Crystal structure of the Orexin-1 receptor in complex with GSK1059865. Determined by X-ray diffraction at 2.13 Å resolution. Released 15 Jan 2020.
Explore 6TOS in 3D Show helices and sheets RCSB PDB PDBe
6TOS contains 32 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 | 28-35 | 8 | |
| α-helix | 36-40 | 5 | |
| α-helix | 41-73 | 33 | |
| α-helix | 75-77 | 3 | |
| α-helix | 80-94 | 15 | |
| α-helix | 95-99 | 5 | |
| α-helix | 100-109 | 10 | |
| α-helix | 115-148 | 34 | |
| α-helix | 158-175 | 18 | |
| α-helix | 177-182 | 6 | |
| β-strand | 183-187 | 5 | 1 |
| β-strand | 200-204 | 5 | 1 |
| α-helix | 211-220 | 10 | |
| α-helix | 221-225 | 5 | |
| α-helix | 226-242 | 17 | |
| α-helix | 287-322 | 36 | |
| α-helix | 333-361 | 29 | |
| α-helix | 363-375 | 13 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 45-73 | 29 | |
| 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 | 2 |
| α-helix | 190-194 | 5 | |
| β-strand | 200-204 | 5 | 2 |
| α-helix | 210-220 | 11 | |
| α-helix | 221-225 | 5 | |
| α-helix | 226-243 | 18 | |
| α-helix | 245-247 | 3 | |
| α-helix | 252-322 | 39 | |
| α-helix | 333-361 | 29 | |
| α-helix | 363-376 | 14 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Orexin receptor type 1 | A, B | protein | 336 | Homo sapiens | O43613 (AlphaFold model) |
>6TOS_1 Orexin receptor type 1 (chains A, B) AASEDEFLRYLWRDYLYPKQYAWVLIAAYVAVFVVALVGNTLVCLAVWRNHHMRTVTNYF LVNLSLADVLATAICLPASLLVDITESWLFGHALCKVIPYLQAVSVSVAVLTLSFIALDR WYAICHPLLFKSTARRALGSILGIWAVSLAIMVPQAAVMECSSVLPELAARTRAFSVCDE RWADDLAPKIYHSCFFIVTYLAPLGLMAMAYFQIFRKLWGRQIPGTTSAEVKQMRARRKT AKMLMVVVLVFALCYLPISVLNVLKRVFGMFRQASDREAVYAAFTFSHWLVYANSAANPI IYNFLSGKFREQFKAAFSWWLPGLAAAHHHHHHHHH
| ID | Name | Formula | Copies |
|---|---|---|---|
| NRE | [(2~{S},5~{S})-2-[[(5-bromanylpyridin-2-yl)amino]methyl]-5-methyl-piperidin-1-y… | C20 H23 Br F N3 O2 | 2 |
| CIT | Citric acid | C6 H8 O7 | 2 |
| SOG | octyl 1-thio-beta-D-glucopyranoside | C14 H28 O5 S | 27 |
| PGW | (1R)-2-{[(S)-{[(2S)-2,3-dihydroxypropyl]oxy}(hydroxy)phosphoryl]oxy}-1-[(hexade… | C40 H77 O10 P | 2 |
Water and common crystallization additives (PG4, SO4, 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:
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