Beta-Lactamase DataBase
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Beta-Lactamase DataBase

Structures

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
ABlaA-15E2E1.902015-10-28A1JML9 pdb MSE P 21 21 2142.116 93.513 122.219 ♦ 90.00 90.00 90.008
ABlaA-18IWV2.402024-04-03Q01166 pdb PO4 C 1 2 189.450 72.647 43.887 ♦ 90.00 94.30 90.004
ABlaA-18IX81.502024-04-03Q01166 pdb *TEB PO4 C 1 2 191.342 72.182 43.543 ♦ 90.00 96.09 90.004
ABlaA-18IXX1.702024-04-03Q01166 pdb *1RG PO4 C 1 2 191.743 72.818 43.700 ♦ 90.00 95.78 90.004
ABlaA-18IY42.002024-04-03Q01166 pdb *MER PO4 C 1 2 191.774 72.619 43.707 ♦ 90.00 94.95 90.004
Legend for ligands: * Ligand covalently-bound to active site residues; $ Non-covalent ligand (Michaelis complex); # Ligand coordinated to active site metal ions.

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

Live statistics (since December 3rd, 2023)