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MolNFT v1 · #151566 · protein

Structure of a far-red fluorescent biliprotein derived from a far-red induced allophycocyanin F subunit from a thermophilic cyanobacterium chroococcidiopsis thermalis

6HRK · Allophycocyanin beta-18 subunit apoprotein: “Structure of a far-red fluorescent biliprotein derived from a far-red induced allophycocyanin F subunit from…”. X-ray diffraction, 1 ligand (BLA), 7 pockets (best druggability 0.60).…

PDB
6HRK
Type
protein
Length
540 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Allophycocyanin beta-18 subunit apoprotein
UniProt
K9TY40
Ligands
BLA
Pockets
7 · best druggability 0.60

Structure

x-ray diffraction · 1 distinct chain · 80% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DAllophycocyanin beta-18 subunit apoproteinprotein13580% helix, 0% strandK9TY40

Ligands and binding sites

  • BLA · Biliverdine IX alpha · ligand · 4 copies · chains A, C, B, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11330.600.8426BLA
21750.590.8226BLA
3950.560.8521BLA
4780.540.8620BLA
51280.540.8124BLA

Interfaces

4 interfaces between chains.

  • A–C · 702 Ų buried · 3 hydrogen bonds · protein-protein
  • A–D · 428 Ų buried · 10 hydrogen bonds · protein-protein
  • B–D · 396 Ų buried · 5 hydrogen bonds · protein-protein
  • A–B · 48 Ų buried · 0 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 cofactor (biliverdin attachment).

Compared structures

  • 6HRK · Structure of a far-red fluorescent biliprotein derived from a far-red induced… · the same entry in another collection · chain A against A, TM-score 1.00

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