HLA-DRB1*1402 in complex with Vimentin59-71. Determined by X-ray diffraction at 1.9 Å resolution. Released 13 Sept 2017.
Explore 6ATF in 3D Show helices and sheets RCSB PDB PDBe
6ATF contains 32 α-helices and 64 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 | 5-15 | 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 | 80-84 | 5 | |
| 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 | 161-166 | 6 | 5 |
| β-strand | 174-178 | 5 | 5 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 7-18 | 12 | 1 |
| β-strand | 23-32 | 10 | 1 |
| β-strand | 35-41 | 7 | 1 |
| β-strand | 47-49 | 3 | 1 |
| α-helix | 52-54 | 3 | |
| α-helix | 55-62 | 8 | |
| α-helix | 65-72 | 8 | |
| α-helix | 74 | 1 | |
| 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 | 98-104 | 7 | 7 |
| β-strand | 114-122 | 9 | 7 |
| β-strand | 123 | 1 | 6 |
| β-strand | 128-133 | 6 | 8 |
| β-strand | 136-138 | 3 | 8 |
| β-strand | 142-144 | 3 | 7 |
| α-helix | 147 | 1 | |
| β-strand | 148-149 | 2 | 7 |
| β-strand | 155-162 | 8 | 7 |
| β-strand | 170-176 | 7 | 8 |
| β-strand | 184-189 | 6 | 8 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 2 | 1 | 2 |
| α-helix | 3-5 | 3 | |
| α-helix | 10-12 | 3 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 5-15 | 11 | 9 |
| β-strand | 19-26 | 8 | 9 |
| β-strand | 29-35 | 7 | 9 |
| β-strand | 40-43 | 4 | 9 |
| α-helix | 46-50 | 5 | |
| β-strand | 53 | 1 | 10 |
| α-helix | 56-76 | 21 | |
| α-helix | 80-84 | 5 | |
| β-strand | 85 | 1 | 11 |
| α-helix | 86-87 | 2 | |
| β-strand | 88-93 | 6 | 12 |
| β-strand | 103-112 | 10 | 12 |
| β-strand | 113 | 1 | 11 |
| β-strand | 118-123 | 6 | 13 |
| β-strand | 126-128 | 3 | 13 |
| β-strand | 133-134 | 2 | 12 |
| α-helix | 137 | 1 | |
| β-strand | 138-139 | 2 | 12 |
| β-strand | 145-153 | 9 | 12 |
| β-strand | 160-166 | 7 | 13 |
| β-strand | 174-179 | 6 | 13 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| HLA class II histocompatibility antigen, DR alpha chain | A, D | protein | 189 | Homo sapiens | P01903 (AlphaFold model) |
| MHC class II antigen | B, E | protein | 200 | Homo sapiens | A0A0A1I7H6 (AlphaFold model) |
| Vimentin59-71 | C, F | protein | 13 | synthetic construct | P08670 (AlphaFold model) |
>6ATF_1 HLA class II histocompatibility antigen, DR alpha chain (chains A, D) IKEEHVIIQAEFYLNPDQSGEFMFDFDGDEIFHVDMAKKETVWRLEEFGRFASFEAQGAL ANIAVDKANLEIMTKRSNYTPITNVPPEVTVLTNSPVELREPNVLICFIDKFTPPVVNVT WLRNGKPVTTGVSETVFLPREDHLFRKFHYLPFLPSTEDVYDCRVEHWGLDEPLLKHWEF DTSGDDDDK
>6ATF_2 MHC class II antigen (chains B, E) GSGDTRPRFLEYSTSECHFFNGTERVRFLERYFHNQEENVRFDSDVGEYRAVTELGRPDA EYWNSQKDLLEQRRAAVDTYCRHNYGVGESFTVQRRVHPKVTVYPSKTQPLQHHNLLVCS VSGFYPGSIEVRWFRNGQEEKTGVVSTGLIHNGDWTFQTLVMLETVPRSGEVYTCQVEHP SVTSPLTVEWRATGGDDDDK
>6ATF_3 Vimentin59-71 (chains C, F) GVYATRSSAVRLR
| ID | Name | Formula | Copies |
|---|---|---|---|
| NAG | 2-acetamido-2-deoxy-beta-D-glucopyranose | C8 H15 N O6 | 2 |
Water and common crystallization additives (PGE, EDO) are not listed.
Molecular basis for increased susceptibility of Indigenous North Americans to seropositive rheumatoid arthritis. Scally, S.W., Law, S.C., Ting, Y.T. et al. Ann Rheum Dis (2017) 76:1915-1923. DOI 10.1136/annrheumdis-2017-211300 · PubMed
Other PDB entries of the same protein (UniProt P01903 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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