Crystal structure of the CD8 alpha beta/H-2Dd complex. Determined by X-ray diffraction at 2.6 Å resolution. Released 14 Jul 2009.
Explore 3DMM in 3D Show helices and sheets RCSB PDB PDBe
3DMM contains 12 α-helices and 50 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 | 3-12 | 10 | 1 |
| α-helix | 20 | 1 | |
| β-strand | 21-28 | 8 | 1 |
| β-strand | 31-37 | 7 | 1 |
| β-strand | 46-47 | 2 | 1 |
| α-helix | 52-54 | 3 | |
| α-helix | 57-84 | 28 | |
| β-strand | 94-103 | 10 | 1 |
| β-strand | 109-118 | 10 | 1 |
| β-strand | 121-126 | 6 | 1 |
| β-strand | 133-135 | 3 | 1 |
| α-helix | 138-150 | 13 | |
| α-helix | 152-161 | 10 | |
| α-helix | 163-179 | 17 | |
| β-strand | 183 | 1 | 2 |
| β-strand | 186-193 | 8 | 3 |
| β-strand | 199-208 | 10 | 3 |
| β-strand | 209 | 1 | 2 |
| β-strand | 214-219 | 6 | 4 |
| β-strand | 229-230 | 2 | 3 |
| α-helix | 231-233 | 3 | |
| β-strand | 234-235 | 2 | 3 |
| β-strand | 241-249 | 9 | 3 |
| α-helix | 254-256 | 3 | |
| β-strand | 257-262 | 6 | 4 |
| β-strand | 270-272 | 3 | 4 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 3-5 | 3 | |
| β-strand | 6-11 | 6 | 5 |
| β-strand | 21-30 | 10 | 5 |
| β-strand | 36-41 | 6 | 6 |
| β-strand | 44-45 | 2 | 6 |
| α-helix | 46 | 1 | |
| β-strand | 50-51 | 2 | 5 |
| β-strand | 55-56 | 2 | 5 |
| β-strand | 62-70 | 9 | 5 |
| β-strand | 78-83 | 6 | 6 |
| β-strand | 91-94 | 4 | 6 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 6-10 | 5 | 7 |
| β-strand | 14 | 1 | 8 |
| β-strand | 22-29 | 8 | 7 |
| β-strand | 35-42 | 8 | 8 |
| β-strand | 51-57 | 7 | 8 |
| β-strand | 63-65 | 3 | 8 |
| α-helix | 67-69 | 3 | |
| β-strand | 75-78 | 4 | 7 |
| β-strand | 84-89 | 6 | 7 |
| β-strand | 98-105 | 8 | 8 |
| β-strand | 110-112 | 3 | 8 |
| β-strand | 114 | 1 | 9 |
| β-strand | 116-118 | 3 | 8 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 2-4 | 3 | 10 |
| β-strand | 7-11 | 5 | 9 |
| β-strand | 16-21 | 6 | 10 |
| β-strand | 30-37 | 8 | 9 |
| β-strand | 44-52 | 9 | 9 |
| β-strand | 56-59 | 4 | 9 |
| β-strand | 69-72 | 4 | 10 |
| β-strand | 80-83 | 4 | 10 |
| α-helix | 88-90 | 3 | |
| β-strand | 92-99 | 8 | 9 |
| β-strand | 104-106 | 3 | 9 |
| β-strand | 110-115 | 6 | 9 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| H-2 class I histocompatibility antigen, D-D alpha chain | A | protein | 275 | Mus musculus | P01900 (AlphaFold model) |
| Beta-2 microglobulin | B | protein | 100 | Mus musculus | P01887 (AlphaFold model) |
| Synthetic peptide | P | protein | 10 | ||
| T-cell surface glycoprotein CD8 alpha chain | C | protein | 166 | Mus musculus | P01731 (AlphaFold model) |
| T-cell surface glycoprotein CD8 beta chain | D | protein | 150 | Mus musculus | P10300 (AlphaFold model) |
>3DMM_1 H-2 class I histocompatibility antigen, D-D alpha chain (chains A) MSHSLRYFVTAVSRPGFGEPRYMEVGYVDNTEFVRFDSDAENPRYEPRARWIEQEGPEYW ERETRRAKGNEQSFRVDLRTALRYYNQSAGGSHTLQWMAGCDVESDGRLLRGYWQFAYDG CDYIALNEDLKTWTAADMAAQITRRKWEQAGAAERDRAYLEGECVEWLRRYLKNGNATLL RTDPPKAHVTHHRRPEGDVTLRCWALGFYPADITLTWQLNGEELTQEMELVETRPAGDGT FQKWASVVVPLGKEQKYTCHVEHEGLPEPLTLRWG
>3DMM_2 Beta-2 microglobulin (chains B) MIQKTPQIQVYSRHPPENGKPNILNCYVTQFHPPHIEIQMLKNGKKIPKVEMSDMSFSKD WSFYILAHTEFTPTETDTYACRVKHASMAEPKTVYWDRDM
>3DMM_3 Synthetic peptide (chains P) RGPGRAFVTI
>3DMM_4 T-cell surface glycoprotein CD8 alpha chain (chains C) GSGEAKPQAPELRIFPKKMDAELGQKVDLVCEVLGSVSQGCSWLFQNSSSKLPQPTFVVY MASSHNKITWDEKLNSSKLFSAMRDTNNKYVLTLNKFSKENEGYYFCSVISNSVMYFSSV VPVLQKVNSTTTKPVLRTPSPVHPTGTSQPQRPEDCRPRGSVKGTG
>3DMM_5 T-cell surface glycoprotein CD8 beta chain (chains D) SSALIQTPSSLLVQTNHTAKMSCEVKSISKLTSIYWLRERQDPKDKYFEFLASWSSSKGV LYGESVDKKRNIILESSDSRRPFLSIMNVKPEDSDFYFCATVGSPKMVFGTGTKLTVVDV LPTTAPTKKTTLKMKKKKQCPFPHPETQKG
Structural basis of the CD8alphabeta/MHC class i interaction: focused recognition orients CD8beta to a T cell proximal position. Wang, R., Natarajan, K., Margulies, D.H. J Immunol (2009) 183:2554-2564. DOI 10.4049/jimmunol.0901276 · PubMed
Other PDB entries of the same protein (UniProt P01900 (AlphaFold model), which also has an AlphaFold model), best resolution first:
MolViewer shows 3DMM 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.