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
APenA-13W4Q1.202013-05-15A0A0H3KN52 2365801510.1074/JBC.M113.458315pdb C 1 2 1121.017 69.910 84.350 ♦ 90.00 90.00 90.0012
APenA-17D5J1.512021-03-17A0A0H3KN52 3372398510.1021/ACSINFECDIS.0C00682pdb MES C 1 2 1123.343 71.158 84.541 ♦ 90.00 90.05 90.0012
APenA-17DOO1.602020-12-23A0A0H3KN52 2826456010.1021/ACSINFECDIS.7B00020pdb *NXL C 1 2 1120.108 69.425 84.632 ♦ 90.00 90.05 90.0012
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)