EC Number   |
|---|
    3.5.1.19 | a trapped nicotinoyl-thioester complexed with wild type enzyme and C136S mutant in complex with nicotinamide, hanging drop vapor diffusion method, using 18-22% (w/v) polyethylene glycol 3350, 0.2-0.3 M NaCl and 0.2 M sodium malonate, pH 6.3, at 18°C |
| 3.5.1.19 | crystal structure (PDB ID 2WT9) analysis, and modeling of substrate binding and unbinding, overview |
| 3.5.1.19 | crystal structure (PDB ID 3O94) analysis, and modeling of substrate binding and unbinding, overview |
| 3.5.1.19 | in complex with nicotinaldehyde, hanging drop vapor diffusion method, using 1.6 M NaOAc, 10% (w/v) ethylene glycol, and 0.1 M HEPES (pH 7.4) |
| 3.5.1.19 | resolution 2.9 Angstrom |
| 3.5.1.19 | sitting-drop vapor-diffusion method at 14°C. The crystal structure is determined at 2.0 A resolution. The structure of BsPncA consists of an alpha/beta domain and a subdomain. The subdomain of BsPncA has a different conformation than that of PncA enzymes from other organisms. The B-factor analysis revealed a rigid structure of the alpha/beta domain, while the subdomain is highly flexible. Both dimers and tetramers are observed in crystals, but only dimers are observed in solution |
| 3.5.1.19 | sitting-drop-based and sparse-matrix screening , using 0.7 M Na-citrate and 0.1 M HEPES (pH 7.5) |
