Research workbench
Structure of mitoxantrone-bound ABCG2
Analyse Structure of mitoxantrone-bound ABCG2 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 7NFD
- Type
- protein
- Length
- 1,582 residues
- Chains
- 6
- Method
- electron microscopy
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- ATP-binding cassette sub-family G member 2; 5D3(FAB) light chain variable domain…
- EC
- 7.6.2.2
- UniProt
- Q9UNQ0
- Ligands
- MIX, NAG
- Pockets
- 20 · best druggability 0.85
Structure
electron microscopy · 3 distinct chains · 36% helix, 11% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B | ATP-binding cassette sub-family G member 2 (EC 7.6.2.2) | protein | 566 | 50% helix, 6% strand | Q9UNQ0 |
| C, E | 5D3(FAB) light chain variable domain | protein | 107 | 3% helix, 29% strand | — |
| D, F | 5D3(FAB) heavy chain variable domain | protein | 118 | 3% helix, 21% strand | — |
Ligands and binding sites
- MIX · 1,4-dihydroxy-5,8-bis({2-[(2-hydroxyethyl) amino]ethyl}amino)-9,10-anthracenedione · ligand · chains A, B
- NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 4 copies · chains A, D, F, B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
20 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 379 | 0.85 | 0.93 | 36 | empty |
| 2 | 902 | 0.79 | 0.81 | 80 | MIX |
| 3 | 597 | 0.71 | 0.79 | 65 | empty |
| 4 | 600 | 0.71 | 0.79 | 67 | empty |
| 5 | 506 | 0.70 | 0.80 | 49 | empty |
Interfaces
11 interfaces between chains.
- A–B · 2312 Ų buried · 24 hydrogen bonds · protein-protein
- C–D · 772 Ų buried · 8 hydrogen bonds · protein-protein
- E–F · 761 Ų buried · 6 hydrogen bonds · protein-protein
- C–B · 426 Ų buried · 4 hydrogen bonds · protein-protein
- A–E · 425 Ų buried · 2 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 7 disulfide, 2 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 Q9UNQ0
- Elsewhere: RCSB PDB 7NFD · PDBe 7NFD · UniProt Q9UNQ0
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