Research workbench
Crystal structure of the mam-MHC complex
Analyse Crystal structure of the mam-MHC complex in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 1R5I
- Type
- protein
- Length
- 1,196 residues
- Chains
- 8
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- HLA class II histocompatibility antigen, dr alpha chain; HLA class II histocompatibility…
- UniProt
- P01903, P04229, P11133, Q48898
- Ligands
- PO4
- Pockets
- 14 · best druggability 0.64
Structure
x-ray diffraction · 4 distinct chains · 34% helix, 28% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, E | HLA class II histocompatibility antigen, dr alpha chain | protein | 181 | 14% helix, 45% strand | P01903 |
| B, F | HLA class II histocompatibility antigen, DRB1-1 beta chain | protein | 190 | 19% helix, 45% strand | P04229 |
| C, G | Hemagglutinin peptide | protein | 13 | 0% helix, 8% strand | P11133 |
| D, H | Superantigen | protein | 214 | 68% helix, 0% strand | Q48898 |
Ligands and binding sites
- PO4 · Phosphate ion · ion · 4 copies · chains A, C, D, E, G, H
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
14 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 354 | 0.64 | 0.79 | 41 | PO4 |
| 2 | 307 | 0.62 | 0.80 | 41 | empty |
| 3 | 235 | 0.59 | 0.80 | 30 | PO4 |
| 4 | 262 | 0.56 | 0.77 | 31 | empty |
| 5 | 136 | 0.54 | 0.81 | 18 | empty |
Interfaces
13 interfaces between chains.
- A–B · 2608 Ų buried · 46 hydrogen bonds · protein-protein
- E–F · 2576 Ų buried · 42 hydrogen bonds · protein-protein
- D–H · 901 Ų buried · 5 hydrogen bonds · protein-protein
- A–D · 788 Ų buried · 14 hydrogen bonds · protein-protein
- E–H · 763 Ų buried · 13 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 6 disulfide, 6 modified (disulfide, engineered).
Compared structures
Analyse
- Open in the research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides and crosslinks on the 3D structure
- Every structure of UniProt P01903
- Every structure of UniProt P04229
- Every structure of UniProt P11133
- Every structure of UniProt Q48898
- Elsewhere: RCSB PDB 1R5I · PDBe 1R5I · UniProt P01903 · UniProt P04229 · UniProt P11133 · UniProt Q48898
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