Crystal structure of the Orexin-1 receptor in complex with EMPA. Determined by X-ray diffraction at 2.11 Å resolution. Released 1 Jan 2020.
Explore 6TOD in 3D Show helices and sheets RCSB PDB PDBe
6TOD contains 36 α-helices and 4 β-strands across 2 chains. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 46-73 | 28 | |
| α-helix | 75-77 | 3 | |
| α-helix | 80-94 | 15 | |
| α-helix | 95-99 | 5 | |
| α-helix | 100-109 | 10 | |
| α-helix | 115-149 | 35 | |
| α-helix | 158-175 | 18 | |
| α-helix | 177-182 | 6 | |
| β-strand | 183-187 | 5 | 1 |
| α-helix | 190-192 | 3 | |
| β-strand | 200-204 | 5 | 1 |
| α-helix | 211-220 | 10 | |
| α-helix | 221-225 | 5 | |
| α-helix | 226-242 | 17 | |
| α-helix | 245-247 | 3 | |
| α-helix | 287-322 | 36 | |
| α-helix | 330-332 | 3 | |
| α-helix | 333-361 | 29 | |
| α-helix | 363-371 | 9 | |
| α-helix | 372-376 | 5 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 30-35 | 6 | |
| α-helix | 36-45 | 10 | |
| α-helix | 46-72 | 27 | |
| α-helix | 75-77 | 3 | |
| α-helix | 80-94 | 15 | |
| α-helix | 95-99 | 5 | |
| α-helix | 100-109 | 10 | |
| α-helix | 115-149 | 35 | |
| α-helix | 158-175 | 18 | |
| α-helix | 177-182 | 6 | |
| β-strand | 183-186 | 4 | 2 |
| β-strand | 201-204 | 4 | 2 |
| α-helix | 211-220 | 10 | |
| α-helix | 221-225 | 5 | |
| α-helix | 226-242 | 17 | |
| α-helix | 253-322 | 38 | |
| α-helix | 333-361 | 29 | |
| α-helix | 363-371 | 9 | |
| α-helix | 372-376 | 5 | |
| α-helix | 377-382 | 6 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Orexin receptor type 1 | A, B | protein | 336 | Homo sapiens | O43613 (AlphaFold model) |
>6TOD_1 Orexin receptor type 1 (chains A, B) AASEDEFLRYLWRDYLYPKQYAWVLIAAYVAVFVVALVGNTLVCLAVWRNHHMRTVTNYF LVNLSLADVLATAICLPASLLVDITESWLFGHALCKVIPYLQTVSVSVAVLTLSFIALDR WYAICHPLLFKSTARRALGSILGIWAVSLAIMVPQAAVMECSSVLPELAARTRAFSVCDE RWADDLAPKIYHSCFFIVTYLAPLGLMAMAYFQIFRKLWGRQIPGTTSAEVKQMRARRKT AKMLMVVVLVFALCYLPISVLNVLKRVFGMFRQASDREAVYAAFTFSHWLVYANSAANPI IYNFLSGKFREQFKAAFSWWLPGLAAAHHHHHHHHH
| ID | Name | Formula | Copies |
|---|---|---|---|
| 7MA | N-ethyl-2-[(6-methoxypyridin-3-yl)-(2-methylphenyl)sulfonyl-amino]-N-(pyridin-3… | C23 H26 N4 O4 S | 2 |
| CIT | Citric acid | C6 H8 O7 | 1 |
| SOG | octyl 1-thio-beta-D-glucopyranoside | C14 H28 O5 S | 47 |
| PGW | (1R)-2-{[(S)-{[(2S)-2,3-dihydroxypropyl]oxy}(hydroxy)phosphoryl]oxy}-1-[(hexade… | C40 H77 O10 P | 2 |
Water and common crystallization additives (SO4, PG4, NA) are not listed.
Comparison of Orexin 1 and Orexin 2 Ligand Binding Modes Using X-ray Crystallography and Computational Analysis. Rappas, M., Ali, A.A.E., Bennett, K.A. et al. J Med Chem (2020) 63:1528-1543. DOI 10.1021/acs.jmedchem.9b01787 · PubMed
Other PDB entries of the same protein (UniProt O43613 (AlphaFold model), which also has an AlphaFold model), best resolution first:
MolViewer shows 6TOD directly in your browser with nothing to install. Switch between cartoon, ball-and-stick, spacefill and surface views, color by chain, secondary structure or B-factor, measure distances, angles and dihedrals, and share or embed the view.