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Crystal structure of alkb in complex with FE(II), 2-oxoglutarate, and methylated trinucleotide T-mea-T (air 9 days)

Analyse Crystal structure of alkb in complex with FE(II), 2-oxoglutarate, and… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2FDK
Type
protein + DNA
Length
201 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
5'-D(P*TP*(MA7)P*T)-3'; Alkylated DNA repair protein alkb
UniProt
P05050
Ligands
AKG, FE2
Pockets
1 · best druggability 0.78

Structure

x-ray diffraction · 2 distinct chains · 16% helix, 34% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
B5'-D(P*TP*(MA7)P*T)-3'dna3——
AAlkylated DNA repair protein alkbprotein19816% helix, 34% strandP05050

Ligands and binding sites

  • AKG · 2-oxoglutaric acid · ligand · chains B, A
  • FE2 · Fe (II) ion · metal · chains B, A
  • SIN · Succinic acid · additive · chains B, A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11020.780.9826FE2, AKG, SIN

Interfaces

1 interface between chains.

  • B–A · 530 Ų buried · 14 hydrogen bonds · protein-nucleic

Modifications

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

Compared structures

  • 2FDK · Crystal Structure of AlkB in complex with Fe(II), 2-oxoglutarate, and methylated… · the same entry in another collection · chain B against B, TM-score 1.00
  • P05050 · AlphaFold monomer V2.0 prediction for alpha-ketoglutarate-dependent dioxygenase alkb… · a predicted model of the same protein · chain A against A, TM-score 0.98

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