5UJT: Human HLA-DQ8
Crystal structure of human HLA-DQ8 in complex with insulin mimotope binding in register 3. Determined by X-ray diffraction at 1.94 Å resolution. Released 20 Dec 2017.
- Method
- X-ray diffraction
- Resolution
- 1.94 Å
- Organism
- Homo sapiens
- Chains
- 9
- Atoms
- 10,035
- Mol. weight
- 136.19 kDa
- Ligands
- NAG
- Released
- 20 Dec 2017
Explore 5UJT in 3D
Show helices and sheets
RCSB PDB
PDBe
Secondary structure: helices and β-sheets
5UJT contains 37 α-helices and 84 β-strands across 9 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.
Chain A: 5 helices, 13 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 5-14 | 11 | 1 |
| β-strand | 19-26 | 8 | 1 |
| β-strand | 29-35 | 7 | 1 |
| β-strand | 40-43 | 4 | 1 |
| α-helix | 46-51 | 6 | |
| α-helix | 56-76 | 21 | |
| α-helix | 80-85 | 6 | |
| β-strand | 88-93 | 6 | 2 |
| β-strand | 103-112 | 10 | 2 |
| β-strand | 118-123 | 6 | 3 |
| β-strand | 126-127 | 2 | 3 |
| α-helix | 128 | 1 | |
| β-strand | 132-134 | 3 | 2 |
| α-helix | 137 | 1 | |
| β-strand | 138-139 | 2 | 2 |
| β-strand | 145-153 | 9 | 2 |
| β-strand | 161-166 | 6 | 3 |
| β-strand | 174-178 | 5 | 3 |
Chain B: 7 helices, 15 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 8-18 | 11 | 1 |
| β-strand | 23-32 | 10 | 1 |
| β-strand | 35-41 | 7 | 1 |
| β-strand | 47-49 | 3 | 1 |
| α-helix | 55-63 | 9 | |
| α-helix | 65-74 | 10 | |
| α-helix | 75-80 | 6 | |
| α-helix | 81-88 | 8 | |
| α-helix | 90-92 | 3 | |
| β-strand | 95 | 1 | 4 |
| α-helix | 96-97 | 2 | |
| β-strand | 98-103 | 6 | 5 |
| β-strand | 113-122 | 10 | 5 |
| β-strand | 123 | 1 | 4 |
| β-strand | 128-133 | 6 | 6 |
| β-strand | 136-137 | 2 | 6 |
| β-strand | 142-144 | 3 | 5 |
| α-helix | 145-147 | 3 | |
| β-strand | 148-149 | 2 | 5 |
| β-strand | 155-163 | 9 | 5 |
| β-strand | 170-176 | 7 | 6 |
| β-strand | 184-189 | 6 | 6 |
Chains C, F and I: 1 helix, 0 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 6-9 | 4 | |
Chain D: 4 helices, 13 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 5-14 | 11 | 7 |
| β-strand | 19-26 | 8 | 7 |
| β-strand | 29-35 | 7 | 7 |
| β-strand | 40-43 | 4 | 7 |
| α-helix | 46-51 | 6 | |
| α-helix | 56-76 | 21 | |
| α-helix | 80-87 | 8 | |
| β-strand | 88-93 | 6 | 8 |
| β-strand | 103-112 | 10 | 8 |
| β-strand | 118-123 | 6 | 9 |
| β-strand | 126-128 | 3 | 9 |
| β-strand | 132-134 | 3 | 8 |
| α-helix | 137 | 1 | |
| β-strand | 138-139 | 2 | 8 |
| β-strand | 145-153 | 9 | 8 |
| β-strand | 161-166 | 6 | 9 |
| β-strand | 174-177 | 4 | 9 |
Chain E: 7 helices, 15 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 8-18 | 11 | 7 |
| β-strand | 23-32 | 10 | 7 |
| β-strand | 35-41 | 7 | 7 |
| β-strand | 47-49 | 3 | 7 |
| α-helix | 55-62 | 8 | |
| α-helix | 65-74 | 10 | |
| α-helix | 75-80 | 6 | |
| α-helix | 81-88 | 8 | |
| α-helix | 90-92 | 3 | |
| β-strand | 95 | 1 | 10 |
| α-helix | 96-97 | 2 | |
| β-strand | 98-103 | 6 | 11 |
| β-strand | 113-122 | 10 | 11 |
| β-strand | 123 | 1 | 10 |
| β-strand | 128-133 | 6 | 12 |
| β-strand | 136-137 | 2 | 12 |
| β-strand | 142-144 | 3 | 11 |
| α-helix | 145-147 | 3 | |
| β-strand | 148-149 | 2 | 11 |
| β-strand | 155-163 | 9 | 11 |
| β-strand | 170-176 | 7 | 12 |
| β-strand | 184-189 | 6 | 12 |
Chain G: 4 helices, 13 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 5-14 | 11 | 13 |
| β-strand | 19-26 | 8 | 13 |
| β-strand | 29-35 | 7 | 13 |
| β-strand | 40-43 | 4 | 13 |
| α-helix | 46-51 | 6 | |
| α-helix | 56-76 | 21 | |
| α-helix | 81-85 | 5 | |
| β-strand | 88-93 | 6 | 14 |
| β-strand | 103-112 | 10 | 14 |
| β-strand | 118-123 | 6 | 15 |
| β-strand | 126-128 | 3 | 15 |
| β-strand | 132-134 | 3 | 14 |
| α-helix | 137 | 1 | |
| β-strand | 138-139 | 2 | 14 |
| β-strand | 145-153 | 9 | 14 |
| β-strand | 161-166 | 6 | 15 |
| β-strand | 174-177 | 4 | 15 |
Chain H: 7 helices, 15 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 8-18 | 11 | 13 |
| β-strand | 23-32 | 10 | 13 |
| β-strand | 35-41 | 7 | 13 |
| β-strand | 47-49 | 3 | 13 |
| α-helix | 55-63 | 9 | |
| α-helix | 65-74 | 10 | |
| α-helix | 75-80 | 6 | |
| α-helix | 81-88 | 8 | |
| α-helix | 90-92 | 3 | |
| β-strand | 95 | 1 | 16 |
| α-helix | 96-97 | 2 | |
| β-strand | 98-102 | 5 | 17 |
| β-strand | 114-122 | 9 | 17 |
| β-strand | 123 | 1 | 16 |
| β-strand | 128-133 | 6 | 18 |
| β-strand | 137 | 1 | 18 |
| β-strand | 142-144 | 3 | 17 |
| α-helix | 145-147 | 3 | |
| β-strand | 148-149 | 2 | 17 |
| β-strand | 155-162 | 8 | 17 |
| β-strand | 170-176 | 7 | 18 |
| β-strand | 184-189 | 6 | 18 |
Molecules and chains
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|
| MHC class II antigen | A, D, G | protein | 185 | Homo sapiens | Q5Y7C3 (AlphaFold model) |
| MHC class II HLA-DQ-beta-1 | B, E, H | protein | 189 | Homo sapiens | O19707 (AlphaFold model) |
| insulin mimotope | C, F, I | protein | 16 | Homo sapiens | |
Sequence of entity 1 (A, D, G), FASTA
>5UJT_1 MHC class II antigen (chains A, D, G)
GEDIVADHVASYGVNLYQSYGPSGQYSHEFDGDEEFYVDLERKETVWQLPLFRRFRRFDP
QFALTNIAVLKHNLNCVIKRSNSTAATNEVPEVTVFSKSPVTLGQPNTLICLVDNIFPPV
VNITWLSNGHSVTEGVSETSFLSKSDHSFFKISYLTFLPSDDEIYDCKVEHWGLDEPLLK
HWEPE
Sequence of entity 2 (B, E, H), FASTA
>5UJT_2 MHC class II HLA-DQ-beta-1 (chains B, E, H)
SPEDFVYQFKGMCYFTNGTERVRLVTRYIYNREEYARFDSDVGVYRAVTPLGPPAAEYWN
SQKEVLERTRAELDTVCRHNYQLELRTTLQRRVEPTVTISPSRTEALNHHNLLVCSVTDF
YPAQIKVRWFRNDQEETTGVVSTPLIRNGDWTFQILVMLEMTPQRGDVYTCHVEHPSLQN
PIIVEWRAQ
Sequence of entity 3 (C, F, I), FASTA
>5UJT_3 insulin mimotope (chains C, F, I)
GVEELYLVAGEEGCGG
Ligands and cofactors
| ID | Name | Formula | Copies |
|---|
| NAG | 2-acetamido-2-deoxy-beta-D-glucopyranose | C8 H15 N O6 | 3 |
Primary citation
C-terminal modification of the insulin B:11-23 peptide creates superagonists in mouse and human type 1 diabetes. Wang, Y., Sosinowski, T., Novikov, A. et al. Proc Natl Acad Sci U S A (2018) 115:162-167. DOI 10.1073/pnas.1716527115 · PubMed
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