Research workbench

E. COLI (lacz) beta-galactosidase (E537Q) in complex with onpg

Analyse E. COLI (lacz) beta-galactosidase (E537Q) in complex with onpg in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB: 1JYV
Type: protein
Length: 4,044 residues
Chains: 4
Method: x-ray diffraction
Collection: MolNFT v1 / PDB
Contract: 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner: 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule: Beta-galactosidase
EC: 3.2.1.23
UniProt: P00722
Ligands: 145, MG, NA
Pockets: 20 · best druggability 0.80

Structure

x-ray diffraction · 1 distinct chain · 14% helix, 41% strand (DSSP).

Chain	Molecule	Type	Residues	Secondary structure	UniProt
A, B, C, D	Beta-galactosidase (EC 3.2.1.23)	protein	1011	14% helix, 41% strand	P00722

Ligands and binding sites

145 · 2-nitrophenyl beta-D-galactopyranoside · ligand · 8 copies · chains A, D, B, C
MG · Magnesium ion · metal · 17 copies · chains A, B, C, D
NA · Sodium ion · metal · 16 copies · chains A, B, C, D
DMS · Dimethyl sulfoxide · additive · 107 copies · chains A, D, B, C

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

20 pockets found on a 1 Å grid, 20 with a druggability of 0.5 or more.

Pocket	Volume (Å³)	Druggability	Buriedness	Lining residues	Inside
1	861	0.80	0.83	86	empty
2	703	0.79	0.83	97	DMS
3	671	0.77	0.83	76	empty
4	1061	0.76	0.79	107	DMS
5	1106	0.75	0.78	95	DMS

Interfaces

6 interfaces between chains.

A–D · 2364 Å² buried · 33 hydrogen bonds · protein-protein
B–C · 2340 Å² buried · 37 hydrogen bonds · protein-protein
A–B · 2019 Å² buried · 33 hydrogen bonds · protein-protein
C–D · 1993 Å² buried · 31 hydrogen bonds · protein-protein
B–D · 138 Å² buried · 3 hydrogen bonds · protein-protein

Compared structures

1JYV · E. COLI (lacZ) BETA-GALACTOSIDASE (E537Q) IN COMPLEX WITH ONPG · the same entry in another collection · chain D against D, TM-score 1.00
P00722 · AlphaFold monomer V2.0 prediction for beta-galactosidase (P00722) · a predicted model of the same protein · chain D against A, TM-score 1.00

Analyse

Open in the research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides and crosslinks on the 3D structure
Every structure of UniProt P00722
Elsewhere: RCSB PDB 1JYV · PDBe 1JYV · UniProt P00722

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