Structures of the human OX1 orexin receptor bound to selective and dual antagonists. Determined by X-ray diffraction at 2.83 Å resolution. Released 9 Mar 2016.
Explore 4ZJC in 3D Show helices and sheets RCSB PDB PDBe
4ZJC contains 25 α-helices and 10 β-strands across 1 chain. 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 | 47-73 | 27 | |
| α-helix | 80-94 | 15 | |
| α-helix | 95-99 | 5 | |
| α-helix | 100-109 | 10 | |
| α-helix | 118-149 | 32 | |
| α-helix | 151-153 | 3 | |
| 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 | 1009-1011 | 3 | |
| α-helix | 1016-1026 | 11 | |
| β-strand | 1033-1038 | 6 | 2 |
| β-strand | 1041 | 1 | 3 |
| α-helix | 1048-1057 | 10 | |
| α-helix | 1064-1066 | 3 | |
| β-strand | 1067-1072 | 6 | 2 |
| β-strand | 1075 | 1 | 3 |
| α-helix | 1077-1089 | 13 | |
| β-strand | 1093-1096 | 4 | 2 |
| α-helix | 1102-1109 | 8 | |
| β-strand | 1114-1117 | 4 | 2 |
| α-helix | 1126-1133 | 8 | |
| α-helix | 1136 | 1 | |
| β-strand | 1137-1141 | 5 | 2 |
| α-helix | 1145-1149 | 5 | |
| β-strand | 1156-1158 | 3 | 2 |
| α-helix | 1163-1176 | 14 | |
| α-helix | 1182-322 | 50 | |
| α-helix | 336-361 | 26 | |
| α-helix | 363-371 | 9 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| human OX1R fusion protein to P.abysii glycogen synthase | A | protein | 553 | Homo sapiens, Pyrococcus abyssi (strain GE5 / Orsay) | O43613 (AlphaFold model), Q9V2J8 (AlphaFold model) |
>4ZJC_1 human OX1R fusion protein to P.abysii glycogen synthase (chains A) DYKDDDDAMEPSATPGAQMGVPPGSREPSPVPPDYEDEFLRYLWRDYLYPKQYEWVLIAA YVAVFVVALVGNTLVCLAVWRNHHMRTVTNYFIVNLSLADVLVTAICLPASLLVDITESW LFGHALCKVIPYLQAVSVSVAVLTLSFIALDRWYAICHPLLFKSTARRARGSILGIWAVS LAIMVPQAAVMECSSVLPELANRTRLFSVCDERWADDLYPKIYHSCFFIVTYLAPLGLMA MAYFQIFRKLWGRQGIDCSFWNESYLTGSRDERKKSLLSKFGMDEGVTFMFIGRFDRGQK GVDVLLKAIEILSSKKEFQEMRFIIIGKGDPELEGWARSLEEKHGNVKVITEMLSREFVR ELYGSVDFVIIPSYFEPFGLVALEAMCLGAIPIASAVGGLRDIITNETGILVKAGDPGEL ANAILKALELSRSDLSKFRENCKKRAMSFSKQMRARRKTAKMLMVVLLVFALCYLPISVL NILKRVFGMFRQASDREAVYACFTFSHWLVYANSAANPIIYNFLSGKFREQFKAAFSCCL PGLHHHHHHHHHH
| ID | Name | Formula | Copies |
|---|---|---|---|
| OLA | Oleic acid | C18 H34 O2 | 2 |
| 4OT | [5-(2-fluorophenyl)-2-methyl-1,3-thiazol-4-yl]{(2S)-2-[(5-phenyl-1,3,4-oxadiazo… | C24 H21 F N4 O2 S | 1 |
Structure and ligand-binding mechanism of the human OX1 and OX2 orexin receptors. Yin, J., Babaoglu, K., Brautigam, C.A. et al. Nat Struct Mol Biol (2016) 23:293-299. DOI 10.1038/nsmb.3183 · 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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