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Crystal structure of muconate lactonizing enzyme from mucobacterium smegmatis complexed with muconolactone

Analyse Crystal structure of muconate lactonizing enzyme from mucobacterium smegmatis… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3DG7
Type
protein
Length
1,464 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Muconate cycloisomerase
EC
5.5.1.-
UniProt
A0QTN8
Ligands
MUC, MG
Pockets
15 · best druggability 0.87

Structure

x-ray diffraction · 1 distinct chain · 42% helix, 22% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DMuconate cycloisomerase (EC 5.5.1.-)protein36642% helix, 22% strandA0QTN8

Ligands and binding sites

  • MUC · [(2S)-5-oxo-2,5-dihydrofuran-2-yl]acetic acid · ligand · 4 copies · chains A, B, 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

15 pockets found on a 1 Å grid, 7 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18580.870.90107empty
21670.820.9733empty
31610.820.9734empty
42830.670.8347empty
52970.660.8237empty

Interfaces

5 interfaces between chains.

  • B–D · 1234 Ų buried · 16 hydrogen bonds · protein-protein
  • C–D · 1198 Ų buried · 19 hydrogen bonds · protein-protein
  • A–B · 1198 Ų buried · 19 hydrogen bonds · protein-protein
  • B–C · 550 Ų buried · 11 hydrogen bonds · protein-protein
  • A–D · 550 Ų buried · 11 hydrogen bonds · protein-protein

Compared structures

  • 3DG7 · Crystal structure of muconate lactonizing enzyme from Mucobacterium Smegmatis complexed… · the same entry in another collection · chain A against A, TM-score 1.00

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