9TMP
Crystal Structure of Native Cytochrome b562 in complex with the synthetic anti-BRIL antibody BAG2.
Summary for 9TMP
| Entry DOI | 10.2210/pdb9tmp/pdb |
| Descriptor | Soluble cytochrome b562, anti-BRIL antibody - heavy chain, anti-BRIL antibody - light chain, ... (5 entities in total) |
| Functional Keywords | cytochrome, fab, bril, protein binding |
| Biological source | synthetic construct More |
| Total number of polymer chains | 3 |
| Total formula weight | 62502.62 |
| Authors | Cooper, B.F.,Isom, G.L. (deposition date: 2025-12-15, release date: 2026-03-25, Last modification date: 2026-04-01) |
| Primary citation | Cooper, B.F.,Isom, G.L. Optimized bacterial expression of a synthetic BRIL antibody. Acta Crystallogr.,Sect.F, 2026 Cited by PubMed Abstract: The use of monoclonal fragments antigen binding (Fabs) is a prevalent methodology facilitating protein structure determination via both crystallography and cryo-EM. The development of a synthetic Fab against the BRIL domain improved the accessibility of this approach, providing a general fiducial applicable to any protein of interest via the simple curation of a BRIL fusion protein. Here, we document the generation of a T7 Express ΔcybC strain allowing contaminant-free bacterial expression of the synthetic anti-BRIL Fab BAG2. We also report the crystal structure of BAG2 in complex with native cytochrome b, a complex arising from expression in canonical Escherichia coli strains. PubMed: 41842660DOI: 10.1107/S2053230X26001548 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (2.65 Å) |
Structure validation
Download full validation report






