HLA-DR1 in complex with a synthetic peptide (AAYSDQATPLLLSPR) and the superantigen SEC3-3B2. Determined by X-ray diffraction at 2.5 Å resolution. Released 17 Aug 2004.
Explore 1T5X in 3D Show helices and sheets RCSB PDB PDBe
1T5X contains 23 α-helices and 49 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 | 5-15 | 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 | |
| β-strand | 53 | 1 | 2 |
| α-helix | 56-76 | 21 | |
| α-helix | 81-84 | 4 | |
| β-strand | 85 | 1 | 3 |
| α-helix | 86-87 | 2 | |
| β-strand | 88-93 | 6 | 4 |
| β-strand | 103-112 | 10 | 4 |
| β-strand | 113 | 1 | 3 |
| β-strand | 118-123 | 6 | 5 |
| β-strand | 126-128 | 3 | 5 |
| β-strand | 133-134 | 2 | 4 |
| α-helix | 137 | 1 | |
| β-strand | 138-139 | 2 | 4 |
| β-strand | 145-153 | 9 | 4 |
| β-strand | 160-166 | 7 | 5 |
| β-strand | 174-179 | 6 | 5 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 7-18 | 12 | 1 |
| β-strand | 23-31 | 9 | 1 |
| β-strand | 36-41 | 6 | 1 |
| β-strand | 46-49 | 4 | 1 |
| α-helix | 52-54 | 3 | |
| α-helix | 55-62 | 8 | |
| α-helix | 65-74 | 10 | |
| α-helix | 75-80 | 6 | |
| α-helix | 81-86 | 6 | |
| α-helix | 87-89 | 3 | |
| β-strand | 95 | 1 | 6 |
| α-helix | 96-97 | 2 | |
| β-strand | 98-103 | 6 | 7 |
| β-strand | 113-122 | 10 | 7 |
| β-strand | 123 | 1 | 6 |
| β-strand | 128-133 | 6 | 8 |
| β-strand | 136-137 | 2 | 8 |
| β-strand | 142-144 | 3 | 7 |
| β-strand | 148-149 | 2 | 7 |
| β-strand | 155-163 | 9 | 7 |
| β-strand | 170-176 | 7 | 8 |
| β-strand | 184-189 | 6 | 8 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 1 | 1 | 2 |
| α-helix | 2-3 | 2 | |
| α-helix | 5-10 | 6 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 2-6 | 5 | |
| α-helix | 8-10 | 3 | |
| α-helix | 14-16 | 3 | |
| β-strand | 17 | 1 | 9 |
| α-helix | 22-25 | 4 | |
| β-strand | 33-38 | 6 | 10 |
| β-strand | 42 | 1 | 11 |
| β-strand | 48-52 | 5 | 11 |
| β-strand | 63-67 | 5 | 11 |
| α-helix | 71-78 | 8 | |
| β-strand | 82-86 | 5 | 10 |
| β-strand | 89 | 1 | 11 |
| β-strand | 108-112 | 5 | 11 |
| β-strand | 115-117 | 3 | 10 |
| β-strand | 129-137 | 9 | 12 |
| β-strand | 140-149 | 10 | 12 |
| β-strand | 153-155 | 3 | 13 |
| α-helix | 156-171 | 16 | |
| β-strand | 183-189 | 7 | 12 |
| β-strand | 195-199 | 5 | 12 |
| α-helix | 202-203 | 2 | |
| β-strand | 205 | 1 | 9 |
| α-helix | 210-214 | 5 | |
| α-helix | 215-219 | 5 | |
| β-strand | 222-224 | 3 | 13 |
| β-strand | 229-235 | 7 | 12 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| HLA class II histocompatibility antigen, DR alpha chain | A | protein | 181 | Homo sapiens | P01903 (AlphaFold model) |
| HLA class II histocompatibility antigen, DRB1-1 beta chain | B | protein | 190 | Homo sapiens | P01911 (AlphaFold model) |
| 15-mer peptide fragment of Regulatory protein MIG1 | C | protein | 15 | P27705 (AlphaFold model) | |
| Enterotoxin type C-3 | D | protein | 239 | Staphylococcus aureus | P0A0L5 (AlphaFold model) |
>1T5X_1 HLA class II histocompatibility antigen, DR alpha chain (chains A) KEEHVIIQAEFYLNPDQSGEFMFDFDGDEIFHVDMAKKETVWRLEEFGRFASFEAQGALA NIAVDKANLEIMTKRSNYTPITNVPPEVTVLTNSPVELREPNVLICFIDKFTPPVVNVTW LRNGKPVTTGVSETVFLPREDHLFRKFHYLPFLPSTEDVYDCRVEHWGLDEPLLKHWEFD A
>1T5X_2 HLA class II histocompatibility antigen, DRB1-1 beta chain (chains B) GDTRPRFLWQLKFECHFFNGTERVRLLERCIYNQEESVRFDSDVGEYRAVTELGRPDAEY WNSQKDLLEQRRAAVDTYCRHNYGVGESFTVQRRVEPKVTVYPSKTQPLQHHNLLVCSVS GFYPGSIEVRWFRNGQEEKAGVVSTGLIQNGDWTFQTLVMLETVPRSGEVYTCQVEHPSV TSPLTVEWRA
>1T5X_3 15-mer peptide fragment of Regulatory protein MIG1 (chains C) AAYSDQATPLLLSPR
>1T5X_4 Enterotoxin type C-3 (chains D) ESQPDPMPDDLHKSSEFTGTMGNMKYLYDDHYVSATKVKSVDSFFKWDLIYNISDKKLKN YDKVKTELLNEDLAKKYKDEVVDVYGSNYYVNCYFSSKDNVGKVTGGKTCMYGGITKHEG NHFDNGNLQNVLVRVYENKRNTISFEVQTDKKSVTAQELDIKARNFLINKKNLYEFNSSP YETGYIKFIENNGNTFWYDMMPAPGDKFDQSKYLMMYNDNKTVDSKSVKIEVHLTTKNG
A Polymorphic Pocket at the P10 Position Contributes to Peptide Binding Specificity in Class II MHC Proteins. Zavala-Ruiz, Z., Strug, I., Anderson, M.W. et al. Chem Biol (2004) 11:1395-1402. DOI 10.1016/j.chembiol.2004.08.007 · PubMed
Other PDB entries of the same protein (UniProt P01903 (AlphaFold model), which also has an AlphaFold model), best resolution first:
MolViewer shows 1T5X directly in your browser with nothing to install. Switch between cartoon, ball-and-stick, spacefill and surface views, color by chain, secondary structure or B-factor, measure distances, angles and dihedrals, and share or embed the view.