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N288Q-N321Q mutant beta-lactamase derived from chromohalobacter SP.560 (condition-1C)

Analyse N288Q-N321Q mutant beta-lactamase derived from chromohalobacter SP.560… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3WS2
Type
protein
Length
1,080 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Beta-lactamase
EC
3.5.2.6
UniProt
Q76LX5
Ligands
CA, CS
Pockets
6 · best druggability 0.71

Structure

x-ray diffraction · 2 distinct chains · 39% helix, 22% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ABeta-lactamase (EC 3.5.2.6)protein36040% helix, 22% strandQ76LX5
B, CBeta-lactamase (EC 3.5.2.6)protein36039% helix, 22% strandQ76LX5

Ligands and binding sites

  • CA · Calcium ion · metal · 10 copies · chains A, B, C
  • CS · Cesium ion · metal · chains A

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

Pockets

6 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17930.710.7770empty
27470.700.7771CA
33280.570.7641empty
42800.550.7639empty
52840.550.7641empty

Interfaces

2 interfaces between chains.

  • A–B · 367 Ų buried · 7 hydrogen bonds · protein-protein
  • A–C · 335 Ų buried · 2 hydrogen bonds · protein-protein

Compared structures

  • 3WS2 · N288Q-N321Q mutant BETA-LACTAMASE DERIVED FROM CHROMOHALOBACTER SP.560 (Condition-1C) · the same entry in another collection · chain A against A, TM-score 1.00

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