Arylsulfate sulfotransferase from Desulfosporosinos orientis

Enzyme Description

Extremophile
No
EC Number

Sequence

Length: 621 amino acids
MSVKFKSFDHIITEQYQAEQAFLTEYQKGEYSFNNPYVKLNPYIIAPLTALVMFKTAQPTTVTITVKGKDKNGDICFNFPTAIEHLIPVYGLYANYANKVELALGDGKTNVITIQTEAAPEIVKLPTQINTTADYFEDNIMFVSPTSTAATAGYDYNGDVRWYGSLNFAFDIKRAKNGRLLLGTHRLVTPPYHTTGLYEMGMIGKIYKEYRLPSGYHHDQFEMEDGNLLILSQDLPRGTVEDMCVLVDRKTGQIIKSWDYQKVLPTNAGGSGSQDSHDWFHNNAVWYDKKTNSLTLSGRHQDIIINLDFETGALNWIIGDPEGWPKELVDNYFFKPVGKGEFDWQYEQHACVVCPNGDIMAFDNGHWRSKIKENYVTANDNFSRGVRYRIDTKKMEIEQVWQYGKERGAEFFSTYICNVEYYDEGHYLIHSGGIGSIDGEALNKPPVQFRGEDEKKVVFNSITVELKDDVMMYEMQLPANYYRAEKLKLYAAEDVLTLGKGELLGTLGVTEEFTTIPPAEEGGMVPEKYNVKLGLEEDRLIFKATFEKGQMVLLQLEGETTHSYFVPTTKRPFLAMCVGTFQESDDRAVEFPVSREGLAGGFRVSLIVDAYKYETGVTIKL
Isabel Oroz-Guinea et al. (2024) β€” Biocatalytic sulfation of aromatic and aliphatic alcohols catalyzed by arylsulfate sulfotransferases
Applied Microbiology and Biotechnology  Β· doi:10.1007/s00253-024-13354-5 β†—  Β· Activity - Classical
6 measurements
Database ID
β€”
Sequence Annotation
Explicit - Provided
Protein Source
Recombinant, host bacterium Escherichia coli BL21 (DE3)

Experimental Data (6 measurements)

6 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, 410 nm) in the presence of organic solvent Dimethyl Sulfoxide (DMSO) 10% 100.0 51.0 % 50 mM Tris-HCl buffer 8 30Β°C 1 mM p-Nitrophenyl sulfate, 1 mM Phenol p-Nitrophenol , phenyl sulfate β€” β€” Classical aqueous control (in %)
Activity - Classical Activity measured by absorbance spectrophotometry (p-nitrophenol absorbance measurement, 410 nm) in the presence of organic solvent Acetone 10% 100.0 72.4 % 50 mM Tris-HCl buffer 8 30Β°C 1 mM p-Nitrophenyl sulfate, 1 mM Phenol p-Nitrophenol , phenyl sulfate β€” β€” Classical aqueous control (in %)
Activity - Classical Activity measured by absorbance spectrophotometry (p-nitrophenol absorbance measurement, 410 nm) in the presence of organic solvent Methanol 10% 100.0 55.1 % 50 mM Tris-HCl buffer 8 30Β°C 1 mM p-Nitrophenyl sulfate, 1 mM Phenol p-Nitrophenol , phenyl sulfate β€” β€” Classical aqueous control (in %)
Activity - Classical Activity measured by absorbance spectrophotometry (p-nitrophenol absorbance measurement, 410 nm) in the presence of organic solvent Isopropanol 10% 100.0 71.8 % 50 mM Tris-HCl buffer 8 30Β°C 1 mM p-Nitrophenyl sulfate, 1 mM Phenol p-Nitrophenol , phenyl sulfate β€” β€” Classical aqueous control (in %)
Activity - Classical Activity measured by absorbance spectrophotometry (p-nitrophenol absorbance measurement, 410 nm) in the presence of organic solvent Dimethylformamide (DMF) 10% 100.0 6.1 % 50 mM Tris-HCl buffer 8 30Β°C 1 mM p-Nitrophenyl sulfate, 1 mM Phenol p-Nitrophenol , phenyl sulfate β€” β€” Classical aqueous control (in %)
Activity - Classical Activity measured by absorbance spectrophotometry (p-nitrophenol absorbance measurement, 410 nm) in the presence of organic solvent 1,2-Dimethoxyethane 10% 100.0 25.0 % 50 mM Tris-HCl buffer 8 30Β°C 1 mM p-Nitrophenyl sulfate, 1 mM Phenol p-Nitrophenol , phenyl sulfate β€” β€” Classical aqueous control (in %)

Visualization : Activity β€” Classical

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

Structure

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