Research workbench
Crystal structure of unbound anti-glycan antibody FAB14.22 at 2.2 a
Analyse Crystal structure of unbound anti-glycan antibody FAB14.22 at 2.2 a in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 5JOR
- Type
- protein
- Length
- 1,708 residues
- Chains
- 8
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- FAB14.22 heavy chain; Fab 14.22 light chain
- Ligands
- SO4
- Pockets
- 20 · best druggability 0.82
Structure
x-ray diffraction · 5 distinct chains · 5% helix, 54% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| B | FAB14.22 heavy chain | protein | 207 | 9% helix, 54% strand | — |
| A, L, C | Fab 14.22 light chain | protein | 218 | 5% helix, 52% strand | — |
| F, H | FAB14.22 heavy chain | protein | 211 | 3% helix, 56% strand | — |
| D | FAB14.22 heavy chain | protein | 208 | 3% helix, 54% strand | — |
| E | Fab 14.22 light chain | protein | 217 | 6% helix, 52% strand | — |
Ligands and binding sites
- SO4 · Sulfate ion · ion · 19 copies · chains B, C, A, D, F, L, H, E
- GOL · Glycerol · additive · 33 copies · chains B, C, A, L, D, F, E, H
- 1PE · Pentaethylene glycol · additive · 15 copies · chains B, C, A, F, H, D, L, E
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
20 pockets found on a 1 Å grid, 9 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 812 | 0.82 | 0.85 | 81 | 1PE, GOL |
| 2 | 349 | 0.71 | 0.83 | 46 | GOL |
| 3 | 641 | 0.67 | 0.77 | 56 | empty |
| 4 | 590 | 0.67 | 0.77 | 54 | SO4, GOL, 1PE |
| 5 | 148 | 0.67 | 0.88 | 29 | GOL |
Interfaces
13 interfaces between chains.
- H–L · 1887 Ų buried · 20 hydrogen bonds · protein-protein
- F–E · 1870 Ų buried · 21 hydrogen bonds · protein-protein
- A–D · 1815 Ų buried · 17 hydrogen bonds · protein-protein
- B–C · 1812 Ų buried · 17 hydrogen bonds · protein-protein
- L–D · 563 Ų buried · 5 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 16 disulfide, 2 covalent (disulfide, additive adduct).
Compared structures
- 5JOR · Crystal structure of unbound anti-glycan antibody Fab14.22 at 2.2 A · the same entry in another collection · chain E against E, 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
- Elsewhere: RCSB PDB 5JOR · PDBe 5JOR
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