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Crystal structures of D-allulose 3-epimerase with D-fructose from sinorhizobium fredii

Analyse Crystal structures of D-allulose 3-epimerase with D-fructose from sinorhizobium… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7DZ3
Type
protein
Length
1,136 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
D-tagatose 3-epimerase
EC
5.1.3.-
UniProt
A0A249Q1V1
Ligands
FUD, MG
Pockets
12 · best druggability 0.87

Structure

x-ray diffraction · 2 distinct chains · 46% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BD-tagatose 3-epimerase (EC 5.1.3.-)protein28345% helix, 15% strandA0A249Q1V1
C, DD-tagatose 3-epimerase (EC 5.1.3.-)protein28546% helix, 15% strandA0A249Q1V1

Ligands and binding sites

  • FUD · D-fructose · ligand · 2 copies · chains C, D
  • MG · Magnesium 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

12 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16050.870.9257empty
2610.740.9923FUD
3700.740.9823FUD
42960.690.8334empty
52600.680.8435empty

Interfaces

6 interfaces between chains.

  • A–D · 1630 Ų buried · 26 hydrogen bonds · protein-protein
  • B–C · 1627 Ų buried · 27 hydrogen bonds · protein-protein
  • C–D · 570 Ų buried · 12 hydrogen bonds · protein-protein
  • A–B · 559 Ų buried · 11 hydrogen bonds · protein-protein
  • A–C · 435 Ų buried · 8 hydrogen bonds · protein-protein

Compared structures

  • 7DZ3 · Crystal structures of D-allulose 3-epimerase with D-fructose from Sinorhizobium fredii · the same entry in another collection · chain A against A, TM-score 1.00

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