3E3Q: 3alpham13 high-affinity mutant of the 2C TCR

Structure of the 3alpham13 high-affinity mutant of the 2C TCR in complex with Ld/QL9. Determined by X-ray diffraction at 2.95 Å resolution. Released 4 Nov 2008.

Method
X-ray diffraction
Resolution
2.95 Å
Organism
Mus musculus
Chains
32
Atoms
25,808
Mol. weight
365.72 kDa
Released
4 Nov 2008

Explore 3E3Q in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

3E3Q contains 80 α-helices and 250 β-strands across 32 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.

Chains a, e, E, F, N, S and W: 1 helix, 11 β-strands

ElementResiduesLengthSheet
β-strand4-7414
β-strand10-14515
β-strand19-25714
β-strand31-37715
β-strand44-49615
β-strand56-57215
β-strand65-68414
β-strand74-79614
α-helix84-863
β-strand88-95815
β-strand107-108215
β-strand112-117615
Chains A and B: 7 helices, 8 β-strands
ElementResiduesLengthSheet
β-strand3-13111
α-helix201
β-strand21-2881
β-strand31-3771
β-strand45-4731
α-helix50-545
α-helix57-8428
β-strand93-103111
β-strand109-118101
β-strand121-12661
β-strand133-13531
α-helix138-14912
α-helix152-1587
α-helix159-1646
α-helix165-17410
Chains b, f, K and O: 1 helix, 0 β-strands
ElementResiduesLengthSheet
α-helix3-86
Chains c, H, L, P, U and Y: 7 helices, 8 β-strands
ElementResiduesLengthSheet
β-strand3-131120
α-helix201
β-strand21-28820
β-strand31-37720
β-strand45-47320
α-helix50-545
α-helix57-8428
β-strand93-1031120
β-strand109-1181020
β-strand121-126620
β-strand133-135320
α-helix138-14912
α-helix152-1587
α-helix159-1646
α-helix165-1739
Chains C, d, I, R, V and Z: 1 helix, 12 β-strands
ElementResiduesLengthSheet
β-strand3-4216
β-strand9-12417
β-strand18-20316
β-strand23-24216
β-strand32-37617
β-strand44-49617
β-strand55-58416
β-strand62-67616
β-strand72-77616
α-helix82-843
β-strand86-93817
β-strand104-106317
β-strand110-114517
Chain D: 1 helix, 12 β-strands
ElementResiduesLengthSheet
β-strand3-426
β-strand9-1247
β-strand18-2036
β-strand23-2426
β-strand32-3767
β-strand44-4967
β-strand55-5736
β-strand63-6756
β-strand72-7766
α-helix82-843
β-strand86-9387
β-strand104-10637
β-strand110-11457
Chains G, Q and X: 1 helix, 0 β-strands
ElementResiduesLengthSheet
α-helix2-87
Chain J: 1 helix, 13 β-strands
ElementResiduesLengthSheet
β-strand4-7428
β-strand10-14529
β-strand19-21330
β-strand22-25428
β-strand31-37729
β-strand44-49629
β-strand56-57229
β-strand65-68430
β-strand74128
β-strand76-79430
α-helix84-863
β-strand88-95829
β-strand107-108229
β-strand112-117629

2 more chain groups are not listed. Open the entry in the viewer and use the sequence panel to see them.

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
H-2 class I histocompatibility antigen, L-D alpha chainA, B, H, L, P, U, Y, cprotein175Mus musculusP01897 (AlphaFold model)
QL9 peptideG, K, O, Q, T, X, b, fprotein9
T-cell receptor alpha chain V region PHDS58C, D, I, M, R, V, Z, dprotein109Mus musculusP01738 (AlphaFold model)
TCR beta chainE, F, J, N, S, W, a, eprotein111Mus musculus
Sequence of entity 1 (A, B, H, L, P, U, Y, c), FASTA
>3E3Q_1 H-2 class I histocompatibility antigen, L-D alpha chain (chains A, B, H, L, P, U, Y, c)
GPHSMRYYETATSRRGLGEPRYTSVGYVDDKEFVRFDSDAENPRYEPQVPWMEQEGPEYW
ERITQVAKGQEQWFRVNLRTLLGYYNQSAGGTHTLQRMYGCDVGSDGRLLRGYEQFAYDG
CDYIALNEDLRTWTAADMAAQITRRKWEQAGAAEYYRAYLEGECVEWLHRYLKNG
Sequence of entity 2 (G, K, O, Q, T, X, b, f), FASTA
>3E3Q_2 QL9 peptide (chains G, K, O, Q, T, X, b, f)
QLSPFPFDL
Sequence of entity 3 (C, D, I, M, R, V, Z, d), FASTA
>3E3Q_3 T-cell receptor alpha chain V region PHDS58 (chains C, D, I, M, R, V, Z, d)
SVTQPDARVTVSEGASLQLRCKYSYSATPYLFWYVQYPRQGPQLLLKYYSGDPVVQGVNG
FEAEFSKSNSSFHLRKASVHRSDSAVYFCAVSDPPPLLTFGSGTKVIVL
Sequence of entity 4 (E, F, J, N, S, W, a, e), FASTA
>3E3Q_4 TCR beta chain (chains E, F, J, N, S, W, a, e)
EAAVTQSPRNKVAVTGEKVTLSCNQTNNHNNMYWYRQDTGHELRLIYYSYGAGSTEKGDI
PDGYKASRPSQENFSLTLESATPSQTSVYFCASGGGGTLYFGAGTRLSVLS

Primary citation

Distinct CDR3 conformations in TCRs determine the level of cross-reactivity for diverse antigens, but not the docking orientation. Jones, L.L., Colf, L.A., Stone, J.D. et al. J Immunol (2008) 181:6255-6264. PubMed

Other PDB entries of the same protein (UniProt P01897 (AlphaFold model), which also has an AlphaFold model), best resolution first:

Browse structure collections

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