GL1X · GenesisL1 explorer

Research workbench

Crystal structure of AmpC Ent385 complex form with avibactam

Analyse Crystal structure of AmpC Ent385 complex form with avibactam in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6LC8
Type
protein
Length
675 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
1.6
Source
Enterobacter cloacae
Molecule
Beta-lactamase
EC
3.5.2.6
Ligands
NXL, SO4
Pockets
7 · best druggability 0.65

Structure

x-ray diffraction · resolution 1.6 · 2 distinct chains · 39% helix, 24% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ABeta-lactamase (EC 3.5.2.6)protein35738% helix, 23% strand—
BBeta-lactamase (EC 3.5.2.6)protein31841% helix, 25% strand—

Ligands and binding sites

  • NXL · (2S,5R)-1-formyl-5-[(sulfooxy)amino]piperidine-2-carboxamide · ligand · 2 copies · chains A, B
  • SO4 · Sulfate ion · ion · 11 copies · chains A, B
  • DIO · 1,4-diethylene dioxide · additive · 4 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15760.650.7673NXL, SO4
21490.440.7527empty
31220.380.7432DIO
4650.380.7916empty
5700.330.7518empty

Interfaces

1 interface between chains.

  • A–B · 708 Ų buried · 6 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 covalent (covalent ligand).

Compared structures

  • 6LC8 · Crystal structure of ampc ENT385 complex form with avibactam · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.