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MolNFT v1 · #15391 · protein + DNA

Structural and biochemical exploration of a critical amino acid in human 8-oxoguanine glycosylase

1N3C · DNA complement strand: “Structural and biochemical exploration of a critical amino acid in human 8-oxoguanine glycosylase”. X-ray diffraction, 1 ligand (CA), 5 pockets (best druggability 0.62). MolNFT v1 #15391 on GenesisL1: 3D…

PDB
1N3C
Type
protein + DNA
Length
344 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
DNA complement strand; 8-oxog-containing DNA; N-GLYCOSYLASE/DNA lyase
UniProt
O15527
Ligands
CA
Pockets
5 · best druggability 0.62

Structure

x-ray diffraction · 3 distinct chains · 51% helix, 11% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
BDNA complement stranddna15——
C8-oxog-containing DNAdna15——
AN-GLYCOSYLASE/DNA lyaseprotein31451% helix, 11% strandO15527

Ligands and binding sites

  • CA · Calcium ion · metal · chains C, A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14430.620.7641CA
2720.480.8318empty
31480.460.7720empty
4780.300.7314empty
5580.270.7411empty

Interfaces

3 interfaces between chains.

  • C–A · 782 Ų buried · 25 hydrogen bonds · protein-nucleic
  • B–C · 616 Ų buried · 58 hydrogen bonds · nucleic-nucleic
  • B–A · 410 Ų buried · 15 hydrogen bonds · protein-nucleic

Modifications

Observed in the structure: 1 modified (nucleotide modification).

Compared structures

  • 1N3C · Structural and biochemical exploration of a critical amino acid in human 8-oxoguanine… · the same entry in another collection · chain B against B, TM-score 1.00
  • O15527 · AlphaFold monomer V2.0 prediction for N-GLYCOSYLASE/DNA lyase (O15527) · a predicted model of the same protein · chain A against A, TM-score 0.99

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