MolNFT v1 · #71674 · protein
A complex between DISHEVELLED2 and clathrin adaptor ap-2
3ML6 · Chimeric complex between protein DISHEVELLED2 homolog dvl-2…: “A complex between DISHEVELLED2 and clathrin adaptor ap-2”. X-ray diffraction, 20 pockets (best druggability 0.73). MolNFT v1 #71674 on GenesisL1: 3D structure, binding…
- PDB
- 3ML6
- Type
- protein
- Length
- 2,054 residues
- Chains
- 6
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Chimeric complex between protein DISHEVELLED2 homolog dvl-2 and clathrin adaptor ap-2…
- UniProt
- Q60838, P84092
- Pockets
- 20 · best druggability 0.73
Structure
x-ray diffraction · 6 distinct chains · 11% helix, 47% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Chimeric complex between protein DISHEVELLED2 homolog dvl-2 and clathrin adaptor ap-2 complex subunit mu | protein | 351 | 11% helix, 47% strand | Q60838, P84092 |
| B | Chimeric complex between protein DISHEVELLED2 homolog dvl-2 and clathrin adaptor ap-2 complex subunit mu | protein | 339 | 12% helix, 48% strand | Q60838, P84092 |
| C | Chimeric complex between protein DISHEVELLED2 homolog dvl-2 and clathrin adaptor ap-2 complex subunit mu | protein | 350 | 11% helix, 47% strand | Q60838, P84092 |
| D | Chimeric complex between protein DISHEVELLED2 homolog dvl-2 and clathrin adaptor ap-2 complex subunit mu | protein | 336 | 12% helix, 48% strand | Q60838, P84092 |
| E | Chimeric complex between protein DISHEVELLED2 homolog dvl-2 and clathrin adaptor ap-2 complex subunit mu | protein | 338 | 12% helix, 48% strand | Q60838, P84092 |
| F | Chimeric complex between protein DISHEVELLED2 homolog dvl-2 and clathrin adaptor ap-2 complex subunit mu | protein | 340 | 11% helix, 48% strand | Q60838, P84092 |
Pockets
20 pockets found on a 1 Å grid, 13 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 581 | 0.73 | 0.81 | 45 | empty |
| 2 | 263 | 0.59 | 0.79 | 31 | empty |
| 3 | 282 | 0.59 | 0.78 | 36 | empty |
| 4 | 235 | 0.57 | 0.78 | 36 | empty |
| 5 | 98 | 0.55 | 0.84 | 26 | empty |
Interfaces
6 interfaces between chains.
- A–E · 1353 Ų buried · 22 hydrogen bonds · protein-protein
- B–F · 1327 Ų buried · 18 hydrogen bonds · protein-protein
- B–E · 578 Ų buried · 4 hydrogen bonds · protein-protein
- A–F · 571 Ų buried · 4 hydrogen bonds · protein-protein
- A–C · 548 Ų buried · 6 hydrogen bonds · protein-protein
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 Q60838
- Every structure of UniProt P84092
- Elsewhere: RCSB PDB 3ML6 · PDBe 3ML6 · UniProt Q60838 · UniProt P84092
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