Crystal structure of HLA-DQ2 complexed with deamidated gliadin peptide. Determined by X-ray diffraction at 2.22 Å resolution. Released 2 Mar 2004.
Explore 1S9V in 3D Show helices and sheets RCSB PDB PDBe
1S9V contains 27 α-helices and 56 β-strands across 6 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 | 5-14 | 11 | 1 |
| β-strand | 19-26 | 8 | 1 |
| β-strand | 29-35 | 7 | 1 |
| β-strand | 40-43 | 4 | 1 |
| α-helix | 46-50 | 5 | |
| α-helix | 56-76 | 21 | |
| α-helix | 81-87 | 7 | |
| β-strand | 88-93 | 6 | 2 |
| β-strand | 103-112 | 10 | 2 |
| β-strand | 118-123 | 6 | 3 |
| β-strand | 126-127 | 2 | 3 |
| 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 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 8-18 | 11 | 1 |
| β-strand | 23-32 | 10 | 1 |
| β-strand | 35-41 | 7 | 1 |
| β-strand | 46-49 | 4 | 1 |
| α-helix | 52-54 | 3 | |
| α-helix | 55-63 | 9 | |
| α-helix | 65-71 | 7 | |
| α-helix | 74 | 1 | |
| α-helix | 75-80 | 6 | |
| α-helix | 81-87 | 7 | |
| α-helix | 90-92 | 3 | |
| β-strand | 95 | 1 | 4 |
| α-helix | 96-97 | 2 | |
| β-strand | 98-103 | 6 | 5 |
| β-strand | 114-122 | 9 | 5 |
| β-strand | 123 | 1 | 4 |
| β-strand | 128-132 | 5 | 6 |
| β-strand | 137-138 | 2 | 6 |
| β-strand | 142-144 | 3 | 5 |
| β-strand | 148-149 | 2 | 5 |
| β-strand | 155-162 | 8 | 5 |
| β-strand | 170-176 | 7 | 6 |
| β-strand | 184-189 | 6 | 6 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 3-10 | 8 |
| 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 | 46-50 | 5 | |
| α-helix | 57-76 | 20 | |
| α-helix | 81-87 | 7 | |
| β-strand | 88-93 | 6 | 8 |
| β-strand | 103-112 | 10 | 8 |
| β-strand | 118-123 | 6 | 9 |
| β-strand | 126-127 | 2 | 9 |
| α-helix | 128 | 1 | |
| 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 |
| 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 | 52-54 | 3 | |
| 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 | 114-122 | 9 | 11 |
| β-strand | 123 | 1 | 10 |
| β-strand | 128-133 | 6 | 12 |
| β-strand | 136-138 | 3 | 12 |
| β-strand | 142-144 | 3 | 11 |
| α-helix | 145-147 | 3 | |
| β-strand | 148-149 | 2 | 11 |
| β-strand | 155-162 | 8 | 11 |
| β-strand | 170-176 | 7 | 12 |
| β-strand | 184-189 | 6 | 12 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| HLA class II histocompatibility antigen, DQ(3) alpha chain | A, D | protein | 193 | Homo sapiens | P01909 (AlphaFold model) |
| HLA class II histocompatibility antigen, DQ(1) beta chain | B, E | protein | 198 | Homo sapiens | P01920 (AlphaFold model) |
| alpha-I gliadin | C, F | protein | 11 |
>1S9V_1 HLA class II histocompatibility antigen, DQ(3) alpha chain (chains A, D) EDIVADHVASYGVNLYQSYGPSGQYTHEFDGDEQFYVDLGRKETVWCLPVLRQFRFDPQF ALTNIAVLKHNLNSLIKRSNSTAATNEVPEVTVFSKSPVTLGQPNILICLVDNIFPPVVN ITWLSNGHSVTEGVSETSFLSKSDHSFFKISYLTLLPSAEESYDCKVEHWGLDKPLLKHW EPEIPAPMSELTE
>1S9V_2 HLA class II histocompatibility antigen, DQ(1) beta chain (chains B, E) RDSPEDFVYQFKGMCYFTNGTERVRLVSRSIYNREEIVRFDSDVGEFRAVTLLGLPAAEY WNSQKDILERKRAAVDRVCRHNYQLELRTTLQRRVEPTVTISPSRTEALNHHNLLVCSVT DFYPAQIKVRWFRNDQEETAGVVSTPLIRNGDWTFQILVMLEMTPQRGDVYTCHVEHPSL QSPITVEWRAQSESAQSK
>1S9V_3 alpha-I gliadin (chains C, F) LQPFPQPELPY
Structural basis for HLA-DQ2-mediated presentation of gluten epitopes in celiac disease. Kim, C.-Y., Quarsten, H., Bergseng, E. et al. Proc Natl Acad Sci U S A (2004) 101:4175-4179. DOI 10.1073/pnas.0306885101 · PubMed
Other PDB entries of the same protein (UniProt P01909 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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