Research workbench
Crystal structure of DLN1 complexed with sucrose
Analyse Crystal structure of DLN1 complexed with sucrose in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 4ZNO
- Type
- protein
- Length
- 636 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Natterin-like protein
- UniProt
- Q5CZR5
- Ligands
- GLC, FRU, CL
- Pockets
- 9 · best druggability 0.51
Structure
x-ray diffraction · 1 distinct chain · 2% helix, 64% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B | Natterin-like protein | protein | 318 | 2% helix, 64% strand | Q5CZR5 |
Ligands and binding sites
- GLC · alpha-D-glucopyranose · sugar · 2 copies · chains A, B
- FRU · beta-D-fructofuranose · sugar · 2 copies · chains A, B
- CL · Chloride ion · ion · 2 copies · chains A, B
- EPE · 4-(2-hydroxyethyl)-1-piperazine ethanesulfonic acid · additive · chains B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
9 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 103 | 0.51 | 0.82 | 23 | empty |
| 2 | 87 | 0.49 | 0.83 | 23 | empty |
| 3 | 109 | 0.42 | 0.77 | 25 | empty |
| 4 | 143 | 0.41 | 0.74 | 29 | empty |
| 5 | 98 | 0.39 | 0.77 | 18 | empty |
Interfaces
1 interface between chains.
- A–B · 1532 Ų buried · 22 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 Q5CZR5
- Elsewhere: RCSB PDB 4ZNO · PDBe 4ZNO · UniProt Q5CZR5
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