MolNFT v1 · #163540 · protein
Dark-adapted structure of archaerhodopsin-3 obtained from lcp crystals using a thin-film sandwich at room temperature
6S63: “Dark-adapted structure of archaerhodopsin-3 obtained from lcp crystals using a thin-film sandwich at room…”. X-ray diffraction, 5 ligands (R16, RET, CA), 1 pocket (best druggability 0.81). MolNFT v1 #163540 on GenesisL1: 3D…
- PDB
- 6S63
- Type
- protein
- Length
- 241 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Archaerhodopsin-3
- UniProt
- P96787
- Ligands
- R16, RET, CA, NA, CL
- Pockets
- 1 · best druggability 0.81
Structure
x-ray diffraction · 1 distinct chain · 74% helix, 5% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Archaerhodopsin-3 | protein | 241 | 74% helix, 5% strand | P96787 |
Ligands and binding sites
- R16 · Hexadecane · ligand · 4 copies · chains A
- RET · Retinal · ligand · chains A
- CA · Calcium ion · metal · chains A
- NA · Sodium ion · metal · chains A
- CL · Chloride ion · ion · 3 copies · chains A
- DD9 · nonane · additive · 5 copies · chains A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
1 pocket found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 143 | 0.81 | 0.97 | 23 | RET |
Modifications
Observed in the structure: 1 cofactor, 1 modified (retinal Schiff base, cyclization).
Compared structures
- 6S63 · Dark-adapted structure of Archaerhodopsin-3 obtained from LCP crystals using a thin-film… · the same entry in another collection · chain A against A, TM-score 1.00
- P96787 · AlphaFold monomer V2.0 prediction for archaerhodopsin-3 (P96787) · a predicted model of the same protein · chain A against A, TM-score 0.97
Analyse
- Open in the research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides and crosslinks on the 3D structure
- Every structure of UniProt P96787
- Elsewhere: RCSB PDB 6S63 · PDBe 6S63 · UniProt P96787
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