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
CEC-1446WHF1.4022/04/2020Q104Z6 pdb *9EP EDO C 1 2 1155.185 46.298 108.854 ♦ 90.00 116.58 90.008
CEC-1446XFS2.7015/07/2020Q104Z6 pdb *TBE EDO PEG PGE P 1 21 146.915 170.299 89.947 ♦ 90.00 89.98 90.008
CEC-1446XG11.2224/06/2020Q104Z6 pdb EDO C 1 2 1154.865 46.176 108.909 ♦ 90.00 116.54 90.008
CEC-1448TTP1.432023-09-06Q104Z6 pdb *NXL EDO IPA PEG C 1 2 1155.614 46.457 109.126 ♦ 90.00 116.58 90.008
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 (1663); class A (626); subclass B1 (403); subclass B2 (16); subclass B3 (104); class C (246); class D (268).

Last updated: January 08, 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 is 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)