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Crystal structure of pcya V225D-biliverdin xiii alpha complex

Analyse Crystal structure of pcya V225D-biliverdin xiii alpha complex in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3AJH
Type
protein
Length
481 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
PHYCOCYANOBILIN:FERREDOXIN oxidoreductase
EC
1.3.7.5
UniProt
Q55891
Ligands
BL3
Pockets
3 · best druggability 0.73

Structure

x-ray diffraction · 2 distinct chains · 38% helix, 25% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APHYCOCYANOBILIN:FERREDOXIN oxidoreductase (EC 1.3.7.5)protein24038% helix, 25% strandQ55891
BPHYCOCYANOBILIN:FERREDOXIN oxidoreductase (EC 1.3.7.5)protein24137% helix, 24% strandQ55891

Ligands and binding sites

  • BL3 · 3-[2-[(Z)-[3-(2-carboxyethyl)-5-[(Z)-(3-ethenyl-4-methyl-5-oxo-pyrrol-2-ylidene)methyl]-4-methyl-pyrrol-2-ylidene]methy l]-5-[(Z)-(3-ethenyl-4-methyl-5-oxo-pyrrol-2-ylidene)methyl]-4-methyl-1H-pyrrol-3-yl]propanoic acid · ligand · 2 copies · chains A, B

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

Pockets

3 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13580.730.8438BL3
23850.720.8350BL3
31610.510.7829empty

Interfaces

1 interface between chains.

  • A–B · 431 Ų buried · 3 hydrogen bonds · protein-protein

Compared structures

  • 3AJH · Crystal structure of PcyA V225D-biliverdin XIII alpha complex · the same entry in another collection · chain A against A, TM-score 1.00
  • Q55891 · AlphaFold monomer V2.0 prediction for PHYCOCYANOBILIN:FERREDOXIN oxidoreductase (Q55891) · a predicted model of the same protein · chain A against A, TM-score 0.98

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