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Oxa-48 in complex with compound 6B

Analyse Oxa-48 in complex with compound 6B in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5QAB
Type
protein
Length
966 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Beta-lactamase
EC
3.5.2.6
UniProt
Q6XEC0
Ligands
XEV, CL
Pockets
9 · best druggability 0.72

Structure

x-ray diffraction · 2 distinct chains · 40% helix, 20% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, DBeta-lactamase (EC 3.5.2.6)protein24240% helix, 20% strandQ6XEC0
B, CBeta-lactamase (EC 3.5.2.6)protein24140% helix, 20% strandQ6XEC0

Ligands and binding sites

  • XEV · 3-(3-methoxyphenyl)benzoic acid · ligand · 3 copies · chains A, B, D
  • CL · Chloride ion · ion · chains D
  • EDO · 1,2-ethanediol · additive · 4 copies · chains B, C, D

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

Pockets

9 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15660.720.8168XEV
24500.720.8253empty
33580.640.7939EDO
41670.470.7626empty
51030.360.7420empty

Interfaces

5 interfaces between chains.

  • A–B · 515 Ų buried · 5 hydrogen bonds · protein-protein
  • B–C · 375 Ų buried · 6 hydrogen bonds · protein-protein
  • C–D · 341 Ų buried · 5 hydrogen bonds · protein-protein
  • A–C · 268 Ų buried · 4 hydrogen bonds · protein-protein
  • B–D · 24 Ų buried · 0 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 modified (carboxylation).

Compared structures

  • 5QAB · OXA-48 IN COMPLEX WITH COMPOUND 6b · the same entry in another collection · chain A against A, TM-score 1.00

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