Research workbench
Crystal structure of aedes aegypti nibbler ntd domain
Analyse Crystal structure of aedes aegypti nibbler ntd domain in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 7JW3
- Type
- protein
- Length
- 727 residues
- Chains
- 3
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Exonuclease mut-7 homolog
- EC
- 3.1.-.-
- UniProt
- Q179T2
- Pockets
- 5 · best druggability 0.64
Structure
x-ray diffraction · 3 distinct chains · 66% helix, 0% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| C | Exonuclease mut-7 homolog (EC 3.1.-.-) | protein | 244 | 67% helix, 0% strand | Q179T2 |
| A | Exonuclease mut-7 homolog (EC 3.1.-.-) | protein | 240 | 69% helix, 0% strand | Q179T2 |
| B | Exonuclease mut-7 homolog (EC 3.1.-.-) | protein | 243 | 62% helix, 0% strand | Q179T2 |
Pockets
5 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 75 | 0.64 | 0.91 | 21 | empty |
| 2 | 172 | 0.51 | 0.78 | 29 | empty |
| 3 | 175 | 0.45 | 0.74 | 21 | empty |
| 4 | 63 | 0.35 | 0.77 | 16 | empty |
| 5 | 78 | 0.31 | 0.74 | 17 | empty |
Interfaces
2 interfaces between chains.
- A–B · 468 Ų buried · 1 hydrogen bond · protein-protein
- C–B · 417 Ų buried · 14 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 24 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 Q179T2
- Elsewhere: RCSB PDB 7JW3 · PDBe 7JW3 · UniProt Q179T2
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