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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 | TRU-1 | 6FM6 | 1.05 | 2018-05-30 | B2BSN6 | 29786960 | 10.1002/CMDC.201800213 | pdb | PGE SO4 | P 1 21 1 | 45.885 78.345 48.190 ♦ 90.00 106.63 90.00 | 2 | |
| C | TRU-1 | 6FM7 | 1.04 | 2018-05-30 | B2BSN6 | 29786960 | 10.1002/CMDC.201800213 | pdb | *NXL EDO SO4 | P 1 21 1 | 45.552 78.248 48.306 ♦ 90.00 106.54 90.00 | 2 |
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: July 23, 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