Sortase A (gene SrtA) from Staphylococcus aureus

Enzyme Description

Extremophile
No
EC Number

Sequence

Length: 206 amino acids
MKKWTNRLMTIAGVVLILVAAYLFAKPHIDNYLHDKDKDEKIEQYDKNVKEQASKDKKQQAKPQIPKDKSKVAGYIEIPDADIKEPVYPGPATPEQLNRGVSFAEENESLDDQNISIAGHTFIDRPNYQFTNLKAAKKGSMVYFKVGNETRKYKMTSIRDVKPTDVGVLDEQKGKDKQLTLITCDDYNEKTGVWEKRKIFVATEVK
Zhimeng Wu et al. (2017) β€” Efficient expression of sortase A from Staphylococcus aureus in Escherichia coli and its enzymatic characterizations
Bioresources and Bioprocessing  Β· doi:10.1186/s40643-017-0143-y β†—  Β· Activity - Classical
25 measurements
Database ID
UniProt: Q2FV99 β†—
Sequence Annotation
Inferred - from protein name
Protein Source
Recombinant, host bacterium Escherichia coli BL21 (DE3)

Experimental Data (25 measurements)

25 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 fluorescence spectrophotometry (cleavage separates dabcyl quencher from edans acceptor, thus removing the quencher and increasing fluoresccence, 350 nm excitation, 495 nm measurement) in the presence of organic solvent Acetonitrile 30% 100 0 % 50 mM Tris–HCl buffer, 150 mM NaCl, 30 mM CaCl2 7.8 37Β°C 0.5 Mg Dabcyl-QALPETGEE-Edans Dabcyl-QALPET , GEE-Edans β€” β€” Classical aqueous control (in %)
Activity - Classical Activity measured by fluorescence spectrophotometry (cleavage separates dabcyl quencher from edans acceptor, thus removing the quencher and increasing fluoresccence, 350 nm excitation, 495 nm measurement) in the presence of organic solvent Dimethyl Sulfoxide (DMSO) 50% 100 10 % 50 mM Tris–HCl buffer, 150 mM NaCl, 30 mM CaCl2 7.8 37Β°C 0.5 Mg Dabcyl-QALPETGEE-Edans Dabcyl-QALPET , GEE-Edans β€” β€” Classical aqueous control (in %)
Activity - Classical Activity measured by fluorescence spectrophotometry (cleavage separates dabcyl quencher from edans acceptor, thus removing the quencher and increasing fluoresccence, 350 nm excitation, 495 nm measurement) in the presence of organic solvent Dimethyl Sulfoxide (DMSO) 40% 100 70 % 50 mM Tris–HCl buffer, 150 mM NaCl, 30 mM CaCl2 7.8 37Β°C 0.5 Mg Dabcyl-QALPETGEE-Edans Dabcyl-QALPET , GEE-Edans β€” β€” Classical aqueous control (in %)
Activity - Classical Activity measured by fluorescence spectrophotometry (cleavage separates dabcyl quencher from edans acceptor, thus removing the quencher and increasing fluoresccence, 350 nm excitation, 495 nm measurement) in the presence of organic solvent Dimethyl Sulfoxide (DMSO) 30% 100 96 % 50 mM Tris–HCl buffer, 150 mM NaCl, 30 mM CaCl2 7.8 37Β°C 0.5 Mg Dabcyl-QALPETGEE-Edans Dabcyl-QALPET , GEE-Edans β€” β€” Classical aqueous control (in %)
Activity - Classical Activity measured by fluorescence spectrophotometry (cleavage separates dabcyl quencher from edans acceptor, thus removing the quencher and increasing fluoresccence, 350 nm excitation, 495 nm measurement) in the presence of organic solvent Dimethyl Sulfoxide (DMSO) 20% 100 98 % 50 mM Tris–HCl buffer, 150 mM NaCl, 30 mM CaCl2 7.8 37Β°C 0.5 Mg Dabcyl-QALPETGEE-Edans Dabcyl-QALPET , GEE-Edans β€” β€” Classical aqueous control (in %)
Activity - Classical Activity measured by fluorescence spectrophotometry (cleavage separates dabcyl quencher from edans acceptor, thus removing the quencher and increasing fluoresccence, 350 nm excitation, 495 nm measurement) in the presence of organic solvent Dimethyl Sulfoxide (DMSO) 10% 100 98 % 50 mM Tris–HCl buffer, 150 mM NaCl, 30 mM CaCl2 7.8 37Β°C 0.5 Mg Dabcyl-QALPETGEE-Edans Dabcyl-QALPET , GEE-Edans β€” β€” Classical aqueous control (in %)
Activity - Classical Activity measured by fluorescence spectrophotometry (cleavage separates dabcyl quencher from edans acceptor, thus removing the quencher and increasing fluoresccence, 350 nm excitation, 495 nm measurement) in the presence of organic solvent Acetone 50% 100 0 % 50 mM Tris–HCl buffer, 150 mM NaCl, 30 mM CaCl2 7.8 37Β°C 0.5 Mg Dabcyl-QALPETGEE-Edans Dabcyl-QALPET , GEE-Edans β€” β€” Classical aqueous control (in %)
Activity - Classical Activity measured by fluorescence spectrophotometry (cleavage separates dabcyl quencher from edans acceptor, thus removing the quencher and increasing fluoresccence, 350 nm excitation, 495 nm measurement) in the presence of organic solvent Acetone 40% 100 2 % 50 mM Tris–HCl buffer, 150 mM NaCl, 30 mM CaCl2 7.8 37Β°C 0.5 Mg Dabcyl-QALPETGEE-Edans Dabcyl-QALPET , GEE-Edans β€” β€” Classical aqueous control (in %)
Activity - Classical Activity measured by fluorescence spectrophotometry (cleavage separates dabcyl quencher from edans acceptor, thus removing the quencher and increasing fluoresccence, 350 nm excitation, 495 nm measurement) in the presence of organic solvent Acetone 30% 100 25 % 50 mM Tris–HCl buffer, 150 mM NaCl, 30 mM CaCl2 7.8 37Β°C 0.5 Mg Dabcyl-QALPETGEE-Edans Dabcyl-QALPET , GEE-Edans β€” β€” Classical aqueous control (in %)
Activity - Classical Activity measured by fluorescence spectrophotometry (cleavage separates dabcyl quencher from edans acceptor, thus removing the quencher and increasing fluoresccence, 350 nm excitation, 495 nm measurement) in the presence of organic solvent Acetone 20% 100 50 % 50 mM Tris–HCl buffer, 150 mM NaCl, 30 mM CaCl2 7.8 37Β°C 0.5 Mg Dabcyl-QALPETGEE-Edans Dabcyl-QALPET , GEE-Edans β€” β€” Classical aqueous control (in %)
Activity - Classical Activity measured by fluorescence spectrophotometry (cleavage separates dabcyl quencher from edans acceptor, thus removing the quencher and increasing fluoresccence, 350 nm excitation, 495 nm measurement) in the presence of organic solvent Acetone 10% 100 74 % 50 mM Tris–HCl buffer, 150 mM NaCl, 30 mM CaCl2 7.8 37Β°C 0.5 Mg Dabcyl-QALPETGEE-Edans Dabcyl-QALPET , GEE-Edans β€” β€” Classical aqueous control (in %)
Activity - Classical Activity measured by fluorescence spectrophotometry (cleavage separates dabcyl quencher from edans acceptor, thus removing the quencher and increasing fluoresccence, 350 nm excitation, 495 nm measurement) in the presence of organic solvent Acetonitrile 50% 100 0 % 50 mM Tris–HCl buffer, 150 mM NaCl, 30 mM CaCl2 7.8 37Β°C 0.5 Mg Dabcyl-QALPETGEE-Edans Dabcyl-QALPET , GEE-Edans β€” β€” Classical aqueous control (in %)
Activity - Classical Activity measured by fluorescence spectrophotometry (cleavage separates dabcyl quencher from edans acceptor, thus removing the quencher and increasing fluoresccence, 350 nm excitation, 495 nm measurement) in the presence of organic solvent Acetonitrile 40% 100 0 % 50 mM Tris–HCl buffer, 150 mM NaCl, 30 mM CaCl2 7.8 37Β°C 0.5 Mg Dabcyl-QALPETGEE-Edans Dabcyl-QALPET , GEE-Edans β€” β€” Classical aqueous control (in %)
Activity - Classical Activity measured by fluorescence spectrophotometry (cleavage separates dabcyl quencher from edans acceptor, thus removing the quencher and increasing fluoresccence, 350 nm excitation, 495 nm measurement) in the presence of organic solvent Methanol 10% 100 73 % 50 mM Tris–HCl buffer, 150 mM NaCl, 30 mM CaCl2 7.8 37Β°C 0.5 Mg Dabcyl-QALPETGEE-Edans Dabcyl-QALPET , GEE-Edans β€” β€” Classical aqueous control (in %)
Activity - Classical Activity measured by fluorescence spectrophotometry (cleavage separates dabcyl quencher from edans acceptor, thus removing the quencher and increasing fluoresccence, 350 nm excitation, 495 nm measurement) in the presence of organic solvent Acetonitrile 20% 100 26 % 50 mM Tris–HCl buffer, 150 mM NaCl, 30 mM CaCl2 7.8 37Β°C 0.5 Mg Dabcyl-QALPETGEE-Edans Dabcyl-QALPET , GEE-Edans β€” β€” Classical aqueous control (in %)
Activity - Classical Activity measured by fluorescence spectrophotometry (cleavage separates dabcyl quencher from edans acceptor, thus removing the quencher and increasing fluoresccence, 350 nm excitation, 495 nm measurement) in the presence of organic solvent Acetonitrile 10% 100 68 % 50 mM Tris–HCl buffer, 150 mM NaCl, 30 mM CaCl2 7.8 37Β°C 0.5 Mg Dabcyl-QALPETGEE-Edans Dabcyl-QALPET , GEE-Edans β€” β€” Classical aqueous control (in %)
Activity - Classical Activity measured by fluorescence spectrophotometry (cleavage separates dabcyl quencher from edans acceptor, thus removing the quencher and increasing fluoresccence, 350 nm excitation, 495 nm measurement) in the presence of organic solvent Ethanol 50% 100 0 % 50 mM Tris–HCl buffer, 150 mM NaCl, 30 mM CaCl2 7.8 37Β°C 0.5 Mg Dabcyl-QALPETGEE-Edans Dabcyl-QALPET , GEE-Edans β€” β€” Classical aqueous control (in %)
Activity - Classical Activity measured by fluorescence spectrophotometry (cleavage separates dabcyl quencher from edans acceptor, thus removing the quencher and increasing fluoresccence, 350 nm excitation, 495 nm measurement) in the presence of organic solvent Ethanol 40% 100 0 % 50 mM Tris–HCl buffer, 150 mM NaCl, 30 mM CaCl2 7.8 37Β°C 0.5 Mg Dabcyl-QALPETGEE-Edans Dabcyl-QALPET , GEE-Edans β€” β€” Classical aqueous control (in %)
Activity - Classical Activity measured by fluorescence spectrophotometry (cleavage separates dabcyl quencher from edans acceptor, thus removing the quencher and increasing fluoresccence, 350 nm excitation, 495 nm measurement) in the presence of organic solvent Ethanol 30% 100 1 % 50 mM Tris–HCl buffer, 150 mM NaCl, 30 mM CaCl2 7.8 37Β°C 0.5 Mg Dabcyl-QALPETGEE-Edans Dabcyl-QALPET , GEE-Edans β€” β€” Classical aqueous control (in %)
Activity - Classical Activity measured by fluorescence spectrophotometry (cleavage separates dabcyl quencher from edans acceptor, thus removing the quencher and increasing fluoresccence, 350 nm excitation, 495 nm measurement) in the presence of organic solvent Ethanol 20% 100 17 % 50 mM Tris–HCl buffer, 150 mM NaCl, 30 mM CaCl2 7.8 37Β°C 0.5 Mg Dabcyl-QALPETGEE-Edans Dabcyl-QALPET , GEE-Edans β€” β€” 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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