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Solution structure and base perturbation studies reveal a novel mode of alkylated base recognition by 3-methyladenine DNA glycosylase I

Analyse Solution structure and base perturbation studies reveal a novel mode of… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1P7M
Type
protein
Length
187 residues
Chains
1
Method
solution nmr
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
DNA-3-methyladenine glycosylase I
EC
3.2.2.20
UniProt
P05100
Ligands
ADK, ZN
Pockets
4 · best druggability 0.63

Structure

solution nmr · 1 distinct chain · 55% helix, 2% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ADNA-3-methyladenine glycosylase I (EC 3.2.2.20)protein18755% helix, 2% strandP05100

Ligands and binding sites

  • ADK · 3-methyl-3H-purin-6-ylamine · ligand · chains A
  • ZN · Zinc ion · metal · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11920.630.8324empty
21050.460.7917ADK
3540.420.8215empty
4540.340.7817empty

Compared structures

  • 1P7M · Solution structure and base perturbation studies reveal a novel mode of alkylated base… · 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 0.90

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