Crystal structure of the Orexin-1 receptor in complex with SB-408124. Determined by X-ray diffraction at 2.65 Å resolution. Released 1 Jan 2020.
Explore 6TQ9 in 3D Show helices and sheets RCSB PDB PDBe
6TQ9 contains 35 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 | 80-93 | 14 | |
| α-helix | 94-99 | 6 | |
| α-helix | 100-109 | 10 | |
| α-helix | 115-144 | 30 | |
| α-helix | 145-149 | 5 | |
| α-helix | 158-175 | 18 | |
| α-helix | 177-182 | 6 | |
| β-strand | 183-186 | 4 | 1 |
| β-strand | 201-204 | 4 | 1 |
| α-helix | 210-220 | 11 | |
| α-helix | 221-225 | 5 | |
| α-helix | 226-242 | 17 | |
| α-helix | 252-322 | 39 | |
| α-helix | 333-361 | 29 | |
| α-helix | 363-375 | 13 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 46-73 | 28 | |
| α-helix | 75-77 | 3 | |
| α-helix | 80-93 | 14 | |
| α-helix | 94-99 | 6 | |
| α-helix | 100-109 | 10 | |
| α-helix | 115-144 | 30 | |
| α-helix | 145-149 | 5 | |
| 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 | 211-220 | 10 | |
| α-helix | 221-225 | 5 | |
| α-helix | 226-239 | 14 | |
| α-helix | 240-244 | 5 | |
| α-helix | 252-322 | 39 | |
| α-helix | 330-332 | 3 | |
| 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) |
>6TQ9_1 Orexin receptor type 1 (chains A, B) AASEDEFLRYLWRDYLYPKQYAWVLIAAYVAVFVVALVGNTLVCLAVWRNHHMRTVTNYF LVNLSLADVLATAICLPASLLVDITESWLFGHALCKVIPYLQAVSVSVAVLTLSFIALDR WYAICHPLLFKSTARRALGSILGIWAVSLAIMVPQAAVMECSSVLPELAARTRAFSVCDE RWADDLAPKIYHSCFFIVTYLAPLGLMAMAYFQIFRKLWGRQIPGTTSAEVKQMRARRKT AKMLMVVVLVFALCYLPISVLNVLKRVFGMFRQASDREAVYAAFTFSHWLVYANSAANPI IYNFLSGKFREQFKAAFSWWLPGLAAAHHHHHHHHH
| ID | Name | Formula | Copies |
|---|---|---|---|
| NVN | 1-[6,8-bis(fluoranyl)-2-methyl-quinolin-4-yl]-3-[4-(dimethylamino)phenyl]urea | C19 H18 F2 N4 O | 3 |
| SOG | octyl 1-thio-beta-D-glucopyranoside | C14 H28 O5 S | 10 |
| 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) 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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