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Human APE1 substrate complex with an T/C mismatch adjacent the thf

Analyse Human APE1 substrate complex with an T/C mismatch adjacent the thf in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6BOU
Type
protein + DNA
Length
578 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
DNA-(apurinic or apyrimidinic site) lyase; 21-mer DNA
EC
3.1.-.-, 4.2.99.18
UniProt
P27695
Pockets
8 · best druggability 0.60

Structure

x-ray diffraction · 4 distinct chains · 27% helix, 25% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ADNA-(apurinic or apyrimidinic site) lyase (EC 3.1.-.-, 4.2.99.18)protein26726% helix, 25% strandP27695
BDNA-(apurinic or apyrimidinic site) lyase (EC 3.1.-.-, 4.2.99.18)protein26928% helix, 25% strandP27695
P21-mer DNAdna21——
V21-mer DNAdna21——

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13940.600.7654empty
22240.520.7634empty
31590.500.7929empty
41090.480.8017empty
51650.470.7729empty

Interfaces

4 interfaces between chains.

  • P–V · 910 Ų buried · 89 hydrogen bonds · nucleic-nucleic
  • A–P · 729 Ų buried · 9 hydrogen bonds · protein-nucleic
  • A–V · 556 Ų buried · 5 hydrogen bonds · protein-nucleic
  • A–B · 529 Ų buried · 6 hydrogen bonds · protein-protein

Modifications

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

Compared structures

  • 6BOU · Human APE1 substrate complex with an T/C mismatch adjacent the THF · the same entry in another collection · chain A against A, TM-score 1.00
  • P27695 · AlphaFold monomer V2.0 prediction for DNA-(apurinic or apyrimidinic site) endonuclease… · a predicted model of the same protein · chain B against A, TM-score 0.99

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