme Description

Extremophile
No
EC Number

Sequence

Length: 205 amino acids
MADGEAAGQQADAVMPTGPAIDVLAFGDSLFAGYRLDRDESYPARLQAALRERGLNVNVTNAGVSGDTTAAGLQRIDFVLDSMAGEPDLVLLELGANDMLRGLPAEEARRNLDTILQRLDQRDIPVMVYGMRAAPNLGGDYGRSFDSIFPDLADKYDAELVPFFIEPLIFDRSLVQQDQLHPTAQGVDAMVEQTVEQVEDRIDDL
Zhengyang Li et al. (2020) β€” Structure-guided protein engineering increases enzymatic activities of the SGNH family esterases
Biotechnology for Biofuels  Β· doi:10.1186/s13068-020-01742-8 β†—  Β· Activity - Classical
8 measurements
Database ID
Sequence Annotation
Explicit - Provided GenBank Accession Number
Protein Source
Recombinant, host bacterium Escherichia coli DH5alpha

Experimental Data (8 measurements)

8 measurements
Property Assay Solvent Solvent Volume Aqueous Reference Measured Value Units Solution pH Temperature Substrate(s) Product(s) Cofactor(s) Shaking Comments
Activity - Classical Activity measured by absorbance spectrophotometry (p-nitrophenol absorbance measurement, 405 nm) in the presence of organic solvent Acetone 15% 100 23 % 100 mM Tris–HCl buffer 7.5 20Β°C 1 mM p-Nitrophenyl hexanoate Hexanoic Acid , p-Nitrophenol β€” β€” Classical aqueous control (in %)
Activity - Classical Activity measured by absorbance spectrophotometry (p-nitrophenol absorbance measurement, 405 nm) in the presence of organic solvent Acetonitrile 15% 100 0 % 100 mM Tris–HCl buffer 7.5 20Β°C 1 mM p-Nitrophenyl hexanoate Hexanoic Acid , p-Nitrophenol β€” β€” Classical aqueous control (in %)
Activity - Classical Activity measured by absorbance spectrophotometry (p-nitrophenol absorbance measurement, 405 nm) in the presence of organic solvent Ethanol 15% 100 59 % 100 mM Tris–HCl buffer 7.5 20Β°C 1 mM p-Nitrophenyl hexanoate Hexanoic Acid , p-Nitrophenol β€” β€” Classical aqueous control (in %)
Activity - Classical Activity measured by absorbance spectrophotometry (p-nitrophenol absorbance measurement, 405 nm) in the presence of organic solvent Dimethylformamide (DMF) 15% 100 22 % 100 mM Tris–HCl buffer 7.5 20Β°C 1 mM p-Nitrophenyl hexanoate Hexanoic Acid , p-Nitrophenol β€” β€” Classical aqueous control (in %)
Activity - Classical Activity measured by absorbance spectrophotometry (p-nitrophenol absorbance measurement, 405 nm) in the presence of organic solvent Dimethyl Sulfoxide (DMSO) 15% 100 104 % 100 mM Tris–HCl buffer 7.5 20Β°C 1 mM p-Nitrophenyl hexanoate Hexanoic Acid , p-Nitrophenol β€” β€” Classical aqueous control (in %)
Activity - Classical Activity measured by absorbance spectrophotometry (p-nitrophenol absorbance measurement, 405 nm) in the presence of organic solvent Glycerol 15% 100 155 % 100 mM Tris–HCl buffer 7.5 20Β°C 1 mM p-Nitrophenyl hexanoate Hexanoic Acid , p-Nitrophenol β€” β€” Classical aqueous control (in %)
Activity - Classical Activity measured by absorbance spectrophotometry (p-nitrophenol absorbance measurement, 405 nm) in the presence of organic solvent Isopropanol 15% 100 75 % 100 mM Tris–HCl buffer 7.5 20Β°C 1 mM p-Nitrophenyl hexanoate Hexanoic Acid , p-Nitrophenol β€” β€” Classical aqueous control (in %)
Activity - Classical Activity measured by absorbance spectrophotometry (p-nitrophenol absorbance measurement, 405 nm) in the presence of organic solvent Methanol 15% 100 77 % 100 mM Tris–HCl buffer 7.5 20Β°C 1 mM p-Nitrophenyl hexanoate Hexanoic Acid , p-Nitrophenol β€” β€” Classical aqueous control (in %)

Visualization : Activity β€” Classical

One bar per measurement. Colour = solvent, shade = solvent volume.

Structure

Drag to rotate Β· Scroll to zoom Β· Right-click drag to pan Β· Powered by Mol*