KM Value [mM] | KM Value Maximum [mM] | Substrate | Comment | Organism | Structure |
---|---|---|---|---|---|
0.67 | - |
4-hydroxyphenylpyruvate | - |
Berberis stolonifera |
Molecular Weight [Da] | Molecular Weight Maximum [Da] | Comment | Organism |
---|---|---|---|
30000 | - |
HPLC gel filtration | Berberis stolonifera |
Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
---|---|---|---|---|---|---|
4-hydroxyphenylpyruvate | Berberis stolonifera | involved in tyrosine metabolism, precursor of tyrosine, early steps of isoquinoline alkaloid biosynthesis | 4-hydroxyphenylacetaldehyde + CO2 | phenylacetaldehydes furnish the benzylic moiety of the isoquinoline alkaloids in their biosynthesis, formation of the 1-benzylisoquinoline structure requires the condensation of p-hydroxyphenylacetaldehyde with dopamine to form norcoclaurine | ? | |
4-hydroxyphenylpyruvate | Berberis canadensis | involved in tyrosine metabolism, precursor of tyrosine, early steps of isoquinoline alkaloid biosynthesis | 4-hydroxyphenylacetaldehyde + CO2 | phenylacetaldehydes furnish the benzylic moiety of the isoquinoline alkaloids in their biosynthesis, formation of the 1-benzylisoquinoline structure requires the condensation of p-hydroxyphenylacetaldehyde with dopamine to form norcoclaurine | ? |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Berberis aristata | - |
- |
- |
Berberis canadensis | - |
produces large amounts of protoberberine alkaloids of the jatrorrhizine type | - |
Berberis julianae | - |
- |
- |
Berberis regeliana | - |
- |
- |
Berberis stolonifera | - |
- |
- |
Eschscholzia californica | - |
- |
- |
Hyalosepalum caffrum | - |
- |
- |
Thalictrum dipterocarpum | - |
- |
- |
Thalictrum minus | - |
- |
- |
Tinospora cordifolia | - |
- |
- |
Purification (Comment) | Organism |
---|---|
29fold partial purification | Berberis stolonifera |
Source Tissue | Comment | Organism | Textmining |
---|---|---|---|
callus | - |
Berberis canadensis | - |
cell suspension culture | - |
Eschscholzia californica | - |
cell suspension culture | - |
Berberis regeliana | - |
cell suspension culture | - |
Thalictrum minus | - |
cell suspension culture | - |
Berberis stolonifera | - |
cell suspension culture | - |
Berberis julianae | - |
cell suspension culture | - |
Thalictrum dipterocarpum | - |
cell suspension culture | - |
Hyalosepalum caffrum | - |
cell suspension culture | - |
Tinospora cordifolia | - |
cell suspension culture | - |
Berberis aristata | - |
Specific Activity Minimum [µmol/min/mg] | Specific Activity Maximum [µmol/min/mg] | Comment | Organism |
---|---|---|---|
additional information | - |
values given as pkat/litre of suspension culture | Eschscholzia californica |
additional information | - |
values given as pkat/litre of suspension culture | Berberis regeliana |
additional information | - |
values given as pkat/litre of suspension culture | Thalictrum minus |
additional information | - |
values given as pkat/litre of suspension culture | Berberis julianae |
additional information | - |
values given as pkat/litre of suspension culture | Thalictrum dipterocarpum |
additional information | - |
values given as pkat/litre of suspension culture | Hyalosepalum caffrum |
additional information | - |
values given as pkat/litre of suspension culture | Tinospora cordifolia |
additional information | - |
values given as pkat/litre of suspension culture | Berberis aristata |
0.001271 | - |
- |
Berberis stolonifera |
Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|
4-hydroxyphenylpyruvate | - |
Berberis stolonifera | 4-hydroxyphenylacetaldehyde + CO2 | - |
? | |
4-hydroxyphenylpyruvate | - |
Berberis canadensis | 4-hydroxyphenylacetaldehyde + CO2 | - |
? | |
4-hydroxyphenylpyruvate | involved in tyrosine metabolism, precursor of tyrosine, early steps of isoquinoline alkaloid biosynthesis | Berberis stolonifera | 4-hydroxyphenylacetaldehyde + CO2 | phenylacetaldehydes furnish the benzylic moiety of the isoquinoline alkaloids in their biosynthesis, formation of the 1-benzylisoquinoline structure requires the condensation of p-hydroxyphenylacetaldehyde with dopamine to form norcoclaurine | ? | |
4-hydroxyphenylpyruvate | involved in tyrosine metabolism, precursor of tyrosine, early steps of isoquinoline alkaloid biosynthesis | Berberis canadensis | 4-hydroxyphenylacetaldehyde + CO2 | phenylacetaldehydes furnish the benzylic moiety of the isoquinoline alkaloids in their biosynthesis, formation of the 1-benzylisoquinoline structure requires the condensation of p-hydroxyphenylacetaldehyde with dopamine to form norcoclaurine | ? |
Temperature Optimum [°C] | Temperature Optimum Maximum [°C] | Comment | Organism |
---|---|---|---|
30 | - |
assay at | Berberis stolonifera |
pH Optimum Minimum | pH Optimum Maximum | Comment | Organism |
---|---|---|---|
6.5 | - |
- |
Berberis stolonifera |