Protease from Bacillus amyloliquefaciens CMW1

Enzyme Description

Extremophile
No
EC Number

Sequence

Length: 382 amino acids
MRGKKVWISLLFALALIFTMAFGSTSSAQAAGKSNGEKKYIVGFKQTMSTMSAAKKKDVISEKGGKVQKQFKYVDAASATLNEKAVKELKKDPSVAYVEEDHVAHAYAQSVPYGVSQIKAPALHSQGYTGSNVKVAVIDSGIDSSHPDLKVAGGASMVPSETNPFQDNNSHGTHVAGTVAALNNSIGVLGVAPSASLYAVKVLGADGSGQYSWIINGIEWAIANNMDVINMSLGGPSGSAALKAAVDKAVASGVVVVAAAGNEGTSGSSSTVGYPGKYPSVIAVGAVDSSNQRASFSSVGPELDVMAPGVSIQSTLPGNKYGAYNGTSMASPHVAGAAALILSKHPNWTNTQVRSSLENTTTKLGDSFYYGKGLINVQAAAQ
Atsushi Kurata et al. (2016) β€” Properties of an ionic liquid-tolerant Bacillus amyloliquefaciens CMW1 and its extracellular protease
Extremophiles  Β· doi:10.1007/s00792-016-0832-z β†—  Β· Activity - Classical
26 measurements
Database ID
UniProt: D4PBI3 β†—
Sequence Annotation
Explicit - Provided GenBank Accession Number
Protein Source
Purified, bacterium Bacillus amyloliquefaciens CMW1

Experimental Data (26 measurements)

26 measurements β€” page 1 of 2
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 (colorimetric assay, azo-peptide absorbance measurement, 440 nm) in the presence of organic solvent Isopropanol 50% 90 14 % 100 mM glycine-NaOH buffer, without CaCl2 9 55Β°C 0.25% (w/v) Azocasein azopeptides , Peptides β€” Yes, "vortex used" Classical aqueous control (in %)
Activity - Classical Activity measured by absorbance spectrophotometry (colorimetric assay, azo-peptide absorbance measurement, 440 nm) in the presence of organic solvent 1-Octanol 50% 90 66 % 100 mM glycine-NaOH buffer, without CaCl2 9 55Β°C 0.25% (w/v) Azocasein azopeptides , Peptides β€” Yes, "vortex used" Classical aqueous control (in %)
Activity - Classical Activity measured by absorbance spectrophotometry (colorimetric assay, azo-peptide absorbance measurement, 440 nm) in the presence of organic solvent 1-Octanol 50% 100 72 % 100 mM glycine-NaOH buffer, with 2 mM CaCl2 9 55Β°C 0.25% (w/v) Azocasein azopeptides , Peptides β€” Yes, "vortex used" Classical aqueous control (in %)
Activity - Classical Activity measured by absorbance spectrophotometry (colorimetric assay, azo-peptide absorbance measurement, 440 nm) in the presence of organic solvent Toluene 50% 90 52 % 100 mM glycine-NaOH buffer, without CaCl2 9 55Β°C 0.25% (w/v) Azocasein azopeptides , Peptides β€” Yes, "vortex used" Classical aqueous control (in %)
Activity - Classical Activity measured by absorbance spectrophotometry (colorimetric assay, azo-peptide absorbance measurement, 440 nm) in the presence of organic solvent Toluene 50% 100 72 % 100 mM glycine-NaOH buffer, with 2 mM CaCl2 9 55Β°C 0.25% (w/v) Azocasein azopeptides , Peptides β€” Yes, "vortex used" Classical aqueous control (in %)
Activity - Classical Activity measured by absorbance spectrophotometry (colorimetric assay, azo-peptide absorbance measurement, 440 nm) in the presence of organic solvent Chloroform 50% 90 36 % 100 mM glycine-NaOH buffer, without CaCl2 9 55Β°C 0.25% (w/v) Azocasein azopeptides , Peptides β€” Yes, "vortex used" Classical aqueous control (in %)
Activity - Classical Activity measured by absorbance spectrophotometry (colorimetric assay, azo-peptide absorbance measurement, 440 nm) in the presence of organic solvent Chloroform 50% 100 44 % 100 mM glycine-NaOH buffer, with 2 mM CaCl2 9 55Β°C 0.25% (w/v) Azocasein azopeptides , Peptides β€” Yes, "vortex used" Classical aqueous control (in %)
Activity - Classical Activity measured by absorbance spectrophotometry (colorimetric assay, azo-peptide absorbance measurement, 440 nm) in the presence of organic solvent Butyl Acetate 50% 90 79 % 100 mM glycine-NaOH buffer, without CaCl2 9 55Β°C 0.25% (w/v) Azocasein azopeptides , Peptides β€” Yes, "vortex used" Classical aqueous control (in %)
Activity - Classical Activity measured by absorbance spectrophotometry (colorimetric assay, azo-peptide absorbance measurement, 440 nm) in the presence of organic solvent Butyl Acetate 50% 100 107 % 100 mM glycine-NaOH buffer, with 2 mM CaCl2 9 55Β°C 0.25% (w/v) Azocasein azopeptides , Peptides β€” Yes, "vortex used" Classical aqueous control (in %)
Activity - Classical Activity measured by absorbance spectrophotometry (colorimetric assay, azo-peptide absorbance measurement, 440 nm) in the presence of organic solvent Diethyl Ether 50% 90 106 % 100 mM glycine-NaOH buffer, without CaCl2 9 55Β°C 0.25% (w/v) Azocasein azopeptides , Peptides β€” Yes, "vortex used" Classical aqueous control (in %)
Activity - Classical Activity measured by absorbance spectrophotometry (colorimetric assay, azo-peptide absorbance measurement, 440 nm) in the presence of organic solvent Diethyl Ether 50% 100 111 % 100 mM glycine-NaOH buffer, with 2 mM CaCl2 9 55Β°C 0.25% (w/v) Azocasein azopeptides , Peptides β€” Yes, "vortex used" Classical aqueous control (in %)
Activity - Classical Activity measured by absorbance spectrophotometry (colorimetric assay, azo-peptide absorbance measurement, 440 nm) in the presence of organic solvent Ethyl Acetate 50% 90 40 % 100 mM glycine-NaOH buffer, without CaCl2 9 55Β°C 0.25% (w/v) Azocasein azopeptides , Peptides β€” Yes, "vortex used" Classical aqueous control (in %)
Activity - Classical Activity measured by absorbance spectrophotometry (colorimetric assay, azo-peptide absorbance measurement, 440 nm) in the presence of organic solvent Ethyl Acetate 50% 100 54 % 100 mM glycine-NaOH buffer, with 2 mM CaCl2 9 55Β°C 0.25% (w/v) Azocasein azopeptides , Peptides β€” Yes, "vortex used" Classical aqueous control (in %)
Activity - Classical Activity measured by absorbance spectrophotometry (colorimetric assay, azo-peptide absorbance measurement, 440 nm) in the presence of organic solvent Formamide 50% 100 35 % 100 mM glycine-NaOH buffer, with 2 mM CaCl2 9 55Β°C 0.25% (w/v) Azocasein azopeptides , Peptides β€” Yes, "vortex used" Classical aqueous control (in %)
Activity - Classical Activity measured by absorbance spectrophotometry (colorimetric assay, azo-peptide absorbance measurement, 440 nm) in the presence of organic solvent Isopropanol 50% 100 23 % 100 mM glycine-NaOH buffer, with 2 mM CaCl2 9 55Β°C 0.25% (w/v) Azocasein azopeptides , Peptides β€” Yes, "vortex used" Classical aqueous control (in %)
Activity - Classical Activity measured by absorbance spectrophotometry (colorimetric assay, azo-peptide absorbance measurement, 440 nm) in the presence of organic solvent Ethanol 50% 90 9 % 100 mM glycine-NaOH buffer, without CaCl2 9 55Β°C 0.25% (w/v) Azocasein azopeptides , Peptides β€” Yes, "vortex used" Classical aqueous control (in %)
Activity - Classical Activity measured by absorbance spectrophotometry (colorimetric assay, azo-peptide absorbance measurement, 440 nm) in the presence of organic solvent Ethanol 50% 100 15 % 100 mM glycine-NaOH buffer, with 2 mM CaCl2 9 55Β°C 0.25% (w/v) Azocasein azopeptides , Peptides β€” Yes, "vortex used" Classical aqueous control (in %)
Activity - Classical Activity measured by absorbance spectrophotometry (colorimetric assay, azo-peptide absorbance measurement, 440 nm) in the presence of organic solvent Acetonitrile 50% 90 8 % 100 mM glycine-NaOH buffer, without CaCl2 9 55Β°C 0.25% (w/v) Azocasein azopeptides , Peptides β€” Yes, "vortex used" Classical aqueous control (in %)
Activity - Classical Activity measured by absorbance spectrophotometry (colorimetric assay, azo-peptide absorbance measurement, 440 nm) in the presence of organic solvent Acetonitrile 50% 100 21 % 100 mM glycine-NaOH buffer, with 2 mM CaCl2 9 55Β°C 0.25% (w/v) Azocasein azopeptides , Peptides β€” Yes, "vortex used" Classical aqueous control (in %)
Activity - Classical Activity measured by absorbance spectrophotometry (colorimetric assay, azo-peptide absorbance measurement, 440 nm) in the presence of organic solvent Methanol 50% 90 25 % 100 mM glycine-NaOH buffer, without CaCl2 9 55Β°C 0.25% (w/v) Azocasein azopeptides , Peptides β€” Yes, "vortex used" Classical aqueous control (in %)
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Visualization : Activity β€” Classical

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

Structure

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