Fructose-6-phosphate aldolase (gene fsaA) from Escherichia coli

Enzyme Description

Extremophile
No
EC Number

Sequence

Length: 220 amino acids
MELYLDTSDVVAVKALSRIFPLAGVTTNPSIIAAGKKPLDVVLPQLHEAMGGQGRLFAQVMATTAEGMVNDALKLRSIIADIVVKVPVTAEGLAAIKMLKAEGIPTLGTAVYGAAQGLLSALAGAEYVAPYVNRIDAQGGSGIQTVTDLHQLLKMHAPQAKVLAASFKTPRQALDCLLAGCESITLPLDVAQQMISYPAVDAAVAKFEQDWQGAFGRTSI
Martina Sudar et al. (2013) β€” Aldol addition of dihydroxyacetone to N-Cbz-3-aminopropanal catalyzed by two aldolases variants in microreactors
Enzyme and Microbial Technology  Β· doi:10.1016/j.enzmictec.2013.03.013 β†—  Β· Activity - Classical
36 measurements
Database ID
UniProt: P78055 β†—
Sequence Annotation
Inferred - from protein name
Protein Source
Recombinant, host bacterium Escherichia coli

Experimental Data (36 measurements)

36 measurements β€” page 2 of 2
Mutation Property Assay Solvent Solvent Volume Aqueous ReferenceWT Reference Measured Value Units Solution pH Temperature Substrate(s) Product(s) Cofactor(s) Shaking Comments
A129S Activity - Classical Activity (in U*mg^-1) measured by HPLC in the presence of organic solvent Ethyl Acetate 20% 5.7 β€” 1.1 U/mg 50 mM TEA-HCl buffer 7.5 25Β°C 100 mM Dihydroxyacetone, 100 mM N-Cbz-3-aminopropanal 6-(N-Cbz-amino)-4-hydroxyhexan-2-one β€” 1000 rpm Classical aqueous control (in U/mg) with 5% organic solvent due to N-Cbz-3-aminopropanal low solubility in water | Control in low (5%) ethyl acetate content solution
A129S Activity - Classical Activity (in U*mg^-1) measured by HPLC in the presence of organic solvent Ethyl Acetate 30% 5.7 β€” 0.7 U/mg 50 mM TEA-HCl buffer 7.5 25Β°C 100 mM Dihydroxyacetone, 100 mM N-Cbz-3-aminopropanal 6-(N-Cbz-amino)-4-hydroxyhexan-2-one β€” 1000 rpm Classical aqueous control (in U/mg) with 5% organic solvent due to N-Cbz-3-aminopropanal low solubility in water | Control in low (5%) ethyl acetate content solution
A129S Activity - Classical Activity (in U*mg^-1) measured by HPLC in the presence of organic solvent Ethyl Acetate 40% 5.7 β€” 0.3 U/mg 50 mM TEA-HCl buffer 7.5 25Β°C 100 mM Dihydroxyacetone, 100 mM N-Cbz-3-aminopropanal 6-(N-Cbz-amino)-4-hydroxyhexan-2-one β€” 1000 rpm Classical aqueous control (in U/mg) with 5% organic solvent due to N-Cbz-3-aminopropanal low solubility in water | Control in low (5%) ethyl acetate content solution
A129S Activity - Classical Activity (in U*mg^-1) measured by HPLC in the presence of organic solvent Ethyl Acetate 50% 5.7 β€” 0.0 U/mg 50 mM TEA-HCl buffer 7.5 25Β°C 100 mM Dihydroxyacetone, 100 mM N-Cbz-3-aminopropanal 6-(N-Cbz-amino)-4-hydroxyhexan-2-one β€” 1000 rpm Classical aqueous control (in U/mg) with 5% organic solvent due to N-Cbz-3-aminopropanal low solubility in water | Control in low (5%) ethyl acetate content solution
A129S Activity - Classical Activity (in U*mg^-1) measured by HPLC in the presence of organic solvent Acetonitrile 5% 4.0 β€” 4.0 U/mg 50 mM TEA-HCl buffer 7.5 25Β°C 100 mM Dihydroxyacetone, 100 mM N-Cbz-3-aminopropanal 6-(N-Cbz-amino)-4-hydroxyhexan-2-one β€” 1000 rpm Classical aqueous control (in U/mg) with 5% organic solvent due to N-Cbz-3-aminopropanal low solubility in water | Control in low (5%) acetonitrile content solution
A129S Activity - Classical Activity (in U*mg^-1) measured by HPLC in the presence of organic solvent Acetonitrile 10% 4.0 β€” 3.7 U/mg 50 mM TEA-HCl buffer 7.5 25Β°C 100 mM Dihydroxyacetone, 100 mM N-Cbz-3-aminopropanal 6-(N-Cbz-amino)-4-hydroxyhexan-2-one β€” 1000 rpm Classical aqueous control (in U/mg) with 5% organic solvent due to N-Cbz-3-aminopropanal low solubility in water | Control in low (5%) acetonitrile content solution
A129S Activity - Classical Activity (in U*mg^-1) measured by HPLC in the presence of organic solvent Acetonitrile 20% 4.0 β€” 2.4 U/mg 50 mM TEA-HCl buffer 7.5 25Β°C 100 mM Dihydroxyacetone, 100 mM N-Cbz-3-aminopropanal 6-(N-Cbz-amino)-4-hydroxyhexan-2-one β€” 1000 rpm Classical aqueous control (in U/mg) with 5% organic solvent due to N-Cbz-3-aminopropanal low solubility in water | Control in low (5%) acetonitrile content solution
A129S Activity - Classical Activity (in U*mg^-1) measured by HPLC in the presence of organic solvent Ethyl Acetate 5% 5.7 β€” 5.7 U/mg 50 mM TEA-HCl buffer 7.5 25Β°C 100 mM Dihydroxyacetone, 100 mM N-Cbz-3-aminopropanal 6-(N-Cbz-amino)-4-hydroxyhexan-2-one β€” 1000 rpm Classical aqueous control (in U/mg) with 5% organic solvent due to N-Cbz-3-aminopropanal low solubility in water | Control in low (5%) ethyl acetate content solution
A129S Activity - Classical Activity (in U*mg^-1) measured by HPLC in the presence of organic solvent Acetonitrile 40% 4.0 β€” 0.7 U/mg 50 mM TEA-HCl buffer 7.5 25Β°C 100 mM Dihydroxyacetone, 100 mM N-Cbz-3-aminopropanal 6-(N-Cbz-amino)-4-hydroxyhexan-2-one β€” 1000 rpm Classical aqueous control (in U/mg) with 5% organic solvent due to N-Cbz-3-aminopropanal low solubility in water | Control in low (5%) acetonitrile content solution
A129S Activity - Classical Activity (in U*mg^-1) measured by HPLC in the presence of organic solvent Acetonitrile 50% 4.0 β€” 0.3 U/mg 50 mM TEA-HCl buffer 7.5 25Β°C 100 mM Dihydroxyacetone, 100 mM N-Cbz-3-aminopropanal 6-(N-Cbz-amino)-4-hydroxyhexan-2-one β€” 1000 rpm Classical aqueous control (in U/mg) with 5% organic solvent due to N-Cbz-3-aminopropanal low solubility in water | Control in low (5%) acetonitrile content solution
A129S Activity - Classical Activity (in U*mg^-1) measured by HPLC in the presence of organic solvent Dimethylformamide (DMF) 5% 3.4 β€” 3.4 U/mg 50 mM TEA-HCl buffer 7.5 25Β°C 100 mM Dihydroxyacetone, 100 mM N-Cbz-3-aminopropanal 6-(N-Cbz-amino)-4-hydroxyhexan-2-one β€” 1000 rpm Classical aqueous control (in U/mg) with 5% organic solvent due to N-Cbz-3-aminopropanal low solubility in water | Control in low (5%) DMF content solution
A129S Activity - Classical Activity (in U*mg^-1) measured by HPLC in the presence of organic solvent Dimethylformamide (DMF) 10% 3.4 β€” 3.2 U/mg 50 mM TEA-HCl buffer 7.5 25Β°C 100 mM Dihydroxyacetone, 100 mM N-Cbz-3-aminopropanal 6-(N-Cbz-amino)-4-hydroxyhexan-2-one β€” 1000 rpm Classical aqueous control (in U/mg) with 5% organic solvent due to N-Cbz-3-aminopropanal low solubility in water | Control in low (5%) DMF content solution
A129S Activity - Classical Activity (in U*mg^-1) measured by HPLC in the presence of organic solvent Dimethylformamide (DMF) 20% 3.4 β€” 2.0 U/mg 50 mM TEA-HCl buffer 7.5 25Β°C 100 mM Dihydroxyacetone, 100 mM N-Cbz-3-aminopropanal 6-(N-Cbz-amino)-4-hydroxyhexan-2-one β€” 1000 rpm Classical aqueous control (in U/mg) with 5% organic solvent due to N-Cbz-3-aminopropanal low solubility in water | Control in low (5%) DMF content solution
A129S Activity - Classical Activity (in U*mg^-1) measured by HPLC in the presence of organic solvent Dimethylformamide (DMF) 30% 3.4 β€” 1.1 U/mg 50 mM TEA-HCl buffer 7.5 25Β°C 100 mM Dihydroxyacetone, 100 mM N-Cbz-3-aminopropanal 6-(N-Cbz-amino)-4-hydroxyhexan-2-one β€” 1000 rpm Classical aqueous control (in U/mg) with 5% organic solvent due to N-Cbz-3-aminopropanal low solubility in water | Control in low (5%) DMF content solution
A129S Activity - Classical Activity (in U*mg^-1) measured by HPLC in the presence of organic solvent Dimethylformamide (DMF) 40% 3.4 β€” 0.8 U/mg 50 mM TEA-HCl buffer 7.5 25Β°C 100 mM Dihydroxyacetone, 100 mM N-Cbz-3-aminopropanal 6-(N-Cbz-amino)-4-hydroxyhexan-2-one β€” 1000 rpm Classical aqueous control (in U/mg) with 5% organic solvent due to N-Cbz-3-aminopropanal low solubility in water | Control in low (5%) DMF content solution
A129S Activity - Classical Activity (in U*mg^-1) measured by HPLC in the presence of organic solvent Dimethylformamide (DMF) 50% 3.4 β€” 0.4 U/mg 50 mM TEA-HCl buffer 7.5 25Β°C 100 mM Dihydroxyacetone, 100 mM N-Cbz-3-aminopropanal 6-(N-Cbz-amino)-4-hydroxyhexan-2-one β€” 1000 rpm Classical aqueous control (in U/mg) with 5% organic solvent due to N-Cbz-3-aminopropanal low solubility in water | Control in low (5%) DMF content solution
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Mutations in this dataset (2)

A129S A129S/A165G

Visualization : Activity β€” Classical

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

Structure

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