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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
▲ ▼ | ▲ ▼ | ▲ ▼ | ▲ ▼ | ▲ ▼ | ▲ ▼ | ||||||||
D | BPU-1 | 5CTM | 1.00 | 2015-11-18 | A8FFI9 | 26551395 | 10.1038/NCHEMBIO.1950 | pdb | EDO FLC KCX PEG | P 1 21 1 | 47.660 79.870 65.010 ♦ 90.00 92.29 90.00 | 4 | |
D | BPU-1 | 5CTN | 1.35 | 2015-11-25 | A8FFI9 | 26551395 | 10.1038/NCHEMBIO.1950 | pdb | *5R7 FLC | P 1 21 1 | 47.802 80.002 64.949 ♦ 90.00 92.85 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