Beta-Lactamase DataBase (BLDB): Structure and Function

Ambler class	Protein name	PDB code	Resolution (Å)	Release date	UniProt code	PDB	Ligands	Space group	Unit cell parameters	Z value
▲ ▼	▲ ▼	▲ ▼	▲ ▼	▲ ▼				▲ ▼
B1	ElBla2-1	6V3U	2.00	2020-01-15	Q2N9N3	pdb	EDO IPA MSE OCS SO4 ZN	P 41	80.043 80.043 72.502 ♦ 90.00 90.00 90.00	8
B1	ElBla2-1	6V72	1.50	2019-12-25	Q2N9N3	pdb	CA CL EDO FMT MSE	P 3 2 1	96.985 96.985 45.186 ♦ 90.00 90.00 120.00	6
B1	ElBla2-1	6V73	2.40	2019-12-25	Q2N9N3	pdb	^#BME CL FMT ZN	P 63 2 2	121.139 121.139 90.551 ♦ 90.00 90.00 120.00	12

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)

Structures