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Structure of L-2-haloacid dehalogenase from xanthobacter autotrophicus

Analyse Structure of L-2-haloacid dehalogenase from xanthobacter autotrophicus in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1AQ6
Type
protein
Length
490 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
L-2-haloacid dehalogenase
EC
3.8.1.2
UniProt
Q60099
Pockets
4 · best druggability 0.66

Structure

x-ray diffraction · 1 distinct chain · 56% helix, 12% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BL-2-haloacid dehalogenase (EC 3.8.1.2)protein24556% helix, 12% strandQ60099

Ligands and binding sites

  • FMT · Formic acid · additive · 3 copies · chains A, 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, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11620.660.8723empty
21540.650.8622FMT
3790.350.7623empty
4910.330.7420empty

Interfaces

1 interface between chains.

  • A–B · 2264 Ų buried · 39 hydrogen bonds · protein-protein

Compared structures

  • 1AQ6 · Structure of L-2-haloacid dehalogenase from xanthobacter autotrophicus · the same entry in another collection · chain A against A, TM-score 1.00
  • Q60099 · AlphaFold monomer V2.0 prediction for (S)-2-haloacid dehalogenase (Q60099) · a predicted model of the same protein · chain A against A, TM-score 0.99

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