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Anion-free blue form of pharaonis halorhodopsin

Analyse Anion-free blue form of pharaonis halorhodopsin in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3QBG
Type
protein
Length
781 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Halorhodopsin
UniProt
Q3ITX1
Ligands
BNG, RET, 22B
Pockets
8 · best druggability 0.79

Structure

x-ray diffraction · 2 distinct chains · 73% helix, 4% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AHalorhodopsinprotein26172% helix, 4% strandQ3ITX1
B, DHalorhodopsinprotein26073% helix, 5% strandQ3ITX1

Ligands and binding sites

  • BNG · nonyl beta-D-glucopyranoside · ligand · 4 copies · chains A, D, B
  • RET · Retinal · ligand · 3 copies · chains A, B, D
  • 22B · Bacterioruberin · ligand · 2 copies · chains A, B, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11300.790.9722RET
21270.790.9624RET
31170.780.9623RET
44990.710.8051empty
55490.710.795222B

Interfaces

3 interfaces between chains.

  • A–D · 808 Ų buried · 6 hydrogen bonds · protein-protein
  • A–B · 781 Ų buried · 6 hydrogen bonds · protein-protein
  • B–D · 757 Ų buried · 6 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 3 cofactor (retinal Schiff base).

Compared structures

  • 3QBG · Anion-free blue form of pharaonis halorhodopsin · the same entry in another collection · chain A against A, TM-score 1.00

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