Crystal structure of the mCD1d/NC-aGC/iNKTCR ternary complex. Determined by X-ray diffraction at 2.6 Å resolution. Released 3 Jun 2015.
Explore 4Y16 in 3D Show helices and sheets RCSB PDB PDBe
4Y16 contains 20 α-helices and 72 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 | 9-18 | 10 | 1 |
| β-strand | 24-32 | 9 | 1 |
| β-strand | 35-40 | 6 | 1 |
| α-helix | 47 | 1 | |
| β-strand | 48-49 | 2 | 1 |
| α-helix | 60-88 | 29 | |
| β-strand | 96-106 | 11 | 1 |
| β-strand | 112-120 | 9 | 1 |
| β-strand | 123-129 | 7 | 1 |
| β-strand | 132-135 | 4 | 1 |
| α-helix | 136 | 1 | |
| α-helix | 141-143 | 3 | |
| α-helix | 144-151 | 8 | |
| α-helix | 154-162 | 9 | |
| α-helix | 163-167 | 5 | |
| α-helix | 168-178 | 11 | |
| α-helix | 180-183 | 4 | |
| β-strand | 187 | 1 | 2 |
| β-strand | 190-196 | 7 | 3 |
| β-strand | 205-213 | 9 | 3 |
| β-strand | 214 | 1 | 2 |
| β-strand | 219-224 | 6 | 4 |
| β-strand | 227-228 | 2 | 4 |
| β-strand | 233-234 | 2 | 3 |
| β-strand | 238-239 | 2 | 3 |
| β-strand | 245-252 | 8 | 3 |
| β-strand | 261-266 | 6 | 4 |
| β-strand | 275-278 | 4 | 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 | 3-6 | 4 | 8 |
| β-strand | 9-13 | 5 | 9 |
| β-strand | 18-24 | 7 | 8 |
| β-strand | 31-37 | 7 | 9 |
| β-strand | 44-49 | 6 | 9 |
| β-strand | 53-58 | 6 | 8 |
| β-strand | 61-66 | 6 | 8 |
| β-strand | 71-76 | 6 | 8 |
| α-helix | 81-83 | 3 | |
| β-strand | 85-92 | 8 | 9 |
| β-strand | 101-103 | 3 | 9 |
| β-strand | 107-112 | 6 | 9 |
| β-strand | 121-127 | 7 | 10 |
| β-strand | 134-139 | 6 | 10 |
| β-strand | 155-157 | 3 | 10 |
| α-helix | 158-160 | 3 | |
| β-strand | 163-165 | 3 | 11 |
| α-helix | 166-168 | 3 | |
| β-strand | 170-172 | 3 | 11 |
| β-strand | 174-179 | 6 | 10 |
| α-helix | 186-188 | 3 | |
| β-strand | 200 | 1 | 10 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 4-7 | 4 | 12 |
| β-strand | 10-14 | 5 | 13 |
| β-strand | 19-25 | 7 | 12 |
| β-strand | 31-37 | 7 | 13 |
| β-strand | 44-49 | 6 | 13 |
| β-strand | 56-57 | 2 | 13 |
| β-strand | 65-70 | 6 | 12 |
| β-strand | 73-78 | 6 | 12 |
| α-helix | 83-85 | 3 | |
| β-strand | 87-94 | 8 | 13 |
| β-strand | 101-102 | 2 | 13 |
| β-strand | 106-111 | 6 | 13 |
| β-strand | 118 | 1 | 14 |
| β-strand | 121-126 | 6 | 10 |
| α-helix | 127-128 | 2 | |
| α-helix | 129-135 | 7 | |
| β-strand | 137-147 | 11 | 10 |
| β-strand | 148 | 1 | 14 |
| β-strand | 152-158 | 7 | 15 |
| β-strand | 161-163 | 3 | 15 |
| β-strand | 167-169 | 3 | 10 |
| α-helix | 173 | 1 | |
| β-strand | 174-175 | 2 | 10 |
| β-strand | 185-194 | 10 | 10 |
| α-helix | 195-199 | 5 | |
| β-strand | 204-211 | 8 | 15 |
| β-strand | 214 | 1 | 16 |
| β-strand | 228 | 1 | 16 |
| β-strand | 230-237 | 8 | 15 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Antigen-presenting glycoprotein CD1d1 | A | protein | 285 | Mus musculus | P11609 (AlphaFold model) |
| Beta-2-microglobulin | B | protein | 99 | Mus musculus | P01887 (AlphaFold model) |
| Chimeric TCR Valpha14/Jalpha18 chain (mouse variable domain, human constant domain) | C | protein | 209 | Mus musculus, Homo sapiens | A0A0B4J1J9 (AlphaFold model), P01848 (AlphaFold model) |
| Chimeric TCR Vbeta8.2 chain (mouse variable domain, human constant domain) | D | protein | 241 | Mus musculus, Homo sapiens | A0A5B9, A2NTY6 |
>4Y16_1 Antigen-presenting glycoprotein CD1d1 (chains A) SEAQQKNYTFRCLQMSSFANRSWSRTDSVVWLGDLQTHRWSNDSATISFTKPWSQGKLSN QQWEKLQHMFQVYRVSFTRDIQELVKMMSPKEDYPIEIQLSAGCEMYPGNASESFLHVAF QGKYVVRFWGTSWQTVPGAPSWLDLPIKVLNADQGTSATVQMLLNDTCPLFVRGLLEAGK SDLEKQEKPVAWLSSVPSSAHGHRQLVCHVSGFYPKPVWVMWMRGDQEQQGTHRGDFLPN ADETWYLQATLDVEAGEEAGLACRVKHSSLGGQDIILYWHHHHHH
>4Y16_2 Beta-2-microglobulin (chains B) IQKTPQIQVYSRHPPENGKPNILNCYVTQFHPPHIEIQMLKNGKKIPKVEMSDMSFSKDW SFYILAHTEFTPTETDTYACRVKHASMAEPKTVYWDRDM
>4Y16_3 Chimeric TCR Valpha14/Jalpha18 chain (mouse variable domain, human constant domain) (chains C) MKTQVEQSPQSLVVRQGENCVLQCNYSVTPDNHLRWFKQDTGKGLVSLTVLVDQKDKTSN GRYSATLDKDAKHSTLHITATLLDDTATYICVVGDRGSALGRLHFGAGTQLIVIPDIQNP DPAVYQLRDSKSSDKSVCLFTDFDSQTNVSQSKDSDVYITDKCVLDMRSMDFKSNSAVAW SNKSDFACANAFNNSIIPEDTFFPSPESS
>4Y16_4 Chimeric TCR Vbeta8.2 chain (mouse variable domain, human constant domain) (chains D) MEAAVTQSPRNKVAVTGGKVTLSCNQTNNHNNMYWYRQDTGHGLRLIHYSYGAGSTEKGD IPDGYKASRPSQENFSLILELATPSQTSVYFCASGDEGYTQYFGPGTRLLVLEDLRNVTP PKVSLFEPSKAEISHTQKATLVCLATGFYPDHVELSWWVNGKEVHSGVCTDPQPLKEQPA LNDSRYSLSSRLRVSATFWQNPRNHFRCQVQFYGLSENDEWTQDRAKPVTQIVSAEAWGR A
| ID | Name | Formula | Copies |
|---|---|---|---|
| NAG | 2-acetamido-2-deoxy-beta-D-glucopyranose | C8 H15 N O6 | 1 |
| 48G | N-[(2S,3S,4R)-3,4-dihydroxy-1-{[6-O-(naphthalen-1-ylcarbamoyl)-alpha-D-galactop… | C61 H106 N2 O10 | 1 |
Lipid and Carbohydrate Modifications of alpha-Galactosylceramide Differently Influence Mouse and Human Type I Natural Killer T Cell Activation. Birkholz, A., Nemcovic, M., Yu, E.D. et al. J Biol Chem (2015) 290:17206-17217. DOI 10.1074/jbc.M115.654814 · PubMed
Other PDB entries of the same protein (UniProt P11609 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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