Research workbench
Structure of full-length CD20 in complex with obinutuzumab Fab
Analyse Structure of full-length CD20 in complex with obinutuzumab Fab in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 6Y9A
- Type
- protein
- Length
- 775 residues
- Chains
- 4
- Method
- electron microscopy
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- B-lymphocyte antigen CD20; Obinutuzumab Fab heavy chain; Obinutuzumab Fab light chain
- UniProt
- P11836
- Pockets
- 19 · best druggability 0.77
Structure
electron microscopy · 3 distinct chains · 23% helix, 32% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B | B-lymphocyte antigen CD20 | protein | 169 | 70% helix, 0% strand | P11836 |
| H | Obinutuzumab Fab heavy chain | protein | 218 | 6% helix, 43% strand | — |
| L | Obinutuzumab Fab light chain | protein | 219 | 5% helix, 45% strand | — |
Pockets
19 pockets found on a 1 Å grid, 14 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 954 | 0.77 | 0.79 | 76 | empty |
| 2 | 169 | 0.74 | 0.91 | 40 | empty |
| 3 | 179 | 0.73 | 0.89 | 36 | empty |
| 4 | 129 | 0.72 | 0.91 | 37 | empty |
| 5 | 302 | 0.72 | 0.85 | 42 | empty |
Interfaces
5 interfaces between chains.
- H–L · 1821 Ų buried · 12 hydrogen bonds · protein-protein
- A–B · 1366 Ų buried · 4 hydrogen bonds · protein-protein
- A–H · 331 Ų buried · 4 hydrogen bonds · protein-protein
- B–H · 272 Ų buried · 3 hydrogen bonds · protein-protein
- A–L · 238 Ų buried · 2 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 6 disulfide (disulfide).
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 P11836
- Elsewhere: RCSB PDB 6Y9A · PDBe 6Y9A · UniProt P11836
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