| Cloned (Comment) | Organism |
|---|---|
| expression in Escherichia coli BL21(DE3) | Acinetobacter baumannii |
| Crystallization (Comment) | Organism |
|---|---|
| sitting drop vapor-diffusion method at 18°C, high-resolution cocrystal structure of CatB8 with chloramphenicol | Acinetobacter baumannii |
| Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
|---|---|---|---|---|---|---|
| acetyl-CoA + chloramphenicol | Acinetobacter baumannii | - |
CoA + chloramphenicol 3-acetate | - |
? |
| Organism | UniProt | Comment | Textmining |
|---|---|---|---|
| Acinetobacter baumannii | Q6Q627 | - |
- |
| Purification (Comment) | Organism |
|---|---|
- |
Acinetobacter baumannii |
| Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
|---|---|---|---|---|---|---|
| acetyl-CoA + chloramphenicol | - |
Acinetobacter baumannii | CoA + chloramphenicol 3-acetate | - |
? | |
| acetyl-CoA + chloramphenicol | chloramphenicol is recruited through the key residues D41, Q77, and E94. chloramphenicol and acetyl-CoA enter the catalytic pocket of CatB8, where an acetylation reaction takes place | Acinetobacter baumannii | CoA + chloramphenicol 3-acetate | - |
? |
| Synonyms | Comment | Organism |
|---|---|---|
| catB8 | - |
Acinetobacter baumannii |