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Crystal structure of the gracilariopsis lemaneiformis alpha-1,4- glucan lyase covalent intermediate complex with 5-fluoro-glucosyl- fluoride

Analyse Crystal structure of the gracilariopsis lemaneiformis alpha-1,4- glucan lyase… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4AMX
Type
protein
Length
4,100 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Alpha-1,4-glucan lyase isozyme 1
EC
4.2.2.13
UniProt
Q9STC1
Ligands
5GF, AFR
Pockets
20 · best druggability 0.77

Structure

x-ray diffraction · 1 distinct chain · 19% helix, 29% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DAlpha-1,4-glucan lyase isozyme 1 (EC 4.2.2.13)protein102519% helix, 29% strandQ9STC1

Ligands and binding sites

  • 5GF · 5-fluoro-beta-D-glucopyranose · ligand · 3 copies · chains A, B, C
  • AFR · alpha-D-threo-hexo-2,5-diulo-5,1-pyranosyl fluoride · ligand · chains D
  • GOL · Glycerol · additive · 5 copies · chains A, B, 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, 20 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11020.770.9730empty
21030.760.9737empty
3600.751.0019empty
4630.700.9630empty
5650.700.9625empty

Interfaces

3 interfaces between chains.

  • A–C · 788 Ų buried · 25 hydrogen bonds · protein-protein
  • B–D · 133 Ų buried · 6 hydrogen bonds · protein-protein
  • A–B · 79 Ų buried · 0 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 modified, 3 covalent (oxidation, covalent ligand).

Compared structures

  • 4AMX · CRYSTAL STRUCTURE OF THE GRACILARIOPSIS LEMANEIFORMIS ALPHA-1,4- GLUCAN LYASE Covalent… · the same entry in another collection · chain A against A, TM-score 1.00

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