Research workbench
Histocompatibility antigen I-AG7
Analyse Histocompatibility antigen I-AG7 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 1F3J
- Type
- protein
- Length
- 766 residues
- Chains
- 6
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- H-2 class II histocompatibility antigen; MHC class II nod; Lysozyme C
- UniProt
- P04228, Q31135, P00698
- Ligands
- NAG
- Pockets
- 10 · best druggability 0.75
Structure
x-ray diffraction · 3 distinct chains · 13% helix, 42% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, D | H-2 class II histocompatibility antigen | protein | 182 | 11% helix, 44% strand | P04228 |
| B, E | MHC class II nod | protein | 187 | 16% helix, 44% strand | Q31135 |
| P, Q | Lysozyme C | protein | 14 | 0% helix, 0% strand | P00698 |
Ligands and binding sites
- NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 6 copies · chains A, B, D, E
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
10 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 867 | 0.75 | 0.79 | 82 | empty |
| 2 | 504 | 0.68 | 0.79 | 51 | empty |
| 3 | 615 | 0.66 | 0.76 | 57 | empty |
| 4 | 66 | 0.44 | 0.81 | 16 | empty |
| 5 | 123 | 0.43 | 0.77 | 23 | empty |
Interfaces
9 interfaces between chains.
- A–B · 2517 Ų buried · 42 hydrogen bonds · protein-protein
- D–E · 2510 Ų buried · 43 hydrogen bonds · protein-protein
- B–P · 809 Ų buried · 17 hydrogen bonds · protein-protein
- E–Q · 808 Ų buried · 16 hydrogen bonds · protein-protein
- A–P · 730 Ų buried · 12 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 6 disulfide, 6 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 P04228
- Every structure of UniProt Q31135
- Every structure of UniProt P00698
- Elsewhere: RCSB PDB 1F3J · PDBe 1F3J · UniProt P04228 · UniProt Q31135 · UniProt P00698
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