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Crystal structure of apocarotenoid cleavage oxygenase from synechocystis, native enzyme

Analyse Crystal structure of apocarotenoid cleavage oxygenase from synechocystis… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2BIW
Type
protein
Length
1,916 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Apocarotenoid-cleaving oxygenase
UniProt
P74334
Ligands
3ON, FE
Pockets
20 · best druggability 0.86

Structure

x-ray diffraction · 1 distinct chain · 8% helix, 41% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DApocarotenoid-cleaving oxygenaseprotein4798% helix, 41% strandP74334

Ligands and binding sites

  • 3ON · (3R)-3-hydroxy-8'-apocarotenol · ligand · 4 copies · chains A, B, C, D
  • FE · Fe (III) 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

20 pockets found on a 1 Å grid, 17 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111230.860.87983ON
211180.860.87933ON
311410.850.86823ON
411590.850.85783ON
54160.800.8837empty

Interfaces

3 interfaces between chains.

  • A–C · 582 Ų buried · 7 hydrogen bonds · protein-protein
  • B–D · 505 Ų buried · 7 hydrogen bonds · protein-protein
  • A–B · 437 Ų buried · 5 hydrogen bonds · protein-protein

Compared structures

  • 2BIW · Crystal structure of apocarotenoid cleavage oxygenase from Synechocystis, native enzyme · the same entry in another collection · chain D against D, TM-score 1.00
  • P74334 · AlphaFold monomer V2.0 prediction for apocarotenoid-15,15'-oxygenase (P74334) · a predicted model of the same protein · chain D against A, TM-score 1.00

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