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Crystal structure of the K142Q mutant of E.COLI muty (core fragment)

Analyse Crystal structure of the K142Q mutant of E.COLI muty (core fragment) in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1KG5
Type
protein
Length
225 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
A/G-specific adenine glycosylase
EC
3.2.2.-
UniProt
P17802
Ligands
SF4, SO4
Pockets
2 · best druggability 0.68

Structure

x-ray diffraction · 1 distinct chain · 62% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AA/G-specific adenine glycosylase (EC 3.2.2.-)protein22562% helix, 0% strandP17802

Ligands and binding sites

  • SF4 · Iron/sulfur cluster · ligand · chains A
  • SO4 · Sulfate ion · ion · chains A
  • GOL · Glycerol · additive · 4 copies · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1520.680.9615SF4
21550.500.7824GOL

Compared structures

  • 1KG5 · Crystal structure of the K142Q mutant of E.coli MutY (core fragment) · the same entry in another collection · chain A against A, TM-score 1.00
  • P17802 · AlphaFold monomer V2.0 prediction for adenine DNA glycosylase (P17802) · a predicted model of the same protein · chain A against A, TM-score 0.99

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