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Crystal structure of 0.5M urea unfolded yage, a kdg aldolase protein in complex with pyruvate

Analyse Crystal structure of 0.5M urea unfolded yage, a kdg aldolase protein in complex… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4U4M
Type
protein
Length
1,192 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Yage
Ligands
URE, PYR
Pockets
6 · best druggability 0.74

Structure

x-ray diffraction · 1 distinct chain · 51% helix, 12% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DYageprotein29851% helix, 12% strand—

Ligands and binding sites

  • URE · Urea · ligand · 10 copies · chains A, C, B, D
  • PYR · Pyruvic acid · ligand · 4 copies · chains A, B, C, D
  • EDO · 1,2-ethanediol · additive · 10 copies · chains A, B, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11580.740.9236empty
22040.700.8841URE
32870.650.8140URE, PYR
42660.650.8239PYR
53080.640.8043URE, PYR

Interfaces

4 interfaces between chains.

  • C–D · 1720 Ų buried · 29 hydrogen bonds · protein-protein
  • A–B · 1714 Ų buried · 30 hydrogen bonds · protein-protein
  • B–D · 990 Ų buried · 23 hydrogen bonds · protein-protein
  • A–C · 963 Ų buried · 24 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 covalent (covalent ligand).

Compared structures

  • 4U4M · Crystal structure of 0.5M urea unfolded YagE, a KDG aldolase protein in complex with… · the same entry in another collection · chain A against A, TM-score 1.00

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