Application | Comment | Organism |
---|---|---|
synthesis | the enzyme might be useful for enzymatic synthesis of galactosylfuranoside-containing pharmacophores to be used in mammals | Acetivibrio thermocellus |
Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
---|---|---|---|---|---|---|
alpha-L-arabinofuranosyl-1,4-alpha-D-xylopyranoside + H2O | Acetivibrio thermocellus | - |
L-arabinofuranose + D-xylopyranose | - |
? |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Acetivibrio thermocellus | - |
- |
- |
Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|
4-nitrophenyl alpha-L-arabinofuranoside + H2O | - |
Acetivibrio thermocellus | 4-nitrophenol + L-arabinofuranose | also synthesis of regioisomers of di- to pentaarabinofuranosides | ? | |
alpha-L-arabinofuranosyl-1,4-alpha-D-xylopyranoside + H2O | - |
Acetivibrio thermocellus | L-arabinofuranose + D-xylopyranose | - |
? | |
additional information | the enzyme recognizes both the L-Araf motif and its D-Galf analogue. The arabinofuranosidase is also able to hydrolyze galactosyl derivatives and is efficient in catalyzing oligomerisations using 4-nitrophenyl furanosides as donors. Molecular dynamics and active site structure determination and analysis by NMR, substrate specificity, and product structures by mass spectrometry and NMR.overview | Acetivibrio thermocellus | ? | - |
? |
Synonyms | Comment | Organism |
---|---|---|
arabinofuranosyl hydrolase | - |
Acetivibrio thermocellus |
Araf 51 | - |
Acetivibrio thermocellus |
Temperature Optimum [°C] | Temperature Optimum Maximum [°C] | Comment | Organism |
---|---|---|---|
82 | - |
- |
Acetivibrio thermocellus |
pH Optimum Minimum | pH Optimum Maximum | Comment | Organism |
---|---|---|---|
7 | 8 | - |
Acetivibrio thermocellus |