MolNFT v1 · #102882 · protein
S16 protein complex
4OZH · HLA class II histocompatibility antigen, dq alpha 1 chain: “S16 protein complex”. X-ray diffraction, 2 ligands (NAG, CA), 20 pockets (best druggability 0.79). MolNFT v1 #102882 on GenesisL1: 3D structure, binding sites and pockets…
- PDB
- 4OZH
- Type
- protein
- Length
- 1,619 residues
- Chains
- 10
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- HLA class II histocompatibility antigen, dq alpha 1 chain; HLA class II…
- UniProt
- P01909, Q5Y7D3
- Ligands
- NAG, CA
- Pockets
- 20 · best druggability 0.79
Structure
x-ray diffraction · 6 distinct chains · 9% helix, 44% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, C | HLA class II histocompatibility antigen, dq alpha 1 chain | protein | 181 | 14% helix, 44% strand | P01909 |
| B, D | HLA class II histocompatibility antigen, dq beta 1 chain | protein | 181 | 19% helix, 45% strand | Q5Y7D3 |
| E, G | T-cell receptor, S16, alpha chain | protein | 195 | 2% helix, 42% strand | — |
| F, H | T-cell receptor, S16, beta chain | protein | 240 | 7% helix, 49% strand | — |
| I | Gliadin-ALPHA2 peptide | protein | 12 | 0% helix, 0% strand | — |
| J | Gliadin-ALPHA2 peptide | protein | 13 | 0% helix, 0% strand | — |
Ligands and binding sites
- NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 3 copies · chains A, C
- CA · Calcium ion · metal · chains G
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
20 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 903 | 0.79 | 0.82 | 110 | empty |
| 2 | 847 | 0.78 | 0.81 | 80 | empty |
| 3 | 162 | 0.60 | 0.83 | 36 | empty |
| 4 | 209 | 0.57 | 0.79 | 32 | empty |
| 5 | 113 | 0.47 | 0.79 | 23 | empty |
Interfaces
24 interfaces between chains.
- C–D · 2638 Ų buried · 43 hydrogen bonds · protein-protein
- A–B · 2590 Ų buried · 49 hydrogen bonds · protein-protein
- G–H · 2089 Ų buried · 23 hydrogen bonds · protein-protein
- E–F · 2088 Ų buried · 22 hydrogen bonds · protein-protein
- A–J · 671 Ų buried · 6 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 16 disulfide, 3 glycan (disulfide, N-glycosylation).
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 P01909
- Every structure of UniProt Q5Y7D3
- Elsewhere: RCSB PDB 4OZH · PDBe 4OZH · UniProt P01909 · UniProt Q5Y7D3
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