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
DOXA-11M6K1.502003-01-14P13661 1249383110.1110/PS.0224303pdb KCX MPD P 136.020 51.620 72.890 ♦ 70.19 84.11 81.512
DOXA-13ISG1.402009-12-01P13661 1991910110.1021/BI901690Rpdb *DRW KCX MPD P 1 21 135.041 71.613 93.139 ♦ 90.00 99.18 90.004
DOXA-14MLL1.372013-10-09P13661 2416518010.1128/AAC.01483-13pdbK70D *1S6 MPD PO4 P 150.919 72.609 73.446 ♦ 80.90 69.87 71.444
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)