MAGE-A3 reactive TCR in complex with MAGE-A3 in HLA-A1. Determined by X-ray diffraction at 2.62 Å resolution. Released 2 Mar 2016.
Explore 5BRZ in 3D Show helices and sheets RCSB PDB PDBe
5BRZ contains 21 α-helices and 71 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 | 3-14 | 12 | 1 |
| β-strand | 18-28 | 11 | 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 | 94-103 | 10 | 1 |
| β-strand | 109-118 | 10 | 1 |
| β-strand | 121-126 | 6 | 1 |
| β-strand | 133-135 | 3 | 1 |
| α-helix | 138-149 | 12 | |
| α-helix | 152-161 | 10 | |
| α-helix | 163-174 | 12 | |
| α-helix | 176-179 | 4 | |
| β-strand | 183 | 1 | 2 |
| α-helix | 184-185 | 2 | |
| β-strand | 186-193 | 8 | 3 |
| β-strand | 198-208 | 11 | 3 |
| β-strand | 209 | 1 | 2 |
| β-strand | 213-219 | 7 | 4 |
| β-strand | 222-223 | 2 | 4 |
| β-strand | 228-230 | 3 | 3 |
| α-helix | 231-233 | 3 | |
| β-strand | 234-235 | 2 | 3 |
| β-strand | 241-250 | 10 | 3 |
| β-strand | 257-263 | 7 | 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 |
| α-helix | 46 | 1 | |
| β-strand | 50-51 | 2 | 6 |
| β-strand | 55-56 | 2 | 6 |
| β-strand | 62-70 | 9 | 6 |
| β-strand | 78-83 | 6 | 7 |
| β-strand | 91-94 | 4 | 7 |
| α-helix | 95-96 | 2 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 5-6 | 2 | 8 |
| β-strand | 11-15 | 5 | 9 |
| β-strand | 20-26 | 7 | 8 |
| β-strand | 31-39 | 9 | 9 |
| β-strand | 45-51 | 7 | 9 |
| β-strand | 57-60 | 4 | 8 |
| β-strand | 63-68 | 6 | 8 |
| β-strand | 73-78 | 6 | 8 |
| β-strand | 87-95 | 9 | 9 |
| β-strand | 104-105 | 2 | 9 |
| β-strand | 109-114 | 6 | 9 |
| β-strand | 123-129 | 7 | 10 |
| β-strand | 136-141 | 6 | 10 |
| α-helix | 151-153 | 3 | |
| β-strand | 158-159 | 2 | 10 |
| α-helix | 160-162 | 3 | |
| β-strand | 165-166 | 2 | 11 |
| β-strand | 173-174 | 2 | 11 |
| β-strand | 176-180 | 5 | 10 |
| α-helix | 188-191 | 4 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 6-8 | 3 | 12 |
| β-strand | 11-15 | 5 | 13 |
| β-strand | 20-25 | 6 | 12 |
| α-helix | 26-27 | 2 | |
| β-strand | 32-39 | 8 | 13 |
| β-strand | 43-51 | 9 | 13 |
| β-strand | 54-58 | 5 | 13 |
| β-strand | 65-69 | 5 | 12 |
| β-strand | 75-79 | 5 | 12 |
| α-helix | 84-86 | 3 | |
| β-strand | 88-95 | 8 | 13 |
| β-strand | 102-104 | 3 | 13 |
| β-strand | 108-113 | 6 | 13 |
| α-helix | 116-118 | 3 | |
| β-strand | 120 | 1 | 14 |
| β-strand | 123-128 | 6 | 10 |
| α-helix | 129-130 | 2 | |
| α-helix | 131-137 | 7 | |
| β-strand | 139-149 | 11 | 10 |
| β-strand | 150 | 1 | 14 |
| β-strand | 154-160 | 7 | 15 |
| β-strand | 163-165 | 3 | 15 |
| β-strand | 169-171 | 3 | 10 |
| β-strand | 176-177 | 2 | 10 |
| β-strand | 187-196 | 10 | 10 |
| α-helix | 197-200 | 4 | |
| β-strand | 206-213 | 8 | 15 |
| β-strand | 216 | 1 | 16 |
| α-helix | 227-228 | 2 | |
| β-strand | 230 | 1 | 16 |
| β-strand | 232-239 | 8 | 15 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| HLA class I histocompatibility antigen, A-1 alpha chain | A | protein | 275 | Homo sapiens | P04439 (AlphaFold model) |
| Beta-2-microglobulin | B | protein | 100 | Homo sapiens | P61769 (AlphaFold model) |
| Glu-val-asp-pro-ile-gly-his-leu-tyr | C | protein | 9 | Homo sapiens | P43357 (AlphaFold model) |
| Protein TRAV21,T-cell receptor alpha chain C region | D | protein | 197 | Homo sapiens | A0A0B4J279 (AlphaFold model), P01848 |
| Protein TRBV5-1,Human nkt tcr beta chain | E | protein | 241 | Homo sapiens | A0A578, A0A5B9 |
>5BRZ_1 HLA class I histocompatibility antigen, A-1 alpha chain (chains A) GSHSMRYFFTSVSRPGRGEPRFIAVGYVDDTQFVRFDSDAASQKMEPRAPWIEQEGPEYW DQETRNMKAHSQTDRANLGTLRGYYNQSEDGSHTIQIMYGCDVGPDGRFLRGYRQDAYDG KDYIALNEDLRSWTAADMAAQITKRKWEAVHAAEQRRVYLEGRCVDGLRRYLENGKETLQ RTDPPKTHMTHHPISDHEATLRCWALGFYPAEITLTWQRDGEDQTQDTELVETRPAGDGT FQKWAAVVVPSGEEQRYTCHVQHEGLPKPLTLRWP
>5BRZ_2 Beta-2-microglobulin (chains B) MIQRTPKIQVYSRHPAENGKSNFLNCYVSGFHPSDIEVDLLKNGERIEKVEHSDLSFSKD WSFYLLYYTEFTPTEKDEYACRVNHVTLSQPKIVKWDRDM
>5BRZ_3 GLU-VAL-ASP-PRO-ILE-GLY-HIS-LEU-TYR (chains C) EVDPIGHLY
>5BRZ_4 Protein TRAV21,T-cell receptor alpha chain C region (chains D) AQEVTQIPAALSVPEGENLVLNCSFTDSAIYNLQWFRQDPGKGLTSLLYVRPYQREQTSG RLNASLDKSSGRSTLYIAASQPGDSATYLCAVRPGGAGPFFVVFGKGTKLSVIPNIQNPD PAVYQLRDSKSSDKSVCLFTDFDSQTNVSQSKDSDVYITDKCVLDMRSMDFKSNSAVAWS NKSDFACANAFNNSIIP
>5BRZ_5 Protein TRBV5-1,Human nkt tcr beta chain (chains E) AGVTQTPRYLIKTRGQQVTLSCSPISGHRSVSWYQQTPGQGLQFLFEYFSETQRNKGNFP GRFSGRQFSNSRSEMNVSTLELGDSALYLCASSFNMATGQYFGPGTRLTVTEDLKNVFPP EVAVFEPSEAEISHTQKATLVCLATGFYPDHVELSWWVNGKEVHSGVCTDPQPLKEQPAL NDSRYALSSRLRVSATFWQDPRNHFRCQVQFYGLSENDEWTQDRAKPVTQIVSAEAWGRA D
Direct molecular mimicry enables off-target cardiovascular toxicity by an enhanced affinity TCR designed for cancer immunotherapy. Raman, M.C., Rizkallah, P.J., Simmons, R. et al. Sci Rep (2016) 6:18851-18851. DOI 10.1038/srep18851 · PubMed
Other PDB entries of the same protein (UniProt P04439 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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