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ECAII(D90T,K162T) mutant in complex with citrate at pH 5

Analyse ECAII(D90T,K162T) mutant in complex with citrate at pH 5 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6NX6
Type
protein
Length
625 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
2.15
Source
Escherichia coli (strain K12)
Molecule
L-asparaginase 2
EC
3.5.1.1
UniProt
P00805
Pockets
4 · best druggability 0.61

Structure

x-ray diffraction · resolution 2.15 · 2 distinct chains · 34% helix, 21% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AL-asparaginase 2 (EC 3.5.1.1)protein31334% helix, 21% strandP00805
BL-asparaginase 2 (EC 3.5.1.1)protein31234% helix, 21% strandP00805

Ligands and binding sites

  • ACY · Acetic acid · additive · chains A
  • CIT · Citric acid · additive · chains B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13780.610.7759empty
21350.470.7821empty
3650.290.7417CIT
4590.290.7518ACY

Interfaces

1 interface between chains.

  • A–B · 990 Ų buried · 15 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 disulfide (disulfide).

Compared structures

  • 6NX6 · ECAII(D90T,K162T) mutant in complex with citrate at pH 5 · the same entry in another collection · chain A against A, TM-score 1.00
  • P00805 · AlphaFold monomer V2.0 prediction for L-asparaginase 2 (P00805) · a predicted model of the same protein · chain B against A, TM-score 0.99

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