MolNFT v2 · #190172 · protein
Cryo-EM structure of human TTYH2 in GDN
7P54 · Protein tweety homolog 2: “Cryo-EM structure of human TTYH2 in GDN”. Electron microscopy at 3.3, 1 ligand (NAG), 6 pockets (best druggability 0.78). MolNFT v2 #190172 on GenesisL1: 3D structure, binding sites and pockets in GL1X.
- PDB
- 7P54
- Type
- protein
- Length
- 794 residues
- Chains
- 2
- Method
- electron microscopy
- Collection
- MolNFT v2 / PDB Bank
- Contract
- 0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
- Owner
- 0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
- Resolution
- 3.3
- Source
- Homo sapiens
- Molecule
- Protein tweety homolog 2
- UniProt
- Q9BSA4
- Ligands
- NAG
- Pockets
- 6 · best druggability 0.78
Structure
electron microscopy · resolution 3.3 · 1 distinct chain · 83% helix, 0% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B | Protein tweety homolog 2 | protein | 397 | 83% helix, 0% strand | Q9BSA4 |
Ligands and binding sites
- NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 12 copies · chains A, B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
6 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 762 | 0.78 | 0.81 | 49 | empty |
| 2 | 860 | 0.78 | 0.81 | 101 | empty |
| 3 | 714 | 0.77 | 0.81 | 47 | empty |
| 4 | 459 | 0.76 | 0.84 | 69 | empty |
| 5 | 88 | 0.36 | 0.75 | 19 | empty |
Interfaces
1 interface between chains.
- A–B · 1329 Ų buried · 11 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 8 glycan, 4 disulfide (N-glycosylation, disulfide).
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 Q9BSA4
- Elsewhere: RCSB PDB 7P54 · PDBe 7P54 · UniProt Q9BSA4
GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.