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Crystal structure of a putative gamma-carboxymuconolactone decarboxylase subunit (BXE_B0980) from burkholderia xenovorans LB400 at 1.70 a resolution

Analyse Crystal structure of a putative gamma-carboxymuconolactone decarboxylase… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2Q0T
Type
protein
Length
756 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Putative gamma-carboxymuconolactone decarboxylase subunit
UniProt
Q13LR5
Pockets
7 · best druggability 0.77

Structure

x-ray diffraction · 2 distinct chains · 76% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APutative gamma-carboxymuconolactone decarboxylase subunitprotein25875% helix, 0% strandQ13LR5
B, CPutative gamma-carboxymuconolactone decarboxylase subunitprotein24978% helix, 0% strandQ13LR5

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11260.770.9624empty
21280.770.9527empty
31630.740.9130empty
42550.640.8235empty
52030.520.7725empty

Interfaces

3 interfaces between chains.

  • A–B · 2358 Ų buried · 27 hydrogen bonds · protein-protein
  • B–C · 2096 Ų buried · 24 hydrogen bonds · protein-protein
  • A–C · 2052 Ų buried · 16 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 7 modified (engineered).

Compared structures

  • 2Q0T · Crystal structure of a putative gamma-carboxymuconolactone decarboxylase subunit… · the same entry in another collection · chain A against A, TM-score 1.00

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