Research workbench
Crystal structure of D-tagatose 3-epimerase-like protein
Analyse Crystal structure of D-tagatose 3-epimerase-like protein in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 3WQO
- Type
- protein
- Length
- 538 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v2 / PDB Bank
- Contract
- 0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
- Owner
- 0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
- Resolution
- 2.64
- Source
- Methanocaldococcus jannaschii DSM 2661
- Molecule
- Uncharacterized protein MJ1311
- UniProt
- Q58707
- Ligands
- MN
- Pockets
- 3 · best druggability 0.83
Structure
x-ray diffraction · resolution 2.64 · 2 distinct chains · 45% helix, 16% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Uncharacterized protein MJ1311 | protein | 271 | 47% helix, 16% strand | Q58707 |
| B | Uncharacterized protein MJ1311 | protein | 267 | 44% helix, 16% strand | Q58707 |
Ligands and binding sites
- MN · Manganese (II) ion · metal · 4 copies · chains A, B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
3 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1181 | 0.83 | 0.84 | 101 | MN |
| 2 | 50 | 0.32 | 0.78 | 15 | empty |
| 3 | 63 | 0.31 | 0.75 | 18 | empty |
Interfaces
1 interface between chains.
- A–B · 1038 Ų buried · 7 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 Q58707
- Elsewhere: RCSB PDB 3WQO · PDBe 3WQO · UniProt Q58707
GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.