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Biuret Hydrolase (BiuH) from Rhodococcus sp. Mel C169S bound with biuret

Analyse Biuret Hydrolase (BiuH) from Rhodococcus sp. Mel C169S bound with biuret in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6XJM
Type
protein
Length
911 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
2.05
Source
Rhodococcus sp. Mel
Molecule
Biuret hydrolase
UniProt
H8ZKV9
Ligands
C5J
Pockets
5 · best druggability 0.87

Structure

x-ray diffraction · resolution 2.05 · 4 distinct chains · 39% helix, 21% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ABiuret hydrolaseprotein22640% helix, 22% strandH8ZKV9
BBiuret hydrolaseprotein22738% helix, 19% strandH8ZKV9
CBiuret hydrolaseprotein22838% helix, 22% strandH8ZKV9
DBiuret hydrolaseprotein23039% helix, 20% strandH8ZKV9

Ligands and binding sites

  • C5J · dicarbonimidic diamide · ligand · 4 copies · chains A, D, B, C

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15130.870.9444empty
22860.610.8033empty
32820.610.7934empty
42820.600.7933empty
53160.590.7736empty

Interfaces

6 interfaces between chains.

  • B–C · 2019 Ų buried · 40 hydrogen bonds · protein-protein
  • A–D · 2009 Ų buried · 38 hydrogen bonds · protein-protein
  • A–B · 858 Ų buried · 11 hydrogen bonds · protein-protein
  • C–D · 846 Ų buried · 11 hydrogen bonds · protein-protein
  • A–C · 234 Ų buried · 8 hydrogen bonds · protein-protein

Compared structures

  • 6XJM · Biuret hydrolase (biuh) from rhodococcus sp. mel C169S bound with biuret · the same entry in another collection · chain A against A, TM-score 1.00

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