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Structure of E.COLI rhomboid protease glpg in complex with monobactam L29

Analyse Structure of E.COLI rhomboid protease glpg in complex with monobactam L29 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3ZMI
Type
protein
Length
174 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Rhomboid protease glpg
EC
3.4.21.105
UniProt
P09391
Ligands
BNG, L6C
Pockets
2 · best druggability 0.65

Structure

x-ray diffraction · 1 distinct chain · 78% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ARhomboid protease glpg (EC 3.4.21.105)protein17478% helix, 0% strandP09391

Ligands and binding sites

  • BNG · nonyl beta-D-glucopyranoside · ligand · 6 copies · chains A
  • L6C · phenyl N-[(1R)-3-oxidanylidene-1-phenyl-propyl]carbamate · ligand · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12640.650.8230L6C
2850.390.7616BNG

Modifications

Observed in the structure: 1 covalent (covalent ligand).

Compared structures

  • 3ZMI · Structure of E.coli rhomboid protease GlpG in complex with monobactam L29 · the same entry in another collection · chain A against A, TM-score 1.00
  • P09391 · AlphaFold monomer V2.0 prediction for rhomboid protease glpg (P09391) · a predicted model of the same protein · chain A against A, TM-score 0.99

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