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Triazine hydrolase from arthobacter aurescens modified for maximum expression in E.COLI

Analyse Triazine hydrolase from arthobacter aurescens modified for maximum expression… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4LH8
Type
protein
Length
911 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Triazine hydrolase
EC
3.8.1.8
UniProt
Q6SJY7
Ligands
ZN
Pockets
9 · best druggability 0.80

Structure

x-ray diffraction · 2 distinct chains · 39% helix, 23% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ATriazine hydrolase (EC 3.8.1.8)protein45639% helix, 23% strandQ6SJY7
BTriazine hydrolase (EC 3.8.1.8)protein45538% helix, 23% strandQ6SJY7

Ligands and binding sites

  • ZN · Zinc ion · metal · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11410.800.9835empty
21190.780.9727empty
32530.740.8840empty
42070.580.8025empty
51980.530.7824empty

Interfaces

1 interface between chains.

  • A–B · 2730 Ų buried · 39 hydrogen bonds · protein-protein

Compared structures

  • 4LH8 · Triazine hydrolase from Arthobacter aurescens modified for maximum expression in E.coli · the same entry in another collection · chain A against A, TM-score 1.00

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