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Crystal structure of TM1821, the 8-oxoguanine DNA glycosylase of thermotoga maritima

Analyse Crystal structure of TM1821, the 8-oxoguanine DNA glycosylase of thermotoga… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3N0U
Type
protein
Length
626 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Probable N-GLYCOSYLASE/DNA lyase
EC
3.2.2.-, 4.2.99.18
UniProt
Q9X2E1
Ligands
NA
Pockets
9 · best druggability 0.72

Structure

x-ray diffraction · 2 distinct chains · 72% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BProbable N-GLYCOSYLASE/DNA lyase (EC 3.2.2.-, 4.2.99.18)protein20972% helix, 0% strandQ9X2E1
CProbable N-GLYCOSYLASE/DNA lyase (EC 3.2.2.-, 4.2.99.18)protein20872% helix, 0% strandQ9X2E1

Ligands and binding sites

  • NA · Sodium ion · metal · 3 copies · chains A, B, C

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17570.720.7872NA
21840.610.8328empty
31890.610.8228empty
41100.520.8225empty
51890.430.7321empty

Interfaces

2 interfaces between chains.

  • A–C · 582 Ų buried · 8 hydrogen bonds · protein-protein
  • A–B · 335 Ų buried · 5 hydrogen bonds · protein-protein

Compared structures

  • 3N0U · Crystal structure of Tm1821, the 8-oxoguanine DNA glycosylase of Thermotoga maritima · the same entry in another collection · chain A against A, TM-score 1.00
  • Q9X2E1 · AlphaFold monomer V2.0 prediction for 8-oxoguanine DNA GLYCOSYLASE/AP lyase (Q9X2E1) · a predicted model of the same protein · chain C against A, TM-score 0.98

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