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Ambler class |
Protein name |
PDB code |
Resolution (Å) |
Release date |
UniProt code |
PubMed ID |
DOI |
PDB |
Mutations |
Ligands |
Space group |
Unit cell parameters |
Z value |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| ▲ ▼ | ▲ ▼ | ▲ ▼ | ▲ ▼ | ▲ ▼ | ▲ ▼ | ||||||||
| C | ADC-212 | 8FQR | 1.24 | 2023-07-05 | 37358467 | 10.1021/ACS.JMEDCHEM.3C00144 | pdb | GLY PO4 | P 1 21 1 | 49.388 69.805 55.124 ♦ 90.00 114.96 90.00 | 2 | ||
| C | ADC-212 | 8FQS | 1.21 | 2023-07-05 | 37358467 | 10.1021/ACS.JMEDCHEM.3C00144 | pdb | *YDB DMS PO4 | P 21 21 21 | 46.483 71.818 103.964 ♦ 90.00 90.00 90.00 | 4 |
Statistics (number of structures): Overall (1805); class A (681); subclass B1 (470); subclass B2 (16); subclass B3 (104); class C (249); class D (285).
Last updated: January 22, 2025.
If you use BLDB please cite: Naas, T.; Oueslati, S.; Bonnin, R. A.; Dabos, M. L.; Zavala, A.; Dortet, L.; Retailleau, P.; Iorga, B. I., Beta-Lactamase DataBase (BLDB) – Structure and Function. J. Enzyme Inhib. Med. Chem. 2017, 32, 917-919.
The development of the BLDB database was funded in part by the JPIAMR transnational project DesInMBL, the Région Ile-de-France (DIM Malinf) and the Laboratory of Excellence in Research on Medication and Innovative Therapeutics (LERMIT).
Contact: contact@bldb.eu
