Crystal structure of the Orexin-2 receptor in complex with EMPA at 2.74 A resolution. Determined by X-ray diffraction at 2.74 Å resolution. Released 1 Jan 2020.
Explore 6TPG in 3D Show helices and sheets RCSB PDB PDBe
6TPG 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 | 38-45 | 8 | |
| α-helix | 54-81 | 28 | |
| α-helix | 83-85 | 3 | |
| α-helix | 88-106 | 19 | |
| α-helix | 108-117 | 10 | |
| α-helix | 124-156 | 33 | |
| α-helix | 166-183 | 18 | |
| α-helix | 185-190 | 6 | |
| β-strand | 191-194 | 4 | 1 |
| β-strand | 209-212 | 4 | 1 |
| α-helix | 219-228 | 10 | |
| α-helix | 229-233 | 5 | |
| α-helix | 234-247 | 14 | |
| α-helix | 248-253 | 6 | |
| α-helix | 1009-1011 | 3 | |
| α-helix | 1016-1026 | 11 | |
| β-strand | 1033-1038 | 6 | 2 |
| β-strand | 1041 | 1 | 3 |
| α-helix | 1048-1058 | 11 | |
| α-helix | 1062-1066 | 5 | |
| 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 | 1144-1149 | 6 | |
| β-strand | 1156-1158 | 3 | 2 |
| α-helix | 1163-1177 | 15 | |
| α-helix | 1182-328 | 50 | |
| α-helix | 339-367 | 29 | |
| α-helix | 369-383 | 15 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Orexin receptor type 2,GlgA glycogen synthase,Hypocretin receptor-2 | A | protein | 564 | Homo sapiens, Pyrococcus abyssi GE5 | O43614 (AlphaFold model), Q9V2J8 (AlphaFold model) |
>6TPG_1 Orexin receptor type 2,GlgA glycogen synthase,Hypocretin receptor-2 (chains A) QDLDYKDDDDKMSGTKLEDSPPCRDWSSASELDETQEPLLDPTDYDDEEFLRYLWREYLH PKEYAWVLIAGYIIVFVVALIGNVLVCVAVWKNHHMRTVTNLFIVNLSLAAVLVTITCLP ATLVVDITETWFFGQSLCKVIPYLQTVSVSVSALTLSCIALDRWYAICHPLMFKSTAKRA LNSIVIIWIVSCIIMIPQAIVMECSTVFPGLADKTTAFTVCDERWGGEIAPKMYHICFFL VTYAAPLCLMVLLYLQIFRKLWCRQGIDCSFWNESYLTGSRDERKKSLLSKFGMDEGVTF MFIGRFDRGQKGVDVLLKAIEILSSKKEFQEMRFIIIGKGDPELEGWARSLEEKHGNVKV ITEMLSREFVRELYGSVDFVIIPSYFEPFGLVALEAMCLGAIPIASAVGGLRDIITNETG ILVKAGDPGELANAILKALELSRSDLSKFRENCKKRAMSFSKQIRARRKTARMLMVVVLV FAICYAPISILNVLKRVFGMFAHTEDRETVYAWFAFSHWLVYANSAANPIIYNFLSGKFR EEFKAAFSWWWLGVHHHHHHHHHH
| ID | Name | Formula | Copies |
|---|---|---|---|
| 7MA | N-ethyl-2-[(6-methoxypyridin-3-yl)-(2-methylphenyl)sulfonyl-amino]-N-(pyridin-3… | C23 H26 N4 O4 S | 1 |
| OLA | Oleic acid | C18 H34 O2 | 1 |
Water and common crystallization additives (PG4) 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 O43614 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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