GL1X · GenesisL1 explorer

MolNFT v1 · #131650 · protein

Oxa-48 in complex with compound 26B

5QAV · Beta-lactamase: “Oxa-48 in complex with compound 26B”. X-ray diffraction, 2 ligands (L43, CL), 11 pockets (best druggability 0.78). MolNFT v1 #131650 on GenesisL1: 3D structure, binding sites and pockets in GL1X.

PDB
5QAV
Type
protein
Length
968 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
L43, CL
Pockets
11 · best druggability 0.78

Structure

x-ray diffraction · 1 distinct chain · 40% helix, 21% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DBeta-lactamase (EC 3.5.2.6)protein24240% helix, 21% strandQ6XEC0

Ligands and binding sites

  • L43 · 3-[4-(1~{H}-1,2,3,4-tetrazol-5-yl)phenyl]benzoic acid · ligand · 2 copies · chains C, D
  • CL · Chloride ion · ion · 2 copies · chains C, D
  • EDO · 1,2-ethanediol · additive · 9 copies · chains A, B, C, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110410.780.8091empty
28420.740.7991EDO
31790.490.7627empty
4610.370.7918empty
5570.360.7917empty

Interfaces

5 interfaces between chains.

  • A–B · 454 Ų buried · 5 hydrogen bonds · protein-protein
  • B–C · 397 Ų buried · 8 hydrogen bonds · protein-protein
  • C–D · 271 Ų buried · 1 hydrogen bond · protein-protein
  • A–C · 265 Ų buried · 4 hydrogen bonds · protein-protein
  • B–D · 11 Ų buried · 0 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 modified (carboxylation).

Compared structures

  • 5QAV · OXA-48 IN COMPLEX WITH COMPOUND 26b · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

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