42F3 TCR pCPA12/H-2Ld complex. Determined by X-ray diffraction at 3.06 Å resolution. Released 19 Aug 2015.
Explore 4N5E in 3D Show helices and sheets RCSB PDB PDBe
4N5E contains 15 α-helices and 51 β-strands across 3 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 | 3-12 | 10 | 10 |
| α-helix | 13-14 | 2 | |
| β-strand | 21-28 | 8 | 10 |
| β-strand | 31-37 | 7 | 10 |
| β-strand | 45-47 | 3 | 10 |
| α-helix | 51-54 | 4 | |
| α-helix | 57-84 | 28 | |
| β-strand | 94-103 | 10 | 10 |
| β-strand | 109-118 | 10 | 10 |
| β-strand | 121-126 | 6 | 10 |
| β-strand | 133-135 | 3 | 10 |
| α-helix | 139-150 | 12 | |
| α-helix | 152-158 | 7 | |
| α-helix | 159-163 | 5 | |
| α-helix | 164-173 | 10 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 3-4 | 2 | 1 |
| β-strand | 9-13 | 5 | 2 |
| β-strand | 18-20 | 3 | 1 |
| β-strand | 23-24 | 2 | 1 |
| β-strand | 31-37 | 7 | 2 |
| β-strand | 44-49 | 6 | 2 |
| β-strand | 55-57 | 3 | 1 |
| β-strand | 62-67 | 6 | 1 |
| β-strand | 72-77 | 6 | 1 |
| α-helix | 82-84 | 3 | |
| β-strand | 87-93 | 7 | 2 |
| β-strand | 102-103 | 2 | 2 |
| β-strand | 107-112 | 6 | 2 |
| β-strand | 121-127 | 7 | 3 |
| β-strand | 134-139 | 6 | 3 |
| β-strand | 156-157 | 2 | 3 |
| α-helix | 158-160 | 3 | |
| β-strand | 163-165 | 3 | 4 |
| α-helix | 166-168 | 3 | |
| β-strand | 170-172 | 3 | 4 |
| β-strand | 174-178 | 5 | 3 |
| β-strand | 199 | 1 | 3 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 4-7 | 4 | 5 |
| β-strand | 10-14 | 5 | 6 |
| β-strand | 19-25 | 7 | 5 |
| β-strand | 31-38 | 8 | 6 |
| β-strand | 42-50 | 9 | 6 |
| β-strand | 56-57 | 2 | 6 |
| β-strand | 65-67 | 3 | 5 |
| β-strand | 73-78 | 6 | 5 |
| α-helix | 83-85 | 3 | |
| β-strand | 87-96 | 10 | 6 |
| β-strand | 99-102 | 4 | 6 |
| β-strand | 106-111 | 6 | 6 |
| β-strand | 118 | 1 | 7 |
| α-helix | 119-120 | 2 | |
| β-strand | 121-126 | 6 | 3 |
| α-helix | 127-128 | 2 | |
| α-helix | 129-135 | 7 | |
| β-strand | 137-147 | 11 | 3 |
| β-strand | 148 | 1 | 7 |
| β-strand | 152-158 | 7 | 8 |
| β-strand | 161-163 | 3 | 8 |
| β-strand | 167-169 | 3 | 3 |
| β-strand | 174-175 | 2 | 3 |
| β-strand | 185-194 | 10 | 3 |
| α-helix | 195-198 | 4 | |
| β-strand | 204-211 | 8 | 8 |
| β-strand | 214 | 1 | 9 |
| β-strand | 228 | 1 | 9 |
| β-strand | 230-237 | 8 | 8 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| 42F3 alpha VmCh | C | protein | 212 | Mus musculus, Homo sapiens | A0A0G2JFA3, P01738 (AlphaFold model), P01848 (AlphaFold model) |
| 42F3 beta VmCh | D | protein | 243 | Mus musculus, Homo sapiens | A0A0A6YX08, A0A5B9 |
| H-2 class I histocompatibility antigen, L-D alpha chain | A | protein | 180 | Mus musculus | P01897 |
| pCPA12 | B | protein | 9 |
>4N5E_1 42F3 alpha VmCh (chains C) GSHMAQSVTQPDARVTVSEGASLQLRCKYSYSATPYLFWYVQYPRQGLQMLLKYYSGDPV VQGVNGFEAEFSKSDSSFHLRKASVHWSDSAVYFCAVSAKGTGSKLSFGKGAKLTVSPNI QNPDPAVYQLRDSKSSDKSVCLFTDFDSQTNVSQSKDSDVYITDKCVLDMRSMDFKSNSA VAWSNKSDFACANAFNNSIIPEDTFFPSPESS
>4N5E_2 42F3 beta VmCh (chains D) MGEAAVTQSPRNKVTVTGGNVTLSCRQTNSHNYMYWYRQDTGHGLRLIHYSYGAGNLQIG DVPDGYKATRTTQEDFFLLLELASPSQTSLYFCASSDAPGQLYFGEGSKLTVLEDLKNVF PPEVAVFEPSEAEISHTQKATLVCLATGFYPDHVELSWWVNGKEVHSGVCTDPQPLKEQP ALNDSRYALSSRLRVSATFWQNPRNHFRCQVQFYGLSENDEWTQDRAKPVTQIVSAEAWG RAD
>4N5E_3 H-2 class I histocompatibility antigen, L-D alpha chain (chains A) MGPHSMRYYETATSRRGLGEPRYTSVGYVDDKEFVRFDSDAENPRYEPQVPWMEQEGPEY WERITQIAKGQEQWFRVNLRTLLGYYNQSAGGTHTLQWMYGCDVGSDGRLLRGYEQFAYD GCDYIALNEDLRTWTAADMAAQITRRKWEQAGAAEYYRAYLEGECVEWLHRYLKNGNATL
>4N5E_4 pCPA12 (chains B) VPYMAEFGM
Structural interplay between germline interactions and adaptive recognition determines the bandwidth of TCR-peptide-MHC cross-reactivity. Adams, J.J., Narayanan, S., Birnbaum, M.E. et al. Nat Immunol (2016) 17:87-94. DOI 10.1038/ni.3310 · PubMed
Other PDB entries of the same protein (UniProt A0A0G2JFA3), best resolution first:
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