GL1X · GenesisL1 explorer

Research workbench

Crystal structure of N2C/D282C stabilized opsin bound to RS08

Analyse Crystal structure of N2C/D282C stabilized opsin bound to RS08 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6FK8
Type
protein
Length
326 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Rhodopsin
UniProt
P02699
Ligands
ACE, PLM, DNZ, NAG, MAN, BMA
Pockets
4 · best druggability 0.83

Structure

x-ray diffraction · 1 distinct chain · 67% helix, 4% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ARhodopsinprotein32667% helix, 4% strandP02699

Ligands and binding sites

  • ACE · Acetyl group · ligand · chains A
  • PLM · Palmitic acid · ligand · chains A
  • DNZ · (2~{R},3~{S})-3-azanyl-2-(4-chlorophenyl)-1-spiro[1,3-benzodioxole-2,4'-piperidine]-1'-yl-butan-1-one · ligand · chains A
  • NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 2 copies · chains A
  • MAN · alpha-D-mannopyranose · sugar · 2 copies
  • BMA · beta-D-mannopyranose · sugar
  • BOG · octyl beta-D-glucopyranoside · additive · 2 copies · chains A

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

Pockets

4 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17950.830.8663DNZ, BOG
2990.570.8520empty
32130.500.7529empty
4630.320.7510empty

Modifications

Observed in the structure: 2 disulfide, 1 covalent, 1 glycan, 1 lipid (disulfide, covalent ligand, N-glycosylation, palmitoylation).

Compared structures

  • 6FK8 · Crystal structure of N2C/D282C stabilized opsin bound to RS08 · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.