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Crystal structure of the proton pumping rhodopsin AR2 from marine alga acetabularia acetabulum

Analyse Crystal structure of the proton pumping rhodopsin AR2 from marine alga… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3AM6
Type
protein
Length
896 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Rhodopsin-2
Ligands
CLR, RET
Pockets
10 · best druggability 0.82

Structure

x-ray diffraction · 1 distinct chain · 79% helix, 2% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, DRhodopsin-2protein22479% helix, 2% strand—

Ligands and binding sites

  • CLR · Cholesterol · ligand · 8 copies · chains A, B, C, D
  • RET · Retinal · ligand · 4 copies · chains A, B, C, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19650.820.8369empty
21300.800.9723RET
31270.800.9723RET
41250.800.9723RET
51290.790.9624RET

Interfaces

5 interfaces between chains.

  • B–D · 591 Ų buried · 2 hydrogen bonds · protein-protein
  • A–C · 585 Ų buried · 2 hydrogen bonds · protein-protein
  • C–D · 295 Ų buried · 1 hydrogen bond · protein-protein
  • A–B · 295 Ų buried · 1 hydrogen bond · protein-protein
  • B–C · 162 Ų buried · 1 hydrogen bond · protein-protein

Modifications

Observed in the structure: 4 cofactor (retinal Schiff base).

Compared structures

  • 3AM6 · Crystal structure of the proton pumping rhodopsin AR2 from marine alga Acetabularia… · the same entry in another collection · chain A against A, TM-score 1.00

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