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The crystal structure of allophycocyanin from the red algae gracilaria chilensis

Analyse The crystal structure of allophycocyanin from the red algae gracilaria chilensis in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5TJF
Type
protein
Length
318 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Allophycocyanin alpha subunit; Allophycocyanin beta subunit
UniProt
A0A141SEH2, A0A141SEH3
Ligands
CYC, NA, CL
Pockets
3 · best druggability 0.59

Structure

x-ray diffraction · 2 distinct chains · 78% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AAllophycocyanin alpha subunitprotein15878% helix, 0% strandA0A141SEH2
BAllophycocyanin beta subunitprotein16078% helix, 0% strandA0A141SEH3

Ligands and binding sites

  • CYC · Phycocyanobilin · ligand · 2 copies · chains A, B
  • NA · Sodium ion · metal · 17 copies · chains A, B
  • CL · Chloride ion · ion · 5 copies · chains A, B
  • PEG · Di(hydroxyethyl)ether · additive · 4 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, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11040.590.8620CYC
2830.560.8618CYC
3550.290.7514empty

Interfaces

1 interface between chains.

  • A–B · 1527 Ų buried · 11 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 cofactor, 1 modified (phycocyanobilin attachment, nonstandard).

Compared structures

  • 5TJF · The crystal structure of Allophycocyanin from the red algae Gracilaria chilensis · the same entry in another collection · chain A against A, TM-score 1.00

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