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MolNFT v2 · #15977 · protein

NMR Solution Structure of Zinc-binding protein 3-methyladenine DNA glycosylase I (TAG)

1NKU: “NMR Solution Structure of Zinc-binding protein 3-methyladenine DNA glycosylase I (TAG)”. Solution nmr at NOT, 1 ligand (ZN), 3 pockets (best druggability 0.46). MolNFT v2 #15977 on GenesisL1: 3D structure, binding sites and pockets…

PDB
1NKU
Type
protein
Length
187 residues
Chains
1
Method
solution nmr
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
NOT
Source
Escherichia coli
Molecule
3-Methyladenine Dna Glycosylase I (TAG)
EC
3.2.2.20
UniProt
P05100
Ligands
ZN
Pockets
3 · best druggability 0.46

Structure

solution nmr · resolution NOT · 1 distinct chain · 57% helix, 2% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A3-Methyladenine Dna Glycosylase I (TAG) (EC 3.2.2.20)protein18757% helix, 2% strandP05100

Ligands and binding sites

  • ZN · Zinc ion · metal · chains A

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

Pockets

3 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11250.460.7821empty
2980.340.7214empty
3500.330.7815empty

Compared structures

  • 1NKU · NMR solution structure of zinc-binding protein 3-methyladenine DNA glycosylase I (tag) · the same entry in another collection · chain A against A, TM-score 1.00
  • P05100 · AlphaFold monomer V2.0 prediction for DNA-3-methyladenine glycosylase 1 (P05100) · a predicted model of the same protein · chain A against A, TM-score 0.89

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