Crystal structure of intracellular B30.2 domain of BTN3A3 mutant in complex with HMBPP. Determined by X-ray diffraction at 1.6 Å resolution. Released 3 Apr 2019.
Explore 6J0G in 3D Show helices and sheets RCSB PDB PDBe
6J0G contains 26 α-helices and 66 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 |
|---|---|---|---|
| α-helix | 297-306 | 10 | |
| β-strand | 308-309 | 2 | 1 |
| α-helix | 310 | 1 | |
| β-strand | 314 | 1 | 2 |
| β-strand | 323-325 | 3 | 1 |
| β-strand | 331-334 | 4 | 1 |
| β-strand | 353-355 | 3 | 3 |
| β-strand | 356 | 1 | 2 |
| β-strand | 360 | 1 | 3 |
| β-strand | 364-370 | 7 | 1 |
| β-strand | 377-383 | 7 | 3 |
| α-helix | 397-399 | 3 | |
| β-strand | 401-407 | 7 | 3 |
| β-strand | 411-414 | 4 | 3 |
| α-helix | 419 | 1 | |
| β-strand | 420-421 | 2 | 3 |
| β-strand | 430-436 | 7 | 1 |
| β-strand | 441-446 | 6 | 1 |
| β-strand | 452-455 | 4 | 1 |
| α-helix | 456 | 1 | |
| α-helix | 458-459 | 2 | |
| β-strand | 465-470 | 6 | 3 |
| α-helix | 477-478 | 2 | |
| β-strand | 479-481 | 3 | 1 |
| α-helix | 482-484 | 3 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 298-306 | 9 | |
| β-strand | 308-309 | 2 | 4 |
| α-helix | 310 | 1 | |
| β-strand | 314-315 | 2 | 5 |
| β-strand | 323-325 | 3 | 4 |
| β-strand | 331-334 | 4 | 4 |
| β-strand | 353-356 | 4 | 5 |
| β-strand | 360 | 1 | 5 |
| β-strand | 364-370 | 7 | 4 |
| β-strand | 377-383 | 7 | 5 |
| α-helix | 397-399 | 3 | |
| β-strand | 401-407 | 7 | 5 |
| β-strand | 411-414 | 4 | 5 |
| α-helix | 419 | 1 | |
| β-strand | 420-422 | 3 | 5 |
| β-strand | 430-436 | 7 | 4 |
| β-strand | 441-446 | 6 | 4 |
| β-strand | 452-455 | 4 | 4 |
| β-strand | 465-470 | 6 | 5 |
| β-strand | 479-481 | 3 | 4 |
| α-helix | 482-483 | 2 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 298-306 | 9 | |
| β-strand | 308-309 | 2 | 6 |
| β-strand | 314-315 | 2 | 7 |
| β-strand | 323-325 | 3 | 6 |
| β-strand | 331-334 | 4 | 6 |
| β-strand | 353-356 | 4 | 7 |
| β-strand | 360 | 1 | 7 |
| β-strand | 364-370 | 7 | 6 |
| β-strand | 377-383 | 7 | 7 |
| α-helix | 397-399 | 3 | |
| β-strand | 401-407 | 7 | 7 |
| β-strand | 411-414 | 4 | 7 |
| β-strand | 420-421 | 2 | 7 |
| β-strand | 430-436 | 7 | 6 |
| β-strand | 441-446 | 6 | 6 |
| β-strand | 452-455 | 4 | 6 |
| β-strand | 465-470 | 6 | 7 |
| α-helix | 477-478 | 2 | |
| β-strand | 479-481 | 3 | 6 |
| α-helix | 482-483 | 2 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 298-306 | 9 | |
| β-strand | 308-309 | 2 | 8 |
| α-helix | 310 | 1 | |
| β-strand | 314 | 1 | 9 |
| β-strand | 323-325 | 3 | 8 |
| β-strand | 331-334 | 4 | 8 |
| β-strand | 353-355 | 3 | 10 |
| β-strand | 356 | 1 | 9 |
| β-strand | 360 | 1 | 10 |
| β-strand | 364-370 | 7 | 8 |
| β-strand | 377-383 | 7 | 10 |
| α-helix | 397-399 | 3 | |
| β-strand | 401-407 | 7 | 10 |
| β-strand | 411-414 | 4 | 10 |
| α-helix | 419 | 1 | |
| β-strand | 420-421 | 2 | 10 |
| α-helix | 422 | 1 | |
| β-strand | 430-436 | 7 | 8 |
| β-strand | 441-446 | 6 | 8 |
| β-strand | 452-455 | 4 | 8 |
| α-helix | 456 | 1 | |
| α-helix | 458-459 | 2 | |
| β-strand | 465-470 | 6 | 10 |
| α-helix | 477-478 | 2 | |
| β-strand | 479-481 | 3 | 8 |
| α-helix | 482-483 | 2 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Butyrophilin subfamily 3 member A3 | A, B, C, D | protein | 221 | Homo sapiens | O00478 (AlphaFold model) |
>6J0G_1 Butyrophilin subfamily 3 member A3 (chains A, B, C, D) MGSSHHHHHHSSGLVPRGSHMENLYFQGAGAGAAYHEWKMALFKPADVILDPDTANAILL VSEDQRSVQRAEEPRDLPDNPERFEWHYCVLGCENFTSGRHYWEVEVGDRKEWHIGVCSK NVERKKGWVKMTPENGYWTMGLTDGNKYRALTEPRTNLKLPEPPRKVGIFLDYETGEISF YNATDGSHIYTFPHASFSEPLYPVFRILTLEPTALTICPIP
| ID | Name | Formula | Copies |
|---|---|---|---|
| H6P | (2E)-4-hydroxy-3-methylbut-2-en-1-yl trihydrogen diphosphate | C5 H12 O8 P2 | 4 |
A Structural Change in Butyrophilin upon Phosphoantigen Binding Underlies Phosphoantigen-Mediated V gamma 9V delta 2 T Cell Activation. Yang, Y., Li, L., Yuan, L. et al. Immunity (2019) 50:1043. DOI 10.1016/j.immuni.2019.02.016 · PubMed
Other PDB entries of the same protein (UniProt O00478 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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