MolNFT v1 · #37240 · protein
UGL_D88N/DGLCA-glc-rha-glc
2FV0 · Unsaturated glucuronyl hydrolase: “UGL_D88N/DGLCA-glc-rha-glc”. X-ray diffraction, 3 ligands (GAD, BGC, RAM), 5 pockets (best druggability 0.57). MolNFT v1 #37240 on GenesisL1: 3D structure, binding sites and pockets in GL1X.
- PDB
- 2FV0
- Type
- protein
- Length
- 754 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Unsaturated glucuronyl hydrolase
- EC
- 3.2.1.-
- UniProt
- Q9RC92
- Ligands
- GAD, BGC, RAM
- Pockets
- 5 · best druggability 0.57
Structure
x-ray diffraction · 1 distinct chain · 53% helix, 10% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B | Unsaturated glucuronyl hydrolase (EC 3.2.1.-) | protein | 377 | 53% helix, 10% strand | Q9RC92 |
Ligands and binding sites
- GAD · 2,6-anhydro-3-deoxy-L-threo-hex-2-enonic acid · ligand · chains A
- BGC · beta-D-glucopyranose · sugar · 2 copies · chains A
- RAM · alpha-L-rhamnopyranose · sugar · chains A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
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 | 187 | 0.57 | 0.80 | 23 | BGC, GAD |
| 2 | 126 | 0.52 | 0.81 | 20 | empty |
| 3 | 146 | 0.37 | 0.72 | 23 | empty |
| 4 | 83 | 0.30 | 0.72 | 14 | empty |
| 5 | 54 | 0.25 | 0.73 | 14 | empty |
Interfaces
1 interface between chains.
- A–B · 949 Ų buried · 19 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 Q9RC92
- Elsewhere: RCSB PDB 2FV0 · PDBe 2FV0 · UniProt Q9RC92
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