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Protocatechuate 3,4-dioxygenase Y408E mutant

Analyse Protocatechuate 3,4-dioxygenase Y408E mutant in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1YKM
Type
protein
Length
2,628 residues
Chains
12
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Protocatechuate 3,4-dioxygenase alpha chain; Protocatechuate 3,4-dioxygenase beta chain
EC
1.13.11.3
UniProt
P00436, P00437
Ligands
FE
Pockets
20 · best druggability 0.82

Structure

x-ray diffraction · 2 distinct chains · 9% helix, 31% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, C, E, G, I, KProtocatechuate 3,4-dioxygenase alpha chain (EC 1.13.11.3)protein2009% helix, 32% strandP00436
B, D, F, H, J, LProtocatechuate 3,4-dioxygenase beta chain (EC 1.13.11.3)protein2388% helix, 30% strandP00437

Ligands and binding sites

  • FE · Fe (III) ion · metal · 6 copies · chains B, D, F, H, J, L

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

Pockets

20 pockets found on a 1 Å grid, 14 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18970.820.8486empty
28980.810.8389empty
31290.800.9840empty
47940.800.8377empty
55380.800.8655empty

Interfaces

35 interfaces between chains.

  • I–J · 3784 Ų buried · 65 hydrogen bonds · protein-protein
  • A–B · 3774 Ų buried · 65 hydrogen bonds · protein-protein
  • C–D · 3773 Ų buried · 65 hydrogen bonds · protein-protein
  • K–L · 3764 Ų buried · 69 hydrogen bonds · protein-protein
  • E–F · 3764 Ų buried · 64 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 6 modified (artifact).

Compared structures

  • 1YKM · Protocatechuate 3,4-Dioxygenase Y408E mutant · the same entry in another collection · chain L against L, TM-score 1.00

Analyse

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