2-deoxy-D-ribose-5- phosphate aldolase from Haloarcula japonica TR-1

Enzyme Description

Extremophile
Yes "extreme halophilic" archaeon
EC Number

Sequence

Length: 231 amino acids
MDDIPDRIEHTVLGPTTTPDDVRTCLDEALQYGMRACIPPWALPLATEYANVQLTAVIDFPHGQGQTDSVCQAAKLAWDAGADELDMVCNIGLLKAGEDDAVRNHITEVVASVPVPVKVIVEAPLLSDDELERVGQLVADADAAYLKTATGFSEGGATVHDVEILSKYLPVKASGGVGSWADAQAMFEAGAERIGASSGDTIVREWQAATEGETVTEPERDRDDPDTTDGY
Tatsuya Ohshida et al. (2016) β€” First characterization of extremely halophilic 2-deoxy-D-ribose-5-phosphate aldolase
Protein Expression and Purification  Β· doi:10.1016/j.pep.2016.05.009 β†—  Β· Stability - Incubation
44 measurements
Database ID
Sequence Annotation
Explicit - Provided GenBank Accession Number
Protein Source
Recombinant, host bacterium Escherichia coli BL21 (DE3)

Experimental Data (44 measurements)

44 measurements β€” page 2 of 3
Property Assay Solvent Solvent Volume Aqueous Reference Measured Value Units Solution pH Temperature Substrate(s) Product(s) Cofactor(s) Shaking Comments
Stability - Incubation Activity after incubation (50 minutes at 25Β°C), measured by absorbance spectrophotometry NADH absorbance measurement in a coupled reaction with TIM and GPDH, with TIM converting G3P into DHAP, and GPDH reducing DHAP, 340 nm) in aqueous phase Dimethyl Sulfoxide (DMSO) 50% 100 101 % Incubation: 10 mM Tris-HCl buffer, 2M NaCl, Assay: 100 mM citrate-Na citrate buffer, 1 M NaCl, 0.15 mM NADH, 8 U/ml triose-phosphate isomerase (rabbit muscle), 2.5 U/ml glycerol-3-phosphate dehydrogenase (rabbit muscle) Incubation: 8, Assay: 6.4 Incubation: 25Β°C, Assay: 37Β°C 2 mM 2-Deoxyribose-5-phosphate Acetaldehyde , Glyceraldehyde 3-phosphate β€” β€” Non-incubated control (in %), assay measured in aqueous phase | Clear about assay in aqueous phase
Stability - Incubation Activity after incubation (60 minutes at 25Β°C), measured by absorbance spectrophotometry NADH absorbance measurement in a coupled reaction with TIM and GPDH, with TIM converting G3P into DHAP, and GPDH reducing DHAP, 340 nm) in aqueous phase Dimethyl Sulfoxide (DMSO) 50% 100 97 % Incubation: 10 mM Tris-HCl buffer, 2M NaCl, Assay: 100 mM citrate-Na citrate buffer, 1 M NaCl, 0.15 mM NADH, 8 U/ml triose-phosphate isomerase (rabbit muscle), 2.5 U/ml glycerol-3-phosphate dehydrogenase (rabbit muscle) Incubation: 8, Assay: 6.4 Incubation: 25Β°C, Assay: 37Β°C 2 mM 2-Deoxyribose-5-phosphate Acetaldehyde , Glyceraldehyde 3-phosphate β€” β€” Non-incubated control (in %), assay measured in aqueous phase | Clear about assay in aqueous phase
Stability - Incubation Activity after incubation (10 minutes at 25Β°C), measured by absorbance spectrophotometry NADH absorbance measurement in a coupled reaction with TIM and GPDH, with TIM converting G3P into DHAP, and GPDH reducing DHAP, 340 nm) in aqueous phase Acetonitrile 20% 100 81 % Incubation: 10 mM Tris-HCl buffer, 2M NaCl, Assay: 100 mM citrate-Na citrate buffer, 1 M NaCl, 0.15 mM NADH, 8 U/ml triose-phosphate isomerase (rabbit muscle), 2.5 U/ml glycerol-3-phosphate dehydrogenase (rabbit muscle) Incubation: 8, Assay: 6.4 Incubation: 25Β°C, Assay: 37Β°C 2 mM 2-Deoxyribose-5-phosphate Acetaldehyde , Glyceraldehyde 3-phosphate β€” β€” Non-incubated control (in %), assay measured in aqueous phase | Clear about assay in aqueous phase
Stability - Incubation Activity after incubation (10 minutes at 25Β°C), measured by absorbance spectrophotometry NADH absorbance measurement in a coupled reaction with TIM and GPDH, with TIM converting G3P into DHAP, and GPDH reducing DHAP, 340 nm) in aqueous phase Ethanol 20% 100 87 % Incubation: 10 mM Tris-HCl buffer, 2M NaCl, Assay: 100 mM citrate-Na citrate buffer, 1 M NaCl, 0.15 mM NADH, 8 U/ml triose-phosphate isomerase (rabbit muscle), 2.5 U/ml glycerol-3-phosphate dehydrogenase (rabbit muscle) Incubation: 8, Assay: 6.4 Incubation: 25Β°C, Assay: 37Β°C 2 mM 2-Deoxyribose-5-phosphate Acetaldehyde , Glyceraldehyde 3-phosphate β€” β€” Non-incubated control (in %), assay measured in aqueous phase | Clear about assay in aqueous phase
Stability - Incubation Activity after incubation (10 minutes at 25Β°C), measured by absorbance spectrophotometry NADH absorbance measurement in a coupled reaction with TIM and GPDH, with TIM converting G3P into DHAP, and GPDH reducing DHAP, 340 nm) in aqueous phase Ethanol 30% 100 60 % Incubation: 10 mM Tris-HCl buffer, 2M NaCl, Assay: 100 mM citrate-Na citrate buffer, 1 M NaCl, 0.15 mM NADH, 8 U/ml triose-phosphate isomerase (rabbit muscle), 2.5 U/ml glycerol-3-phosphate dehydrogenase (rabbit muscle) Incubation: 8, Assay: 6.4 Incubation: 25Β°C, Assay: 37Β°C 2 mM 2-Deoxyribose-5-phosphate Acetaldehyde , Glyceraldehyde 3-phosphate β€” β€” Non-incubated control (in %), assay measured in aqueous phase | Clear about assay in aqueous phase
Stability - Incubation Activity after incubation (10 minutes at 25Β°C), measured by absorbance spectrophotometry NADH absorbance measurement in a coupled reaction with TIM and GPDH, with TIM converting G3P into DHAP, and GPDH reducing DHAP, 340 nm) in aqueous phase Ethanol 40% 100 46 % Incubation: 10 mM Tris-HCl buffer, 2M NaCl, Assay: 100 mM citrate-Na citrate buffer, 1 M NaCl, 0.15 mM NADH, 8 U/ml triose-phosphate isomerase (rabbit muscle), 2.5 U/ml glycerol-3-phosphate dehydrogenase (rabbit muscle) Incubation: 8, Assay: 6.4 Incubation: 25Β°C, Assay: 37Β°C 2 mM 2-Deoxyribose-5-phosphate Acetaldehyde , Glyceraldehyde 3-phosphate β€” β€” Non-incubated control (in %), assay measured in aqueous phase | Clear about assay in aqueous phase
Stability - Incubation Activity after incubation (10 minutes at 25Β°C), measured by absorbance spectrophotometry NADH absorbance measurement in a coupled reaction with TIM and GPDH, with TIM converting G3P into DHAP, and GPDH reducing DHAP, 340 nm) in aqueous phase Ethanol 50% 100 30 % Incubation: 10 mM Tris-HCl buffer, 2M NaCl, Assay: 100 mM citrate-Na citrate buffer, 1 M NaCl, 0.15 mM NADH, 8 U/ml triose-phosphate isomerase (rabbit muscle), 2.5 U/ml glycerol-3-phosphate dehydrogenase (rabbit muscle) Incubation: 8, Assay: 6.4 Incubation: 25Β°C, Assay: 37Β°C 2 mM 2-Deoxyribose-5-phosphate Acetaldehyde , Glyceraldehyde 3-phosphate β€” β€” Non-incubated control (in %), assay measured in aqueous phase | Clear about assay in aqueous phase
Stability - Incubation Activity after incubation (10 minutes at 25Β°C), measured by absorbance spectrophotometry NADH absorbance measurement in a coupled reaction with TIM and GPDH, with TIM converting G3P into DHAP, and GPDH reducing DHAP, 340 nm) in aqueous phase Methanol 10% 100 82 % Incubation: 10 mM Tris-HCl buffer, 2M NaCl, Assay: 100 mM citrate-Na citrate buffer, 1 M NaCl, 0.15 mM NADH, 8 U/ml triose-phosphate isomerase (rabbit muscle), 2.5 U/ml glycerol-3-phosphate dehydrogenase (rabbit muscle) Incubation: 8, Assay: 6.4 Incubation: 25Β°C, Assay: 37Β°C 2 mM 2-Deoxyribose-5-phosphate Acetaldehyde , Glyceraldehyde 3-phosphate β€” β€” Non-incubated control (in %), assay measured in aqueous phase | Clear about assay in aqueous phase
Stability - Incubation Activity after incubation (10 minutes at 25Β°C), measured by absorbance spectrophotometry NADH absorbance measurement in a coupled reaction with TIM and GPDH, with TIM converting G3P into DHAP, and GPDH reducing DHAP, 340 nm) in aqueous phase Methanol 20% 100 99 % Incubation: 10 mM Tris-HCl buffer, 2M NaCl, Assay: 100 mM citrate-Na citrate buffer, 1 M NaCl, 0.15 mM NADH, 8 U/ml triose-phosphate isomerase (rabbit muscle), 2.5 U/ml glycerol-3-phosphate dehydrogenase (rabbit muscle) Incubation: 8, Assay: 6.4 Incubation: 25Β°C, Assay: 37Β°C 2 mM 2-Deoxyribose-5-phosphate Acetaldehyde , Glyceraldehyde 3-phosphate β€” β€” Non-incubated control (in %), assay measured in aqueous phase | Clear about assay in aqueous phase
Stability - Incubation Activity after incubation (10 minutes at 25Β°C), measured by absorbance spectrophotometry NADH absorbance measurement in a coupled reaction with TIM and GPDH, with TIM converting G3P into DHAP, and GPDH reducing DHAP, 340 nm) in aqueous phase Methanol 30% 100 94 % Incubation: 10 mM Tris-HCl buffer, 2M NaCl, Assay: 100 mM citrate-Na citrate buffer, 1 M NaCl, 0.15 mM NADH, 8 U/ml triose-phosphate isomerase (rabbit muscle), 2.5 U/ml glycerol-3-phosphate dehydrogenase (rabbit muscle) Incubation: 8, Assay: 6.4 Incubation: 25Β°C, Assay: 37Β°C 2 mM 2-Deoxyribose-5-phosphate Acetaldehyde , Glyceraldehyde 3-phosphate β€” β€” Non-incubated control (in %), assay measured in aqueous phase | Clear about assay in aqueous phase
Stability - Incubation Activity after incubation (10 minutes at 25Β°C), measured by absorbance spectrophotometry NADH absorbance measurement in a coupled reaction with TIM and GPDH, with TIM converting G3P into DHAP, and GPDH reducing DHAP, 340 nm) in aqueous phase Methanol 40% 100 60 % Incubation: 10 mM Tris-HCl buffer, 2M NaCl, Assay: 100 mM citrate-Na citrate buffer, 1 M NaCl, 0.15 mM NADH, 8 U/ml triose-phosphate isomerase (rabbit muscle), 2.5 U/ml glycerol-3-phosphate dehydrogenase (rabbit muscle) Incubation: 8, Assay: 6.4 Incubation: 25Β°C, Assay: 37Β°C 2 mM 2-Deoxyribose-5-phosphate Acetaldehyde , Glyceraldehyde 3-phosphate β€” β€” Non-incubated control (in %), assay measured in aqueous phase | Clear about assay in aqueous phase
Stability - Incubation Activity after incubation (10 minutes at 25Β°C), measured by absorbance spectrophotometry NADH absorbance measurement in a coupled reaction with TIM and GPDH, with TIM converting G3P into DHAP, and GPDH reducing DHAP, 340 nm) in aqueous phase Methanol 50% 100 23 % Incubation: 10 mM Tris-HCl buffer, 2M NaCl, Assay: 100 mM citrate-Na citrate buffer, 1 M NaCl, 0.15 mM NADH, 8 U/ml triose-phosphate isomerase (rabbit muscle), 2.5 U/ml glycerol-3-phosphate dehydrogenase (rabbit muscle) Incubation: 8, Assay: 6.4 Incubation: 25Β°C, Assay: 37Β°C 2 mM 2-Deoxyribose-5-phosphate Acetaldehyde , Glyceraldehyde 3-phosphate β€” β€” Non-incubated control (in %), assay measured in aqueous phase | Clear about assay in aqueous phase
Stability - Incubation Activity after incubation (10 minutes at 25Β°C), measured by absorbance spectrophotometry NADH absorbance measurement in a coupled reaction with TIM and GPDH, with TIM converting G3P into DHAP, and GPDH reducing DHAP, 340 nm) in aqueous phase Acetonitrile 10% 100 96 % Incubation: 10 mM Tris-HCl buffer, 2M NaCl, Assay: 100 mM citrate-Na citrate buffer, 1 M NaCl, 0.15 mM NADH, 8 U/ml triose-phosphate isomerase (rabbit muscle), 2.5 U/ml glycerol-3-phosphate dehydrogenase (rabbit muscle) Incubation: 8, Assay: 6.4 Incubation: 25Β°C, Assay: 37Β°C 2 mM 2-Deoxyribose-5-phosphate Acetaldehyde , Glyceraldehyde 3-phosphate β€” β€” Non-incubated control (in %), assay measured in aqueous phase | Clear about assay in aqueous phase
Stability - Incubation Activity after incubation (10 minutes at 25Β°C), measured by absorbance spectrophotometry NADH absorbance measurement in a coupled reaction with TIM and GPDH, with TIM converting G3P into DHAP, and GPDH reducing DHAP, 340 nm) in aqueous phase Ethanol 10% 100 86 % Incubation: 10 mM Tris-HCl buffer, 2M NaCl, Assay: 100 mM citrate-Na citrate buffer, 1 M NaCl, 0.15 mM NADH, 8 U/ml triose-phosphate isomerase (rabbit muscle), 2.5 U/ml glycerol-3-phosphate dehydrogenase (rabbit muscle) Incubation: 8, Assay: 6.4 Incubation: 25Β°C, Assay: 37Β°C 2 mM 2-Deoxyribose-5-phosphate Acetaldehyde , Glyceraldehyde 3-phosphate β€” β€” Non-incubated control (in %), assay measured in aqueous phase | Clear about assay in aqueous phase
Stability - Incubation Activity after incubation (10 minutes at 25Β°C), measured by absorbance spectrophotometry NADH absorbance measurement in a coupled reaction with TIM and GPDH, with TIM converting G3P into DHAP, and GPDH reducing DHAP, 340 nm) in aqueous phase Acetonitrile 30% 100 85 % Incubation: 10 mM Tris-HCl buffer, 2M NaCl, Assay: 100 mM citrate-Na citrate buffer, 1 M NaCl, 0.15 mM NADH, 8 U/ml triose-phosphate isomerase (rabbit muscle), 2.5 U/ml glycerol-3-phosphate dehydrogenase (rabbit muscle) Incubation: 8, Assay: 6.4 Incubation: 25Β°C, Assay: 37Β°C 2 mM 2-Deoxyribose-5-phosphate Acetaldehyde , Glyceraldehyde 3-phosphate β€” β€” Non-incubated control (in %), assay measured in aqueous phase | Clear about assay in aqueous phase
Stability - Incubation Activity after incubation (10 minutes at 25Β°C), measured by absorbance spectrophotometry NADH absorbance measurement in a coupled reaction with TIM and GPDH, with TIM converting G3P into DHAP, and GPDH reducing DHAP, 340 nm) in aqueous phase Acetonitrile 40% 100 83 % Incubation: 10 mM Tris-HCl buffer, 2M NaCl, Assay: 100 mM citrate-Na citrate buffer, 1 M NaCl, 0.15 mM NADH, 8 U/ml triose-phosphate isomerase (rabbit muscle), 2.5 U/ml glycerol-3-phosphate dehydrogenase (rabbit muscle) Incubation: 8, Assay: 6.4 Incubation: 25Β°C, Assay: 37Β°C 2 mM 2-Deoxyribose-5-phosphate Acetaldehyde , Glyceraldehyde 3-phosphate β€” β€” Non-incubated control (in %), assay measured in aqueous phase | Clear about assay in aqueous phase
Stability - Incubation Activity after incubation (10 minutes at 25Β°C), measured by absorbance spectrophotometry NADH absorbance measurement in a coupled reaction with TIM and GPDH, with TIM converting G3P into DHAP, and GPDH reducing DHAP, 340 nm) in aqueous phase Acetonitrile 50% 100 84 % Incubation: 10 mM Tris-HCl buffer, 2M NaCl, Assay: 100 mM citrate-Na citrate buffer, 1 M NaCl, 0.15 mM NADH, 8 U/ml triose-phosphate isomerase (rabbit muscle), 2.5 U/ml glycerol-3-phosphate dehydrogenase (rabbit muscle) Incubation: 8, Assay: 6.4 Incubation: 25Β°C, Assay: 37Β°C 2 mM 2-Deoxyribose-5-phosphate Acetaldehyde , Glyceraldehyde 3-phosphate β€” β€” Non-incubated control (in %), assay measured in aqueous phase | Clear about assay in aqueous phase
Stability - Incubation Activity after incubation (10 minutes at 25Β°C), measured by absorbance spectrophotometry NADH absorbance measurement in a coupled reaction with TIM and GPDH, with TIM converting G3P into DHAP, and GPDH reducing DHAP, 340 nm) in aqueous phase Dimethyl Sulfoxide (DMSO) 10% 100 94 % Incubation: 10 mM Tris-HCl buffer, 2M NaCl, Assay: 100 mM citrate-Na citrate buffer, 1 M NaCl, 0.15 mM NADH, 8 U/ml triose-phosphate isomerase (rabbit muscle), 2.5 U/ml glycerol-3-phosphate dehydrogenase (rabbit muscle) Incubation: 8, Assay: 6.4 Incubation: 25Β°C, Assay: 37Β°C 2 mM 2-Deoxyribose-5-phosphate Acetaldehyde , Glyceraldehyde 3-phosphate β€” β€” Non-incubated control (in %), assay measured in aqueous phase | Clear about assay in aqueous phase
Stability - Incubation Activity after incubation (10 minutes at 25Β°C), measured by absorbance spectrophotometry NADH absorbance measurement in a coupled reaction with TIM and GPDH, with TIM converting G3P into DHAP, and GPDH reducing DHAP, 340 nm) in aqueous phase Dimethyl Sulfoxide (DMSO) 20% 100 96 % Incubation: 10 mM Tris-HCl buffer, 2M NaCl, Assay: 100 mM citrate-Na citrate buffer, 1 M NaCl, 0.15 mM NADH, 8 U/ml triose-phosphate isomerase (rabbit muscle), 2.5 U/ml glycerol-3-phosphate dehydrogenase (rabbit muscle) Incubation: 8, Assay: 6.4 Incubation: 25Β°C, Assay: 37Β°C 2 mM 2-Deoxyribose-5-phosphate Acetaldehyde , Glyceraldehyde 3-phosphate β€” β€” Non-incubated control (in %), assay measured in aqueous phase | Clear about assay in aqueous phase
Stability - Incubation Activity after incubation (10 minutes at 25Β°C), measured by absorbance spectrophotometry NADH absorbance measurement in a coupled reaction with TIM and GPDH, with TIM converting G3P into DHAP, and GPDH reducing DHAP, 340 nm) in aqueous phase Dimethyl Sulfoxide (DMSO) 30% 100 98 % Incubation: 10 mM Tris-HCl buffer, 2M NaCl, Assay: 100 mM citrate-Na citrate buffer, 1 M NaCl, 0.15 mM NADH, 8 U/ml triose-phosphate isomerase (rabbit muscle), 2.5 U/ml glycerol-3-phosphate dehydrogenase (rabbit muscle) Incubation: 8, Assay: 6.4 Incubation: 25Β°C, Assay: 37Β°C 2 mM 2-Deoxyribose-5-phosphate Acetaldehyde , Glyceraldehyde 3-phosphate β€” β€” Non-incubated control (in %), assay measured in aqueous phase | Clear about assay in aqueous phase
1 2 3

Visualization : Stability β€” Incubation

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*