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Crystal structure of the epimerase snon in complex with FE3+, alpha ketoglutarate and nogalamycin ro

Analyse Crystal structure of the epimerase snon in complex with FE3+, alpha… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5EQU
Type
protein
Length
1,024 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
SNON,SNON
UniProt
Q9RN67, Q9EYI0
Ligands
AKG, 5R6, FE
Pockets
13 · best druggability 0.82

Structure

x-ray diffraction · 1 distinct chain · 29% helix, 27% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DSNON,SNONprotein25629% helix, 27% strandQ9RN67, Q9EYI0

Ligands and binding sites

  • AKG · 2-oxoglutaric acid · ligand · 4 copies · chains A, B, C, D
  • 5R6 · Nogalamycin RO · ligand · 4 copies · chains A, B, C, D
  • FE · Fe (III) ion · metal · 4 copies · chains A, B, C, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19620.820.8494empty
22960.760.8734FE, AKG, 5R6
33050.750.8736FE, AKG, 5R6
410810.740.7780empty
52860.740.8641AKG, 5R6

Interfaces

5 interfaces between chains.

  • A–D · 684 Ų buried · 4 hydrogen bonds · protein-protein
  • A–B · 625 Ų buried · 5 hydrogen bonds · protein-protein
  • C–D · 603 Ų buried · 4 hydrogen bonds · protein-protein
  • A–C · 143 Ų buried · 0 hydrogen bonds · protein-protein
  • B–D · 99 Ų buried · 1 hydrogen bond · protein-protein

Compared structures

  • 5EQU · Crystal structure of the epimerase SnoN in complex with Fe3+, alpha ketoglutarate and… · the same entry in another collection · chain A against A, TM-score 1.00

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