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Crystal structure of mid domain from HAGO2
Analyse Crystal structure of mid domain from HAGO2 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 3LUK
- Type
- protein
- Length
- 402 residues
- Chains
- 3
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Protein argonaute-2
- UniProt
- Q9UKV8
- Ligands
- PO4
- Pockets
- 4 · best druggability 0.38
Structure
x-ray diffraction · 3 distinct chains · 48% helix, 16% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Protein argonaute-2 | protein | 136 | 49% helix, 16% strand | Q9UKV8 |
| B | Protein argonaute-2 | protein | 133 | 47% helix, 17% strand | Q9UKV8 |
| C | Protein argonaute-2 | protein | 133 | 49% helix, 17% strand | Q9UKV8 |
Ligands and binding sites
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
4 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 53 | 0.38 | 0.81 | 15 | empty |
| 2 | 104 | 0.37 | 0.75 | 25 | empty |
| 3 | 50 | 0.37 | 0.80 | 13 | empty |
| 4 | 58 | 0.26 | 0.73 | 13 | empty |
Interfaces
2 interfaces between chains.
- B–C · 664 Ų buried · 3 hydrogen bonds · protein-protein
- A–B · 644 Ų buried · 11 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 12 modified (engineered).
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 Q9UKV8
- Elsewhere: RCSB PDB 3LUK · PDBe 3LUK · UniProt Q9UKV8
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