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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-219 | 8FQT | 1.89 | 2023-07-05 | 37358467 | 10.1021/ACS.JMEDCHEM.3C00144 | pdb | PO4 | P 21 21 21 | 43.041 83.567 206.469 ♦ 90.00 90.00 90.00 | 8 | ||
| C | ADC-219 | 8FQU | 1.49 | 2023-07-05 | 37358467 | 10.1021/ACS.JMEDCHEM.3C00144 | pdb | *YDB DMS | P 1 21 1 | 45.517 172.435 49.470 ♦ 90.00 111.68 90.00 | 4 |
Statistics (number of structures): Overall (1663); class A (626); subclass B1 (403); subclass B2 (16); subclass B3 (104); class C (246); class D (268).
Last updated: November 20, 2024.
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