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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
▲ ▼ | ▲ ▼ | ▲ ▼ | ▲ ▼ | ▲ ▼ | ▲ ▼ | ||||||||
A | KPC-3 | 6QWA | 1.06 | 2019-08-21 | Q93DC4 | 31383664 | 10.1128/AAC.00564-19 | pdb | *MK7 EOH GOL JJT SO4 | P 21 21 2 | 60.128 78.717 55.806 ♦ 90.00 90.00 90.00 | 4 | |
A | KPC-3 | 6QWD | 1.20 | 2019-08-21 | A0A220QIS6 | 31383664 | 10.1128/AAC.00564-19 | pdb | GOL SO4 | P 21 21 2 | 60.006 78.624 56.008 ♦ 90.00 90.00 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