Beta-Lactamase DataBase (BLDB): Structure and Function

Ambler class	Protein name	PDB code	Resolution (Å)	Release date	UniProt code	PubMed ID	DOI	PDB	Ligands	Space group	Unit cell parameters	Z value
▲ ▼	▲ ▼	▲ ▼	▲ ▼	▲ ▼						▲ ▼
C	MOX-1	3W8K	1.50	2014-04-23	Q51578	24777102	10.1128/AAC.02363-13	pdb	ACT SEP ZN	P 1 21 1	49.617 59.378 62.685 ♦ 90.00 102.19 90.00	2
C	MOX-1	4WBG	1.90	2015-07-01	Q51578	26055361	10.1128/AAC.04428-14	pdb	*AZR ACT ZN	P 1 21 1	49.540 59.250 62.480 ♦ 90.00 102.72 90.00	2
C	MOX-1	5ZYB	2.13	2019-06-26	Q51578			pdb	^$ZXM ACT ZN	P 1 21 1	49.640 59.200 62.890 ♦ 90.00 102.03 90.00	2

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: 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

Live statistics (since December 3rd, 2023)

Structures