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Ndm-1 metallo-beta-lactamase: a parsimonious interpretation of the diffraction data

Analyse Ndm-1 metallo-beta-lactamase: a parsimonious interpretation of the diffraction… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5NBK
Type
protein
Length
463 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Metallo-beta-lactamase type 2
EC
3.5.2.6
UniProt
C7C422
Ligands
ZN, CL
Pockets
3 · best druggability 0.79

Structure

x-ray diffraction · 2 distinct chains · 26% helix, 30% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AMetallo-beta-lactamase type 2 (EC 3.5.2.6)protein23724% helix, 30% strandC7C422
CMetallo-beta-lactamase type 2 (EC 3.5.2.6)protein22627% helix, 30% strandC7C422

Ligands and binding sites

  • ZN · Zinc ion · metal · 4 copies · chains A, C
  • CL · Chloride ion · ion · 2 copies · chains A, C
  • PG4 · Tetraethylene glycol · additive · 3 copies · chains A, C
  • P6G · Hexaethylene glycol · additive · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11060.790.9821empty
2600.310.7616empty
3620.300.7516PG4

Interfaces

1 interface between chains.

  • A–C · 929 Ų buried · 5 hydrogen bonds · protein-protein

Compared structures

  • 5NBK · NDM-1 metallo-beta-lactamase: a parsimonious interpretation of the diffraction data · the same entry in another collection · chain A against A, TM-score 1.00
  • C7C422 · AlphaFold monomer V2.0 prediction for metallo-beta-lactamase type 2 (C7C422) · a predicted model of the same protein · chain C against A, TM-score 0.99

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