5E8O: PDB entry 5E8O

The structure of the TEIPP associated altered peptide ligand Trh4-p2ABU in complex with H-2D(b). Determined by X-ray diffraction at 1.98 Å resolution. Released 3 Feb 2016.

Method
X-ray diffraction
Resolution
1.98 Å
Organism
Mus musculus
Chains
6
Atoms
6,340
Mol. weight
89.66 kDa
Released
3 Feb 2016

Explore 5E8O in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

5E8O 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.

Chain A: 6 helices, 19 β-strands

ElementResiduesLengthSheet
β-strand3-13111
β-strand21-2881
β-strand31-3771
β-strand46-4721
α-helix50-545
α-helix57-8428
β-strand93-103111
β-strand109-118101
β-strand121-12661
β-strand133-13421
α-helix140-15011
α-helix152-16110
α-helix163-17412
β-strand18312
α-helix184-1852
β-strand186-19383
β-strand198-208113
β-strand20912
β-strand214-21964
β-strand22314
β-strand229-23023
β-strand234-23523
β-strand241-250103
β-strand257-26264
β-strand270-27234
Chains B and E: 2 helices, 11 β-strands
ElementResiduesLengthSheet
β-strand315
α-helix4-52
β-strand6-1166
β-strand21-30106
β-strand3115
β-strand36-4167
β-strand44-4527
β-strand50-5126
α-helix52-543
β-strand55-5626
β-strand62-7096
β-strand78-8367
β-strand91-9447
Chain D: 8 helices, 19 β-strands
ElementResiduesLengthSheet
β-strand3-13118
β-strand21-2888
β-strand31-3778
β-strand46-4728
α-helix50-545
α-helix57-8428
α-helix87-882
β-strand93-103118
β-strand109-118108
β-strand121-12668
β-strand133-13428
α-helix138-15013
α-helix152-16110
α-helix163-17513
β-strand18319
β-strand186-193810
α-helix195-1973
β-strand198-2081110
β-strand20919
β-strand214-219611
β-strand222-223211
β-strand228-230310
β-strand234-235210
β-strand241-2501010
α-helix254-2563
β-strand257-262611
β-strand270-272311

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
H-2 class I histocompatibility antigen, D-B alpha chainA, Dprotein276Mus musculusP01899 (AlphaFold model)
Ceramide synthase 5C, Fprotein9Mus musculusQ9D6K9 (AlphaFold model)
Beta-2-microglobulinB, Eprotein99Mus musculusP01887 (AlphaFold model)
Sequence of entity 1 (A, D), FASTA
>5E8O_1 H-2 class I histocompatibility antigen, D-B alpha chain (chains A, D)
GPHSMRYFETAVSRPGLEEPRYISVGYVDNKEFVRFDSDAENPRYEPRAPWMEQEGPEYW
ERETQKAKGQEQWFRVSLRNLLGYYNQSAGGSHTLQQMSGCDLGSDWRLLRGYLQFAYEG
RDYIALNEDLKTWTAADMAAQITRRKWEQSGAAEHYKAYLEGECVEWLHRYLKNGNATLL
RTDSPKAHVTHHPRSKGEVTLRCWALGFYPADITLTWQLNGEELTQDMELVETRPAGDGT
FQKWASVVVPLGKEQNYTCRVYHEGLPEPLTLRWEP
Sequence of entity 2 (C, F), FASTA
>5E8O_2 Ceramide synthase 5 (chains C, F)
MALRMTAVM
Sequence of entity 3 (B, E), FASTA
>5E8O_3 Beta-2-microglobulin (chains B, E)
IQKTPQIQVYSRHPPENGKPNILNCYVTQFHPPHIEIQMLKNGKKIPKVEMSDMSFSKDW
SFYILAHTEFTPTETDTYACRVKHDSMAEPKTVYWDRDM

Primary citation

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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