MolNFT v1 · #90970 · protein
Crystal structure of the human IgE-FC(EPSILON)3-4 bound to its B cell receptor DERCD23
4EZM · Ig epsilon chain C region: “Crystal structure of the human IgE-FC(EPSILON)3-4 bound to its B cell receptor DERCD23”. X-ray diffraction, 3 ligands (MAN, NAG, BMA), 15 pockets (best druggability 0.59). MolNFT v1 #90970 on GenesisL1…
- PDB
- 4EZM
- Type
- protein
- Length
- 2,022 residues
- Chains
- 12
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Ig epsilon chain C region; Low affinity immunoglobulin epsilon Fc receptor
- UniProt
- P01854, P06734
- Ligands
- MAN, NAG, BMA
- Pockets
- 15 · best druggability 0.59
Structure
x-ray diffraction · 9 distinct chains · 11% helix, 43% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Ig epsilon chain C region | protein | 211 | 9% helix, 46% strand | P01854 |
| B | Ig epsilon chain C region | protein | 208 | 10% helix, 46% strand | P01854 |
| C | Ig epsilon chain C region | protein | 197 | 11% helix, 46% strand | P01854 |
| D | Ig epsilon chain C region | protein | 207 | 10% helix, 47% strand | P01854 |
| E | Ig epsilon chain C region | protein | 191 | 8% helix, 41% strand | P01854 |
| F | Ig epsilon chain C region | protein | 208 | 10% helix, 46% strand | P01854 |
| G, H, I, J | Low affinity immunoglobulin epsilon Fc receptor | protein | 133 | 15% helix, 37% strand | P06734 |
| K | Low affinity immunoglobulin epsilon Fc receptor | protein | 134 | 15% helix, 37% strand | P06734 |
| L | Low affinity immunoglobulin epsilon Fc receptor | protein | 134 | 15% helix, 37% strand | P06734 |
Ligands and binding sites
- MAN · alpha-D-mannopyranose · sugar · 14 copies · chains A, B, C, D, E, F
- NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 12 copies · chains A, B, C, D, E, F
- BMA · beta-D-mannopyranose · sugar · 6 copies · chains A, B, C, D, E, F
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
15 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 140 | 0.59 | 0.84 | 30 | empty |
| 2 | 202 | 0.49 | 0.75 | 25 | empty |
| 3 | 181 | 0.44 | 0.74 | 21 | empty |
| 4 | 167 | 0.42 | 0.74 | 20 | empty |
| 5 | 162 | 0.41 | 0.74 | 24 | MAN |
Interfaces
12 interfaces between chains.
- C–D · 1340 Ų buried · 14 hydrogen bonds · protein-protein
- E–F · 1328 Ų buried · 12 hydrogen bonds · protein-protein
- A–B · 1301 Ų buried · 10 hydrogen bonds · protein-protein
- F–L · 963 Ų buried · 19 hydrogen bonds · protein-protein
- E–K · 938 Ų buried · 11 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 5 disulfide (disulfide).
Compared structures
- 4EZM · Crystal structure of the human IgE-Fc(epsilon)3-4 bound to its B cell receptor derCD23 · the same entry in another collection · chain L against L, TM-score 1.00
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 P01854
- Every structure of UniProt P06734
- Elsewhere: RCSB PDB 4EZM · PDBe 4EZM · UniProt P01854 · UniProt P06734
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