| Crystallization (Comment) | Organism |
|---|---|
| structure to 1.9 A resolution | Arabidopsis thaliana |
| KM Value [mM] | KM Value Maximum [mM] | Substrate | Comment | Organism | Structure |
|---|---|---|---|---|---|
| 4.8 | - |
meso-2,6-diaminoheptanedioate | pH 8.0, 30°C | Arabidopsis thaliana | |
| 5.1 | - |
meso-2,6-diaminoheptanedioate | pH 8.0, 30°C | Arabidopsis thaliana |
| Molecular Weight [Da] | Molecular Weight Maximum [Da] | Comment | Organism |
|---|---|---|---|
| 50000 | - |
and 100000, analytical ultracentrifugation | Arabidopsis thaliana |
| 100000 | - |
and 50000, analytical ultracentrifugation | Arabidopsis thaliana |
| Organism | UniProt | Comment | Textmining |
|---|---|---|---|
| Arabidopsis thaliana | Q949X7 | isoform DAPDC1 | - |
| Arabidopsis thaliana | Q94A94 | isoform DAPDC2 | - |
| Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
|---|---|---|---|---|---|---|
| meso-2,6-Diaminoheptanedioate | - |
Arabidopsis thaliana | L-Lysine + CO2 | - |
? |
| Subunits | Comment | Organism |
|---|---|---|
| dimer | and monmer, 2 * 53807, calculated from sequence. Dimer is predominant | Arabidopsis thaliana |
| dimer | and monmer, 2 * 54240, calculated from sequence. Dimer is predominant | Arabidopsis thaliana |
| monomer | and dimer, 1 * 53807, calculated from sequence. Dimer is predominant | Arabidopsis thaliana |
| monomer | and dimer, 1 * 54240, calculated from sequence. Dimer is predominant | Arabidopsis thaliana |
| Synonyms | Comment | Organism |
|---|---|---|
| At3g14390 | locus name | Arabidopsis thaliana |
| At5g11880 | locus name | Arabidopsis thaliana |
| DAPDC1 | - |
Arabidopsis thaliana |
| DAPDC2 | - |
Arabidopsis thaliana |
| LYSA1 | - |
Arabidopsis thaliana |
| LYSA2 | - |
Arabidopsis thaliana |
| Turnover Number Minimum [1/s] | Turnover Number Maximum [1/s] | Substrate | Comment | Organism | Structure |
|---|---|---|---|---|---|
| 0.005 | - |
meso-2,6-diaminoheptanedioate | pH 8.0, 30°C | Arabidopsis thaliana | |
| 0.014 | - |
meso-2,6-diaminoheptanedioate | pH 8.0, 30°C | Arabidopsis thaliana |
| Cofactor | Comment | Organism | Structure |
|---|---|---|---|
| pyridoxal 5'-phosphate | - |
Arabidopsis thaliana |
| General Information | Comment | Organism |
|---|---|---|
| metabolism | binding of PLP initiates rearrangements within the active site, specifically the reorientation of Arg169, His218, and His22, which is propagated to the active-site loop, through Arg169. The substrate, meso-diaminopimelate, is positioned through interactions with conserved active-site residues to form an additional hydrogen bond to His220. This stabilizes the closed active-site loop conformation, mediated through Arg169, and can only occur when the D-stereocenter is oriented for decarboxylation | Arabidopsis thaliana |
| physiological function | expression of DAPDC1 rescues Escherichia coli that harbors a mutation in the gene encoding DAPDC. DAPDC1 is only able to rescue the mutant when its expression is repressed by glucose | Arabidopsis thaliana |
| physiological function | expression of DAPDC2 rescues Escherichia coli that harbors a mutation in the gene encoding DAPDC. DAPDC2 is only able to rescue the mutant when its expression is repressed by glucose | Arabidopsis thaliana |