The structure of the TEIPP associated altered peptide ligand Trh4-p5NLE in complex with H-2D(b). Determined by X-ray diffraction at 2.0 Å resolution. Released 3 Feb 2016.
Explore 5E8P in 3D Show helices and sheets RCSB PDB PDBe
5E8P contains 18 α-helices and 60 β-strands across 4 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 |
|---|---|---|---|
| β-strand | 3-13 | 11 | 1 |
| β-strand | 21-28 | 8 | 1 |
| β-strand | 31-37 | 7 | 1 |
| β-strand | 46-47 | 2 | 1 |
| α-helix | 50-54 | 5 | |
| α-helix | 57-84 | 28 | |
| β-strand | 93-103 | 11 | 1 |
| β-strand | 109-118 | 10 | 1 |
| β-strand | 121-126 | 6 | 1 |
| β-strand | 133-134 | 2 | 1 |
| α-helix | 141-150 | 10 | |
| α-helix | 152-161 | 10 | |
| α-helix | 163-174 | 12 | |
| β-strand | 183 | 1 | 2 |
| β-strand | 186-195 | 10 | 3 |
| β-strand | 198-208 | 11 | 3 |
| β-strand | 209 | 1 | 2 |
| β-strand | 214-218 | 5 | 4 |
| β-strand | 223 | 1 | 4 |
| β-strand | 229-230 | 2 | 3 |
| β-strand | 234-235 | 2 | 3 |
| β-strand | 241-249 | 9 | 3 |
| α-helix | 254-256 | 3 | |
| β-strand | 258-262 | 5 | 4 |
| β-strand | 270-272 | 3 | 4 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 3 | 1 | 5 |
| α-helix | 4-5 | 2 | |
| β-strand | 6-11 | 6 | 6 |
| β-strand | 21-30 | 10 | 6 |
| β-strand | 31 | 1 | 5 |
| β-strand | 36-41 | 6 | 7 |
| β-strand | 44-45 | 2 | 7 |
| β-strand | 50-51 | 2 | 6 |
| α-helix | 52-54 | 3 | |
| β-strand | 55-56 | 2 | 6 |
| β-strand | 62-70 | 9 | 6 |
| β-strand | 78-83 | 6 | 7 |
| β-strand | 91-94 | 4 | 7 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 3-13 | 11 | 8 |
| β-strand | 21-28 | 8 | 8 |
| β-strand | 31-37 | 7 | 8 |
| β-strand | 46-47 | 2 | 8 |
| α-helix | 50-54 | 5 | |
| α-helix | 57-84 | 28 | |
| α-helix | 87-88 | 2 | |
| β-strand | 93-103 | 11 | 8 |
| β-strand | 109-118 | 10 | 8 |
| β-strand | 121-126 | 6 | 8 |
| β-strand | 133-134 | 2 | 8 |
| α-helix | 138-150 | 13 | |
| α-helix | 152-161 | 10 | |
| α-helix | 163-173 | 11 | |
| β-strand | 183 | 1 | 9 |
| α-helix | 184-185 | 2 | |
| β-strand | 186-193 | 8 | 10 |
| β-strand | 199-208 | 10 | 10 |
| β-strand | 209 | 1 | 9 |
| β-strand | 214-218 | 5 | 11 |
| β-strand | 223 | 1 | 11 |
| β-strand | 228-230 | 3 | 10 |
| β-strand | 234-235 | 2 | 10 |
| β-strand | 241-249 | 9 | 10 |
| α-helix | 254-256 | 3 | |
| β-strand | 258-262 | 5 | 11 |
| β-strand | 270-272 | 3 | 11 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| H-2 class I histocompatibility antigen, D-B alpha chain | A, D | protein | 276 | Mus musculus | P01899 (AlphaFold model) |
| Beta-2-microglobulin | B, E | protein | 99 | Mus musculus | P01887 (AlphaFold model) |
| Ceramide synthase 5 | C, F | protein | 9 | Mus musculus | Q9D6K9 (AlphaFold model) |
>5E8P_1 H-2 class I histocompatibility antigen, D-B alpha chain (chains A, D) GPHSMRYFETAVSRPGLEEPRYISVGYVDNKEFVRFDSDAENPRYEPRAPWMEQEGPEYW ERETQKAKGQEQWFRVSLRNLLGYYNQSAGGSHTLQQMSGCDLGSDWRLLRGYLQFAYEG RDYIALNEDLKTWTAADMAAQITRRKWEQSGAAEHYKAYLEGECVEWLHRYLKNGNATLL RTDSPKAHVTHHPRSKGEVTLRCWALGFYPADITLTWQLNGEELTQDMELVETRPAGDGT FQKWASVVVPLGKEQNYTCRVYHEGLPEPLTLRWEP
>5E8P_2 Beta-2-microglobulin (chains B, E) IQKTPQIQVYSRHPPENGKPNILNCYVTQFHPPHIEIQMLKNGKKIPKVEMSDMSFSKDW SFYILAHTEFTPTETDTYACRVKHDSMAEPKTVYWDRDM
>5E8P_3 Ceramide synthase 5 (chains C, F) MCLRLTAVM
The MHC Class I Cancer-Associated Neoepitope Trh4 Linked with Impaired Peptide Processing Induces a Unique Noncanonical TCR Conformer. Hafstrand, I., Doorduijn, E.M., Duru, A.D. et al. J Immunol (2016) 196:2327-2334. DOI 10.4049/jimmunol.1502249 · PubMed
Other PDB entries of the same protein (UniProt P01899 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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