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MolNFT v1 · #91512 · protein

Crystal structure of levan fructotransferase D54N mutant from arthrobacter ureafaciens in complex with sucrose

4FFH: “Crystal structure of levan fructotransferase D54N mutant from arthrobacter ureafaciens in complex with sucrose”. X-ray diffraction, 2 ligands (GLC, FRU), 20 pockets (best druggability 0.61). MolNFT v1 #91512 on GenesisL1: 3D…

PDB
4FFH
Type
protein
Length
1,918 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Levan fructotransferase
EC
4.2.2.16
UniProt
Q9KJD0
Ligands
GLC, FRU
Pockets
20 · best druggability 0.61

Structure

x-ray diffraction · 2 distinct chains · 8% helix, 49% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, CLevan fructotransferase (EC 4.2.2.16)protein4807% helix, 49% strandQ9KJD0
DLevan fructotransferase (EC 4.2.2.16)protein4788% helix, 50% strandQ9KJD0

Ligands and binding sites

  • GLC · alpha-D-glucopyranose · sugar · 6 copies · chains A, B, C, D
  • FRU · beta-D-fructofuranose · sugar · 6 copies · chains A, B, C, D

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

Pockets

20 pockets found on a 1 Å grid, 10 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12810.610.7928empty
22680.590.7935GLC, FRU
33250.590.7739empty
42740.580.7828empty
52490.580.7925empty

Interfaces

4 interfaces between chains.

  • A–B · 416 Ų buried · 3 hydrogen bonds · protein-protein
  • A–D · 329 Ų buried · 6 hydrogen bonds · protein-protein
  • A–C · 284 Ų buried · 3 hydrogen bonds · protein-protein
  • C–D · 51 Ų buried · 1 hydrogen bond · protein-protein

Compared structures

  • 4FFH · Crystal Structure of Levan Fructotransferase D54N mutant from Arthrobacter ureafaciens in… · the same entry in another collection · chain A against A, TM-score 1.00

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